| geneid | 25953 |
|---|---|
| ensemblid | ENSG00000127838.15 |
| hgncid | 9153 |
| symbol | PNKD |
| name | PNKD metallo-beta-lactamase domain containing |
| refseq_nuc | NM_015488.5 |
| refseq_prot | NP_056303.3 |
| ensembl_nuc | ENST00000273077.9 |
| ensembl_prot | ENSP00000273077.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 218270519 |
| end | 218346793 |
| strand | + |
| ver | v1.2 |
| region | chr2:218270519-218346793 |
| region5000 | chr2:218265519-218351793 |
| regionname0 | PNKD_chr2_218270519_218346793 |
| regionname5000 | PNKD_chr2_218265519_218351793 |
| 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 | 385 | 274 | 87 | 58 | 88 | 12 | 27 | 68 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0002 | 0/0 | 385 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0003 | 0/0 | 385 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0004 | 0/0 | 385 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0005 | 0/0 | 385 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| 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 | 1/1 | 1158 | 250 | 75 | 53 | 87 | 8 | 25 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| c0002 | 0/0 | 1158 | 18 | 10 | 4 | 1 | 1 | 2 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| c0003 | 0/0 | 1158 | 3 | 3 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| c0004 | 0/0 | 1158 | 2 | 0 | 1 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| c0005 | 0/0 | 1158 | 2 | 0 | 0 | 0 | 2 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| c0006 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| c0007 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| c0008 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| c0009 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| c0010 | 0/0 | 1158 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1830 | 103 | 12 | 28 | 44 | 6 | 13 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0002 | 0/1 | 1830 | 60 | 23 | 15 | 12 | 5 | 4 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0003 | 0/0 | 1830 | 38 | 24 | 3 | 10 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0004 | 0/0 | 1832 | 21 | 0 | 3 | 14 | 1 | 3 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0005 | 0/0 | 1830 | 20 | 6 | 3 | 4 | 0 | 7 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0006 | 0/0 | 1830 | 8 | 0 | 5 | 3 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0007 | 1/0 | 1830 | 5 | 4 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0008 | 0/0 | 1830 | 4 | 4 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0009 | 0/0 | 1830 | 4 | 4 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0010 | 0/0 | 1830 | 3 | 3 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0011 | 0/0 | 1832 | 3 | 3 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0012 | 0/0 | 1830 | 2 | 2 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0013 | 0/0 | 1830 | 2 | 0 | 0 | 2 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0014 | 0/0 | 1830 | 2 | 2 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0015 | 0/0 | 1830 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0016 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0017 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0018 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| t0019 | 0/0 | 1830 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| 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 | 2 | 2 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0013 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| 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 | 1/1 | 1158 | 250 | 75 | 53 | 87 | 8 | 25 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0002 | 0/0 | 1158 | 18 | 10 | 4 | 1 | 1 | 2 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0004 | 0/0 | 1158 | 2 | 0 | 1 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0005 | 0/0 | 1158 | 2 | 0 | 0 | 0 | 2 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0006 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0008 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0002c0003 | 0/0 | 1158 | 3 | 3 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0003c0009 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0004c0007 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0005c0010 | 0/0 | 1158 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2987 | 101 | 12 | 28 | 42 | 6 | 13 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0002 | 0/1 | 2987 | 41 | 14 | 11 | 11 | 2 | 2 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0003 | 0/0 | 2987 | 37 | 23 | 3 | 10 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0004 | 0/0 | 2989 | 19 | 0 | 2 | 14 | 0 | 3 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0005 | 0/0 | 2987 | 19 | 6 | 3 | 4 | 0 | 6 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0006 | 0/0 | 2987 | 8 | 0 | 5 | 3 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0007 | 1/0 | 2987 | 5 | 4 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0008 | 0/0 | 2987 | 4 | 4 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0009 | 0/0 | 2987 | 4 | 4 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0010 | 0/0 | 2987 | 3 | 3 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0012 | 0/0 | 2987 | 2 | 2 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0013 | 0/0 | 2987 | 2 | 0 | 0 | 2 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0014 | 0/0 | 2987 | 2 | 2 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0015 | 0/0 | 2987 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0018 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0001t0019 | 0/0 | 2987 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0002t0002 | 0/0 | 2987 | 16 | 8 | 4 | 1 | 1 | 2 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0002t0016 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0002t0017 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0004t0004 | 0/0 | 2989 | 2 | 0 | 1 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0005t0002 | 0/0 | 2987 | 2 | 0 | 0 | 0 | 2 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0006t0002 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0001c0008t0003 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0002c0003t0011 | 0/0 | 2989 | 3 | 3 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0003c0009t0001 | 0/0 | 2987 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0004c0007t0001 | 0/0 | 2987 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| a0005c0010t0005 | 0/0 | 2987 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | copy fasta | chr2 | 218265519 | 218351793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0006g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0006g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0006g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0007g0013 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0007g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0008g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0009g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0010g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0010g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0012g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0012g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0013g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0013g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0014g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0014g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0015g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0018g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0001t0019g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0016g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0002t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0004t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0004t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0005t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0005t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0006t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0001c0008t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0002c0003t0011g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0002c0003t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0002c0003t0011g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0003c0009t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0004c0007t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| a0005c0010t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0004 | g0134 | EUR | GBR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0040 | EUR | GBR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | FIN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0220 | EUR | FIN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | CHS | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | CHS | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | CHS | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0131 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0218 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0037 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0210 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0263 | AMR | CLM | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0124 | AMR | CLM | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01433 | hp1 | a0001 | c0004 | t0004 | g0002 | AMR | CLM | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0244 | AMR | CLM | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01515 | hp2 | a0001 | c0005 | t0002 | g0214 | EUR | IBS | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01516 | hp1 | a0001 | c0005 | t0002 | g0221 | EUR | IBS | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0179 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0162 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | KHV | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0240 | EAS | KHV | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | KHV | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02148 | hp1 | a0001 | c0001 | t0006 | g0243 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0117 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | CDX | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CDX | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02258 | hp2 | a0001 | c0001 | t0014 | g0153 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02273 | hp2 | a0001 | c0001 | t0015 | g0120 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02280 | hp2 | a0002 | c0003 | t0011 | g0146 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0047 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02572 | hp2 | a0001 | c0008 | t0003 | g0008 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0091 | SAS | PJL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0253 | SAS | PJL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0026 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0222 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0035 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0028 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02630 | hp2 | a0001 | c0002 | t0016 | g0031 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02717 | hp1 | a0002 | c0003 | t0011 | g0155 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0001 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0200 | SAS | PJL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0001 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0027 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02886 | hp1 | a0001 | c0001 | t0012 | g0268 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0273 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | ESN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | ESN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | ESN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02976 | hp2 | a0001 | c0001 | t0012 | g0272 | AFR | ESN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0030 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | MSL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | MSL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | ESN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0227 | AFR | ESN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | ESN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | ESN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | ESN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | MSL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | MSL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0248 | SAS | PJL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | MSL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | MSL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | ESN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | GWD | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | MSL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | MSL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0245 | SAS | PJL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0128 | SAS | PJL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0249 | SAS | BEB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0246 | SAS | BEB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03942 | hp2 | a0005 | c0010 | t0005 | g0141 | SAS | BEB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0065 | SAS | STU | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0247 | SAS | STU | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | STU | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0256 | SAS | STU | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0112 | SAS | STU | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18522 | hp1 | a0001 | c0001 | t0018 | g0277 | AFR | YRI | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | YRI | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | CHB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | CHB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0149 | AFR | YRI | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18946 | hp1 | a0001 | c0001 | t0013 | g0094 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0259 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18962 | hp1 | a0001 | c0001 | t0013 | g0097 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18962 | hp2 | a0001 | c0001 | t0006 | g0161 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18978 | hp1 | a0001 | c0001 | t0005 | g0258 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0257 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18992 | hp1 | a0001 | c0001 | t0019 | g0139 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19005 | hp1 | a0004 | c0007 | t0001 | g0133 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | LWK | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0266 | AFR | LWK | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0166 | AFR | LWK | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19055 | hp1 | a0001 | c0001 | t0006 | g0165 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0190 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | YRI | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0048 | AFR | YRI | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0230 | AFR | ASW | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA20129 | hp2 | a0002 | c0003 | t0011 | g0236 | AFR | ASW | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0208 | EUR | TSI | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | GIH | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0238 | AMR | CLM | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0067 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02486 | hp1 | a0001 | c0001 | t0014 | g0159 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0032 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02559 | hp1 | a0001 | c0002 | t0017 | g0066 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0265 | AFR | ACB | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03471 | hp1 | a0001 | c0006 | t0002 | g0034 | AFR | MSL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | USA | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | USA | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA18955 | hp2 | a0003 | c0009 | t0001 | g0042 | EAS | JPT | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | USA | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0269 | AFR | USA | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0129 | AFR | LWK | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | LWK | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0215 | REF | REF | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0013 | REF | REF | PNKD_chr2_218265519_218351793 | PNKD | chr2 | 218265519 | 218351793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218270540
|
C | G | 1 | a0005 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.5C>G | p.Ala2Gly | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 1/10 | 22/2987 | 5/1158 | 2/385 | chr2 | 218270540 | ||
| chr2:218271496
|
A | T | 1 | a0003 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.183A>T | p.Glu61Asp | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/10 | 200/2987 | 183/1158 | 61/385 | chr2 | 218271496 | ||
| chr2:218340131
|
G | A | 1 | a0002 | 3 | HG02280.hp2 HG02717.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.455G>A | p.Arg152Gln | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 4/10 | 472/2987 | 455/1158 | 152/385 | chr2 | 218340131 | ||
| chr2:218344925
|
C | T | 1 | a0004 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.1102C>T | p.Arg368Trp | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 1119/2987 | 1102/1158 | 368/385 | chr2 | 218344925 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218340060
|
G | A | 1 | a0001c0006 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.384G>A | p.Ser128Ser | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 4/10 | 401/2987 | 384/1158 | 128/385 | chr2 | 218340060 | ||
| chr2:218340748
|
G | A | 2 | a0001c0002a0001c0006 | 19 | HG00099.hp2 HG00642.hp2 HG01109.hp1 others(16): Show |
synonymous_variant | LOW | c.486G>A | p.Gly162Gly | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 5/10 | 503/2987 | 486/1158 | 162/385 | chr2 | 218340748 | ||
| chr2:218342015
|
C | A | 1 | a0001c0004 | 2 | HG00099.hp1 HG01433.hp1 |
synonymous_variant | LOW | c.652C>A | p.Arg218Arg | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/10 | 669/2987 | 652/1158 | 218/385 | chr2 | 218342015 | ||
| chr2:218343553
|
C | T | 1 | a0001c0008 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.835C>T | p.Leu279Leu | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 8/10 | 852/2987 | 835/1158 | 279/385 | chr2 | 218343553 | ||
| chr2:218344525
|
G | A | 1 | a0001c0005 | 2 | HG01515.hp2 HG01516.hp1 |
synonymous_variant | LOW | c.939G>A | p.Arg313Arg | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 9/10 | 956/2987 | 939/1158 | 313/385 | chr2 | 218344525 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218345073
|
C | A | 11 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(8): Show | 93 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*92C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 92 | chr2 | 218345073 | |||||
| chr2:218345162
|
G | C | 9 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(6): Show | 74 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*181G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 181 | chr2 | 218345162 | |||||
| chr2:218345192
|
C | T | 1 | a0001c0001t0009 | 4 | HG02451.hp2 HG02630.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*211C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 211 | chr2 | 218345192 | |||||
| chr2:218345220
|
G | A | 1 | a0001c0001t0015 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*239G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 239 | chr2 | 218345220 | |||||
| chr2:218345395
|
T | C | 1 | a0001c0001t0012 | 2 | HG02886.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*414T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 414 | chr2 | 218345395 | |||||
| chr2:218345432
|
A | G | 1 | a0001c0001t0006 | 8 | HG01123.hp2 HG01496.hp1 HG01975.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*451A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 451 | chr2 | 218345432 | |||||
| chr2:218345488
|
G | C | 3 | a0001c0001t0005a0001c0001t0015a0005c0010t0005 | 21 | HG01109.hp2 HG01261.hp1 HG01361.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*507G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 507 | chr2 | 218345488 | |||||
| chr2:218345659
|
C | CCT | 3 | a0001c0001t0004a0001c0004t0004a0002c0003t0011 | 24 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*680_*681dupTC | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 682 | INFO_REALIGN_3_PRIME | chr2 | 218345659 | ||||
| chr2:218345845
|
C | T | 1 | a0001c0002t0017 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*864C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 864 | chr2 | 218345845 | |||||
| chr2:218345883
|
T | C | 6 | a0001c0001t0001a0001c0001t0013a0001c0001t0014others(3): Show | 108 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*902T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 902 | chr2 | 218345883 | |||||
| chr2:218345973
|
C | G | 1 | a0001c0001t0010 | 3 | HG02717.hp2 HG02809.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*992C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 992 | chr2 | 218345973 | |||||
| chr2:218346058
|
G | A | 6 | a0001c0001t0001a0001c0001t0013a0001c0001t0014others(3): Show | 108 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1077G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 1077 | chr2 | 218346058 | |||||
| chr2:218346066
|
G | A | 1 | a0001c0002t0017 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1085G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 1085 | chr2 | 218346066 | |||||
| chr2:218346122
|
G | A | 1 | a0001c0001t0019 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1141G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 1141 | chr2 | 218346122 | |||||
| chr2:218346174
|
C | T | 2 | a0001c0001t0004a0001c0004t0004 | 21 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1193C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 1193 | chr2 | 218346174 | |||||
| chr2:218346261
|
C | T | 1 | a0001c0001t0014 | 2 | HG02258.hp2 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1280C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 1280 | chr2 | 218346261 | |||||
| chr2:218346530
|
G | A | 1 | a0001c0001t0013 | 2 | NA18946.hp1 NA18962.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1549G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 1549 | chr2 | 218346530 | |||||
| chr2:218346619
|
T | C | 1 | a0001c0001t0018 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1638T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 1638 | chr2 | 218346619 | |||||
| chr2:218346646
|
G | A | 1 | a0001c0001t0009 | 4 | HG02451.hp2 HG02630.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1665G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 1665 | chr2 | 218346646 | |||||
| chr2:218346704
|
T | C | 1 | a0001c0001t0008 | 4 | HG02615.hp1 NA19043.hp1 NA19240.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1723T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 1723 | chr2 | 218346704 | |||||
| chr2:218346755
|
G | A | 1 | a0001c0002t0016 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1774G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 10/10 | 1774 | chr2 | 218346755 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218270700
|
C | G | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0018g0277 | 3 | NA18522.hp1 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.67+98C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 1/9 | chr2 | 218270700 | ||||||
| chr2:218271207
|
C | T | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-174C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 1/9 | chr2 | 218271207 | ||||||
| chr2:218271251
|
C | G | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0018g0277 | 3 | NA18522.hp1 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.68-130C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 1/9 | chr2 | 218271251 | ||||||
| chr2:218271297
|
C | G | 1 | a0001c0001t0003g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-84C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 1/9 | chr2 | 218271297 | ||||||
| chr2:218271582
|
G | A | 1 | a0001c0001t0003g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.236+33G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218271582 | ||||||
| chr2:218271738
|
A | G | 1 | a0001c0001t0005g0263 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.236+189A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218271738 | ||||||
| chr2:218271780
|
C | T | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+231C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218271780 | ||||||
| chr2:218271845
|
T | A | 1 | a0001c0004t0004g0002 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.236+296T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218271845 | ||||||
| chr2:218271961
|
A | G | 263 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.236+412A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218271961 | ||||||
| chr2:218271976
|
A | G | 1 | a0001c0001t0001g0262 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.236+427A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218271976 | ||||||
| chr2:218272069
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | NA18951.hp1 NA18967.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+520G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218272069 | ||||||
| chr2:218272086
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.236+537G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218272086 | ||||||
| chr2:218272165
|
TAA | T | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+617_236+618del others(2): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218272165 | ||||||
| chr2:218272251
|
G | GTTGCA | 19 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(16): Show | 19 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.236+703_236+707dup others(5): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218272251 | |||||
| chr2:218272270
|
C | T | 2 | a0001c0001t0003g0016a0001c0001t0010g0001 | 3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.236+721C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218272270 | ||||||
| chr2:218272729
|
G | A | 1 | a0001c0001t0004g0022 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.236+1180G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218272729 | ||||||
| chr2:218272787
|
A | C | 1 | a0001c0001t0004g0261 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.236+1238A>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218272787 | ||||||
| chr2:218273246
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.236+1697C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218273246 | ||||||
| chr2:218273263
|
GTTTTGTT | G | 53 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(50): Show | 53 | HG00099.hp2 HG01109.hp1 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.236+1734_236+1740d others(9): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218273263 | |||||
