Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 65268 |
|---|---|
| ensemblid | ENSG00000165238.17 |
| hgncid | 14542 |
| symbol | WNK2 |
| name | WNK lysine deficient protein kinase 2 |
| refseq_nuc | NM_006648.4 |
| refseq_prot | NP_006639.3 |
| ensembl_nuc | ENST00000427277.7 |
| ensembl_prot | ENSP00000411181.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 93184139 |
| end | 93320569 |
| strand | + |
| ver | v1.2 |
| region | chr9:93184139-93320569 |
| region5000 | chr9:93179139-93325569 |
| regionname0 | WNK2_chr9_93184139_93320569 |
| regionname5000 | WNK2_chr9_93179139_93325569 |
| 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 | 2217 | 180 | 44 | 35 | 62 | 9 | 28 | 45 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002 | 0/0 | 2217 | 67 | 9 | 19 | 25 | 7 | 7 | 17 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0003 | 0/0 | 2217 | 15 | 0 | 5 | 10 | 0 | 0 | 8 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0004 | 0/0 | 2217 | 13 | 4 | 1 | 8 | 0 | 0 | 6 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0005 | 0/0 | 2205 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0006 | 0/0 | 2217 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0007 | 0/0 | 2217 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0008 | 0/0 | 2217 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0009 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0010 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0011 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0012 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0013 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0014 | 0/0 | 2217 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0015 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0016 | 0/0 | 2205 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0017 | 0/0 | 2205 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0018 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0019 | 0/0 | 2217 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0020 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0021 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0022 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0023 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0024 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0025 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0026 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0027 | 0/0 | 2217 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 6654 | 53 | 7 | 11 | 24 | 6 | 5 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0002 | 0/0 | 6654 | 44 | 8 | 6 | 25 | 1 | 4 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0003 | 0/0 | 6654 | 38 | 4 | 15 | 14 | 3 | 2 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0004 | 0/1 | 6654 | 20 | 9 | 6 | 0 | 3 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0005 | 0/0 | 6654 | 15 | 0 | 5 | 10 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0006 | 0/0 | 6654 | 13 | 4 | 1 | 8 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0007 | 0/0 | 6654 | 13 | 0 | 0 | 3 | 0 | 10 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0008 | 0/0 | 6654 | 11 | 0 | 3 | 5 | 0 | 3 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0009 | 1/0 | 6654 | 10 | 1 | 2 | 0 | 2 | 4 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0010 | 0/0 | 6654 | 8 | 0 | 7 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0011 | 0/0 | 6654 | 5 | 5 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0012 | 0/0 | 6618 | 5 | 4 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0013 | 0/0 | 6654 | 5 | 0 | 0 | 5 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0014 | 0/0 | 6654 | 5 | 4 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0015 | 0/0 | 6654 | 4 | 4 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0016 | 0/0 | 6654 | 4 | 0 | 0 | 4 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0017 | 0/0 | 6654 | 3 | 0 | 0 | 3 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0018 | 0/0 | 6654 | 3 | 0 | 0 | 3 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0019 | 0/0 | 6618 | 3 | 3 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0020 | 0/0 | 6654 | 3 | 2 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0021 | 0/0 | 6654 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0022 | 0/0 | 6654 | 2 | 0 | 0 | 1 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0023 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0024 | 0/0 | 6654 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0025 | 0/0 | 6654 | 2 | 0 | 0 | 1 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0026 | 0/0 | 6654 | 2 | 0 | 1 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0027 | 0/0 | 6618 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0028 | 0/0 | 6654 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0029 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0030 | 0/0 | 6618 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0031 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0032 | 0/0 | 6654 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0033 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0034 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0035 | 0/0 | 6654 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0036 | 0/0 | 6654 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0037 | 0/0 | 6618 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0038 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0039 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0040 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0041 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0042 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0043 | 0/0 | 6654 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0044 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0045 | 0/0 | 6600 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0046 | 0/0 | 6654 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0047 | 0/0 | 6654 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0048 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0049 | 0/0 | 6654 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0050 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0051 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0052 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0053 | 0/0 | 6618 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0054 | 0/0 | 6654 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0055 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0056 | 0/0 | 6654 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0057 | 0/0 | 6654 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0058 | 0/0 | 6654 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0059 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0060 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0061 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0062 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| c0063 | 0/0 | 6654 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 427 | 287 | 64 | 59 | 114 | 13 | 36 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| t0002 | 0/1 | 427 | 28 | 16 | 7 | 0 | 3 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| t0003 | 0/0 | 427 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| 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 | 0 | 1 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0002 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0021 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 6654 | 44 | 8 | 6 | 25 | 1 | 4 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0003 | 0/0 | 6654 | 38 | 4 | 15 | 14 | 3 | 2 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0004 | 0/1 | 6654 | 20 | 9 | 6 | 0 | 3 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0007 | 0/0 | 6654 | 13 | 0 | 0 | 3 | 0 | 10 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0008 | 0/0 | 6654 | 11 | 0 | 3 | 5 | 0 | 3 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0009 | 1/0 | 6654 | 10 | 1 | 2 | 0 | 2 | 4 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0011 | 0/0 | 6654 | 5 | 5 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0013 | 0/0 | 6654 | 5 | 0 | 0 | 5 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0014 | 0/0 | 6654 | 5 | 4 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0015 | 0/0 | 6654 | 4 | 4 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0017 | 0/0 | 6654 | 3 | 0 | 0 | 3 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0018 | 0/0 | 6654 | 3 | 0 | 0 | 3 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0021 | 0/0 | 6654 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0022 | 0/0 | 6654 | 2 | 0 | 0 | 1 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0024 | 0/0 | 6654 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0025 | 0/0 | 6654 | 2 | 0 | 0 | 1 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0028 | 0/0 | 6654 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0032 | 0/0 | 6654 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0034 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0035 | 0/0 | 6654 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0048 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0049 | 0/0 | 6654 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0052 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0055 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0057 | 0/0 | 6654 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0059 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0001 | 0/0 | 6654 | 53 | 7 | 11 | 24 | 6 | 5 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0010 | 0/0 | 6654 | 8 | 0 | 7 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0038 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0040 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0042 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0043 | 0/0 | 6654 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0046 | 0/0 | 6654 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0063 | 0/0 | 6654 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0003c0005 | 0/0 | 6654 | 15 | 0 | 5 | 10 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0004c0006 | 0/0 | 6654 | 13 | 4 | 1 | 8 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0005c0012 | 0/0 | 6618 | 5 | 4 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0005c0019 | 0/0 | 6618 | 3 | 3 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0005c0027 | 0/0 | 6618 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0005c0030 | 0/0 | 6618 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0006c0016 | 0/0 | 6654 | 4 | 0 | 0 | 4 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0007c0020 | 0/0 | 6654 | 3 | 2 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0008c0026 | 0/0 | 6654 | 2 | 0 | 1 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0008c0061 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0009c0023 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0010c0054 | 0/0 | 6654 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0011c0062 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0012c0044 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0013c0041 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0014c0047 | 0/0 | 6654 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0015c0039 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0016c0037 | 0/0 | 6618 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0017c0053 | 0/0 | 6618 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0018c0036 | 0/0 | 6654 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0019c0058 | 0/0 | 6654 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0020c0051 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0021c0050 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0022c0029 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0023c0033 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0024c0060 | 0/0 | 6654 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0025c0031 | 0/0 | 6654 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0026c0045 | 0/0 | 6600 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0027c0056 | 0/0 | 6654 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 7080 | 44 | 8 | 6 | 25 | 1 | 4 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0003t0001 | 0/0 | 7080 | 38 | 4 | 15 | 14 | 3 | 2 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0004t0002 | 0/1 | 7080 | 20 | 9 | 6 | 0 | 3 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0007t0001 | 0/0 | 7080 | 13 | 0 | 0 | 3 | 0 | 10 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0008t0001 | 0/0 | 7080 | 11 | 0 | 3 | 5 | 0 | 3 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0009t0001 | 1/0 | 7080 | 10 | 1 | 2 | 0 | 2 | 4 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0011t0001 | 0/0 | 