| chr2:218273294
|
G | A | 2 | a0001c0001t0006g0161a0001c0001t0006g0162 | 2 | HG01978.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.236+1745G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218273294 | ||||||
| chr2:218273302
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0004g0163 | 2 | NA18972.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.236+1753G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218273302 | ||||||
| chr2:218273377
|
T | G | 1 | a0001c0001t0001g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.236+1828T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218273377 | ||||||
| chr2:218273445
|
T | TG | 4 | a0001c0001t0001g0020a0001c0001t0001g0140a0001c0001t0019g0139others(1): Show | 4 | HG03669.hp2 HG03942.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+1897dupG | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218273445 | |||||
| chr2:218273446
|
GT | G | 138 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(135): Show | 138 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.236+1913delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218273446 | |||||
| chr2:218273446
|
GTT | G | 21 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(18): Show | 21 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.236+1912_236+1913d others(4): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218273446 | |||||
| chr2:218273447
|
T | G | 102 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.236+1898T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218273447 | ||||||
| chr2:218273448
|
T | G | 1 | a0003c0009t0001g0042 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.236+1899T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218273448 | ||||||
| chr2:218273479
|
ATTT | A | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+1946_236+1948d others(5): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218273479 | |||||
| chr2:218273482
|
T | TA | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | NA18951.hp1 NA18967.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.236+1933_236+1934i others(3): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218273482 | ||||||
| chr2:218273483
|
T | A | 151 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0044others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.236+1934T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218273483 | ||||||
| chr2:218273484
|
T | A | 1 | a0001c0001t0001g0137 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.236+1935T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218273484 | ||||||
| chr2:218273486
|
T | A | 86 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(83): Show | 86 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.236+1937T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218273486 | ||||||
| chr2:218273487
|
T | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG01070.hp1 HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.236+1938T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218273487 | ||||||
| chr2:218273647
|
ATT | A | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+2112_236+2113d others(4): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218273647 | |||||
| chr2:218273820
|
G | A | 1 | a0001c0001t0008g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.236+2271G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218273820 | ||||||
| chr2:218273902
|
A | G | 106 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(103): Show | 106 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.236+2353A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218273902 | ||||||
| chr2:218273967
|
C | T | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0018g0277 | 3 | NA18522.hp1 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+2418C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218273967 | ||||||
| chr2:218274067
|
G | A | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0018g0277 | 3 | NA18522.hp1 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+2518G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218274067 | ||||||
| chr2:218274217
|
C | T | 101 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(98): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.236+2668C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218274217 | ||||||
| chr2:218274321
|
C | A | 1 | a0001c0001t0002g0167 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.236+2772C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218274321 | ||||||
| chr2:218274324
|
C | A | 1 | a0001c0001t0004g0168 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.236+2775C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218274324 | ||||||
| chr2:218274392
|
T | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG03239.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.236+2843T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218274392 | ||||||
| chr2:218274448
|
A | T | 1 | a0003c0009t0001g0042 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.236+2899A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218274448 | ||||||
| chr2:218274536
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.236+2987G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218274536 | ||||||
| chr2:218274587
|
C | T | 10 | a0001c0001t0001g0237a0001c0001t0002g0241a0001c0001t0004g0239others(7): Show | 10 | HG00621.hp2 HG01123.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.236+3038C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218274587 | ||||||
| chr2:218274643
|
T | A | 1 | a0003c0009t0001g0042 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.236+3094T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218274643 | ||||||
| chr2:218274675
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.236+3126A>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218274675 | ||||||
| chr2:218274757
|
T | A | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+3208T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218274757 | ||||||
| chr2:218274850
|
G | A | 259 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.236+3301G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218274850 | ||||||
| chr2:218274851
|
T | A | 1 | a0003c0009t0001g0042 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.236+3302T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218274851 | ||||||
| chr2:218275051
|
T | C | 1 | a0001c0001t0002g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.236+3502T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218275051 | ||||||
| chr2:218275103
|
C | T | 3 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276 | 3 | HG01884.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.236+3554C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218275103 | ||||||
| chr2:218275292
|
G | A | 15 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172others(12): Show | 15 | HG00735.hp2 HG01975.hp2 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.236+3743G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218275292 | ||||||
| chr2:218275561
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.236+4012C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218275561 | ||||||
| chr2:218275565
|
G | C | 105 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(102): Show | 105 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.236+4016G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218275565 | ||||||
| chr2:218275565
|
G | T | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.236+4016G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218275565 | ||||||
| chr2:218275662
|
A | G | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG00099.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.236+4113A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218275662 | ||||||
| chr2:218275680
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.236+4131T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218275680 | ||||||
| chr2:218275739
|
C | T | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0018g0277 | 3 | NA18522.hp1 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+4190C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218275739 | ||||||
| chr2:218275900
|
A | G | 31 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(28): Show | 31 | HG01109.hp1 HG01891.hp2 HG01975.hp1 others(28): Show |
intron_variant | MODIFIER | c.236+4351A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218275900 | ||||||
| chr2:218276144
|
A | G | 1 | a0002c0003t0011g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.236+4595A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218276144 | ||||||
| chr2:218276244
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.236+4695G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218276244 | ||||||
| chr2:218276257
|
C | T | 2 | a0001c0001t0007g0273a0001c0001t0012g0272 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236+4708C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218276257 | ||||||
| chr2:218276421
|
G | A | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0018g0277 | 3 | NA18522.hp1 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+4872G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218276421 | ||||||
| chr2:218276481
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.236+4932G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218276481 | ||||||
| chr2:218276525
|
C | T | 1 | a0001c0001t0002g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.236+4976C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218276525 | ||||||
| chr2:218276596
|
T | C | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.236+5047T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218276596 | ||||||
| chr2:218276641
|
A | AC | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+5097dupC | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218276641 | |||||
| chr2:218276692
|
C | T | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0018g0277 | 3 | NA18522.hp1 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+5143C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218276692 | ||||||
| chr2:218276735
|
C | G | 156 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(153): Show | 156 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.236+5186C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218276735 | ||||||
| chr2:218276823
|
C | T | 265 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.236+5274C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218276823 | ||||||
| chr2:218276863
|
T | C | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0018g0277 | 3 | NA18522.hp1 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+5314T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218276863 | ||||||
| chr2:218276915
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.236+5366G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218276915 | ||||||
| chr2:218276981
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.236+5432C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218276981 | ||||||
| chr2:218277141
|
A | G | 3 | a0001c0001t0005g0257a0001c0001t0005g0258a0001c0001t0005g0259 | 3 | NA18961.hp1 NA18978.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.236+5592A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218277141 | ||||||
| chr2:218277300
|
G | A | 260 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.236+5751G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218277300 | ||||||
| chr2:218277604
|
C | G | 2 | a0001c0001t0007g0273a0001c0001t0012g0272 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236+6055C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218277604 | ||||||
| chr2:218277768
|
C | T | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+6219C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218277768 | ||||||
| chr2:218277769
|
G | A | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 107 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.236+6220G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218277769 | ||||||
| chr2:218277871
|
C | T | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+6322C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218277871 | ||||||
| chr2:218278050
|
C | T | 157 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.236+6501C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218278050 | ||||||
| chr2:218278059
|
C | T | 3 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0008g0048 | 3 | HG02896.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.236+6510C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218278059 | ||||||
| chr2:218278100
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.236+6551T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218278100 | ||||||
| chr2:218278137
|
C | A | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 107 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.236+6588C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218278137 | ||||||
| chr2:218278317
|
T | G | 1 | a0001c0001t0004g0186 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.236+6768T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218278317 | ||||||
| chr2:218278506
|
G | A | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+6957G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218278506 | ||||||
| chr2:218278552
|
C | A | 1 | a0001c0001t0001g0057 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.236+7003C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218278552 | ||||||
| chr2:218278555
|
C | T | 1 | a0001c0001t0002g0184 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.236+7006C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218278555 | ||||||
| chr2:218278604
|
T | C | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+7055T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218278604 | ||||||
| chr2:218278640
|
T | G | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.236+7091T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218278640 | ||||||
| chr2:218278910
|
G | GA | 2 | a0001c0001t0003g0016a0001c0001t0010g0001 | 3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.236+7364dupA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218278910 | |||||
| chr2:218279016
|
C | G | 1 | a0001c0001t0005g0256 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.236+7467C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218279016 | ||||||
| chr2:218279046
|
G | A | 1 | a0001c0001t0003g0187 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.236+7497G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218279046 | ||||||
| chr2:218279185
|
C | T | 6 | a0001c0001t0010g0030a0001c0002t0002g0029a0001c0002t0002g0032others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.236+7636C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218279185 | ||||||
| chr2:218279200
|
A | T | 7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+7651A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218279200 | ||||||
| chr2:218279353
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.236+7804C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218279353 | ||||||
| chr2:218279366
|
G | A | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+7817G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218279366 | ||||||
| chr2:218279395
|
CT | C | 6 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(3): Show | 6 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.236+7847delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218279395 | ||||||
| chr2:218279426
|
G | A | 105 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(102): Show | 105 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.236+7877G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218279426 | ||||||
| chr2:218279507
|
A | T | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+7958A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218279507 | ||||||
| chr2:218279531
|
G | A | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+7982G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218279531 | ||||||
| chr2:218279591
|
TG | T | 3 | a0001c0001t0005g0245a0001c0001t0005g0246a0001c0001t0005g0256 | 3 | HG03669.hp1 HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.236+8043delG | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218279591 | ||||||
| chr2:218279662
|
G | A | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.236+8113G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218279662 | ||||||
| chr2:218279775
|
A | G | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+8226A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218279775 | ||||||
| chr2:218279821
|
T | C | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+8272T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218279821 | ||||||
| chr2:218279843
|
AAG | A | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+8299_236+8300d others(4): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218279843 | |||||
| chr2:218280092
|
T | C | 273 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.236+8543T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218280092 | ||||||
| chr2:218280155
|
G | C | 1 | a0001c0001t0003g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.236+8606G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218280155 | ||||||
| chr2:218280251
|
T | G | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.236+8702T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218280251 | ||||||
| chr2:218280404
|
G | A | 2 | a0001c0001t0003g0016a0001c0001t0010g0001 | 3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.236+8855G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218280404 | ||||||
| chr2:218280555
|
T | C | 1 | a0001c0001t0002g0188 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+9006T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218280555 | ||||||
| chr2:218280654
|
G | T | 3 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276 | 3 | HG01884.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.236+9105G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218280654 | ||||||
| chr2:218280702
|
C | CCCTGAAT others(1): Show |
3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0004g0022 | 3 | NA18943.hp1 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+9173_236+9180d others(10): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218280702 | |||||
| chr2:218280756
|
G | A | 1 | a0001c0001t0004g0186 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.236+9207G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218280756 | ||||||
| chr2:218280805
|
C | CT | 43 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0150others(40): Show | 43 | HG00099.hp2 HG00642.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.236+9279dupT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218280805 | |||||
| chr2:218280805
|
C | CTT | 14 | a0001c0001t0001g0158a0001c0001t0002g0274a0001c0001t0002g0275others(11): Show | 14 | HG01243.hp1 HG01884.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.236+9278_236+9279d others(4): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218280805 | |||||
| chr2:218280805
|
CT | C | 8 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0191others(5): Show | 8 | HG00099.hp1 HG02897.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+9279delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218280805 | |||||
| chr2:218280873
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.236+9324G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218280873 | ||||||
| chr2:218280957
|
G | A | 2 | a0001c0002t0002g0037a0001c0002t0002g0038 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.236+9408G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218280957 | ||||||
| chr2:218280972
|
C | T | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+9423C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218280972 | ||||||
| chr2:218281038
|
C | G | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.236+9489C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281038 | ||||||
| chr2:218281051
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.236+9502T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281051 | ||||||
| chr2:218281124
|
T | TTTTTGTT others(9): Show |
2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.236+9576_236+9591d others(18): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218281124 | |||||
| chr2:218281128
|
T | TGTTTTTT others(8): Show |
1 | a0001c0001t0001g0232 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.236+9590_236+9591i others(17): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218281128 | |||||
| chr2:218281130
|
T | TTTTGTTT others(8): Show |
7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+9584_236+9585i others(17): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218281130 | |||||
| chr2:218281130
|
T | TTTTTGTT others(8): Show |
1 | a0001c0001t0001g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.236+9585_236+9586i others(17): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218281130 | |||||
| chr2:218281130
|
T | TTTTTTTT others(8): Show |
45 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(42): Show | 45 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.236+9591_236+9592i others(17): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218281130 | |||||
| chr2:218281130
|
T | TTTTTTTT others(7): Show |
99 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(96): Show | 99 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.236+9590_236+9591i others(16): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218281130 | |||||
| chr2:218281130
|
T | TTTTTTTT others(8): Show |
1 | a0001c0001t0004g0233 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.236+9590_236+9591i others(17): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218281130 | |||||
| chr2:218281130
|
T | TTTTTTTT others(9): Show |
2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+9590_236+9591i others(18): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218281130 | |||||
| chr2:218281135
|
T | TTTTTGTT others(8): Show |
8 | a0001c0001t0010g0030a0001c0002t0002g0023a0001c0002t0002g0029others(5): Show | 8 | HG01109.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+9591_236+9592i others(17): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218281135 | |||||
| chr2:218281139
|
T | TGTTTTGT others(9): Show |
90 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(87): Show | 90 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.236+9591_236+9592i others(18): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218281139 | |||||
| chr2:218281139
|
T | TTGTTTTG others(10): Show |
1 | a0001c0001t0003g0128 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.236+9590_236+9591i others(19): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281139 | ||||||
| chr2:218281140
|
G | GTTTTGTT others(10): Show |
3 | a0001c0001t0001g0061a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG02074.hp2 NA19002.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.236+9591_236+9592i others(19): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281140 | ||||||
| chr2:218281141
|
G | T | 94 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.236+9592G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281141 | ||||||
| chr2:218281338
|
T | C | 1 | a0001c0001t0002g0274 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.236+9789T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281338 | ||||||
| chr2:218281344
|
C | T | 2 | a0001c0002t0002g0037a0001c0002t0002g0038 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.236+9795C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281344 | ||||||
| chr2:218281375
|
G | T | 1 | a0001c0002t0002g0023 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.236+9826G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281375 | ||||||
| chr2:218281391
|
C | G | 31 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(28): Show | 31 | HG01109.hp1 HG01891.hp2 HG01975.hp1 others(28): Show |
intron_variant | MODIFIER | c.236+9842C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281391 | ||||||
| chr2:218281417
|
G | A | 1 | a0001c0001t0007g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.236+9868G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281417 | ||||||
| chr2:218281428
|
C | T | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+9879C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281428 | ||||||
| chr2:218281433
|
G | A | 1 | a0001c0002t0002g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.236+9884G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281433 | ||||||
| chr2:218281476
|
T | A | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+9927T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281476 | ||||||
| chr2:218281569
|
C | T | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+10020C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281569 | ||||||
| chr2:218281660
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.236+10111G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281660 | ||||||
| chr2:218281737
|
G | C | 7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+10188G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281737 | ||||||
| chr2:218281884
|
T | C | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+10335T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218281884 | ||||||
| chr2:218282001
|
G | A | 7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+10452G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218282001 | ||||||
| chr2:218282055
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.236+10506T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218282055 | ||||||
| chr2:218282080
|
G | A | 101 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(98): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.236+10531G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218282080 | ||||||
| chr2:218282119
|
G | C | 1 | a0001c0001t0002g0167 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.236+10570G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218282119 | ||||||
| chr2:218282145
|
T | C | 106 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(103): Show | 106 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.236+10596T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218282145 | ||||||
| chr2:218282159
|
G | C | 101 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(98): Show | 101 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.236+10610G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218282159 | ||||||
| chr2:218282159
|
G | T | 2 | a0001c0001t0001g0231a0002c0003t0011g0236 | 2 | HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.236+10610G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218282159 | ||||||
| chr2:218282265
|
G | A | 50 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(47): Show | 50 | HG00099.hp2 HG01109.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.236+10716G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218282265 | ||||||
| chr2:218282522
|
T | C | 2 | a0001c0002t0002g0035a0001c0002t0002g0036 | 2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.236+10973T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218282522 | ||||||
| chr2:218282522
|
T | G | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+10973T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218282522 | ||||||
| chr2:218282740
|
A | G | 1 | a0001c0001t0007g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.236+11191A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218282740 | ||||||
| chr2:218282922
|
G | A | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.236+11373G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218282922 | ||||||
| chr2:218283058
|
C | A | 1 | a0001c0001t0002g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.236+11509C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218283058 | ||||||
| chr2:218283179
|
CA | C | 4 | a0001c0001t0003g0021a0001c0001t0003g0049a0001c0001t0003g0050others(1): Show | 4 | HG02896.hp2 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+11631delA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218283179 | ||||||
| chr2:218283205
|
T | G | 6 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0001t0001g0071others(3): Show | 6 | HG00323.hp2 HG00642.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.236+11656T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218283205 | ||||||
| chr2:218283646
|
G | A | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+12097G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218283646 | ||||||
| chr2:218283762
|
G | A | 1 | a0001c0001t0004g0194 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.236+12213G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218283762 | ||||||
| chr2:218283803
|
T | C | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+12254T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218283803 | ||||||
| chr2:218283930
|
A | G | 274 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.236+12381A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218283930 | ||||||
| chr2:218284000
|
C | A | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 107 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.236+12451C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218284000 | ||||||
| chr2:218284045
|
T | A | 2 | a0001c0001t0004g0186a0001c0001t0004g0234 | 2 | HG00609.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.236+12496T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218284045 | ||||||
| chr2:218284072
|
G | A | 1 | a0001c0002t0002g0131 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.236+12523G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218284072 | ||||||
| chr2:218284155
|
C | T | 2 | a0001c0002t0002g0035a0001c0002t0002g0036 | 2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.236+12606C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218284155 | ||||||
| chr2:218284163
|
C | CAA | 94 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0201others(91): Show | 94 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.236+12617_236+1261 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218284163 | |||||
| chr2:218284163
|
C | CAAA | 5 | a0001c0001t0001g0196a0001c0001t0001g0235a0001c0001t0003g0197others(2): Show | 5 | HG01175.hp2 HG06807.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.236+12616_236+1261 others(7): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218284163 | |||||
| chr2:218284168
|
G | A | 102 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(99): Show | 102 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.236+12619G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218284168 | ||||||
| chr2:218284396
|
C | A | 1 | a0001c0001t0004g0233 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.236+12847C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218284396 | ||||||
| chr2:218284440
|
A | G | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+12891A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218284440 | ||||||
| chr2:218284499
|
A | G | 263 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.236+12950A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218284499 | ||||||
| chr2:218284562
|
T | C | 265 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.236+13013T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218284562 | ||||||
| chr2:218284768
|
C | T | 4 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(1): Show | 4 | HG00735.hp2 HG01975.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+13219C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218284768 | ||||||
| chr2:218284916
|
C | T | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+13367C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218284916 | ||||||
| chr2:218284993
|
G | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+13444G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218284993 | ||||||
| chr2:218285005
|
G | A | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 107 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.236+13456G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218285005 | ||||||
| chr2:218285017
|
G | A | 106 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(103): Show | 106 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.236+13468G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218285017 | ||||||
| chr2:218285488
|
A | G | 134 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(131): Show | 134 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.236+13939A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218285488 | ||||||
| chr2:218285515
|
A | G | 104 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(101): Show | 104 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.236+13966A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218285515 | ||||||
| chr2:218285552
|
G | A | 1 | a0001c0001t0003g0025 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.236+14003G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218285552 | ||||||
| chr2:218285584
|
A | G | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+14035A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218285584 | ||||||
| chr2:218285719
|
C | T | 1 | a0001c0001t0007g0014 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.236+14170C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218285719 | ||||||
| chr2:218285726
|
G | A | 5 | a0001c0001t0003g0021a0001c0001t0003g0049a0001c0001t0003g0050others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.236+14177G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218285726 | ||||||
| chr2:218285931
|
G | C | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.236+14382G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218285931 | ||||||
| chr2:218286019
|
G | A | 1 | a0001c0002t0002g0131 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.236+14470G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218286019 | ||||||
| chr2:218286097
|
G | T | 1 | a0001c0001t0003g0187 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.236+14548G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218286097 | ||||||
| chr2:218286442
|
T | C | 3 | a0001c0001t0008g0026a0001c0001t0009g0027a0001c0001t0009g0028 | 3 | HG02615.hp1 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.236+14893T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218286442 | ||||||
| chr2:218286495
|
A | C | 157 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.236+14946A>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218286495 | ||||||
| chr2:218286734
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.236+15185G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218286734 | ||||||
| chr2:218286860
|
GA | G | 260 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.236+15318delA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218286860 | |||||
| chr2:218287044
|
C | T | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+15495C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218287044 | ||||||
| chr2:218287084
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.236+15535C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218287084 | ||||||
| chr2:218287203
|
T | C | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+15654T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218287203 | ||||||
| chr2:218287415
|
A | T | 7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+15866A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218287415 | ||||||
| chr2:218287557
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.236+16008A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218287557 | ||||||
| chr2:218287602
|
C | T | 2 | a0001c0002t0002g0035a0001c0002t0002g0036 | 2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.236+16053C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218287602 | ||||||
| chr2:218287736
|
C | T | 1 | a0001c0001t0003g0271 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.236+16187C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218287736 | ||||||
| chr2:218287854
|
T | C | 1 | a0001c0001t0009g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.236+16305T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218287854 | ||||||
| chr2:218287863
|
C | T | 1 | a0001c0001t0003g0128 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.236+16314C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218287863 | ||||||
| chr2:218287880
|
C | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+16331C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218287880 | ||||||
| chr2:218287925
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.236+16376T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218287925 | ||||||
| chr2:218288166
|
C | T | 38 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(35): Show | 38 | HG00099.hp2 HG01109.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.236+16617C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218288166 | ||||||
| chr2:218288214
|
G | T | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+16665G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218288214 | ||||||
| chr2:218288346
|
A | G | 1 | a0001c0002t0002g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.236+16797A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218288346 | ||||||
| chr2:218288354
|
G | A | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.236+16805G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218288354 | ||||||
| chr2:218288655
|
C | T | 7 | a0001c0001t0002g0009a0001c0001t0005g0003a0001c0001t0005g0004others(4): Show | 7 | HG01884.hp1 HG02572.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.236+17106C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218288655 | ||||||
| chr2:218288661
|
G | A | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.236+17112G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218288661 | ||||||
| chr2:218289160
|
G | T | 3 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0008g0048 | 3 | HG02896.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.236+17611G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218289160 | ||||||
| chr2:218289259
|
T | C | 103 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.236+17710T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218289259 | ||||||
| chr2:218289260
|
GA | G | 265 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.236+17713delA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218289260 | |||||
| chr2:218289362
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0005g0263 | 2 | HG01069.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.236+17813C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218289362 | ||||||
| chr2:218289370
|
G | A | 19 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(16): Show | 19 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.236+17821G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218289370 | ||||||
| chr2:218289417
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.236+17868G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218289417 | ||||||
| chr2:218289625
|
G | GA | 30 | a0001c0001t0001g0254a0001c0001t0002g0009a0001c0001t0002g0274others(27): Show | 31 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.236+18097dupA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218289625 | |||||
| chr2:218289625
|
G | GAA | 124 | a0001c0001t0001g0135a0001c0001t0001g0150a0001c0001t0001g0151others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.236+18096_236+1809 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218289625 | |||||
| chr2:218289625
|
G | GAAA | 92 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.236+18095_236+1809 others(7): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218289625 | |||||
| chr2:218289625
|
G | GAAAA | 23 | a0001c0001t0001g0060a0001c0001t0001g0074a0001c0001t0001g0075others(20): Show | 23 | HG00621.hp1 HG00642.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.236+18094_236+1809 others(8): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218289625 | |||||
| chr2:218290042
|
G | A | 7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+18493G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218290042 | ||||||
| chr2:218290058
|
G | A | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 107 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.236+18509G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218290058 | ||||||
| chr2:218290135
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.236+18586G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218290135 | ||||||
| chr2:218290319
|
C | T | 1 | a0001c0002t0002g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.236+18770C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218290319 | ||||||
| chr2:218290358
|
G | A | 1 | a0001c0001t0009g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.236+18809G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218290358 | ||||||
| chr2:218290434
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.236+18885C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218290434 | ||||||
| chr2:218290435
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.236+18886G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218290435 | ||||||
| chr2:218290796
|
G | A | 7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+19247G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218290796 | ||||||
| chr2:218290981
|
A | G | 1 | a0001c0001t0008g0129 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.236+19432A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218290981 | ||||||
| chr2:218291184
|
A | T | 104 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(101): Show | 104 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.236+19635A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218291184 | ||||||
| chr2:218291186
|
G | T | 104 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(101): Show | 104 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.236+19637G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218291186 | ||||||
| chr2:218291236
|
C | A | 1 | a0001c0001t0001g0087 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.236+19687C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218291236 | ||||||
| chr2:218291353
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.236+19804C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218291353 | ||||||
| chr2:218291655
|
C | T | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.236+20106C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218291655 | ||||||
| chr2:218291744
|
C | G | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+20195C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218291744 | ||||||
| chr2:218291785
|
GGAT | G | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0018g0277 | 3 | NA18522.hp1 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+20238_236+2024 others(7): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218291785 | |||||
| chr2:218291873
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.236+20324G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218291873 | ||||||
| chr2:218291877
|
G | A | 3 | a0001c0001t0005g0245a0001c0001t0005g0246a0001c0001t0005g0256 | 3 | HG03669.hp1 HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.236+20328G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218291877 | ||||||
| chr2:218291924
|
C | T | 1 | a0001c0002t0017g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.236+20375C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218291924 | ||||||
| chr2:218292091
|
C | A | 1 | a0001c0001t0001g0073 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.236+20542C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218292091 | ||||||
| chr2:218292092
|
C | A | 1 | a0001c0001t0001g0073 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.236+20543C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218292092 | ||||||
| chr2:218292100
|
T | A | 1 | a0001c0001t0004g0163 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.236+20551T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218292100 | ||||||
| chr2:218292256
|
G | A | 96 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(93): Show | 96 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.236+20707G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218292256 | ||||||
| chr2:218292325
|
G | A | 13 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0049others(10): Show | 13 | HG01109.hp1 HG02486.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.236+20776G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218292325 | ||||||
| chr2:218292326
|
G | T | 4 | a0001c0001t0003g0265a0001c0001t0003g0270a0001c0001t0005g0269others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+20777G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218292326 | ||||||
| chr2:218292589
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.236+21040C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218292589 | ||||||
| chr2:218292598
|
G | A | 1 | a0001c0002t0002g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.236+21049G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218292598 | ||||||
| chr2:218292620
|
T | C | 37 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(34): Show | 37 | HG01109.hp1 HG01891.hp2 HG01975.hp1 others(34): Show |
intron_variant | MODIFIER | c.236+21071T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218292620 | ||||||
| chr2:218292647
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.236+21098C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218292647 | ||||||
| chr2:218292881
|
C | T | 7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+21332C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218292881 | ||||||
| chr2:218292969
|
C | T | 164 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.236+21420C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218292969 | ||||||
| chr2:218292991
|
A | G | 2 | a0001c0001t0001g0231a0002c0003t0011g0236 | 2 | HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.236+21442A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218292991 | ||||||
| chr2:218293199
|
G | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+21650G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218293199 | ||||||
| chr2:218293236
|
T | C | 164 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.236+21687T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218293236 | ||||||
| chr2:218293580
|
C | CT | 122 | a0001c0001t0001g0073a0001c0001t0001g0100a0001c0001t0001g0101others(119): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.236+22053dupT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218293580 | |||||
| chr2:218293580
|
C | CTT | 67 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(64): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.236+22052_236+2205 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218293580 | |||||
| chr2:218293580
|
C | CTTT | 7 | a0001c0001t0001g0060a0001c0001t0001g0084a0001c0001t0001g0085others(4): Show | 7 | HG01257.hp1 HG02027.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.236+22051_236+2205 others(7): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218293580 | |||||
| chr2:218293580
|
CT | C | 5 | a0001c0001t0001g0061a0001c0001t0001g0092a0001c0001t0003g0278others(2): Show | 5 | HG01516.hp2 HG03098.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.236+22053delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218293580 | |||||
| chr2:218293603
|
C | T | 1 | a0001c0001t0003g0088 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.236+22054C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218293603 | ||||||
| chr2:218293779
|
G | GGTTT | 164 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.236+22239_236+2224 others(8): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218293779 | |||||
| chr2:218293810
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0069a0001c0001t0001g0076 | 3 | HG01081.hp2 HG01175.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.236+22261C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218293810 | ||||||
| chr2:218293927
|
TA | T | 152 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.236+22400delA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218293927 | |||||
| chr2:218293927
|
TAA | T | 15 | a0001c0001t0001g0045a0001c0001t0001g0055a0001c0001t0001g0101others(12): Show | 15 | HG01069.hp1 HG01167.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.236+22399_236+2240 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218293927 | |||||
| chr2:218293927
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0008g0129 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.236+22388_236+2240 others(17): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218293927 | |||||
| chr2:218294134
|
A | G | 273 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.236+22585A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218294134 | ||||||
| chr2:218294250
|
T | C | 266 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.236+22701T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218294250 | ||||||
| chr2:218294379
|
C | T | 266 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.236+22830C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218294379 | ||||||
| chr2:218294490
|
C | G | 1 | a0001c0001t0002g0224 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.236+22941C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218294490 | ||||||
| chr2:218294515
|
T | C | 273 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.236+22966T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218294515 | ||||||
| chr2:218294804
|
T | C | 11 | a0001c0001t0001g0237a0001c0001t0002g0241a0001c0001t0004g0168others(8): Show | 11 | HG00609.hp2 HG00621.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.236+23255T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218294804 | ||||||
| chr2:218294823
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.236+23274G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218294823 | ||||||
| chr2:218294906
|
T | C | 164 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.236+23357T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218294906 | ||||||
| chr2:218294950
|
A | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+23401A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218294950 | ||||||
| chr2:218295047
|
G | A | 125 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(122): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.236+23498G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218295047 | ||||||
| chr2:218295112
|
G | A | 1 | a0001c0001t0004g0022 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.236+23563G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218295112 | ||||||
| chr2:218295449
|
C | G | 2 | a0001c0001t0003g0016a0001c0001t0010g0001 | 3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.236+23900C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218295449 | ||||||
| chr2:218295456
|
G | A | 1 | a0001c0001t0005g0248 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.236+23907G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218295456 | ||||||
| chr2:218295542
|
C | T | 20 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(17): Show | 20 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.236+23993C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218295542 | ||||||
| chr2:218295545
|
A | C | 1 | a0001c0001t0001g0061 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.236+23996A>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218295545 | ||||||
| chr2:218295550
|
G | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+24001G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218295550 | ||||||
| chr2:218295749
|
T | G | 2 | a0001c0001t0003g0016a0001c0001t0010g0001 | 3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.236+24200T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218295749 | ||||||
| chr2:218295811
|
G | A | 3 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276 | 3 | HG01884.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.236+24262G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218295811 | ||||||
| chr2:218295844
|
C | CT | 6 | a0001c0001t0002g0183a0001c0001t0002g0223a0001c0001t0003g0021others(3): Show | 6 | HG02622.hp1 HG02976.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.236+24312dupT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218295844 | |||||
| chr2:218295844
|
CT | C | 101 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(98): Show | 101 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.236+24312delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218295844 | |||||
| chr2:218295898
|
T | C | 125 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(122): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.236+24349T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218295898 | ||||||
| chr2:218296001
|
C | A | 9 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(6): Show | 9 | HG01243.hp1 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.236+24452C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218296001 | ||||||
| chr2:218296009
|
G | A | 2 | a0001c0001t0003g0264a0001c0001t0008g0048 | 2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.236+24460G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218296009 | ||||||
| chr2:218296026
|
T | C | 106 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(103): Show | 107 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.236+24477T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218296026 | ||||||
| chr2:218296084
|
G | C | 7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+24535G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218296084 | ||||||
| chr2:218296141
|
C | A | 102 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(99): Show | 102 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.236+24592C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218296141 | ||||||
| chr2:218296198
|
G | A | 1 | a0001c0002t0002g0039 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.236+24649G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218296198 | ||||||
| chr2:218296442
|
G | C | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.236+24893G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218296442 | ||||||
| chr2:218296518
|