7080 | 5 | 5 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0013t0001 | 0/0 | 7080 | 5 | 0 | 0 | 5 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0014t0002 | 0/0 | 7080 | 5 | 4 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0015t0001 | 0/0 | 7080 | 4 | 4 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0017t0001 | 0/0 | 7080 | 3 | 0 | 0 | 3 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0018t0001 | 0/0 | 7080 | 3 | 0 | 0 | 3 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0021t0002 | 0/0 | 7080 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0022t0001 | 0/0 | 7080 | 2 | 0 | 0 | 1 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0024t0001 | 0/0 | 7080 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0025t0001 | 0/0 | 7080 | 2 | 0 | 0 | 1 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0028t0001 | 0/0 | 7080 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0032t0001 | 0/0 | 7080 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0034t0001 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0035t0001 | 0/0 | 7080 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0048t0001 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0049t0001 | 0/0 | 7080 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0052t0001 | 0/0 | 7080 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0055t0001 | 0/0 | 7080 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0057t0003 | 0/0 | 7080 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0001c0059t0001 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0001t0001 | 0/0 | 7080 | 53 | 7 | 11 | 24 | 6 | 5 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0010t0001 | 0/0 | 7080 | 8 | 0 | 7 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0038t0001 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0040t0002 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0042t0001 | 0/0 | 7080 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0043t0001 | 0/0 | 7080 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0046t0001 | 0/0 | 7080 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0002c0063t0001 | 0/0 | 7080 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0003c0005t0001 | 0/0 | 7080 | 15 | 0 | 5 | 10 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0004c0006t0001 | 0/0 | 7080 | 13 | 4 | 1 | 8 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0005c0012t0001 | 0/0 | 7044 | 5 | 4 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0005c0019t0001 | 0/0 | 7044 | 3 | 3 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0005c0027t0001 | 0/0 | 7044 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0005c0030t0001 | 0/0 | 7044 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0006c0016t0001 | 0/0 | 7080 | 4 | 0 | 0 | 4 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0007c0020t0001 | 0/0 | 7080 | 3 | 2 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0008c0026t0001 | 0/0 | 7080 | 2 | 0 | 1 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0008c0061t0001 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0009c0023t0001 | 0/0 | 7098 | 2 | 2 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0010c0054t0001 | 0/0 | 7080 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0011c0062t0001 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0012c0044t0001 | 0/0 | 7080 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0013c0041t0001 | 0/0 | 7080 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0014c0047t0001 | 0/0 | 7080 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0015c0039t0001 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0016c0037t0001 | 0/0 | 7044 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0017c0053t0001 | 0/0 | 7044 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0018c0036t0001 | 0/0 | 7080 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0019c0058t0001 | 0/0 | 7080 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0020c0051t0001 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0021c0050t0001 | 0/0 | 7080 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0022c0029t0001 | 0/0 | 7080 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0023c0033t0001 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0024c0060t0001 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0025c0031t0001 | 0/0 | 7080 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0026c0045t0001 | 0/0 | 7026 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| a0027c0056t0001 | 0/0 | 7080 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | copy fasta | chr9 | 93179139 | 93325569 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0003t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0002 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0004t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0007t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0007t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0007t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0007t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0007t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0007t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0007t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0007t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0007t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0007t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0007t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0007t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0007t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0008t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0008t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0008t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0008t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0008t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0008t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0008t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0008t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0008t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0008t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0008t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0009t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0009t0001g0021 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0009t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0009t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0009t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0009t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0009t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0009t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0009t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0009t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0011t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0011t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0011t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0011t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0011t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0013t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0013t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0013t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0013t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0013t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0014t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0014t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0014t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0014t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0014t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0015t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0015t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0015t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0015t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0017t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0017t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0017t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0018t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0018t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0018t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0021t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0021t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0022t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0022t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0024t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0024t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0025t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0025t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0028t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0028t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0032t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0034t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0035t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0048t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0049t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0052t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0055t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0057t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0001c0059t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0010t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0010t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0010t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0010t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0010t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0010t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0010t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0010t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0038t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0040t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0042t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0043t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0046t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0002c0063t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0003c0005t0001g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0003c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0003c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0003c0005t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0003c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0003c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0003c0005t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0003c0005t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0003c0005t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0003c0005t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0003c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0003c0005t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0003c0005t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0003c0005t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0004c0006t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0004c0006t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0004c0006t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0004c0006t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0004c0006t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0004c0006t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0004c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0004c0006t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0004c0006t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0004c0006t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0004c0006t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0004c0006t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0004c0006t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0005c0012t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0005c0012t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0005c0012t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0005c0012t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0005c0012t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0005c0019t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0005c0019t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0005c0019t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0005c0027t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0005c0027t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0005c0030t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0006c0016t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0006c0016t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0006c0016t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0006c0016t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0007c0020t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0007c0020t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0007c0020t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0008c0026t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0008c0026t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0008c0061t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0009c0023t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0009c0023t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0010c0054t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0011c0062t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0012c0044t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0013c0041t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0014c0047t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0015c0039t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0016c0037t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0017c0053t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0018c0036t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0019c0058t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0020c0051t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0021c0050t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0022c0029t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0023c0033t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0024c0060t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0025c0031t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0026c0045t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| a0027c0056t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0170 | EUR | GBR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00099 | hp2 | a0002 | c0010 | t0001 | g0191 | EUR | GBR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | GBR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00140 | hp2 | a0001 | c0009 | t0001 | g0204 | EUR | GBR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00280 | hp1 | a0001 | c0009 | t0001 | g0199 | EUR | FIN | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00280 | hp2 | a0002 | c0001 | t0001 | g0189 | EUR | FIN | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0190 | EUR | FIN | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0241 | EUR | FIN | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00438 | hp1 | a0004 | c0006 | t0001 | g0089 | EAS | CHS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00438 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | CHS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0237 | EAS | CHS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00544 | hp2 | a0012 | c0044 | t0001 | g0165 | EAS | CHS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | CHS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0129 | EAS | CHS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00609 | hp1 | a0002 | c0001 | t0001 | g0092 | EAS | CHS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | CHS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0103 | EAS | CHS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | CHS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00639 | hp1 | a0001 | c0004 | t0002 | g0284 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00639 | hp2 | a0001 | c0004 | t0002 | g0258 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0250 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00642 | hp2 | a0001 | c0004 | t0002 | g0288 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0221 | EAS | CHS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00673 | hp2 | a0001 | c0007 | t0001 | g0271 | EAS | CHS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00733 | hp1 | a0002 | c0010 | t0001 | g0185 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0219 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00735 | hp1 | a0002 | c0001 | t0001 | g0175 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01071 | hp1 | a0001 | c0008 | t0001 | g0014 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01071 | hp2 | a0001 | c0008 | t0001 | g0151 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0251 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0168 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01081 | hp1 | a0001 | c0035 | t0001 | g0207 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01081 | hp2 | a0027 | c0056 | t0001 | g0298 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01106 | hp1 | a0002 | c0001 | t0001 | g0146 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01106 | hp2 | a0001 | c0008 | t0001 | g0010 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01109 | hp1 | a0001 | c0004 | t0002 | g0257 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01109 | hp2 | a0001 | c0014 | t0002 | g0302 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0295 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01167 | hp2 | a0002 | c0046 | t0001 | g0187 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01168 | hp1 | a0001 | c0009 | t0001 | g0203 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0252 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01175 | hp1 | a0001 | c0004 | t0002 | g0289 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01175 | hp2 | a0002 | c0001 | t0001 | g0178 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01192 | hp1 | a0002 | c0001 | t0001 | g0179 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0247 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01243 | hp1 | a0005 | c0012 | t0001 | g0196 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01243 | hp2 | a0002 | c0001 | t0001 | g0184 | AMR | PUR | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01255 | hp1 | a0008 | c0026 | t0001 | g0306 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01255 | hp2 | a0004 | c0006 | t0001 | g0081 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01256 | hp1 | a0003 | c0005 | t0001 | g0115 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0169 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0249 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01258 | hp1 | a0003 | c0005 | t0001 | g0114 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0226 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01261 | hp2 | a0002 | c0001 | t0001 | g0297 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0232 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01346 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01358 | hp1 | a0002 | c0001 | t0001 | g0172 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0227 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01361 | hp1 | a0001 | c0004 | t0002 | g0259 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01496 | hp1 | a0003 | c0005 | t0001 | g0113 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | CLM | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01515 | hp1 | a0001 | c0004 | t0002 | g0285 | EUR | IBS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01515 | hp2 | a0002 | c0001 | t0001 | g0149 | EUR | IBS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01517 | hp1 | a0002 | c0001 | t0001 | g0120 | EUR | IBS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01517 | hp2 | a0001 | c0004 | t0002 | g0002 | EUR | IBS | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01884 | hp2 | a0001 | c0015 | t0001 | g0033 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01891 | hp2 | a0001 | c0014 | t0002 | g0300 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01928 | hp1 | a0002 | c0010 | t0001 | g0180 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0220 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0231 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01943 | hp2 | a0001 | c0032 | t0001 | g0017 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01952 | hp1 | a0007 | c0020 | t0001 | g0287 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01952 | hp2 | a0002 | c0010 | t0001 | g0173 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0223 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01975 | hp2 | a0002 | c0001 | t0001 | g0137 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01978 | hp1 | a0014 | c0047 | t0001 | g0183 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01978 | hp2 | a0003 | c0005 | t0001 | g0126 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01981 | hp1 | a0002 | c0010 | t0001 | g0181 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0230 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01993 | hp1 | a0019 | c0058 | t0001 | g0283 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG01993 | hp2 | a0002 | c0010 | t0001 | g0188 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0133 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02040 | hp2 | a0021 | c0050 | t0001 | g0070 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02055 | hp1 | a0007 | c0020 | t0001 | g0286 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02055 | hp2 | a0002 | c0001 | t0001 | g0167 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02056 | hp1 | a0003 | c0005 | t0001 | g0112 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02071 | hp1 | a0001 | c0055 | t0001 | g0064 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02071 | hp2 | a0002 | c0001 | t0001 | g0144 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02074 | hp1 | a0003 | c0005 | t0001 | g0001 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0242 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02080 | hp2 | a0002 | c0001 | t0001 | g0108 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02129 | hp2 | a0001 | c0007 | t0001 | g0281 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02135 | hp1 | a0022 | c0029 | t0001 | g0009 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0118 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02145 | hp1 | a0001 | c0004 | t0002 | g0261 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02145 | hp2 | a0005 | c0027 | t0001 | g0039 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02148 | hp1 | a0002 | c0010 | t0001 | g0177 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0225 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02165 | hp1 | a0001 | c0008 | t0001 | g0132 | EAS | CDX | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | CDX | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02258 | hp1 | a0001 | c0004 | t0002 | g0265 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02258 | hp2 | a0009 | c0023 | t0001 | g0292 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02273 | hp1 | a0002 | c0010 | t0001 | g0182 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0307 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02280 | hp1 | a0001 | c0004 | t0002 | g0206 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02280 | hp2 | a0005 | c0012 | t0001 | g0197 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02300 | hp1 | a0001 | c0009 | t0001 | g0201 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02300 | hp2 | a0003 | c0005 | t0001 | g0001 | AMR | PEL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02451 | hp1 | a0001 | c0014 | t0002 | g0301 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02451 | hp2 | a0001 | c0028 | t0001 | g0310 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02523 | hp1 | a0004 | c0006 | t0001 | g0088 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02523 | hp2 | a0002 | c0001 | t0001 | g0153 | EAS | KHV | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02572 | hp1 | a0001 | c0024 | t0001 | g0054 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02572 | hp2 | a0001 | c0014 | t0002 | g0299 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02615 | hp1 | a0005 | c0012 | t0001 | g0193 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02615 | hp2 | a0001 | c0024 | t0001 | g0056 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02622 | hp1 | a0002 | c0038 | t0001 | g0098 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0233 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02630 | hp1 | a0002 | c0001 | t0001 | g0096 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02630 | hp2 | a0007 | c0020 | t0001 | g0312 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02647 | hp1 | a0002 | c0040 | t0002 | g0162 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02647 | hp2 | a0001 | c0011 | t0001 | g0212 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02717 | hp1 | a0001 | c0011 | t0001 | g0213 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02723 | hp1 | a0015 | c0039 | t0001 | g0097 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02723 | hp2 | a0001 | c0004 | t0002 | g0266 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02735 | hp1 | a0001 | c0004 | t0002 | g0278 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02735 | hp2 | a0002 | c0001 | t0001 | g0174 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02738 | hp1 | a0018 | c0036 | t0001 | g0019 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02738 | hp2 | a0002 | c0001 | t0001 | g0106 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02818 | hp1 | a0004 | c0006 | t0001 | g0079 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02818 | hp2 | a0001 | c0011 | t0001 | g0210 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02886 | hp1 | a0023 | c0033 | t0001 | g0214 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02886 | hp2 | a0005 | c0019 | t0001 | g0041 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02895 | hp1 | a0005 | c0030 | t0001 | g0208 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02895 | hp2 | a0001 | c0011 | t0001 | g0211 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02965 | hp1 | a0001 | c0048 | t0001 | g0069 | AFR | ESN | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | ESN | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02970 | hp1 | a0001 | c0021 | t0002 | g0218 | AFR | ESN | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02970 | hp2 | a0001 | c0059 | t0001 | g0304 | AFR | ESN | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03041 | hp1 | a0001 | c0014 | t0002 | g0255 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0309 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03098 | hp1 | a0002 | c0001 | t0001 | g0095 | AFR | MSL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03098 | hp2 | a0001 | c0034 | t0001 | g0216 | AFR | MSL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03130 | hp1 | a0001 | c0015 | t0001 | g0034 | AFR | ESN | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03130 | hp2 | a0005 | c0019 | t0001 | g0139 | AFR | ESN | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03139 | hp1 | a0024 | c0060 | t0001 | g0254 | AFR | ESN | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03139 | hp2 | a0001 | c0021 | t0002 | g0068 | AFR | ESN | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03209 | hp1 | a0005 | c0027 | t0001 | g0043 | AFR | MSL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03209 | hp2 | a0001 | c0009 | t0001 | g0205 | AFR | MSL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03225 | hp1 | a0017 | c0053 | t0001 | g0042 | AFR | MSL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03225 | hp2 | a0001 | c0004 | t0002 | g0264 | AFR | MSL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03239 | hp1 | a0001 | c0009 | t0001 | g0013 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0209 | AFR | MSL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03453 | hp2 | a0001 | c0004 | t0002 | g0263 | AFR | MSL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03486 | hp1 | a0004 | c0006 | t0001 | g0080 | AFR | MSL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03486 | hp2 | a0005 | c0012 | t0001 | g0194 | AFR | MSL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03490 | hp1 | a0001 | c0008 | t0001 | g0025 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03490 | hp2 | a0002 | c0063 | t0001 | g0276 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03491 | hp1 | a0001 | c0007 | t0001 | g0277 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03491 | hp2 | a0008 | c0026 | t0001 | g0305 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03492 | hp1 | a0001 | c0008 | t0001 | g0026 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03492 | hp2 | a0001 | c0007 | t0001 | g0268 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03516 | hp1 | a0008 | c0061 | t0001 | g0290 | AFR | ESN | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | ESN | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03540 | hp1 | a0001 | c0011 | t0001 | g0215 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03540 | hp2 | a0001 | c0015 | t0001 | g0038 | AFR | GWD | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | MSL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03579 | hp2 | a0026 | c0045 | t0001 | g0294 | AFR | MSL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0044 | SAS | STU | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03688 | hp2 | a0001 | c0009 | t0001 | g0200 | SAS | STU | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03704 | hp1 | a0001 | c0009 | t0001 | g0198 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0313 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0176 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03710 | hp2 | a0001 | c0007 | t0001 | g0272 | SAS | PJL | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03831 | hp1 | a0001 | c0007 | t0001 | g0269 | SAS | BEB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03831 | hp2 | a0001 | c0008 | t0001 | g0011 | SAS | BEB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03834 | hp1 | a0001 | c0007 | t0001 | g0273 | SAS | BEB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03834 | hp2 | a0001 | c0057 | t0003 | g0275 | SAS | BEB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03927 | hp1 | a0001 | c0009 | t0001 | g0202 | SAS | BEB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03927 | hp2 | a0001 | c0007 | t0001 | g0274 | SAS | BEB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03942 | hp1 | a0001 | c0025 | t0001 | g0027 | SAS | BEB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG03942 | hp2 | a0001 | c0022 | t0001 | g0074 | SAS | BEB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0110 | SAS | STU | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0075 | SAS | STU | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG04184 | hp1 | a0001 | c0007 | t0001 | g0270 | SAS | BEB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG04184 | hp2 | a0010 | c0054 | t0001 | g0071 | SAS | BEB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0076 | SAS | STU | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG04199 | hp2 | a0001 | c0049 | t0001 | g0073 | SAS | STU | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG04204 | hp1 | a0001 | c0007 | t0001 | g0028 | SAS | STU | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG04204 | hp2 | a0002 | c0001 | t0001 | g0128 | SAS | STU | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG04228 | hp1 | a0001 | c0007 | t0001 | g0267 | SAS | STU | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0077 | SAS | STU | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18522 | hp1 | a0001 | c0004 | t0002 | g0262 | AFR | YRI | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18522 | hp2 | a0004 | c0006 | t0001 | g0078 | AFR | YRI | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0224 | EAS | CHB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | CHB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18906 | hp1 | a0001 | c0004 | t0002 | g0260 | AFR | YRI | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18906 | hp2 | a0016 | c0037 | t0001 | g0195 | AFR | YRI | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18939 | hp2 | a0013 | c0041 | t0001 | g0154 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18943 | hp1 | a0001 | c0003 | t0001 | g0245 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18944 | hp1 | a0001 | c0013 | t0001 | g0125 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18944 | hp2 | a0006 | c0016 | t0001 | g0143 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0243 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18950 | hp1 | a0006 | c0016 | t0001 | g0142 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18953 | hp2 | a0006 | c0016 | t0001 | g0140 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18954 | hp1 | a0003 | c0005 | t0001 | g0127 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18954 | hp2 | a0001 | c0008 | t0001 | g0023 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18959 | hp1 | a0002 | c0001 | t0001 | g0150 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18959 | hp2 | a0004 | c0006 | t0001 | g0090 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18962 | hp1 | a0025 | c0031 | t0001 | g0235 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18962 | hp2 | a0001 | c0013 | t0001 | g0148 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18963 | hp1 | a0001 | c0018 | t0001 | g0005 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18963 | hp2 | a0004 | c0006 | t0001 | g0087 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0246 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18964 | hp2 | a0002 | c0001 | t0001 | g0102 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18966 | hp1 | a0003 | c0005 | t0001 | g0111 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18968 | hp1 | a0002 | c0001 | t0001 | g0135 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18968 | hp2 | a0001 | c0003 | t0001 | g0234 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18969 | hp1 | a0003 | c0005 | t0001 | g0116 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18970 | hp1 | a0001 | c0013 | t0001 | g0157 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18974 | hp1 | a0002 | c0001 | t0001 | g0131 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18974 | hp2 | a0001 | c0018 | t0001 | g0244 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18983 | hp1 | a0001 | c0022 | t0001 | g0008 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18983 | hp2 | a0002 | c0001 | t0001 | g0160 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18984 | hp1 | a0004 | c0006 | t0001 | g0085 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0236 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18989 | hp1 | a0001 | c0007 | t0001 | g0256 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18989 | hp2 | a0002 | c0001 | t0001 | g0091 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0107 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18993 | hp2 | a0002 | c0001 | t0001 | g0130 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18994 | hp1 | a0001 | c0008 | t0001 | g0016 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18994 | hp2 | a0002 | c0001 | t0001 | g0164 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18995 | hp1 | a0001 | c0017 | t0001 | g0123 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18995 | hp2 | a0001 | c0008 | t0001 | g0024 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18999 | hp1 | a0001 | c0013 | t0001 | g0145 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18999 | hp2 | a0006 | c0016 | t0001 | g0141 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19000 | hp1 | a0003 | c0005 | t0001 | g0105 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19000 | hp2 | a0001 | c0017 | t0001 | g0161 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19005 | hp2 | a0002 | c0001 | t0001 | g0119 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19009 | hp1 | a0003 | c0005 | t0001 | g0101 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19010 | hp1 | a0001 | c0003 | t0001 | g0228 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19010 | hp2 | a0003 | c0005 | t0001 | g0117 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19011 | hp1 | a0001 | c0052 | t0001 | g0156 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19011 | hp2 | a0004 | c0006 | t0001 | g0083 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0253 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19060 | hp2 | a0002 | c0001 | t0001 | g0138 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19064 | hp2 | a0002 | c0001 | t0001 | g0109 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19065 | hp1 | a0002 | c0001 | t0001 | g0136 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19066 | hp1 | a0003 | c0005 | t0001 | g0104 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19066 | hp2 | a0001 | c0018 | t0001 | g0004 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19070 | hp1 | a0001 | c0008 | t0001 | g0063 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19070 | hp2 | a0001 | c0017 | t0001 | g0122 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19079 | hp2 | a0004 | c0006 | t0001 | g0086 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19080 | hp1 | a0002 | c0042 | t0001 | g0147 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19082 | hp2 | a0002 | c0001 | t0001 | g0152 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19085 | hp1 | a0002 | c0001 | t0001 | g0155 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19087 | hp1 | a0004 | c0006 | t0001 | g0084 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19087 | hp2 | a0001 | c0013 | t0001 | g0158 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19090 | hp1 | a0003 | c0005 | t0001 | g0094 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19240 | hp1 | a0001 | c0004 | t0002 | g0282 | AFR | YRI | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0314 | AFR | YRI | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA20129 | hp1 | a0001 | c0028 | t0001 | g0311 | AFR | ASW | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA20129 | hp2 | a0004 | c0006 | t0001 | g0082 | AFR | ASW | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA20752 | hp1 | a0002 | c0001 | t0001 | g0186 | EUR | TSI | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0240 | EUR | TSI | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA20805 | hp1 | a0001 | c0004 | t0002 | g0279 | EUR | TSI | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0171 | EUR | TSI | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA20905 | hp1 | a0001 | c0007 | t0001 | g0280 | SAS | GIH | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA20905 | hp2 | a0002 | c0043 | t0001 | g0121 | SAS | GIH | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02109 | hp1 | a0002 | c0001 | t0001 | g0100 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02109 | hp2 | a0005 | c0012 | t0001 | g0192 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02486 | hp1 | a0002 | c0001 | t0001 | g0296 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02486 | hp2 | a0005 | c0019 | t0001 | g0040 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02559 | hp1 | a0020 | c0051 | t0001 | g0308 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0239 | AFR | ACB | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG06807 | hp1 | a0002 | c0001 | t0001 | g0099 | AFR | USA | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| HG06807 | hp2 | a0009 | c0023 | t0001 | g0291 | AFR | USA | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18955 | hp1 | a0002 | c0001 | t0001 | g0134 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA18955 | hp2 | a0001 | c0025 | t0001 | g0163 | EAS | JPT | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA20300 | hp1 | a0002 | c0001 | t0001 | g0159 | AFR | USA | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA20300 | hp2 | a0001 | c0015 | t0001 | g0293 | AFR | USA | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA21309 | hp1 | a0011 | c0062 | t0001 | g0303 | AFR | LWK | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | LWK | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0002 | g0002 | REF | REF | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| homoSapiens_grch38 | hp1 | a0001 | c0009 | t0001 | g0021 | REF | REF | WNK2_chr9_93179139_93325569 | WNK2 | chr9 | 93179139 | 93325569 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:93185248
|
G | A | 1 | a0027 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.319G>A | p.Ala107Thr | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/30 | 568/7080 | 319/6654 | 107/2217 | chr9 | 93185248 | ||
| chr9:93252954
|
A | G | 1 | a0026 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1906A>G | p.Met636Val | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/30 | 2155/7080 | 1906/6654 | 636/2217 | chr9 | 93252954 | ||
| chr9:93252974
|
C | A | 1 | a0026 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1926C>A | p.Asp642Glu | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/30 | 2175/7080 | 1926/6654 | 642/2217 | chr9 | 93252974 | ||
| chr9:93252975
|
G | A | 1 | a0025 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.1927G>A | p.Ala643Thr | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/30 | 2176/7080 | 1927/6654 | 643/2217 | chr9 | 93252975 | ||
| chr9:93256440
|
C | A | 1 | a0026 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.2176C>A | p.Pro726Thr | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 10/30 | 2425/7080 | 2176/6654 | 726/2217 | chr9 | 93256440 | ||
| chr9:93257029
|
C | G | 1 | a0010 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.2272C>G | p.His758Asp | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/30 | 2521/7080 | 2272/6654 | 758/2217 | chr9 | 93257029 | ||
| chr9:93259030
|
G | A | 8 | a0002a0003a0006others(5): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
missense_variant | MODERATE | c.2482G>A | p.Val828Met | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/30 | 2731/7080 | 2482/6654 | 828/2217 | chr9 | 93259030 | ||
| chr9:93259141
|
C | T | 1 | a0003 | 15 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(12): Show |
missense_variant | MODERATE | c.2593C>T | p.Pro865Ser | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/30 | 2842/7080 | 2593/6654 | 865/2217 | chr9 | 93259141 | ||
| chr9:93259271
|
G | C | 2 | a0007a0026 | 4 | HG01952.hp1 HG02055.hp1 HG02630.hp2 others(1): Show |
missense_variant | MODERATE | c.2723G>C | p.Gly908Ala | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/30 | 2972/7080 | 2723/6654 | 908/2217 | chr9 | 93259271 | ||
| chr9:93259318
|
G | A | 1 | a0011 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.2770G>A | p.Val924Ile | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/30 | 3019/7080 | 2770/6654 | 924/2217 | chr9 | 93259318 | ||
| chr9:93259430
|
CGCTGCCC others(47): Show |
C | 1 | a0026 | 1 | HG03579.hp2 | disruptive_inframe_deletion | MODERATE | c.2892_2945delTCAACC others(48): Show |
p.Gln965_Pro982del | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/30 | 3141/7080 | 2892/6654 | 964/2217 | INFO_REALIGN_3_PRIME | chr9 | 93259430 | |
| chr9:93259450
|
TTGCCCCC others(29): Show |
T | 3 | a0005a0016a0017 | 13 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
disruptive_inframe_deletion | MODERATE | c.2918_2953delCACGGC others(30): Show |
p.Thr973_Pro984del | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/30 | 3167/7080 | 2918/6654 | 973/2217 | INFO_REALIGN_3_PRIME | chr9 | 93259450 | |
| chr9:93259484
|
T | TGCTGCCC others(11): Show |
1 | a0009 | 2 | HG02258.hp2 HG06807.hp2 |
disruptive_inframe_insertion | MODERATE | c.2953_2954insCGCTGC others(12): Show |
p.Pro984_Met985insTh others(16): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/30 | 3203/7080 | 2954/6654 | 985/2217 | INFO_REALIGN_3_PRIME | chr9 | 93259484 | |
| chr9:93262004
|
A | C | 1 | a0012 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.3257A>C | p.Gln1086Pro | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/30 | 3506/7080 | 3257/6654 | 1086/2217 | chr9 | 93262004 | ||
| chr9:93262083
|
G | C | 3 | a0005a0016a0017 | 13 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
missense_variant | MODERATE | c.3336G>C | p.Gln1112His | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/30 | 3585/7080 | 3336/6654 | 1112/2217 | chr9 | 93262083 | ||
| chr9:93267899
|
G | A | 1 | a0024 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.3850G>A | p.Gly1284Ser | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 17/30 | 4099/7080 | 3850/6654 | 1284/2217 | chr9 | 93267899 | ||
| chr9:93267911
|
G | A | 1 | a0015 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.3862G>A | p.Gly1288Arg | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 17/30 | 4111/7080 | 3862/6654 | 1288/2217 | chr9 | 93267911 | ||
| chr9:93288848
|
A | C | 1 | a0016 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.4094A>C | p.Gln1365Pro | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/30 | 4343/7080 | 4094/6654 | 1365/2217 | chr9 | 93288848 | ||
| chr9:93288849
|
G | C | 1 | a0016 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.4095G>C | p.Gln1365His | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/30 | 4344/7080 | 4095/6654 | 1365/2217 | chr9 | 93288849 | ||
| chr9:93288980
|
C | A | 1 | a0023 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.4226C>A | p.Pro1409Gln | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/30 | 4475/7080 | 4226/6654 | 1409/2217 | chr9 | 93288980 | ||
| chr9:93289557
|
C | A | 1 | a0004 | 13 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(10): Show |
missense_variant | MODERATE | c.4803C>A | p.Asp1601Glu | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/30 | 5052/7080 | 4803/6654 | 1601/2217 | chr9 | 93289557 | ||
| chr9:93292513
|
C | A | 1 | a0026 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.5048C>A | p.Pro1683His | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/30 | 5297/7080 | 5048/6654 | 1683/2217 | chr9 | 93292513 | ||
| chr9:93292518
|
C | T | 1 | a0018 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.5053C>T | p.Arg1685Cys | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/30 | 5302/7080 | 5053/6654 | 1685/2217 | chr9 | 93292518 | ||
| chr9:93292812
|
G | A | 1 | a0017 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.5347G>A | p.Asp1783Asn | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/30 | 5596/7080 | 5347/6654 | 1783/2217 | chr9 | 93292812 | ||
| chr9:93292921
|
C | T | 1 | a0019 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.5456C>T | p.Pro1819Leu | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/30 | 5705/7080 | 5456/6654 | 1819/2217 | chr9 | 93292921 | ||
| chr9:93292939
|
C | T | 1 | a0020 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.5474C>T | p.Ser1825Phe | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/30 | 5723/7080 | 5474/6654 | 1825/2217 | chr9 | 93292939 | ||
| chr9:93293020
|
C | T | 1 | a0021 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.5555C>T | p.Ser1852Leu | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/30 | 5804/7080 | 5555/6654 | 1852/2217 | chr9 | 93293020 | ||
| chr9:93293056
|
A | G | 1 | a0022 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.5591A>G | p.Lys1864Arg | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/30 | 5840/7080 | 5591/6654 | 1864/2217 | chr9 | 93293056 | ||
| chr9:93308378
|
G | A | 1 | a0014 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.6310G>A | p.Ala2104Thr | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/30 | 6559/7080 | 6310/6654 | 2104/2217 | chr9 | 93308378 | ||
| chr9:93308387
|
G | A | 1 | a0008 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.6319G>A | p.Val2107Ile | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/30 | 6568/7080 | 6319/6654 | 2107/2217 | chr9 | 93308387 | ||
| chr9:93308546
|
G | A | 1 | a0013 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.6478G>A | p.Ala2160Thr | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/30 | 6727/7080 | 6478/6654 | 2160/2217 | chr9 | 93308546 | ||
| chr9:93317553
|
C | T | 1 | a0006 | 4 | NA18944.hp2 NA18950.hp1 NA18953.hp2 others(1): Show |
missense_variant | MODERATE | c.6550C>T | p.Arg2184Cys | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/30 | 6799/7080 | 6550/6654 | 2184/2217 | chr9 | 93317553 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:93185196
|
C | T | 13 | a0001c0004a0001c0007a0001c0014others(10): Show | 51 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(48): Show |
synonymous_variant | LOW | c.267C>T | p.Ala89Ala | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/30 | 516/7080 | 267/6654 | 89/2217 | chr9 | 93185196 | ||
| chr9:93185220
|
G | T | 1 | a0001c0055 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.291G>T | p.Ala97Ala | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/30 | 540/7080 | 291/6654 | 97/2217 | chr9 | 93185220 | ||
| chr9:93230888
|
A | G | 14 | a0001c0002a0001c0013a0001c0017others(11): Show | 68 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
splice_region_variant&synonymous_variant | LOW | c.855A>G | p.Thr285Thr | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/30 | 1104/7080 | 855/6654 | 285/2217 | chr9 | 93230888 | ||
| chr9:93230933
|
C | T | 4 | a0002c0010a0002c0046a0002c0063others(1): Show | 11 | HG00099.hp2 HG00733.hp1 HG01167.hp2 others(8): Show |
synonymous_variant | LOW | c.900C>T | p.Ser300Ser | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/30 | 1149/7080 | 900/6654 | 300/2217 | chr9 | 93230933 | ||
| chr9:93231044
|
T | C | 7 | a0001c0004a0001c0007a0001c0021others(4): Show | 40 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
synonymous_variant | LOW | c.1011T>C | p.Ser337Ser | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/30 | 1260/7080 | 1011/6654 | 337/2217 | chr9 | 93231044 | ||
| chr9:93231086
|
G | A | 1 | a0005c0030 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.1053G>A | p.Ala351Ala | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/30 | 1302/7080 | 1053/6654 | 351/2217 | chr9 | 93231086 | ||
| chr9:93252974
|
C | T | 15 | a0002c0001a0002c0010a0002c0038others(12): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
synonymous_variant | LOW | c.1926C>T | p.Asp642Asp | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/30 | 2175/7080 | 1926/6654 | 642/2217 | chr9 | 93252974 | ||
| chr9:93252980
|
G | A | 1 | a0002c0038 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1932G>A | p.Ala644Ala | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/30 | 2181/7080 | 1932/6654 | 644/2217 | chr9 | 93252980 | ||
| chr9:93257136
|
G | A | 1 | a0001c0048 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.2379G>A | p.Pro793Pro | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/30 | 2628/7080 | 2379/6654 | 793/2217 | chr9 | 93257136 | ||
| chr9:93258972
|
G | A | 1 | a0001c0032 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.2424G>A | p.Ala808Ala | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/30 | 2673/7080 | 2424/6654 | 808/2217 | chr9 | 93258972 | ||
| chr9:93259029
|