C | T | 102 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(99): Show | 102 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.236+24969C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218296518 | ||||||
| chr2:218296644
|
A | T | 2 | a0001c0001t0003g0016a0001c0001t0010g0001 | 3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.236+25095A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218296644 | ||||||
| chr2:218296669
|
CTT | C | 3 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276 | 3 | HG01884.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.236+25124_236+2512 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218296669 | |||||
| chr2:218296747
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.236+25198C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218296747 | ||||||
| chr2:218296764
|
C | T | 1 | a0001c0001t0003g0025 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.236+25215C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218296764 | ||||||
| chr2:218296944
|
C | G | 1 | a0001c0002t0002g0033 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.236+25395C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218296944 | ||||||
| chr2:218297035
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.236+25486G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297035 | ||||||
| chr2:218297226
|
C | G | 2 | a0001c0001t0003g0024a0001c0001t0003g0025 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.236+25677C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297226 | ||||||
| chr2:218297347
|
G | A | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.236+25798G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297347 | ||||||
| chr2:218297497
|
C | A | 1 | a0001c0001t0001g0061 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.236+25948C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297497 | ||||||
| chr2:218297554
|
G | A | 37 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(34): Show | 37 | HG01109.hp1 HG01891.hp2 HG01975.hp1 others(34): Show |
intron_variant | MODIFIER | c.236+26005G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297554 | ||||||
| chr2:218297599
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.236+26050C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297599 | ||||||
| chr2:218297637
|
A | T | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+26088A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297637 | ||||||
| chr2:218297684
|
C | CA | 86 | a0001c0001t0001g0084a0001c0001t0001g0164a0001c0001t0001g0196others(83): Show | 86 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.236+26158dupA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218297684 | |||||
| chr2:218297684
|
CA | C | 7 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0116others(4): Show | 7 | HG00280.hp2 HG00735.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.236+26158delA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218297684 | |||||
| chr2:218297706
|
A | AC | 50 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(47): Show | 50 | HG00099.hp1 HG00621.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.236+26157_236+2615 others(5): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297706 | ||||||
| chr2:218297706
|
A | C | 109 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0051others(106): Show | 110 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.236+26157A>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297706 | ||||||
| chr2:218297710
|
G | C | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.236+26161G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297710 | ||||||
| chr2:218297760
|
G | T | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+26211G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297760 | ||||||
| chr2:218297761
|
A | T | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+26212A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297761 | ||||||
| chr2:218297796
|
G | A | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+26247G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297796 | ||||||
| chr2:218297822
|
A | C | 1 | a0001c0001t0001g0061 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.236+26273A>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297822 | ||||||
| chr2:218297825
|
C | A | 1 | a0001c0001t0001g0061 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.236+26276C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297825 | ||||||
| chr2:218297930
|
G | A | 11 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0008g0048others(8): Show | 11 | HG01109.hp1 HG02486.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.236+26381G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297930 | ||||||
| chr2:218297994
|
T | G | 2 | a0001c0001t0001g0260a0001c0001t0003g0264 | 2 | HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.236+26445T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218297994 | ||||||
| chr2:218297997
|
C | CA | 155 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(152): Show | 156 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.236+26463dupA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218297997 | |||||
| chr2:218298007
|
A | AG | 6 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037others(3): Show | 6 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.236+26458_236+2645 others(5): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218298007 | ||||||
| chr2:218298061
|
G | A | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+26512G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218298061 | ||||||
| chr2:218298113
|
C | T | 124 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.236+26564C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218298113 | ||||||
| chr2:218298114
|
G | A | 36 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(33): Show | 36 | HG01109.hp1 HG01891.hp2 HG01975.hp1 others(33): Show |
intron_variant | MODIFIER | c.236+26565G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218298114 | ||||||
| chr2:218298119
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.236+26570T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218298119 | ||||||
| chr2:218298586
|
T | C | 7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+27037T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218298586 | ||||||
| chr2:218298761
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.236+27212T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218298761 | ||||||
| chr2:218298765
|
G | A | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.236+27216G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218298765 | ||||||
| chr2:218298929
|
C | T | 2 | a0001c0001t0003g0016a0001c0001t0010g0001 | 3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.236+27380C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218298929 | ||||||
| chr2:218299089
|
C | T | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+27540C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218299089 | ||||||
| chr2:218299205
|
G | A | 1 | a0001c0002t0002g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.236+27656G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218299205 | ||||||
| chr2:218299290
|
C | T | 9 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(6): Show | 9 | HG01243.hp1 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.236+27741C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218299290 | ||||||
| chr2:218299496
|
G | A | 1 | a0001c0001t0009g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.236+27947G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218299496 | ||||||
| chr2:218299523
|
C | T | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+27974C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218299523 | ||||||
| chr2:218299570
|
A | G | 164 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.236+28021A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218299570 | ||||||
| chr2:218299620
|
AT | A | 5 | a0001c0001t0001g0055a0001c0001t0003g0278a0001c0001t0003g0279others(2): Show | 5 | HG01975.hp2 HG02897.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.236+28086delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218299620 | |||||
| chr2:218299864
|
G | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+28315G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218299864 | ||||||
| chr2:218300004
|
G | A | 102 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(99): Show | 102 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.236+28455G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218300004 | ||||||
| chr2:218300152
|
A | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+28603A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218300152 | ||||||
| chr2:218300270
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.236+28721A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218300270 | ||||||
| chr2:218300551
|
C | CT | 263 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.236+29014dupT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218300551 | |||||
| chr2:218300609
|
G | A | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.236+29060G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218300609 | ||||||
| chr2:218300654
|
T | A | 23 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(20): Show | 23 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.236+29105T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218300654 | ||||||
| chr2:218301119
|
T | C | 1 | a0001c0001t0003g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.236+29570T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218301119 | ||||||
| chr2:218301266
|
T | C | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+29717T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218301266 | ||||||
| chr2:218301347
|
G | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+29798G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218301347 | ||||||
| chr2:218301563
|
C | G | 266 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.236+30014C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218301563 | ||||||
| chr2:218301566
|
G | C | 275 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.236+30017G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218301566 | ||||||
| chr2:218301602
|
C | T | 3 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276 | 3 | HG01884.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.236+30053C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218301602 | ||||||
| chr2:218301622
|
T | TA | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+30080dupA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218301622 | |||||
| chr2:218301658
|
G | A | 1 | a0001c0001t0004g0022 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.236+30109G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218301658 | ||||||
| chr2:218301923
|
G | A | 1 | a0001c0001t0010g0001 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.236+30374G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218301923 | ||||||
| chr2:218301924
|
C | T | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+30375C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218301924 | ||||||
| chr2:218301926
|
C | G | 19 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(16): Show | 19 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.236+30377C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218301926 | ||||||
| chr2:218301928
|
C | T | 1 | a0001c0008t0003g0008 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.236+30379C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218301928 | ||||||
| chr2:218301956
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.236+30407G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218301956 | ||||||
| chr2:218302074
|
G | A | 37 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(34): Show | 37 | HG01109.hp1 HG01891.hp2 HG01975.hp1 others(34): Show |
intron_variant | MODIFIER | c.236+30525G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218302074 | ||||||
| chr2:218302157
|
G | C | 7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+30608G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218302157 | ||||||
| chr2:218302254
|
A | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+30705A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218302254 | ||||||
| chr2:218302256
|
G | C | 1 | a0001c0001t0008g0048 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.236+30707G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218302256 | ||||||
| chr2:218302435
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0118 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.236+30886G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218302435 | ||||||
| chr2:218302773
|
C | T | 1 | a0001c0001t0009g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.236+31224C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218302773 | ||||||
| chr2:218302795
|
G | A | 1 | a0001c0001t0012g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.236+31246G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218302795 | ||||||
| chr2:218302806
|
G | A | 161 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.236+31257G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218302806 | ||||||
| chr2:218302829
|
A | G | 266 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.236+31280A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218302829 | ||||||
| chr2:218302840
|
G | C | 104 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.236+31291G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218302840 | ||||||
| chr2:218302852
|
C | A | 1 | a0001c0001t0002g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.236+31303C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218302852 | ||||||
| chr2:218302906
|
C | T | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+31357C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218302906 | ||||||
| chr2:218302939
|
C | CGTTT | 11 | a0001c0001t0001g0150a0001c0001t0003g0142a0001c0001t0003g0143others(8): Show | 12 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+31407_236+3141 others(8): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218302939 | |||||
| chr2:218303019
|
A | T | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+31470A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303019 | ||||||
| chr2:218303069
|
A | C | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+31520A>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303069 | ||||||
| chr2:218303081
|
A | C | 2 | a0001c0001t0003g0266a0001c0001t0003g0267 | 2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.236+31532A>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303081 | ||||||
| chr2:218303110
|
G | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+31561G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303110 | ||||||
| chr2:218303168
|
C | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+31619C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303168 | ||||||
| chr2:218303235
|
A | C | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+31686A>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303235 | ||||||
| chr2:218303237
|
C | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+31688C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303237 | ||||||
| chr2:218303242
|
C | T | 102 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(99): Show | 102 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.236+31693C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303242 | ||||||
| chr2:218303279
|
C | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0127 | 2 | NA18964.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.236+31730C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303279 | ||||||
| chr2:218303430
|
C | T | 1 | a0001c0001t0005g0124 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.236+31881C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303430 | ||||||
| chr2:218303523
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0007g0010 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.236+31974C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303523 | ||||||
| chr2:218303544
|
C | A | 20 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(17): Show | 20 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.236+31995C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303544 | ||||||
| chr2:218303574
|
C | CT | 12 | a0001c0001t0001g0164a0001c0001t0001g0232a0001c0001t0002g0170others(9): Show | 12 | HG01433.hp1 HG01978.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+32046dupT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218303574 | |||||
| chr2:218303574
|
CT | C | 15 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0002g0220others(12): Show | 16 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.236+32046delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218303574 | |||||
| chr2:218303574
|
CTT | C | 112 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.236+32045_236+3204 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218303574 | |||||
| chr2:218303679
|
C | T | 37 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(34): Show | 37 | HG01109.hp1 HG01891.hp2 HG01975.hp1 others(34): Show |
intron_variant | MODIFIER | c.236+32130C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303679 | ||||||
| chr2:218303709
|
G | A | 101 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(98): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.236+32160G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303709 | ||||||
| chr2:218303802
|
C | T | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+32253C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303802 | ||||||
| chr2:218303864
|
A | G | 266 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.236+32315A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303864 | ||||||
| chr2:218303869
|
C | T | 1 | a0001c0001t0003g0128 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.236+32320C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303869 | ||||||
| chr2:218303895
|
C | T | 1 | a0001c0001t0003g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.236+32346C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218303895 | ||||||
| chr2:218304042
|
A | G | 264 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.236+32493A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218304042 | ||||||
| chr2:218304387
|
A | G | 264 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.236+32838A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218304387 | ||||||
| chr2:218304434
|
G | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0074a0001c0001t0001g0100others(1): Show | 4 | HG02080.hp1 HG02132.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+32885G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218304434 | ||||||
| chr2:218304436
|
A | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+32887A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218304436 | ||||||
| chr2:218304480
|
T | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+32931T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218304480 | ||||||
| chr2:218304726
|
G | A | 1 | a0001c0001t0008g0026 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.236+33177G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218304726 | ||||||
| chr2:218304765
|
G | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+33216G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218304765 | ||||||
| chr2:218304849
|
T | C | 164 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.236+33300T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218304849 | ||||||
| chr2:218304850
|
G | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0130a0001c0001t0001g0262 | 3 | HG00323.hp2 HG01261.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.236+33301G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218304850 | ||||||
| chr2:218304854
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0007g0010 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.236+33305C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218304854 | ||||||
| chr2:218304873
|
G | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0025 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.236+33324G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218304873 | ||||||
| chr2:218304911
|
T | C | 1 | a0001c0001t0005g0248 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.236+33362T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218304911 | ||||||
| chr2:218304976
|
G | A | 19 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(16): Show | 19 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.236+33427G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218304976 | ||||||
| chr2:218305202
|
TCTTC | T | 6 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(3): Show | 6 | HG01884.hp1 HG02572.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.236+33659_236+3366 others(8): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218305202 | |||||
| chr2:218305232
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.236+33683T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218305232 | ||||||
| chr2:218305353
|
T | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.236+33804T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218305353 | ||||||
| chr2:218305513
|
A | C | 1 | a0001c0001t0004g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.236+33964A>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218305513 | ||||||
| chr2:218305513
|
A | T | 125 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(122): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.236+33964A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218305513 | ||||||
| chr2:218305587
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.236+34038T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218305587 | ||||||
| chr2:218305605
|
G | A | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.236+34056G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218305605 | ||||||
| chr2:218305622
|
T | C | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+34073T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218305622 | ||||||
| chr2:218305654
|
A | G | 163 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.236+34105A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218305654 | ||||||
| chr2:218305718
|
C | G | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-34065C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218305718 | ||||||
| chr2:218305739
|
G | A | 19 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(16): Show | 19 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.237-34044G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218305739 | ||||||
| chr2:218305802
|
G | A | 126 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(123): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.237-33981G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218305802 | ||||||
| chr2:218306003
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.237-33780G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218306003 | ||||||
| chr2:218306295
|
G | A | 1 | a0001c0001t0010g0001 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.237-33488G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218306295 | ||||||
| chr2:218306468
|
T | C | 163 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.237-33315T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218306468 | ||||||
| chr2:218306474
|
C | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-33309C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218306474 | ||||||
| chr2:218306498
|
C | G | 1 | a0001c0001t0001g0099 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.237-33285C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218306498 | ||||||
| chr2:218306519
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.237-33264T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218306519 | ||||||
| chr2:218306730
|
T | C | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-33053T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218306730 | ||||||
| chr2:218306739
|
G | A | 7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-33044G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218306739 | ||||||
| chr2:218306938
|
T | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0025 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.237-32845T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218306938 | ||||||
| chr2:218307075
|
G | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-32708G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218307075 | ||||||
| chr2:218307090
|
A | G | 266 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.237-32693A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218307090 | ||||||
| chr2:218307274
|
G | A | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.237-32509G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218307274 | ||||||
| chr2:218307281
|
A | T | 2 | a0001c0001t0003g0266a0001c0001t0003g0267 | 2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.237-32502A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218307281 | ||||||
| chr2:218307506
|
G | A | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0007g0230 | 3 | NA18971.hp2 NA19074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.237-32277G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218307506 | ||||||
| chr2:218307672
|
G | A | 7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-32111G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218307672 | ||||||
| chr2:218307689
|
G | A | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-32094G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218307689 | ||||||
| chr2:218307789
|
G | A | 2 | a0001c0001t0001g0231a0002c0003t0011g0236 | 2 | HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.237-31994G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218307789 | ||||||
| chr2:218307890
|
T | C | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-31893T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218307890 | ||||||
| chr2:218307938
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.237-31845C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218307938 | ||||||
| chr2:218308119
|
CA | C | 102 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.237-31657delA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218308119 | |||||
| chr2:218308120
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.237-31663A>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218308120 | ||||||
| chr2:218308151
|
G | A | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.237-31632G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218308151 | ||||||
| chr2:218308188
|
A | AT | 106 | a0001c0001t0001g0057a0001c0001t0001g0084a0001c0001t0001g0126others(103): Show | 106 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.237-31577dupT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218308188 | |||||
| chr2:218308188
|
A | ATT | 9 | a0001c0001t0002g0176a0001c0001t0002g0183a0001c0001t0002g0189others(6): Show | 9 | HG02615.hp2 HG02922.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-31578_237-3157 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218308188 | |||||
| chr2:218308188
|
AT | A | 9 | a0001c0001t0001g0017a0001c0001t0003g0041a0001c0001t0003g0049others(6): Show | 9 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-31577delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218308188 | |||||
| chr2:218308594
|
CT | C | 5 | a0001c0001t0001g0053a0001c0001t0001g0106a0001c0001t0001g0130others(2): Show | 5 | HG01261.hp2 NA18961.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-31177delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218308594 | |||||
| chr2:218308604
|
T | C | 103 | a0001c0001t0001g0084a0001c0001t0001g0164a0001c0001t0001g0191others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.237-31179T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218308604 | ||||||
| chr2:218308722
|
G | T | 1 | a0001c0001t0001g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.237-31061G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218308722 | ||||||
| chr2:218308788
|
T | G | 1 | a0001c0002t0002g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.237-30995T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218308788 | ||||||
| chr2:218308988
|
C | T | 1 | a0001c0001t0004g0233 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.237-30795C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218308988 | ||||||
| chr2:218309093
|
T | C | 1 | a0001c0001t0008g0026 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.237-30690T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218309093 | ||||||
| chr2:218309143
|
G | A | 1 | a0001c0001t0004g0163 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.237-30640G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218309143 | ||||||
| chr2:218309160
|
C | T | 1 | a0001c0001t0007g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.237-30623C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218309160 | ||||||
| chr2:218309293
|
C | G | 1 | a0001c0001t0003g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.237-30490C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218309293 | ||||||
| chr2:218309390
|
G | T | 3 | a0001c0001t0005g0124a0001c0001t0015g0120a0001c0002t0002g0131 | 3 | HG00642.hp2 HG01361.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.237-30393G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218309390 | ||||||
| chr2:218309416
|
CA | C | 115 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0061others(112): Show | 116 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.237-30345delA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218309416 | |||||
| chr2:218309416
|
CAA | C | 147 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.237-30346_237-3034 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218309416 | |||||
| chr2:218309475
|
T | C | 265 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.237-30308T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218309475 | ||||||
| chr2:218309612
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0108 | 2 | HG01074.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.237-30171T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218309612 | ||||||
| chr2:218309840
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG03239.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.237-29943G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218309840 | ||||||
| chr2:218309867
|
G | A | 7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-29916G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218309867 | ||||||
| chr2:218309921
|
G | A | 1 | a0001c0001t0003g0041 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.237-29862G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218309921 | ||||||
| chr2:218309929
|
G | A | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.237-29854G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218309929 | ||||||
| chr2:218309932
|
T | TA | 20 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(17): Show | 20 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.237-29837dupA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218309932 | |||||
| chr2:218310229
|
T | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-29554T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218310229 | ||||||
| chr2:218310371
|
C | T | 1 | a0001c0001t0005g0259 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.237-29412C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218310371 | ||||||
| chr2:218310443
|
C | T | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-29340C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218310443 | ||||||
| chr2:218310514
|
G | T | 1 | a0001c0001t0012g0272 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.237-29269G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218310514 | ||||||
| chr2:218310518
|
G | A | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.237-29265G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218310518 | ||||||
| chr2:218310592
|
C | CT | 11 | a0001c0001t0001g0235a0001c0001t0003g0041a0001c0001t0003g0226others(8): Show | 11 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.237-29174dupT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218310592 | |||||
| chr2:218310592
|
C | CTT | 105 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(102): Show | 106 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.237-29175_237-2917 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218310592 | |||||
| chr2:218310592
|
C | CTTT | 44 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0069others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.237-29176_237-2917 others(7): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218310592 | |||||
| chr2:218310592
|
CT | C | 7 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG01884.hp1 HG02572.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-29174delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218310592 | |||||
| chr2:218310618
|
G | T | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-29165G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218310618 | ||||||
| chr2:218310764
|
A | G | 163 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.237-29019A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218310764 | ||||||
| chr2:218310935
|
T | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0130a0001c0001t0001g0262 | 3 | HG00323.hp2 HG01261.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.237-28848T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218310935 | ||||||
| chr2:218310975
|
C | T | 1 | a0001c0001t0007g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.237-28808C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218310975 | ||||||
| chr2:218310985
|
T | C | 1 | a0001c0001t0003g0271 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.237-28798T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218310985 | ||||||
| chr2:218311002
|
T | C | 4 | a0001c0001t0004g0186a0001c0001t0004g0194a0001c0001t0004g0198others(1): Show | 4 | HG00609.hp1 NA18612.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-28781T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218311002 | ||||||
| chr2:218311030
|
G | T | 1 | a0001c0001t0003g0025 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.237-28753G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218311030 | ||||||
| chr2:218311391
|
G | A | 1 | a0001c0001t0003g0088 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.237-28392G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218311391 | ||||||
| chr2:218311434
|
A | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-28349A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218311434 | ||||||
| chr2:218311653
|
A | G | 265 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.237-28130A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218311653 | ||||||
| chr2:218311727
|
A | C | 125 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(122): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.237-28056A>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218311727 | ||||||
| chr2:218311874
|
T | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-27909T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218311874 | ||||||
| chr2:218311918
|
C | T | 1 | a0001c0002t0002g0023 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.237-27865C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218311918 | ||||||
| chr2:218311996
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.237-27787T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218311996 | ||||||
| chr2:218312172
|
C | A | 125 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(122): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.237-27611C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218312172 | ||||||
| chr2:218312425
|
C | T | 124 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.237-27358C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218312425 | ||||||
| chr2:218312565
|
T | TA | 258 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.237-27202dupA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218312565 | |||||
| chr2:218312667
|
G | C | 1 | a0001c0001t0008g0048 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.237-27116G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218312667 | ||||||
| chr2:218312872
|
T | TA | 7 | a0001c0001t0003g0041a0001c0002t0002g0035a0001c0002t0002g0036others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-26903dupA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218312872 | |||||
| chr2:218313109
|
A | AT | 102 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(99): Show | 102 | HG00099.hp1 HG00323.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.237-26661dupT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218313109 | |||||
| chr2:218313142
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.237-26641C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218313142 | ||||||
| chr2:218313256
|
G | A | 2 | a0001c0001t0003g0080a0001c0001t0003g0109 | 2 | NA18972.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.237-26527G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218313256 | ||||||
| chr2:218313344
|
C | T | 102 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(99): Show | 102 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.237-26439C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218313344 | ||||||
| chr2:218313872
|
A | T | 19 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(16): Show | 19 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.237-25911A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218313872 | ||||||
| chr2:218313877
|
G | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-25906G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218313877 | ||||||
| chr2:218313903
|
CT | C | 188 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(185): Show | 188 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.237-25859delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218313903 | |||||
| chr2:218313903
|
CTT | C | 23 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0068others(20): Show | 23 | HG01515.hp1 HG02027.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.237-25860_237-2585 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218313903 | |||||
| chr2:218313903
|
CTTT | C | 24 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(21): Show | 24 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.237-25861_237-2585 others(7): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218313903 | |||||
| chr2:218313930
|
G | A | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-25853G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218313930 | ||||||
| chr2:218314152
|
G | A | 162 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.237-25631G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218314152 | ||||||
| chr2:218314202
|
C | T | 37 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(34): Show | 37 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(34): Show |
intron_variant | MODIFIER | c.237-25581C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218314202 | ||||||
| chr2:218314222
|
C | CTT | 17 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(14): Show | 17 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.237-25541_237-2554 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218314222 | |||||
| chr2:218314222
|
C | CTTT | 68 | a0001c0001t0001g0191a0001c0001t0001g0196a0001c0001t0001g0201others(65): Show | 68 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.237-25542_237-2554 others(7): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218314222 | |||||
| chr2:218314222
|
C | CTTTT | 39 | a0001c0001t0001g0164a0001c0001t0001g0217a0001c0001t0001g0232others(36): Show | 40 | HG00609.hp1 HG00609.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.237-25543_237-2554 others(8): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218314222 | |||||
| chr2:218314222
|
C | CTTTTTTT | 8 | a0001c0001t0003g0024a0001c0001t0003g0050a0001c0001t0008g0026others(5): Show | 8 | HG02451.hp2 HG02615.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.237-25546_237-2554 others(11): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218314222 | |||||
| chr2:218314222
|
C | CTTTTTTT others(1): Show |
23 | a0001c0001t0001g0150a0001c0001t0001g0154a0001c0001t0001g0156others(20): Show | 23 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.237-25547_237-2554 others(12): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218314222 | |||||
| chr2:218314222
|
CT | C | 87 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(84): Show | 87 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.237-25540delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218314222 | |||||
| chr2:218314222
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0151a0001c0001t0002g0011 | 2 | HG01975.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.237-25549_237-2554 others(14): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218314222 | |||||
| chr2:218314285
|
G | A | 1 | a0001c0001t0008g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.237-25498G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218314285 | ||||||
| chr2:218314424
|
T | C | 3 | a0001c0001t0004g0239a0001c0001t0004g0261a0001c0001t0005g0240 | 3 | HG00621.hp2 HG02080.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.237-25359T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218314424 | ||||||
| chr2:218314692
|
GT | G | 6 | a0001c0001t0001g0062a0001c0001t0001g0069a0001c0001t0001g0076others(3): Show | 6 | HG01081.hp2 HG01175.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-25080delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218314692 | |||||
| chr2:218314719
|
T | C | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-25064T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218314719 | ||||||
| chr2:218314834
|
C | T | 3 | a0001c0001t0003g0041a0001c0001t0003g0278a0001c0001t0003g0279 | 3 | HG03209.hp2 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-24949C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218314834 | ||||||
| chr2:218314932
|
CA | C | 103 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.237-24850delA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218314932 | ||||||
| chr2:218315006
|
C | CTTTCTT | 4 | a0001c0001t0001g0209a0001c0001t0001g0237a0001c0001t0002g0203others(1): Show | 4 | HG02004.hp1 HG02165.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-24769_237-2476 others(10): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315006 | |||||
| chr2:218315012
|
T | TTCTTTCT others(7): Show |
1 | a0001c0001t0001g0096 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.237-24770_237-2476 others(18): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315012 | |||||
| chr2:218315012
|
T | TTTTCTTT others(3): Show |
4 | a0001c0001t0001g0164a0001c0001t0002g0204a0001c0001t0003g0187others(1): Show | 4 | HG01109.hp2 HG02300.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-24764_237-2476 others(14): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315012 | |||||
| chr2:218315012
|
T | TTTTCTTT others(7): Show |
2 | a0001c0001t0001g0235a0001c0001t0002g0189 | 2 | HG01175.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.237-24764_237-2476 others(18): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315012 | |||||
| chr2:218315016
|
C | CTT | 90 | a0001c0001t0001g0191a0001c0001t0001g0196a0001c0001t0001g0201others(87): Show | 90 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.237-24765_237-2476 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315016 | |||||
| chr2:218315025
|
T | A | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.237-24758T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315025 | ||||||
| chr2:218315038
|
T | TTC | 126 | a0001c0001t0001g0075a0001c0001t0001g0096a0001c0001t0001g0100others(123): Show | 126 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.237-24744_237-2474 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315038 | |||||
| chr2:218315038
|
T | TTCTTTC | 12 | a0001c0001t0001g0056a0001c0001t0001g0076a0001c0001t0001g0137others(9): Show | 12 | HG00099.hp2 HG01175.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-24744_237-2474 others(10): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315038 | |||||
| chr2:218315038
|
T | TTCTTTCT others(3): Show |
22 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0062others(19): Show | 22 | HG01074.hp2 HG01081.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.237-24744_237-2474 others(14): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315038 | |||||
| chr2:218315038
|
T | TTCTTTCT others(7): Show |
28 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0044others(25): Show | 28 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.237-24744_237-2474 others(18): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315038 | |||||
| chr2:218315038
|
T | TTCTTTCT others(11): Show |
45 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0059others(42): Show | 46 | HG00099.hp1 HG00323.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.237-24744_237-2474 others(22): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315038 | |||||
| chr2:218315038
|
T | TTCTTTCT others(15): Show |
25 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0043others(22): Show | 25 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.237-24744_237-2474 others(26): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315038 | |||||
| chr2:218315038
|
T | TTCTTTCT others(19): Show |
7 | a0001c0001t0001g0084a0001c0001t0003g0080a0001c0001t0003g0083others(4): Show | 7 | HG01243.hp1 HG02027.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-24744_237-2474 others(30): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315038 | |||||
| chr2:218315038
|
T | TTCTTTCT others(23): Show |
6 | a0001c0001t0001g0087a0001c0001t0001g0093a0001c0001t0001g0260others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-24744_237-2474 others(34): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315038 | |||||
| chr2:218315038
|
T | TTCTTTCT others(27): Show |
1 | a0001c0001t0001g0126 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.237-24744_237-2474 others(38): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315038 | |||||
| chr2:218315038
|
T | TTCTTTCT others(31): Show |
1 | a0001c0001t0001g0135 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.237-24744_237-2474 others(42): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315038 | |||||
| chr2:218315041
|
T | C | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-24742T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315041 | ||||||
| chr2:218315045
|
T | C | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-24738T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315045 | ||||||
| chr2:218315049
|
T | C | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-24734T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315049 | ||||||
| chr2:218315053
|
T | C | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0004g0200 | 3 | HG02738.hp1 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-24730T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315053 | ||||||
| chr2:218315057
|
T | C | 49 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0059others(46): Show | 49 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.237-24726T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315057 | ||||||
| chr2:218315057
|
T | TCTTCCTT others(1): Show |
15 | a0001c0001t0001g0209a0001c0001t0001g0235a0001c0001t0001g0237others(12): Show | 15 | HG01175.hp2 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.237-24714_237-2470 others(12): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTCCTT others(5): Show |
4 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0003g0041others(1): Show | 4 | HG01109.hp2 HG02615.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-24718_237-2470 others(16): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(17): Show |
13 | a0001c0001t0001g0211a0001c0001t0001g0217a0001c0001t0001g0255others(10): Show | 13 | HG00609.hp1 HG00621.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.237-24723_237-2472 others(28): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(17): Show |
15 | a0001c0001t0001g0231a0001c0001t0001g0250a0001c0001t0001g0251others(12): Show | 15 | HG01081.hp1 HG01192.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.237-24723_237-2472 others(28): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(21): Show |
8 | a0001c0001t0001g0191a0001c0001t0001g0228a0001c0001t0001g0232others(5): Show | 8 | HG00609.hp2 HG02040.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.237-24723_237-2472 others(32): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(20): Show |
1 | a0001c0001t0001g0254 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.237-24723_237-2472 others(31): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(17): Show |
9 | a0001c0001t0002g0172a0001c0001t0002g0177a0001c0001t0003g0046others(6): Show | 9 | HG01109.hp1 HG02572.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-24723_237-2472 others(28): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(21): Show |
11 | a0001c0001t0001g0207a0001c0001t0002g0176a0001c0001t0002g0199others(8): Show | 11 | HG00280.hp1 HG01123.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.237-24723_237-2472 others(32): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(25): Show |
7 | a0001c0001t0001g0196a0001c0001t0001g0213a0001c0001t0002g0169others(4): Show | 7 | HG01257.hp2 HG03453.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-24723_237-2472 others(36): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(29): Show |
1 | a0001c0001t0005g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.237-24723_237-2472 others(40): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(21): Show |
5 | a0001c0001t0001g0100a0001c0001t0001g0150a0001c0001t0002g0171others(2): Show | 5 | HG02257.hp2 HG02280.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-24723_237-2472 others(32): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(25): Show |
12 | a0001c0001t0002g0180a0001c0001t0002g0188a0001c0001t0002g0192others(9): Show | 12 | HG00323.hp1 HG01074.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.237-24723_237-2472 others(36): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(29): Show |
1 | a0001c0001t0004g0233 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.237-24723_237-2472 others(40): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(25): Show |
2 | a0001c0001t0002g0170a0001c0001t0002g0178 | 2 | NA18967.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.237-24723_237-2472 others(36): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(29): Show |
11 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0002g0173others(8): Show | 11 | HG00735.hp2 HG01099.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.237-24723_237-2472 others(40): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(33): Show |
1 | a0001c0001t0002g0184 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.237-24723_237-2472 others(44): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315057
|
T | TCTTTCTT others(33): Show |
2 | a0001c0001t0002g0174a0001c0001t0006g0244 | 2 | HG01496.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.237-24723_237-2472 others(44): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315057 | |||||
| chr2:218315061
|
C | T | 9 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(6): Show | 9 | HG01975.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-24722C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315061 | ||||||
| chr2:218315077
|
T | C | 182 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(179): Show | 182 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.237-24706T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315077 | ||||||
| chr2:218315081
|
T | C | 7 | a0001c0001t0001g0164a0001c0001t0001g0209a0001c0001t0001g0237others(4): Show | 7 | HG02004.hp1 HG02165.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-24702T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315081 | ||||||
| chr2:218315084
|
C | T | 182 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(179): Show | 182 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.237-24699C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315084 | ||||||
| chr2:218315088
|
C | T | 7 | a0001c0001t0001g0164a0001c0001t0001g0209a0001c0001t0001g0237others(4): Show | 7 | HG02004.hp1 HG02165.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-24695C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315088 | ||||||
| chr2:218315094
|
C | CTCCT | 3 | a0001c0002t0002g0036a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG01167.hp1 HG01169.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.237-24663_237-2466 others(8): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315094 | |||||
| chr2:218315094
|
C | CTCCTTCC others(5): Show |
2 | a0001c0001t0003g0049a0001c0001t0008g0048 | 2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.237-24671_237-2466 others(16): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315094 | |||||
| chr2:218315094
|
C | CTCCTTCC others(9): Show |
8 | a0001c0001t0003g0050a0001c0001t0010g0030a0001c0002t0002g0029others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.237-24675_237-2466 others(20): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315094 | |||||
| chr2:218315097
|
C | T | 180 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(177): Show | 180 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.237-24686C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315097 | ||||||
| chr2:218315098
|
T | C | 180 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(177): Show | 180 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.237-24685T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315098 | ||||||
| chr2:218315101
|
C | T | 7 | a0001c0001t0001g0164a0001c0001t0001g0209a0001c0001t0001g0237others(4): Show | 7 | HG02004.hp1 HG02165.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-24682C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315101 | ||||||
| chr2:218315102
|