C | T | 1 | a0001c0048 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.2481C>T | p.Pro827Pro | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/30 | 2730/7080 | 2481/6654 | 827/2217 | chr9 | 93259029 | ||
| chr9:93259098
|
G | A | 1 | a0001c0015 | 4 | HG01884.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
synonymous_variant | LOW | c.2550G>A | p.Ala850Ala | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/30 | 2799/7080 | 2550/6654 | 850/2217 | chr9 | 93259098 | ||
| chr9:93259404
|
A | G | 1 | a0026c0045 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.2856A>G | p.Pro952Pro | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/30 | 3105/7080 | 2856/6654 | 952/2217 | chr9 | 93259404 | ||
| chr9:93261861
|
G | A | 1 | a0002c0046 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.3114G>A | p.Gln1038Gln | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/30 | 3363/7080 | 3114/6654 | 1038/2217 | chr9 | 93261861 | ||
| chr9:93261900
|
G | C | 9 | a0001c0004a0001c0011a0001c0014others(6): Show | 41 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(38): Show |
synonymous_variant | LOW | c.3153G>C | p.Ser1051Ser | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/30 | 3402/7080 | 3153/6654 | 1051/2217 | chr9 | 93261900 | ||
| chr9:93262089
|
G | A | 2 | a0001c0059a0004c0006 | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
synonymous_variant | LOW | c.3342G>A | p.Thr1114Thr | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/30 | 3591/7080 | 3342/6654 | 1114/2217 | chr9 | 93262089 | ||
| chr9:93263680
|
G | A | 1 | a0009c0023 | 2 | HG02258.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.3525G>A | p.Thr1175Thr | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 15/30 | 3774/7080 | 3525/6654 | 1175/2217 | chr9 | 93263680 | ||
| chr9:93263961
|
G | A | 5 | a0001c0004a0001c0014a0001c0021others(2): Show | 29 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
synonymous_variant | LOW | c.3624G>A | p.Thr1208Thr | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/30 | 3873/7080 | 3624/6654 | 1208/2217 | chr9 | 93263961 | ||
| chr9:93268629
|
C | T | 1 | a0005c0027 | 2 | HG02145.hp2 HG03209.hp1 |
splice_region_variant&synonymous_variant | LOW | c.3916C>T | p.Leu1306Leu | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/30 | 4165/7080 | 3916/6654 | 1306/2217 | chr9 | 93268629 | ||
| chr9:93268679
|
C | T | 2 | a0008c0026a0008c0061 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.3966C>T | p.Pro1322Pro | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/30 | 4215/7080 | 3966/6654 | 1322/2217 | chr9 | 93268679 | ||
| chr9:93288984
|
G | A | 2 | a0008c0026a0008c0061 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.4230G>A | p.Ala1410Ala | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/30 | 4479/7080 | 4230/6654 | 1410/2217 | chr9 | 93288984 | ||
| chr9:93289239
|
A | G | 54 | a0001c0002a0001c0003a0001c0004others(51): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
synonymous_variant | LOW | c.4485A>G | p.Gln1495Gln | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/30 | 4734/7080 | 4485/6654 | 1495/2217 | chr9 | 93289239 | ||
| chr9:93289503
|
C | T | 1 | a0001c0018 | 3 | NA18963.hp1 NA18974.hp2 NA19066.hp2 |
synonymous_variant | LOW | c.4749C>T | p.Phe1583Phe | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/30 | 4998/7080 | 4749/6654 | 1583/2217 | chr9 | 93289503 | ||
| chr9:93290013
|
C | G | 2 | a0001c0003a0025c0031 | 39 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(36): Show |
synonymous_variant | LOW | c.4902C>G | p.Ala1634Ala | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/30 | 5151/7080 | 4902/6654 | 1634/2217 | chr9 | 93290013 | ||
| chr9:93292315
|
G | A | 3 | a0001c0034a0001c0035a0024c0060 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.4944G>A | p.Ser1648Ser | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 22/30 | 5193/7080 | 4944/6654 | 1648/2217 | chr9 | 93292315 | ||
| chr9:93292691
|
C | G | 2 | a0001c0013a0001c0052 | 6 | NA18944.hp1 NA18962.hp2 NA18970.hp1 others(3): Show |
synonymous_variant | LOW | c.5226C>G | p.Ala1742Ala | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/30 | 5475/7080 | 5226/6654 | 1742/2217 | chr9 | 93292691 | ||
| chr9:93292781
|
C | T | 22 | a0001c0002a0001c0003a0001c0007others(19): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(125): Show |
synonymous_variant | LOW | c.5316C>T | p.Asp1772Asp | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/30 | 5565/7080 | 5316/6654 | 1772/2217 | chr9 | 93292781 | ||
| chr9:93292865
|
C | T | 1 | a0002c0043 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.5400C>T | p.Gly1800Gly | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/30 | 5649/7080 | 5400/6654 | 1800/2217 | chr9 | 93292865 | ||
| chr9:93292877
|
C | T | 3 | a0001c0034a0001c0035a0024c0060 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.5412C>T | p.Pro1804Pro | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/30 | 5661/7080 | 5412/6654 | 1804/2217 | chr9 | 93292877 | ||
| chr9:93292997
|
G | C | 2 | a0001c0049a0010c0054 | 2 | HG04184.hp2 HG04199.hp2 |
synonymous_variant | LOW | c.5532G>C | p.Leu1844Leu | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/30 | 5781/7080 | 5532/6654 | 1844/2217 | chr9 | 93292997 | ||
| chr9:93293030
|
C | T | 1 | a0002c0042 | 1 | NA19080.hp1 | synonymous_variant | LOW | c.5565C>T | p.Pro1855Pro | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/30 | 5814/7080 | 5565/6654 | 1855/2217 | chr9 | 93293030 | ||
| chr9:93293129
|
C | G | 1 | a0026c0045 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.5664C>G | p.Leu1888Leu | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/30 | 5913/7080 | 5664/6654 | 1888/2217 | chr9 | 93293129 | ||
| chr9:93298031
|
C | T | 1 | a0001c0035 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.5887C>T | p.Leu1963Leu | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/30 | 6136/7080 | 5887/6654 | 1963/2217 | chr9 | 93298031 | ||
| chr9:93308395
|
G | A | 2 | a0001c0014a0002c0040 | 6 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(3): Show |
synonymous_variant | LOW | c.6327G>A | p.Ala2109Ala | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/30 | 6576/7080 | 6327/6654 | 2109/2217 | chr9 | 93308395 | ||
| chr9:93308488
|
G | A | 2 | a0001c0017a0001c0052 | 4 | NA18995.hp1 NA19000.hp2 NA19011.hp1 others(1): Show |
synonymous_variant | LOW | c.6420G>A | p.Ala2140Ala | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/30 | 6669/7080 | 6420/6654 | 2140/2217 | chr9 | 93308488 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:93184308
|
C | T | 1 | a0001c0057t0003 | 1 | HG03834.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-80C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 1/30 | chr9 | 93184308 | ||||||
| chr9:93320470
|
G | T | 4 | a0001c0004t0002a0001c0014t0002a0001c0021t0002others(1): Show | 28 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*78G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 30/30 | 78 | chr9 | 93320470 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:93184457
|
C | T | 1 | a0001c0003t0001g0314 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-3+72C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 1/29 | chr9 | 93184457 | ||||||
| chr9:93184564
|
G | C | 1 | a0001c0002t0001g0003 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3+179G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 1/29 | chr9 | 93184564 | ||||||
| chr9:93184674
|
C | T | 1 | a0001c0003t0001g0313 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-2-254C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 1/29 | chr9 | 93184674 | ||||||
| chr9:93184771
|
C | T | 3 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312 | 3 | HG02451.hp2 HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-157C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 1/29 | chr9 | 93184771 | ||||||
| chr9:93184891
|
C | A | 3 | a0001c0002t0001g0006a0001c0018t0001g0004a0001c0018t0001g0005 | 3 | NA18939.hp1 NA18963.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-2-37C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 1/29 | chr9 | 93184891 | ||||||
| chr9:93185765
|
A | G | 294 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0029others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.681+155A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93185765 | ||||||
| chr9:93185900
|
T | C | 294 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0029others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.681+290T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93185900 | ||||||
| chr9:93185996
|
G | A | 1 | a0002c0001t0001g0007 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.681+386G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93185996 | ||||||
| chr9:93186081
|
A | G | 2 | a0001c0002t0001g0309a0020c0051t0001g0308 | 2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.681+471A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93186081 | ||||||
| chr9:93186086
|
C | A | 1 | a0001c0025t0001g0027 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.681+476C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93186086 | ||||||
| chr9:93186590
|
G | A | 1 | a0001c0007t0001g0028 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.681+980G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93186590 | ||||||
| chr9:93186592
|
G | GGCTGGGG others(3): Show |
1 | a0001c0003t0001g0307 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.681+991_681+1000du others(11): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93186592 | |||||
| chr9:93186628
|
C | T | 2 | a0008c0026t0001g0305a0008c0026t0001g0306 | 2 | HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.681+1018C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93186628 | ||||||
| chr9:93186757
|
C | T | 6 | a0001c0014t0002g0299a0001c0014t0002g0300a0001c0014t0002g0301others(3): Show | 6 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+1147C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93186757 | ||||||
| chr9:93186879
|
G | A | 54 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0029others(51): Show | 54 | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.681+1269G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93186879 | ||||||
| chr9:93186995
|
T | C | 2 | a0001c0018t0001g0004a0001c0018t0001g0005 | 2 | NA18963.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.681+1385T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93186995 | ||||||
| chr9:93187085
|
G | C | 232 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.681+1475G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93187085 | ||||||
| chr9:93187125
|
A | G | 2 | a0002c0001t0001g0296a0002c0001t0001g0297 | 2 | HG01261.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.681+1515A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93187125 | ||||||
| chr9:93187257
|
C | T | 1 | a0001c0003t0001g0295 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.681+1647C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93187257 | ||||||
| chr9:93187312
|
C | T | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681+1702C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93187312 | ||||||
| chr9:93187362
|
G | A | 1 | a0001c0003t0001g0077 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.681+1752G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93187362 | ||||||
| chr9:93187373
|
A | G | 4 | a0001c0015t0001g0293a0009c0023t0001g0291a0009c0023t0001g0292others(1): Show | 4 | HG02258.hp2 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+1763A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93187373 | ||||||
| chr9:93187730
|
G | T | 1 | a0008c0061t0001g0290 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.681+2120G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93187730 | ||||||
| chr9:93187796
|
A | G | 2 | a0001c0008t0001g0025a0001c0008t0001g0026 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.681+2186A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93187796 | ||||||
| chr9:93187818
|
T | G | 133 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.681+2208T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93187818 | ||||||
| chr9:93188021
|
A | T | 1 | a0001c0002t0001g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.681+2411A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188021 | ||||||
| chr9:93188032
|
C | T | 133 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.681+2422C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188032 | ||||||
| chr9:93188041
|
G | C | 133 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.681+2431G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188041 | ||||||
| chr9:93188179
|
C | T | 161 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0029others(158): Show | 162 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.681+2569C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188179 | ||||||