T | C | 7 | a0001c0001t0001g0164a0001c0001t0001g0209a0001c0001t0001g0237others(4): Show | 7 | HG02004.hp1 HG02165.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-24681T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315102 | ||||||
| chr2:218315116
|
C | CCTTTCTT others(21): Show |
1 | a0001c0001t0003g0041 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.237-24664_237-2466 others(32): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315116 | |||||
| chr2:218315116
|
CCTTCCTT others(1): Show |
C | 23 | a0001c0001t0001g0191a0001c0001t0001g0196a0001c0001t0001g0211others(20): Show | 23 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.237-24663_237-2465 others(12): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315116 | |||||
| chr2:218315116
|
CCTTCCTT others(5): Show |
C | 1 | a0001c0001t0005g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.237-24663_237-2465 others(16): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315116 | |||||
| chr2:218315120
|
C | CCTTTCTT others(29): Show |
1 | a0001c0001t0003g0278 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.237-24636_237-2463 others(40): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315120 | |||||
| chr2:218315120
|
C | CCTTTCTT others(33): Show |
1 | a0001c0001t0003g0279 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.237-24636_237-2463 others(44): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315120 | |||||
| chr2:218315120
|
C | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0232a0001c0001t0003g0016others(1): Show | 4 | HG02293.hp1 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-24663C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315120 | ||||||
| chr2:218315120
|
CCTTT | C | 6 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0125others(3): Show | 6 | HG02074.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-24639_237-2463 others(8): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218315120 | |||||
| chr2:218315124
|
T | C | 48 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(45): Show | 48 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.237-24659T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315124 | ||||||
| chr2:218315128
|
T | C | 4 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(1): Show | 4 | HG01884.hp2 HG02074.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-24655T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315128 | ||||||
| chr2:218315182
|
A | G | 263 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.237-24601A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315182 | ||||||
| chr2:218315203
|
G | A | 36 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(33): Show | 36 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.237-24580G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315203 | ||||||
| chr2:218315221
|
G | A | 1 | a0001c0002t0002g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.237-24562G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315221 | ||||||
| chr2:218315272
|
G | A | 160 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.237-24511G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315272 | ||||||
| chr2:218315298
|
C | T | 1 | a0001c0001t0003g0041 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.237-24485C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315298 | ||||||
| chr2:218315338
|
C | T | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.237-24445C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315338 | ||||||
| chr2:218315502
|
G | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0025 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.237-24281G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315502 | ||||||
| chr2:218315711
|
C | T | 1 | a0001c0001t0005g0248 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.237-24072C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315711 | ||||||
| chr2:218315747
|
G | A | 10 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0008g0048others(7): Show | 10 | HG02486.hp2 HG02630.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.237-24036G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315747 | ||||||
| chr2:218315998
|
G | A | 1 | a0001c0001t0002g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.237-23785G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218315998 | ||||||
| chr2:218316018
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.237-23765C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218316018 | ||||||
| chr2:218316059
|
G | A | 3 | a0001c0001t0003g0041a0001c0001t0003g0278a0001c0001t0003g0279 | 3 | HG03209.hp2 NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-23724G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218316059 | ||||||
| chr2:218316108
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.237-23675G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218316108 | ||||||
| chr2:218316268
|
C | CTT | 40 | a0001c0001t0001g0125a0001c0001t0001g0150a0001c0001t0001g0151others(37): Show | 40 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(37): Show |
intron_variant | MODIFIER | c.237-23497_237-2349 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218316268 | |||||
| chr2:218316268
|
C | CTTT | 105 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.237-23498_237-2349 others(7): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218316268 | |||||
| chr2:218316268
|
C | CTTTT | 8 | a0001c0001t0001g0060a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 9 | HG02300.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-23499_237-2349 others(8): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218316268 | |||||
| chr2:218316268
|
CTTTTTTT | C | 6 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037others(3): Show | 6 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-23502_237-2349 others(11): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218316268 | |||||
| chr2:218316271
|
T | TC | 100 | a0001c0001t0001g0164a0001c0001t0001g0191a0001c0001t0001g0196others(97): Show | 100 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.237-23512_237-2351 others(5): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218316271 | ||||||
| chr2:218316562
|
T | TGCCCGGC others(789): Show |
1 | a0001c0001t0003g0119 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.237-23202_237-2320 others(800): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218316562 | |||||
| chr2:218316627
|
C | G | 27 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(24): Show | 27 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.237-23156C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218316627 | ||||||
| chr2:218316635
|
G | A | 1 | a0001c0001t0009g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.237-23148G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218316635 | ||||||
| chr2:218316760
|
C | T | 12 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-23023C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218316760 | ||||||
| chr2:218317174
|
C | T | 244 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.237-22609C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218317174 | ||||||
| chr2:218317235
|
G | A | 2 | a0001c0001t0013g0094a0001c0001t0013g0097 | 2 | NA18946.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.237-22548G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218317235 | ||||||
| chr2:218317270
|
A | G | 7 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-22513A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218317270 | ||||||
| chr2:218317291
|
G | A | 15 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0002g0185others(12): Show | 15 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.237-22492G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218317291 | ||||||
| chr2:218317460
|
G | C | 1 | a0001c0001t0003g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.237-22323G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218317460 | ||||||
| chr2:218317675
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.237-22108A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218317675 | ||||||
| chr2:218317697
|
C | T | 2 | a0001c0001t0003g0016a0001c0001t0010g0001 | 3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.237-22086C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218317697 | ||||||
| chr2:218317758
|
G | A | 131 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.237-22025G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218317758 | ||||||
| chr2:218317768
|
T | C | 256 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(253): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.237-22015T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218317768 | ||||||
| chr2:218317913
|
C | T | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.237-21870C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218317913 | ||||||
| chr2:218317987
|
C | T | 3 | a0001c0001t0002g0189a0001c0001t0002g0203a0001c0001t0002g0204 | 3 | HG02615.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.237-21796C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218317987 | ||||||
| chr2:218317988
|
G | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-21795G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218317988 | ||||||
| chr2:218318025
|
T | C | 164 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(161): Show | 165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.237-21758T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218318025 | ||||||
| chr2:218318330
|
GC | G | 142 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(139): Show | 143 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.237-21452delC | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218318330 | ||||||
| chr2:218318370
|
C | T | 1 | a0001c0001t0003g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.237-21413C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218318370 | ||||||
| chr2:218318465
|
A | G | 1 | a0001c0001t0019g0139 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.237-21318A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218318465 | ||||||
| chr2:218318949
|
T | C | 2 | a0001c0001t0003g0016a0001c0001t0010g0001 | 3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.237-20834T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218318949 | ||||||
| chr2:218318950
|
C | CTT | 75 | a0001c0001t0001g0084a0001c0001t0001g0164a0001c0001t0001g0191others(72): Show | 75 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.237-20812_237-2081 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218318950 | |||||
| chr2:218318950
|
C | CTTT | 10 | a0001c0001t0001g0211a0001c0001t0001g0235a0001c0001t0002g0170others(7): Show | 10 | HG01175.hp2 HG03927.hp1 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-20813_237-2081 others(7): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218318950 | |||||
| chr2:218318950
|
C | T | 4 | a0001c0001t0003g0016a0001c0001t0004g0163a0001c0001t0006g0165others(1): Show | 5 | HG02717.hp2 HG02809.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-20833C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218318950 | ||||||
| chr2:218318950
|
CTTTTTTT others(6): Show |
C | 6 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(3): Show | 6 | HG01884.hp1 HG02572.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-20823_237-2081 others(17): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218318950 | |||||
| chr2:218318952
|
T | TTC | 13 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0049others(10): Show | 13 | HG02486.hp2 HG02630.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.237-20830_237-2082 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218318952 | |||||
| chr2:218318955
|
T | C | 2 | a0001c0001t0003g0016a0001c0001t0010g0001 | 3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.237-20828T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218318955 | ||||||
| chr2:218318955
|
T | TC | 20 | a0001c0001t0001g0060a0001c0001t0001g0151a0001c0001t0001g0152others(17): Show | 20 | HG01975.hp1 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.237-20828_237-2082 others(5): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218318955 | ||||||
| chr2:218318956
|
T | C | 126 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.237-20827T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218318956 | ||||||
| chr2:218318957
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0013g0097 | 2 | NA18951.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.237-20826T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218318957 | ||||||
| chr2:218319195
|
C | T | 1 | a0001c0001t0019g0139 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.237-20588C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319195 | ||||||
| chr2:218319196
|
G | A | 2 | a0001c0005t0002g0214a0001c0005t0002g0221 | 2 | HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.237-20587G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319196 | ||||||
| chr2:218319197
|
C | A | 2 | a0001c0001t0004g0261a0001c0001t0005g0240 | 2 | HG02080.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.237-20586C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319197 | ||||||
| chr2:218319371
|
C | CT | 134 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(131): Show | 135 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.237-20390dupT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218319371 | |||||
| chr2:218319371
|
C | CTT | 5 | a0001c0001t0001g0095a0001c0001t0001g0138a0001c0001t0001g0250others(2): Show | 5 | HG02300.hp2 HG04115.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-20391_237-2039 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218319371 | |||||
| chr2:218319371
|
CT | C | 21 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0255others(18): Show | 21 | HG00099.hp1 HG00099.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.237-20390delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218319371 | |||||
| chr2:218319402
|
G | A | 15 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0002g0185others(12): Show | 15 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.237-20381G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319402 | ||||||
| chr2:218319444
|
C | T | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-20339C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319444 | ||||||
| chr2:218319476
|
A | G | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-20307A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319476 | ||||||
| chr2:218319483
|
C | T | 1 | a0001c0002t0002g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.237-20300C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319483 | ||||||
| chr2:218319541
|
G | A | 256 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(253): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.237-20242G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319541 | ||||||
| chr2:218319552
|
C | T | 165 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(162): Show | 166 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.237-20231C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319552 | ||||||
| chr2:218319565
|
A | G | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-20218A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319565 | ||||||
| chr2:218319578
|
A | G | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-20205A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319578 | ||||||
| chr2:218319664
|
G | A | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-20119G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319664 | ||||||
| chr2:218319675
|
C | T | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-20108C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319675 | ||||||
| chr2:218319682
|
T | A | 15 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0002g0185others(12): Show | 15 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.237-20101T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319682 | ||||||
| chr2:218319707
|
A | C | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-20076A>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319707 | ||||||
| chr2:218319709
|
C | T | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-20074C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319709 | ||||||
| chr2:218319713
|
C | T | 91 | a0001c0001t0001g0084a0001c0001t0001g0164a0001c0001t0001g0191others(88): Show | 91 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.237-20070C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319713 | ||||||
| chr2:218319769
|
A | G | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-20014A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319769 | ||||||
| chr2:218319894
|
G | A | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-19889G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319894 | ||||||
| chr2:218319968
|
A | G | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-19815A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319968 | ||||||
| chr2:218319998
|
T | C | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-19785T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218319998 | ||||||
| chr2:218320033
|
G | A | 13 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0049others(10): Show | 13 | HG02486.hp2 HG02630.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.237-19750G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218320033 | ||||||
| chr2:218320051
|
C | T | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.237-19732C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218320051 | ||||||
| chr2:218320149
|
G | T | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-19634G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218320149 | ||||||
| chr2:218320310
|
G | T | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-19473G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218320310 | ||||||
| chr2:218320313
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.237-19470G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218320313 | ||||||
| chr2:218320438
|
C | T | 90 | a0001c0001t0001g0084a0001c0001t0001g0164a0001c0001t0001g0191others(87): Show | 90 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.237-19345C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218320438 | ||||||
| chr2:218320474
|
G | A | 6 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0001t0001g0071others(3): Show | 6 | HG00323.hp2 HG00642.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-19309G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218320474 | ||||||
| chr2:218320726
|
C | T | 3 | a0001c0001t0003g0016a0001c0001t0010g0001a0002c0003t0011g0236 | 4 | HG02717.hp2 HG02809.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-19057C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218320726 | ||||||
| chr2:218320822
|
A | G | 165 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(162): Show | 166 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.237-18961A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218320822 | ||||||
| chr2:218320857
|
T | C | 11 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0271others(8): Show | 11 | HG02486.hp2 HG02630.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.237-18926T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218320857 | ||||||
| chr2:218320989
|
C | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-18794C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218320989 | ||||||
| chr2:218321023
|
A | T | 1 | a0001c0001t0003g0109 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.237-18760A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218321023 | ||||||
| chr2:218321126
|
G | GCTTGAGC others(1): Show |
150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-18656_237-1864 others(12): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218321126 | |||||
| chr2:218321319
|
C | T | 1 | a0001c0002t0017g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.237-18464C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218321319 | ||||||
| chr2:218321359
|
C | A | 1 | a0002c0003t0011g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.237-18424C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218321359 | ||||||
| chr2:218321374
|
G | A | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.237-18409G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218321374 | ||||||
| chr2:218321411
|
C | A | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.237-18372C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218321411 | ||||||
| chr2:218321623
|
C | CT | 9 | a0001c0001t0001g0075a0001c0001t0001g0096a0001c0001t0001g0125others(6): Show | 9 | HG01192.hp2 HG02074.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-18138dupT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218321623 | |||||
| chr2:218321623
|
CT | C | 100 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0079others(97): Show | 100 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.237-18138delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218321623 | |||||
| chr2:218321623
|
CTT | C | 6 | a0001c0001t0001g0211a0001c0001t0001g0228a0001c0001t0002g0229others(3): Show | 6 | HG01975.hp2 HG02040.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-18139_237-1813 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218321623 | |||||
| chr2:218321659
|
AC | A | 278 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.237-18120delC | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218321659 | |||||
| chr2:218321739
|
T | C | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-18044T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218321739 | ||||||
| chr2:218321816
|
T | C | 255 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.237-17967T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218321816 | ||||||
| chr2:218321869
|
G | A | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.237-17914G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218321869 | ||||||
| chr2:218321916
|
T | A | 7 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-17867T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218321916 | ||||||
| chr2:218321926
|
G | T | 6 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(3): Show | 6 | HG01884.hp1 HG02572.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-17857G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218321926 | ||||||
| chr2:218321934
|
C | CT | 7 | a0001c0001t0001g0228a0001c0001t0001g0235a0001c0001t0001g0255others(4): Show | 7 | HG01069.hp2 HG01175.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-17831dupT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218321934 | |||||
| chr2:218321934
|
C | CTT | 81 | a0001c0001t0001g0084a0001c0001t0001g0164a0001c0001t0001g0191others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.237-17832_237-1783 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218321934 | |||||
| chr2:218321934
|
CTT | C | 11 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0041others(8): Show | 11 | HG02630.hp2 HG02818.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.237-17832_237-1783 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218321934 | |||||
| chr2:218321934
|
CTTTT | C | 146 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(143): Show | 147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.237-17834_237-1783 others(8): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218321934 | |||||
| chr2:218322476
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237-17307G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218322476 | ||||||
| chr2:218322540
|
C | A | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.237-17243C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218322540 | ||||||
| chr2:218322546
|
C | G | 1 | a0001c0002t0002g0023 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.237-17237C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218322546 | ||||||
| chr2:218322644
|
T | C | 110 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(107): Show | 111 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.237-17139T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218322644 | ||||||
| chr2:218322693
|
T | C | 1 | a0001c0002t0002g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.237-17090T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218322693 | ||||||
| chr2:218322880
|
C | A | 153 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(150): Show | 154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.237-16903C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218322880 | ||||||
| chr2:218322954
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.237-16829G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218322954 | ||||||
| chr2:218322975
|
G | A | 163 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(160): Show | 164 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.237-16808G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218322975 | ||||||
| chr2:218323015
|
G | A | 1 | a0001c0001t0007g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.237-16768G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323015 | ||||||
| chr2:218323017
|
C | T | 148 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(145): Show | 149 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.237-16766C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323017 | ||||||
| chr2:218323024
|
T | C | 1 | a0001c0001t0004g0194 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.237-16759T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323024 | ||||||
| chr2:218323048
|
C | CGG | 277 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(274): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.237-16733_237-1673 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218323048 | |||||
| chr2:218323112
|
T | C | 15 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0002g0185others(12): Show | 15 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.237-16671T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323112 | ||||||
| chr2:218323169
|
C | G | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.237-16614C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323169 | ||||||
| chr2:218323178
|
C | T | 108 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.237-16605C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323178 | ||||||
| chr2:218323409
|
C | T | 1 | a0001c0002t0002g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.237-16374C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323409 | ||||||
| chr2:218323514
|
G | A | 55 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(52): Show | 56 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(53): Show |
intron_variant | MODIFIER | c.237-16269G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323514 | ||||||
| chr2:218323545
|
G | A | 1 | a0001c0001t0005g0253 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.237-16238G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323545 | ||||||
| chr2:218323553
|
G | A | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.237-16230G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323553 | ||||||
| chr2:218323693
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.237-16090G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323693 | ||||||
| chr2:218323705
|
C | A | 55 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(52): Show | 56 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(53): Show |
intron_variant | MODIFIER | c.237-16078C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323705 | ||||||
| chr2:218323720
|
T | G | 55 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(52): Show | 56 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(53): Show |
intron_variant | MODIFIER | c.237-16063T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323720 | ||||||
| chr2:218323744
|
C | T | 55 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(52): Show | 56 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(53): Show |
intron_variant | MODIFIER | c.237-16039C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323744 | ||||||
| chr2:218323854
|
C | T | 109 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(106): Show | 109 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.237-15929C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323854 | ||||||
| chr2:218323946
|
T | C | 55 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(52): Show | 56 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(53): Show |
intron_variant | MODIFIER | c.237-15837T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218323946 | ||||||
| chr2:218324089
|
C | G | 1 | a0001c0001t0004g0200 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.237-15694C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218324089 | ||||||
| chr2:218324115
|
C | T | 108 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.237-15668C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218324115 | ||||||
| chr2:218324165
|
G | GCA | 91 | a0001c0001t0001g0084a0001c0001t0001g0164a0001c0001t0001g0191others(88): Show | 91 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.237-15616_237-1561 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218324165 | |||||
| chr2:218324589
|
T | A | 11 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0002g0185others(8): Show | 12 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-15194T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218324589 | ||||||
| chr2:218324634
|
T | C | 9 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0002g0185others(6): Show | 9 | HG01884.hp2 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-15149T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218324634 | ||||||
| chr2:218324687
|
C | T | 56 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(53): Show | 57 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(54): Show |
intron_variant | MODIFIER | c.237-15096C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218324687 | ||||||
| chr2:218324729
|
A | G | 56 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(53): Show | 57 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(54): Show |
intron_variant | MODIFIER | c.237-15054A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218324729 | ||||||
| chr2:218324899
|
G | T | 1 | a0001c0001t0003g0144 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.237-14884G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218324899 | ||||||
| chr2:218324930
|
C | T | 56 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(53): Show | 57 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(54): Show |
intron_variant | MODIFIER | c.237-14853C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218324930 | ||||||
| chr2:218324931
|
G | A | 91 | a0001c0001t0001g0084a0001c0001t0001g0164a0001c0001t0001g0191others(88): Show | 91 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.237-14852G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218324931 | ||||||
| chr2:218324943
|
A | C | 1 | a0001c0001t0001g0232 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.237-14840A>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218324943 | ||||||
| chr2:218324957
|
G | GA | 37 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(34): Show | 38 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.237-14817dupA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218324957 | |||||
| chr2:218324965
|
A | AAG | 19 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0049others(16): Show | 19 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.237-14817_237-1481 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218324965 | |||||
| chr2:218324997
|
C | CT | 50 | a0001c0001t0001g0084a0001c0001t0001g0164a0001c0001t0001g0201others(47): Show | 50 | HG00609.hp1 HG00735.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.237-14758dupT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218324997 | |||||
| chr2:218324997
|
C | CTT | 5 | a0001c0001t0001g0202a0001c0001t0002g0193a0001c0001t0003g0046others(2): Show | 5 | HG01346.hp1 HG02074.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-14759_237-1475 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218324997 | |||||
| chr2:218324997
|
C | CTTTT | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0158others(2): Show | 5 | HG01975.hp1 HG02280.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-14761_237-1475 others(8): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218324997 | |||||
| chr2:218324997
|
CTTTTTT | C | 12 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0076others(9): Show | 12 | HG01109.hp2 HG01175.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-14763_237-1475 others(10): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218324997 | |||||
| chr2:218324997
|
CTTTTTTT | C | 94 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(91): Show | 94 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.237-14764_237-1475 others(11): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218324997 | |||||
| chr2:218324997
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-14768_237-1475 others(15): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218324997 | |||||
| chr2:218324997
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.237-14775_237-1475 others(22): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218324997 | |||||
| chr2:218324997
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0010g0001 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.237-14776_237-1475 others(23): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218324997 | |||||
| chr2:218325026
|
G | A | 90 | a0001c0001t0001g0084a0001c0001t0001g0164a0001c0001t0001g0191others(87): Show | 90 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.237-14757G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218325026 | ||||||
| chr2:218325198
|
C | CT | 28 | a0001c0001t0001g0054a0001c0001t0001g0150a0001c0001t0001g0152others(25): Show | 28 | HG01243.hp1 HG02109.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.237-14561dupT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218325198 | |||||
| chr2:218325198
|
C | CTT | 123 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0044others(120): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.237-14562_237-1456 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218325198 | |||||
| chr2:218325198
|
C | CTTT | 80 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0043others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.237-14563_237-1456 others(7): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218325198 | |||||
| chr2:218325198
|
C | CTTTT | 20 | a0001c0001t0001g0061a0001c0001t0001g0095a0001c0001t0001g0164others(17): Show | 20 | HG02080.hp2 HG02300.hp1 HG02300.hp2 others(17): Show |
intron_variant | MODIFIER | c.237-14564_237-1456 others(8): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218325198 | |||||
| chr2:218325198
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.237-14576_237-1456 others(20): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218325198 | |||||
| chr2:218325198
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0003g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.237-14581_237-1456 others(25): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218325198 | |||||
| chr2:218325228
|
G | A | 1 | a0001c0001t0003g0041 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.237-14555G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218325228 | ||||||
| chr2:218325291
|
T | C | 7 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-14492T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218325291 | ||||||
| chr2:218325343
|
G | A | 9 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0002g0185others(6): Show | 9 | HG01884.hp2 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-14440G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218325343 | ||||||
| chr2:218325554
|
G | A | 5 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0039others(2): Show | 5 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-14229G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218325554 | ||||||
| chr2:218325643
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0110 | 3 | HG01070.hp2 HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.237-14140G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218325643 | ||||||
| chr2:218325733
|
G | A | 50 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(47): Show | 51 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(48): Show |
intron_variant | MODIFIER | c.237-14050G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218325733 | ||||||
| chr2:218325867
|
C | T | 4 | a0001c0001t0005g0124a0001c0001t0005g0218a0001c0001t0015g0120others(1): Show | 4 | HG00642.hp2 HG01109.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-13916C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218325867 | ||||||
| chr2:218325892
|
C | T | 17 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0265others(14): Show | 17 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-13891C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218325892 | ||||||
| chr2:218325893
|
G | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0025 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.237-13890G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218325893 | ||||||
| chr2:218325897
|
G | A | 31 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0002g0185others(28): Show | 32 | HG01243.hp1 HG01884.hp2 HG02486.hp2 others(29): Show |
intron_variant | MODIFIER | c.237-13886G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218325897 | ||||||
| chr2:218325990
|
A | G | 57 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(54): Show | 58 | HG00099.hp2 HG01109.hp1 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.237-13793A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218325990 | ||||||
| chr2:218326014
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.237-13769G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218326014 | ||||||
| chr2:218326134
|
G | T | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.237-13649G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218326134 | ||||||
| chr2:218326302
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.237-13481C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218326302 | ||||||
| chr2:218326533
|
T | C | 91 | a0001c0001t0001g0084a0001c0001t0001g0164a0001c0001t0001g0191others(88): Show | 91 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.237-13250T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218326533 | ||||||
| chr2:218326846
|
G | A | 90 | a0001c0001t0001g0084a0001c0001t0001g0164a0001c0001t0001g0191others(87): Show | 90 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.237-12937G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218326846 | ||||||
| chr2:218327247
|
C | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | NA18951.hp1 NA18967.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.237-12536C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218327247 | ||||||
| chr2:218327258
|
C | T | 2 | a0001c0002t0002g0067a0001c0002t0017g0066 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.237-12525C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218327258 | ||||||
| chr2:218327261
|
A | T | 1 | a0001c0001t0001g0020 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.237-12522A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218327261 | ||||||
| chr2:218327382
|
G | A | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.237-12401G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218327382 | ||||||
| chr2:218327463
|
G | A | 7 | a0001c0001t0002g0009a0001c0001t0005g0003a0001c0001t0005g0004others(4): Show | 7 | HG01884.hp1 HG02572.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-12320G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218327463 | ||||||
| chr2:218327840
|
C | T | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0002g0185others(3): Show | 6 | HG02723.hp2 HG02886.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-11943C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218327840 | ||||||
| chr2:218327872
|
G | T | 1 | a0001c0001t0008g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.237-11911G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218327872 | ||||||
| chr2:218327962
|
G | GA | 10 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.237-11804dupA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218327962 | |||||
| chr2:218327962
|
G | GAA | 5 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0260others(2): Show | 6 | HG02717.hp2 HG02809.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-11805_237-1180 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218327962 | |||||
| chr2:218327962
|
G | GAAA | 19 | a0001c0001t0001g0231a0001c0001t0002g0185a0001c0001t0002g0274others(16): Show | 19 | HG00099.hp2 HG01109.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.237-11806_237-1180 others(7): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218327962 | |||||
| chr2:218327962
|
G | GAAAA | 41 | a0001c0001t0001g0150a0001c0001t0002g0009a0001c0001t0003g0021others(38): Show | 41 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.237-11807_237-1180 others(8): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218327962 | |||||
| chr2:218327962
|
G | GAAAAA | 87 | a0001c0001t0001g0084a0001c0001t0001g0164a0001c0001t0001g0191others(84): Show | 87 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.237-11808_237-1180 others(9): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218327962 | |||||
| chr2:218327962
|
GAAA | G | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 107 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.237-11806_237-1180 others(7): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218327962 | |||||
| chr2:218328032
|
G | A | 155 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.237-11751G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218328032 | ||||||
| chr2:218328118
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0003g0016 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.237-11665C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218328118 | ||||||
| chr2:218328502
|
A | G | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.237-11281A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218328502 | ||||||
| chr2:218328774
|
C | T | 3 | a0001c0001t0003g0046a0001c0001t0009g0149a0001c0001t0018g0277 | 3 | HG02572.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.237-11009C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218328774 | ||||||
| chr2:218328804
|
T | G | 1 | a0001c0001t0001g0135 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.237-10979T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218328804 | ||||||
| chr2:218328850
|
G | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237-10933G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218328850 | ||||||
| chr2:218328902
|
C | CTG | 122 | a0001c0001t0001g0084a0001c0001t0001g0191a0001c0001t0001g0196others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.237-10880_237-1087 others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218328902 | |||||
| chr2:218329101
|
CA | C | 9 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0002g0185others(6): Show | 9 | HG01884.hp2 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-10681delA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218329101 | ||||||
| chr2:218329135
|
G | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0110 | 3 | HG01070.hp2 HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.237-10648G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218329135 | ||||||
| chr2:218329240
|
C | T | 118 | a0001c0001t0001g0084a0001c0001t0001g0209a0001c0001t0001g0211others(115): Show | 119 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.237-10543C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218329240 | ||||||
| chr2:218329323
|
G | A | 1 | a0001c0001t0009g0149 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.237-10460G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218329323 | ||||||
| chr2:218329330
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.237-10453G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218329330 | ||||||
| chr2:218329415
|
C | A | 1 | a0001c0001t0001g0255 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.237-10368C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218329415 | ||||||
| chr2:218329471
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.237-10312C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218329471 | ||||||
| chr2:218329513
|
T | C | 2 | a0001c0001t0003g0016a0001c0001t0010g0001 | 3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.237-10270T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218329513 | ||||||
| chr2:218329692
|
T | C | 275 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.237-10091T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218329692 | ||||||
| chr2:218329712
|
C | T | 1 | a0001c0001t0003g0187 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.237-10071C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218329712 | ||||||
| chr2:218329734
|
C | T | 1 | a0001c0001t0002g0173 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.237-10049C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218329734 | ||||||
| chr2:218330026
|
A | AG | 278 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.237-9755dupG | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218330026 | |||||
| chr2:218330047
|
G | C | 1 | a0001c0001t0003g0041 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.237-9736G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218330047 | ||||||
| chr2:218330049
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.237-9734C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218330049 | ||||||
| chr2:218330178
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.237-9605G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218330178 | ||||||
| chr2:218330241
|
G | A | 1 | a0001c0002t0002g0032 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.237-9542G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218330241 | ||||||
| chr2:218330414
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.237-9369A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218330414 | ||||||
| chr2:218330449
|
G | T | 4 | a0001c0001t0001g0064a0001c0001t0001g0074a0001c0001t0001g0100others(1): Show | 4 | HG02080.hp1 HG02132.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-9334G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218330449 | ||||||
| chr2:218330685
|
A | G | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0260others(1): Show | 4 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-9098A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218330685 | ||||||
| chr2:218330987
|
A | G | 11 | a0001c0001t0002g0009a0001c0001t0005g0003a0001c0001t0005g0004others(8): Show | 11 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.237-8796A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218330987 | ||||||
| chr2:218331076
|
G | A | 121 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.237-8707G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218331076 | ||||||
| chr2:218331156
|
T | A | 15 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(12): Show | 15 | HG01109.hp1 HG01975.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-8627T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218331156 | ||||||
| chr2:218331339
|
G | A | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.237-8444G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218331339 | ||||||
| chr2:218331364
|
G | C | 9 | a0001c0001t0001g0150a0001c0001t0003g0142a0001c0001t0003g0143others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-8419G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218331364 | ||||||
| chr2:218331523
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.237-8260C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218331523 | ||||||
| chr2:218331528
|
T | A | 1 | a0001c0001t0003g0222 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.237-8255T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218331528 | ||||||
| chr2:218331572
|
G | A | 9 | a0001c0001t0003g0083a0001c0001t0003g0088a0001c0001t0003g0089others(6): Show | 9 | HG02132.hp2 HG02165.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-8211G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218331572 | ||||||
| chr2:218331621
|
T | C | 154 | a0001c0001t0001g0084a0001c0001t0001g0151a0001c0001t0001g0152others(151): Show | 155 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.237-8162T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218331621 | ||||||
| chr2:218331628
|
C | T | 16 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0265others(13): Show | 16 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.237-8155C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218331628 | ||||||
| chr2:218331654
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG03239.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.237-8129G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218331654 | ||||||
| chr2:218331654
|
G | T | 1 | a0001c0001t0002g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.237-8129G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218331654 | ||||||
| chr2:218331757
|
C | A | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.237-8026C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218331757 | ||||||
| chr2:218332077
|
A | G | 10 | a0001c0001t0003g0046a0001c0001t0009g0149a0001c0001t0018g0277others(7): Show | 10 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-7706A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218332077 | ||||||
| chr2:218332125
|
A | G | 1 | a0001c0001t0003g0041 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.237-7658A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218332125 | ||||||
| chr2:218332128
|
T | C | 275 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.237-7655T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218332128 | ||||||
| chr2:218332145
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0113 | 2 | HG00280.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.237-7638G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218332145 | ||||||
| chr2:218332168
|
G | T | 1 | a0001c0002t0002g0131 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.237-7615G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218332168 | ||||||
| chr2:218332250
|
C | T | 7 | a0001c0001t0003g0083a0001c0001t0003g0088a0001c0001t0003g0089others(4): Show | 7 | HG02132.hp2 HG02165.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-7533C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218332250 | ||||||
| chr2:218332479
|
C | A | 1 | a0001c0002t0002g0227 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.237-7304C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218332479 | ||||||
| chr2:218333069
|
T | C | 7 | a0001c0001t0001g0132a0001c0001t0003g0083a0001c0001t0003g0088others(4): Show | 7 | HG02132.hp2 HG02165.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-6714T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333069 | ||||||
| chr2:218333177
|
T | G | 1 | a0001c0001t0003g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.237-6606T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333177 | ||||||
| chr2:218333273
|
C | T | 1 | a0001c0001t0005g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.237-6510C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333273 | ||||||
| chr2:218333281
|
A | G | 1 | a0001c0001t0003g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.237-6502A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333281 | ||||||
| chr2:218333282
|
A | G | 4 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(1): Show | 4 | HG01243.hp1 HG02559.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-6501A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333282 | ||||||
| chr2:218333302
|
C | T | 91 | a0001c0001t0001g0078a0001c0001t0001g0084a0001c0001t0001g0092others(88): Show | 91 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.237-6481C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333302 | ||||||
| chr2:218333396
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0063 | 2 | HG01243.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.237-6387G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333396 | ||||||
| chr2:218333414
|
C | T | 5 | a0001c0001t0002g0189a0001c0001t0002g0203a0001c0001t0002g0204others(2): Show | 5 | HG02615.hp2 HG02922.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-6369C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333414 | ||||||
| chr2:218333429
|
C | A | 1 | a0001c0001t0003g0041 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.237-6354C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333429 | ||||||
| chr2:218333700
|
A | T | 83 | a0001c0001t0001g0078a0001c0001t0002g0009a0001c0001t0002g0011others(80): Show | 83 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.237-6083A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333700 | ||||||
| chr2:218333848
|
C | T | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.237-5935C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333848 | ||||||
| chr2:218333886
|
G | A | 4 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(1): Show | 4 | HG01243.hp1 HG02559.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-5897G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333886 | ||||||
| chr2:218333917
|
C | A | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.237-5866C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333917 | ||||||
| chr2:218333922
|
T | C | 87 | a0001c0001t0001g0078a0001c0001t0002g0009a0001c0001t0002g0011others(84): Show | 87 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.237-5861T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333922 | ||||||
| chr2:218333960
|
C | CAAAAATT others(316): Show |
81 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0167others(78): Show | 81 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.237-5813_237-5812i others(325): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218333960 | |||||
| chr2:218333960
|
C | CAAAAATT others(317): Show |
8 | a0001c0001t0001g0078a0001c0001t0002g0180a0001c0001t0002g0216others(5): Show | 8 | HG00621.hp1 HG01099.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.237-5813_237-5812i others(326): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218333960 | |||||