| chr9:93188182
|
A | G | 1 | a0001c0002t0001g0309 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.681+2572A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188182 | ||||||
| chr9:93188269
|
G | A | 1 | a0001c0004t0002g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.681+2659G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188269 | ||||||
| chr9:93188405
|
G | A | 12 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0011t0001g0210others(9): Show | 12 | HG01081.hp1 HG02647.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.681+2795G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188405 | ||||||
| chr9:93188465
|
A | G | 2 | a0001c0004t0002g0288a0001c0004t0002g0289 | 2 | HG00642.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.681+2855A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188465 | ||||||
| chr9:93188631
|
G | A | 1 | a0001c0004t0002g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.681+3021G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188631 | ||||||
| chr9:93188722
|
G | A | 2 | a0004c0006t0001g0078a0004c0006t0001g0079 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.681+3112G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188722 | ||||||
| chr9:93188752
|
C | A | 4 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0031others(1): Show | 4 | HG00621.hp2 NA18948.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+3142C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188752 | ||||||
| chr9:93188783
|
A | T | 54 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0029others(51): Show | 54 | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.681+3173A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188783 | ||||||
| chr9:93188833
|
G | A | 4 | a0001c0014t0002g0299a0001c0014t0002g0300a0001c0014t0002g0301others(1): Show | 4 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+3223G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188833 | ||||||
| chr9:93188851
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.681+3241C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188851 | ||||||
| chr9:93188867
|
G | A | 2 | a0008c0026t0001g0305a0008c0026t0001g0306 | 2 | HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.681+3257G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188867 | ||||||
| chr9:93188885
|
C | A | 133 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.681+3275C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93188885 | ||||||
| chr9:93189106
|
G | A | 11 | a0004c0006t0001g0080a0004c0006t0001g0081a0004c0006t0001g0082others(8): Show | 11 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.681+3496G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189106 | ||||||
| chr9:93189195
|
C | T | 161 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0029others(158): Show | 162 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.681+3585C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189195 | ||||||
| chr9:93189278
|
G | T | 4 | a0001c0015t0001g0293a0009c0023t0001g0291a0009c0023t0001g0292others(1): Show | 4 | HG02258.hp2 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+3668G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189278 | ||||||
| chr9:93189340
|
T | A | 81 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(78): Show | 82 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.681+3730T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189340 | ||||||
| chr9:93189343
|
A | T | 12 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0011t0001g0210others(9): Show | 12 | HG01081.hp1 HG02647.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.681+3733A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189343 | ||||||
| chr9:93189433
|
C | T | 1 | a0002c0001t0001g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.681+3823C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189433 | ||||||
| chr9:93189487
|
A | G | 270 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0029others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.681+3877A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189487 | ||||||
| chr9:93189654
|
C | G | 162 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0029others(159): Show | 163 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.681+4044C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189654 | ||||||
| chr9:93189655
|
C | T | 162 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0029others(159): Show | 163 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.681+4045C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189655 | ||||||
| chr9:93189679
|
G | A | 1 | a0001c0003t0001g0219 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.681+4069G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189679 | ||||||
| chr9:93189828
|
C | T | 4 | a0001c0002t0001g0166a0001c0025t0001g0163a0002c0001t0001g0164others(1): Show | 4 | HG00544.hp2 NA18955.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+4218C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189828 | ||||||
| chr9:93189843
|
G | A | 43 | a0001c0002t0001g0238a0001c0002t0001g0248a0001c0002t0001g0249others(40): Show | 43 | HG00323.hp2 HG00544.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.681+4233G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189843 | ||||||
| chr9:93189851
|
C | T | 19 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0003t0001g0077others(16): Show | 19 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.681+4241C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189851 | ||||||
| chr9:93189854
|
G | A | 1 | a0001c0035t0001g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.681+4244G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189854 | ||||||
| chr9:93189862
|
G | A | 3 | a0004c0006t0001g0080a0004c0006t0001g0081a0004c0006t0001g0082 | 3 | HG01255.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.681+4252G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189862 | ||||||
| chr9:93189914
|
A | G | 4 | a0001c0002t0001g0166a0001c0025t0001g0163a0002c0001t0001g0164others(1): Show | 4 | HG00544.hp2 NA18955.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+4304A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189914 | ||||||
| chr9:93189919
|
A | G | 292 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0029others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.681+4309A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93189919 | ||||||
| chr9:93190071
|
T | C | 1 | a0001c0002t0001g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.681+4461T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190071 | ||||||
| chr9:93190258
|
C | T | 4 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0286others(1): Show | 4 | HG01952.hp1 HG02055.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+4648C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190258 | ||||||
| chr9:93190261
|
G | T | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.681+4651G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190261 | ||||||
| chr9:93190268
|
T | C | 1 | a0001c0022t0001g0008 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.681+4658T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190268 | ||||||
| chr9:93190272
|
G | A | 130 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(127): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.681+4662G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190272 | ||||||
| chr9:93190276
|
T | G | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.681+4666T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190276 | ||||||
| chr9:93190289
|
C | T | 1 | a0002c0040t0002g0162 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.681+4679C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190289 | ||||||
| chr9:93190370
|
A | G | 1 | a0001c0022t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.681+4760A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190370 | ||||||
| chr9:93190399
|
C | T | 1 | a0001c0021t0002g0218 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.681+4789C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190399 | ||||||
| chr9:93190434
|
G | A | 133 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.681+4824G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190434 | ||||||
| chr9:93190441
|
T | C | 1 | a0024c0060t0001g0254 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.681+4831T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190441 | ||||||
| chr9:93190448
|
C | T | 133 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.681+4838C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190448 | ||||||
| chr9:93190547
|
A | G | 133 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.681+4937A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190547 | ||||||
| chr9:93190562
|
A | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.681+4952A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190562 | ||||||
| chr9:93190588
|
C | T | 86 | a0001c0002t0001g0238a0001c0002t0001g0248a0001c0002t0001g0249others(83): Show | 87 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.681+4978C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190588 | ||||||
| chr9:93190651
|
C | T | 1 | a0001c0004t0002g0285 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.681+5041C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190651 | ||||||
| chr9:93190656
|
G | A | 98 | a0001c0002t0001g0217a0001c0002t0001g0238a0001c0002t0001g0248others(95): Show | 99 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.681+5046G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190656 | ||||||
| chr9:93190773
|
C | T | 3 | a0001c0002t0001g0217a0001c0034t0001g0216a0001c0035t0001g0207 | 3 | HG01081.hp1 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.681+5163C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190773 | ||||||
| chr9:93190843
|
C | T | 3 | a0001c0002t0001g0072a0001c0049t0001g0073a0010c0054t0001g0071 | 3 | HG03239.hp2 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.681+5233C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190843 | ||||||
| chr9:93190935
|
T | G | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681+5325T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190935 | ||||||
| chr9:93190936
|
A | G | 1 | a0002c0010t0001g0191 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.681+5326A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190936 | ||||||
| chr9:93190970
|
C | A | 2 | a0001c0008t0001g0025a0001c0008t0001g0026 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.681+5360C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93190970 | ||||||
| chr9:93191010
|
A | G | 133 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.681+5400A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191010 | ||||||
| chr9:93191031
|
C | T | 135 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(132): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.681+5421C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191031 | ||||||
| chr9:93191036
|
G | C | 1 | a0002c0001t0001g0007 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.681+5426G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191036 | ||||||
| chr9:93191059
|
A | G | 233 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.681+5449A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191059 | ||||||
| chr9:93191089
|
G | A | 2 | a0001c0015t0001g0033a0001c0015t0001g0034 | 2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.681+5479G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191089 | ||||||
| chr9:93191095
|
G | T | 2 | a0001c0015t0001g0293a0026c0045t0001g0294 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.681+5485G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191095 | ||||||
| chr9:93191103
|
C | T | 4 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0286others(1): Show | 4 | HG01952.hp1 HG02055.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+5493C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191103 | ||||||
| chr9:93191153
|
A | G | 233 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.681+5543A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191153 | ||||||
| chr9:93191221
|
T | A | 1 | a0007c0020t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.681+5611T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191221 | ||||||
| chr9:93191258
|
C | T | 1 | a0001c0009t0001g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.681+5648C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191258 | ||||||
| chr9:93191331
|
T | A | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681+5721T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191331 | ||||||
| chr9:93191378
|
T | C | 1 | a0001c0007t0001g0256 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.681+5768T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191378 | ||||||
| chr9:93191432
|