| chr2:218333971
|
C | T | 89 | a0001c0001t0001g0078a0001c0001t0002g0009a0001c0001t0002g0011others(86): Show | 89 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.237-5812C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333971 | ||||||
| chr2:218333977
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.237-5806T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218333977 | ||||||
| chr2:218334092
|
A | G | 273 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.237-5691A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218334092 | ||||||
| chr2:218334281
|
T | C | 224 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(221): Show | 224 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.237-5502T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218334281 | ||||||
| chr2:218334281
|
T | G | 5 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(2): Show | 5 | HG01884.hp1 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-5502T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218334281 | ||||||
| chr2:218334345
|
A | G | 204 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(201): Show | 204 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.237-5438A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218334345 | ||||||
| chr2:218334499
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.237-5284A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218334499 | ||||||
| chr2:218334771
|
T | G | 1 | a0001c0001t0001g0051 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.237-5012T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218334771 | ||||||
| chr2:218334812
|
C | T | 3 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0008t0003g0008 | 3 | HG02572.hp2 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.237-4971C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218334812 | ||||||
| chr2:218334927
|
T | C | 1 | a0001c0001t0005g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.237-4856T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218334927 | ||||||
| chr2:218335036
|
C | G | 3 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0008t0003g0008 | 3 | HG02572.hp2 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.237-4747C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218335036 | ||||||
| chr2:218335153
|
T | A | 12 | a0001c0001t0003g0021a0001c0001t0003g0041a0001c0001t0003g0115others(9): Show | 12 | HG01943.hp1 HG02257.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.237-4630T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218335153 | ||||||
| chr2:218335156
|
A | AAAAT | 7 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0039others(4): Show | 7 | HG00099.hp2 HG00642.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-4605_237-4602d others(6): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218335156 | |||||
| chr2:218335358
|
G | A | 3 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0008t0003g0008 | 3 | HG02572.hp2 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.237-4425G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218335358 | ||||||
| chr2:218335609
|
G | GAAATGA | 273 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.237-4169_237-4168i others(8): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218335609 | |||||
| chr2:218335667
|
C | T | 47 | a0001c0001t0001g0084a0001c0001t0003g0021a0001c0001t0003g0024others(44): Show | 47 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.237-4116C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218335667 | ||||||
| chr2:218335859
|
C | G | 3 | a0001c0001t0003g0115a0001c0001t0003g0128a0001c0001t0003g0187 | 3 | HG01943.hp1 HG02300.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.237-3924C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218335859 | ||||||
| chr2:218336040
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.237-3743C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218336040 | ||||||
| chr2:218336043
|
T | A | 1 | a0001c0001t0003g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.237-3740T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218336043 | ||||||
| chr2:218336170
|
G | A | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0142others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-3613G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218336170 | ||||||
| chr2:218336213
|
C | CAAAAA | 101 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(98): Show | 102 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(99): Show |
intron_variant | MODIFIER | c.237-3559_237-3555d others(7): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218336213 | |||||
| chr2:218336213
|
C | CAAAAAA | 123 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.237-3560_237-3555d others(8): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218336213 | |||||
| chr2:218336213
|
C | CAAAAAAA | 41 | a0001c0001t0001g0084a0001c0001t0002g0178a0001c0001t0002g0219others(38): Show | 41 | HG00099.hp1 HG00609.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.237-3561_237-3555d others(9): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218336213 | |||||
| chr2:218336299
|
C | T | 1 | a0001c0001t0004g0233 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.237-3484C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218336299 | ||||||
| chr2:218336432
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.237-3351G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218336432 | ||||||
| chr2:218336470
|
T | A | 21 | a0001c0001t0001g0078a0001c0001t0005g0003a0001c0001t0005g0004others(18): Show | 21 | HG00621.hp1 HG01109.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.237-3313T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218336470 | ||||||
| chr2:218336496
|
T | C | 3 | a0002c0003t0011g0146a0002c0003t0011g0155a0002c0003t0011g0236 | 3 | HG02280.hp2 HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.237-3287T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218336496 | ||||||
| chr2:218336615
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.237-3168G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218336615 | ||||||
| chr2:218336631
|
C | A | 1 | a0001c0001t0005g0248 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.237-3152C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218336631 | ||||||
| chr2:218336678
|
G | A | 1 | a0001c0001t0005g0253 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.237-3105G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218336678 | ||||||
| chr2:218336788
|
CT | C | 207 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.237-2970delT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218336788 | |||||
| chr2:218336788
|
CTT | C | 26 | a0001c0001t0001g0054a0001c0001t0002g0229a0001c0001t0003g0016others(23): Show | 27 | HG01243.hp1 HG01891.hp2 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.237-2971_237-2970d others(4): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218336788 | |||||
| chr2:218336788
|
CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0002g0011a0001c0001t0002g0185a0001c0001t0002g0225others(2): Show | 5 | HG01257.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-2981_237-2970d others(14): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218336788 | |||||
| chr2:218336831
|
T | A | 5 | a0001c0001t0001g0068a0001c0001t0001g0096a0001c0001t0001g0099others(2): Show | 5 | HG02074.hp2 NA18948.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-2952T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218336831 | ||||||
| chr2:218336944
|
C | T | 72 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0167others(69): Show | 72 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.237-2839C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218336944 | ||||||
| chr2:218337219
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.237-2564C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218337219 | ||||||
| chr2:218337387
|
C | T | 3 | a0002c0003t0011g0146a0002c0003t0011g0155a0002c0003t0011g0236 | 3 | HG02280.hp2 HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.237-2396C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218337387 | ||||||
| chr2:218337409
|
T | C | 12 | a0001c0001t0003g0021a0001c0001t0003g0041a0001c0001t0003g0115others(9): Show | 12 | HG01943.hp1 HG02257.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.237-2374T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218337409 | ||||||
| chr2:218337549
|
T | G | 10 | a0001c0001t0003g0080a0001c0001t0003g0083a0001c0001t0003g0088others(7): Show | 10 | HG02132.hp2 HG02165.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.237-2234T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218337549 | ||||||
| chr2:218337596
|
C | G | 1 | a0001c0001t0003g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.237-2187C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218337596 | ||||||
| chr2:218337661
|
C | T | 4 | a0001c0001t0003g0016a0001c0001t0003g0197a0001c0001t0003g0222others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-2122C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218337661 | ||||||
| chr2:218337761
|
G | A | 52 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0167others(49): Show | 52 | HG00323.hp1 HG00735.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.237-2022G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218337761 | ||||||
| chr2:218337891
|
G | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0138a0003c0009t0001g0042 | 3 | HG02300.hp2 NA18955.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.237-1892G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218337891 | ||||||
| chr2:218337901
|
C | T | 71 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0167others(68): Show | 71 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.237-1882C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218337901 | ||||||
| chr2:218337931
|
G | A | 10 | a0001c0001t0003g0080a0001c0001t0003g0083a0001c0001t0003g0088others(7): Show | 10 | HG02132.hp2 HG02165.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.237-1852G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218337931 | ||||||
| chr2:218338003
|
T | C | 3 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276 | 3 | HG01884.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.237-1780T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338003 | ||||||
| chr2:218338005
|
G | A | 1 | a0001c0001t0004g0168 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.237-1778G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338005 | ||||||
| chr2:218338020
|
G | A | 45 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0049others(42): Show | 45 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.237-1763G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338020 | ||||||
| chr2:218338034
|
CTACTCAG others(127): Show |
C | 1 | a0001c0001t0003g0088 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.237-1747_237-1614d others(2): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218338034 | |||||
| chr2:218338177
|
T | G | 1 | a0001c0001t0003g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.237-1606T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338177 | ||||||
| chr2:218338214
|
A | G | 3 | a0002c0003t0011g0146a0002c0003t0011g0155a0002c0003t0011g0236 | 3 | HG02280.hp2 HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.237-1569A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338214 | ||||||
| chr2:218338226
|
C | CGAGGCAG others(11): Show |
3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | NA18951.hp1 NA18967.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.237-1556_237-1539d others(20): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218338226 | |||||
| chr2:218338314
|
T | C | 1 | a0001c0001t0002g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.237-1469T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338314 | ||||||
| chr2:218338355
|
G | T | 49 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0167others(46): Show | 49 | HG00323.hp1 HG00735.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.237-1428G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338355 | ||||||
| chr2:218338460
|
C | CA | 87 | a0001c0001t0001g0095a0001c0001t0001g0132a0001c0001t0002g0009others(84): Show | 87 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.237-1307dupA | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218338460 | |||||
| chr2:218338460
|
C | CAA | 9 | a0001c0001t0002g0011a0001c0001t0002g0172a0001c0001t0003g0046others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-1308_237-1307d others(4): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218338460 | |||||
| chr2:218338516
|
T | C | 92 | a0001c0001t0001g0078a0001c0001t0003g0016a0001c0001t0003g0021others(89): Show | 93 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.237-1267T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338516 | ||||||
| chr2:218338565
|
G | A | 1 | a0001c0008t0003g0008 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.237-1218G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338565 | ||||||
| chr2:218338732
|
C | T | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.237-1051C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338732 | ||||||
| chr2:218338791
|
A | AT | 139 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0043others(136): Show | 140 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.237-973dupT | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218338791 | |||||
| chr2:218338791
|
A | ATT | 47 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0045others(44): Show | 47 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.237-974_237-973dup others(2): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218338791 | |||||
| chr2:218338791
|
A | ATTT | 9 | a0001c0001t0001g0095a0001c0001t0001g0156a0001c0001t0003g0266others(6): Show | 9 | HG00621.hp2 HG01433.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-975_237-973dup others(3): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 218338791 | |||||
| chr2:218338880
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.237-903C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338880 | ||||||
| chr2:218338881
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.237-902C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338881 | ||||||
| chr2:218338908
|
T | C | 21 | a0001c0001t0001g0078a0001c0001t0005g0003a0001c0001t0005g0004others(18): Show | 21 | HG00621.hp1 HG01109.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.237-875T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338908 | ||||||
| chr2:218338950
|
G | A | 10 | a0001c0001t0003g0080a0001c0001t0003g0083a0001c0001t0003g0088others(7): Show | 10 | HG02132.hp2 HG02165.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.237-833G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338950 | ||||||
| chr2:218338968
|
T | G | 9 | a0001c0001t0003g0115a0001c0001t0003g0128a0001c0001t0003g0187others(6): Show | 9 | HG01943.hp1 HG02300.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-815T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218338968 | ||||||
| chr2:218339066
|
G | C | 1 | a0001c0001t0007g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.237-717G>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218339066 | ||||||
| chr2:218339190
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.237-593C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218339190 | ||||||
| chr2:218339296
|
T | G | 6 | a0001c0001t0003g0016a0001c0001t0003g0197a0001c0001t0003g0222others(3): Show | 7 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-487T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218339296 | ||||||
| chr2:218339564
|
C | T | 3 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0008t0003g0008 | 3 | HG02572.hp2 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.237-219C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218339564 | ||||||
| chr2:218339752
|
G | T | 6 | a0001c0001t0003g0016a0001c0001t0003g0197a0001c0001t0003g0222others(3): Show | 7 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-31G>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 2/9 | chr2 | 218339752 | ||||||
| chr2:218339958
|
C | T | 1 | a0001c0001t0019g0139 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.352+60C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 3/9 | chr2 | 218339958 | ||||||
| chr2:218339999
|
A | AC | 6 | a0001c0001t0001g0072a0001c0001t0001g0235a0001c0001t0002g0216others(3): Show | 6 | HG01099.hp1 HG01175.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.353-26dupC | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 218339999 | |||||
| chr2:218340005
|
C | T | 24 | a0001c0001t0001g0084a0001c0001t0004g0022a0001c0001t0004g0117others(21): Show | 24 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.353-24C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 3/9 | chr2 | 218340005 | ||||||
| chr2:218340202
|
C | T | 4 | a0001c0001t0003g0080a0001c0001t0003g0109a0001c0001t0003g0278others(1): Show | 4 | NA18971.hp2 NA18972.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+61C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 4/9 | chr2 | 218340202 | ||||||
| chr2:218340341
|
T | A | 1 | a0001c0001t0001g0099 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.465+200T>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 4/9 | chr2 | 218340341 | ||||||
| chr2:218340717
|
C | T | 1 | a0001c0001t0007g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.466-11C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 4/9 | chr2 | 218340717 | ||||||
| chr2:218340859
|
G | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0025 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.524+73G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 5/9 | chr2 | 218340859 | ||||||
| chr2:218340888
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.524+102C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 5/9 | chr2 | 218340888 | ||||||
| chr2:218340894
|
G | A | 6 | a0001c0001t0003g0016a0001c0001t0003g0197a0001c0001t0003g0222others(3): Show | 7 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.524+108G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 5/9 | chr2 | 218340894 | ||||||
| chr2:218340906
|
C | T | 6 | a0001c0001t0003g0016a0001c0001t0003g0197a0001c0001t0003g0222others(3): Show | 7 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.524+120C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 5/9 | chr2 | 218340906 | ||||||
| chr2:218341044
|
A | G | 2 | a0001c0001t0002g0170a0001c0001t0002g0176 | 2 | NA18964.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.524+258A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 5/9 | chr2 | 218341044 | ||||||
| chr2:218341228
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.525-306C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 5/9 | chr2 | 218341228 | ||||||
| chr2:218341231
|
T | C | 22 | a0001c0001t0003g0021a0001c0001t0003g0041a0001c0001t0003g0046others(19): Show | 22 | HG01243.hp1 HG01891.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.525-303T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 5/9 | chr2 | 218341231 | ||||||
| chr2:218341341
|
G | A | 7 | a0001c0001t0003g0143a0001c0001t0003g0144a0001c0001t0003g0145others(4): Show | 7 | HG02257.hp2 HG02965.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.525-193G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 5/9 | chr2 | 218341341 | ||||||
| chr2:218341414
|
C | T | 3 | a0002c0003t0011g0146a0002c0003t0011g0155a0002c0003t0011g0236 | 3 | HG02280.hp2 HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.525-120C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 5/9 | chr2 | 218341414 | ||||||
| chr2:218341427
|
A | T | 4 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0116others(1): Show | 4 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-107A>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 5/9 | chr2 | 218341427 | ||||||
| chr2:218341712
|
C | G | 20 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(17): Show | 20 | HG01109.hp2 HG01261.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.617+86C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 6/9 | chr2 | 218341712 | ||||||
| chr2:218341763
|
G | A | 6 | a0001c0001t0003g0083a0001c0001t0003g0088a0001c0001t0003g0089others(3): Show | 6 | HG02132.hp2 HG02165.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.617+137G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 6/9 | chr2 | 218341763 | ||||||
| chr2:218341769
|
T | C | 4 | a0001c0001t0008g0048a0001c0001t0008g0129a0002c0003t0011g0146others(1): Show | 4 | HG02280.hp2 HG02717.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+143T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 6/9 | chr2 | 218341769 | ||||||
| chr2:218341843
|
C | T | 6 | a0001c0001t0003g0083a0001c0001t0003g0088a0001c0001t0003g0089others(3): Show | 6 | HG02132.hp2 HG02165.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.618-138C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 6/9 | chr2 | 218341843 | ||||||
| chr2:218341922
|
A | G | 20 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(17): Show | 20 | HG01109.hp2 HG01261.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.618-59A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 6/9 | chr2 | 218341922 | ||||||
| chr2:218341923
|
C | T | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0142others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-58C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 6/9 | chr2 | 218341923 | ||||||
| chr2:218342156
|
C | G | 1 | a0001c0001t0003g0279 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.781+12C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218342156 | ||||||
| chr2:218342196
|
C | T | 110 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.781+52C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218342196 | ||||||
| chr2:218342208
|
C | A | 1 | a0001c0001t0012g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.781+64C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218342208 | ||||||
| chr2:218342231
|
C | T | 3 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0008t0003g0008 | 3 | HG02572.hp2 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.781+87C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218342231 | ||||||
| chr2:218342256
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.781+112G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218342256 | ||||||
| chr2:218342312
|
T | C | 1 | a0001c0001t0009g0149 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.781+168T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218342312 | ||||||
| chr2:218342441
|
T | C | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0142others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+297T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218342441 | ||||||
| chr2:218342529
|
G | A | 6 | a0001c0002t0002g0029a0001c0002t0002g0032a0001c0002t0002g0033others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+385G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218342529 | ||||||
| chr2:218342581
|
T | C | 10 | a0001c0001t0003g0080a0001c0001t0003g0083a0001c0001t0003g0088others(7): Show | 10 | HG02132.hp2 HG02165.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.781+437T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218342581 | ||||||
| chr2:218342741
|
C | G | 5 | a0001c0001t0003g0046a0001c0001t0003g0049a0001c0001t0003g0050others(2): Show | 5 | HG01891.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+597C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218342741 | ||||||
| chr2:218342794
|
T | C | 9 | a0001c0001t0003g0046a0001c0001t0003g0049a0001c0001t0003g0050others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.781+650T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218342794 | ||||||
| chr2:218343125
|
A | AGG | 24 | a0001c0001t0003g0021a0001c0001t0003g0024a0001c0001t0003g0025others(21): Show | 24 | HG01243.hp1 HG01891.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.782-374_782-373ins others(2): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 218343125 | |||||
| chr2:218343127
|
T | G | 273 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.782-373T>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218343127 | ||||||
| chr2:218343131
|
T | C | 1 | a0001c0001t0002g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.782-369T>C | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218343131 | ||||||
| chr2:218343157
|
G | A | 13 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0150others(10): Show | 13 | HG01975.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.782-343G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218343157 | ||||||
| chr2:218343197
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.782-303C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218343197 | ||||||
| chr2:218343218
|
G | A | 1 | a0001c0001t0002g0229 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.782-282G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218343218 | ||||||
| chr2:218343254
|
A | G | 92 | a0001c0001t0001g0084a0001c0001t0003g0016a0001c0001t0003g0021others(89): Show | 93 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.782-246A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218343254 | ||||||
| chr2:218343296
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.782-204C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 7/9 | chr2 | 218343296 | ||||||
| chr2:218343666
|
C | T | 4 | a0001c0001t0003g0016a0001c0001t0003g0197a0001c0001t0003g0222others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.868+80C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 8/9 | chr2 | 218343666 | ||||||
| chr2:218343711
|
C | A | 2 | a0001c0002t0002g0023a0001c0002t0002g0067 | 2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.868+125C>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 8/9 | chr2 | 218343711 | ||||||
| chr2:218343754
|
C | G | 35 | a0001c0001t0003g0021a0001c0001t0003g0024a0001c0001t0003g0025others(32): Show | 35 | HG01243.hp1 HG01891.hp2 HG01943.hp1 others(32): Show |
intron_variant | MODIFIER | c.868+168C>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 8/9 | chr2 | 218343754 | ||||||
| chr2:218343917
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.868+331G>A | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 8/9 | chr2 | 218343917 | ||||||
| chr2:218344004
|
T | TATTC | 5 | a0001c0001t0003g0046a0001c0001t0003g0049a0001c0001t0003g0050others(2): Show | 5 | HG01891.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-432_869-429dup others(4): Show |
PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 218344004 | |||||
| chr2:218344172
|
C | T | 1 | a0001c0002t0002g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.869-283C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 8/9 | chr2 | 218344172 | ||||||
| chr2:218344623
|
C | T | 1 | a0001c0001t0018g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.984+53C>T | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 9/9 | chr2 | 218344623 | ||||||
| chr2:218344670
|
A | G | 274 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.984+100A>G | PNKD | ENSG00000127838.15 | transcript | ENST00000273077.9 | protein_coding | 9/9 | chr2 | 218344670 |