C | T | 2 | a0002c0001t0001g0296a0002c0001t0001g0297 | 2 | HG01261.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.681+5822C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191432 | ||||||
| chr9:93191433
|
C | T | 2 | a0001c0009t0001g0204a0001c0017t0001g0161 | 2 | HG00140.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.681+5823C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191433 | ||||||
| chr9:93191438
|
T | G | 4 | a0005c0012t0001g0192a0005c0012t0001g0193a0005c0012t0001g0194others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+5828T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191438 | ||||||
| chr9:93191656
|
C | T | 1 | a0021c0050t0001g0070 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.681+6046C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191656 | ||||||
| chr9:93191696
|
G | A | 28 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(25): Show | 28 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.681+6086G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191696 | ||||||
| chr9:93191715
|
C | T | 1 | a0001c0014t0002g0302 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.681+6105C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191715 | ||||||
| chr9:93191736
|
A | C | 1 | a0001c0003t0001g0253 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.681+6126A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191736 | ||||||
| chr9:93191943
|
C | T | 1 | a0001c0004t0002g0284 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.681+6333C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191943 | ||||||
| chr9:93191980
|
G | A | 4 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(1): Show | 5 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+6370G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93191980 | ||||||
| chr9:93192103
|
C | A | 37 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(34): Show | 38 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.681+6493C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93192103 | ||||||
| chr9:93192127
|
A | G | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681+6517A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93192127 | ||||||
| chr9:93192174
|
C | T | 85 | a0001c0002t0001g0238a0001c0002t0001g0248a0001c0002t0001g0249others(82): Show | 86 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.681+6564C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93192174 | ||||||
| chr9:93192183
|
A | G | 54 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0029others(51): Show | 54 | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.681+6573A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93192183 | ||||||
| chr9:93192259
|
G | A | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02080.hp1 HG02129.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.681+6649G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93192259 | ||||||
| chr9:93192560
|
G | T | 4 | a0001c0015t0001g0293a0009c0023t0001g0291a0009c0023t0001g0292others(1): Show | 4 | HG02258.hp2 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+6950G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93192560 | ||||||
| chr9:93192578
|
G | A | 1 | a0007c0020t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.681+6968G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93192578 | ||||||
| chr9:93192737
|
T | C | 3 | a0001c0003t0001g0170a0002c0001t0001g0168a0002c0001t0001g0169 | 3 | HG00099.hp1 HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.681+7127T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93192737 | ||||||
| chr9:93192870
|
C | A | 1 | a0001c0015t0001g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.681+7260C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93192870 | ||||||
| chr9:93193013
|
T | C | 1 | a0011c0062t0001g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.681+7403T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93193013 | ||||||
| chr9:93193083
|
T | C | 293 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0029others(290): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.681+7473T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93193083 | ||||||
| chr9:93193251
|
C | T | 1 | a0021c0050t0001g0070 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.681+7641C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93193251 | ||||||
| chr9:93193286
|
C | T | 1 | a0007c0020t0001g0287 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.681+7676C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93193286 | ||||||
| chr9:93193444
|
G | C | 5 | a0005c0019t0001g0040a0005c0019t0001g0041a0005c0027t0001g0039others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.681+7834G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93193444 | ||||||
| chr9:93193462
|
C | T | 2 | a0001c0008t0001g0023a0001c0008t0001g0024 | 2 | NA18954.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.681+7852C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93193462 | ||||||
| chr9:93193689
|
C | T | 2 | a0004c0006t0001g0078a0004c0006t0001g0079 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.681+8079C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93193689 | ||||||
| chr9:93193704
|
A | G | 37 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(34): Show | 38 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.681+8094A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93193704 | ||||||
| chr9:93193885
|
T | G | 1 | a0002c0001t0001g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.681+8275T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93193885 | ||||||
| chr9:93194009
|
A | C | 95 | a0001c0002t0001g0217a0001c0002t0001g0238a0001c0002t0001g0248others(92): Show | 96 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.681+8399A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93194009 | ||||||
| chr9:93194101
|
A | G | 5 | a0001c0015t0001g0293a0007c0020t0001g0312a0009c0023t0001g0291others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.681+8491A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93194101 | ||||||
| chr9:93194168
|
A | T | 1 | a0001c0002t0001g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.681+8558A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93194168 | ||||||
| chr9:93194350
|
T | C | 233 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.681+8740T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93194350 | ||||||
| chr9:93194383
|
TA | T | 5 | a0001c0015t0001g0293a0007c0020t0001g0312a0009c0023t0001g0291others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.681+8780delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93194383 | |||||
| chr9:93194733
|
G | C | 1 | a0001c0002t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.681+9123G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93194733 | ||||||
| chr9:93194755
|
G | A | 6 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(3): Show | 7 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.681+9145G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93194755 | ||||||
| chr9:93194781
|
A | C | 2 | a0009c0023t0001g0291a0009c0023t0001g0292 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.681+9171A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93194781 | ||||||
| chr9:93194861
|
A | G | 3 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038 | 3 | HG01884.hp2 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.681+9251A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93194861 | ||||||
| chr9:93194862
|
T | C | 1 | a0001c0014t0002g0299 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.681+9252T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93194862 | ||||||
| chr9:93194970
|
A | G | 11 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0011t0001g0210others(8): Show | 11 | HG01081.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.681+9360A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93194970 | ||||||
| chr9:93194985
|
T | C | 217 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.681+9375T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93194985 | ||||||
| chr9:93195006
|
A | G | 11 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0011t0001g0210others(8): Show | 11 | HG01081.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.681+9396A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93195006 | ||||||
| chr9:93195022
|
T | TA | 61 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0029others(58): Show | 61 | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.681+9427dupA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195022 | |||||
| chr9:93195038
|
G | C | 1 | a0001c0035t0001g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.681+9428G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93195038 | ||||||
| chr9:93195241
|
A | G | 11 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0011t0001g0210others(8): Show | 11 | HG01081.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.681+9631A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93195241 | ||||||
| chr9:93195424
|
C | T | 1 | a0002c0001t0001g0159 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.681+9814C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93195424 | ||||||
| chr9:93195427
|
G | A | 1 | a0001c0002t0001g0309 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.681+9817G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93195427 | ||||||
| chr9:93195605
|
A | G | 1 | a0001c0048t0001g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.681+9995A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93195605 | ||||||
| chr9:93195653
|
C | A | 1 | a0001c0025t0001g0163 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.681+10043C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93195653 | ||||||
| chr9:93195655
|
T | C | 52 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0004t0002g0002others(49): Show | 53 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.681+10045T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93195655 | ||||||
| chr9:93195681
|
A | G | 7 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(4): Show | 7 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.681+10071A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93195681 | ||||||
| chr9:93195699
|
C | CA | 27 | a0001c0002t0001g0044a0001c0002t0001g0045a0001c0002t0001g0046others(24): Show | 27 | HG00099.hp1 HG00323.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.681+10114dupA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAA | 68 | a0001c0002t0001g0124a0001c0002t0001g0166a0001c0003t0001g0103others(65): Show | 69 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.681+10113_681+1011 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAA | 11 | a0001c0025t0001g0027a0001c0025t0001g0163a0002c0001t0001g0102others(8): Show | 11 | HG00735.hp1 HG01358.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.681+10112_681+1011 others(7): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAA | 11 | a0001c0003t0001g0209a0001c0003t0001g0219a0001c0004t0002g0278others(8): Show | 11 | HG00733.hp2 HG01168.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.681+10110_681+1011 others(9): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAA | 37 | a0001c0003t0001g0077a0001c0003t0001g0250a0001c0003t0001g0251others(34): Show | 38 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.681+10109_681+1011 others(10): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA | 7 | a0001c0003t0001g0234a0001c0004t0002g0257a0001c0004t0002g0260others(4): Show | 7 | HG00639.hp1 HG01081.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.681+10108_681+1011 others(11): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(1): Show |
20 | a0001c0003t0001g0222a0001c0003t0001g0223a0001c0003t0001g0224others(17): Show | 20 | HG01243.hp1 HG01261.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.681+10107_681+1011 others(12): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(3): Show |
6 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0003t0001g0220others(3): Show | 6 | HG00673.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.681+10105_681+1011 others(14): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(4): Show |
2 | a0001c0003t0001g0247a0001c0003t0001g0295 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.681+10104_681+1011 others(15): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(6): Show |
4 | a0001c0002t0001g0217a0001c0003t0001g0245a0001c0003t0001g0246others(1): Show | 4 | NA18943.hp1 NA18964.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+10102_681+1011 others(17): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(7): Show |
2 | a0001c0034t0001g0216a0001c0059t0001g0304 | 2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.681+10101_681+1011 others(18): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(8): Show |
3 | a0001c0002t0001g0093a0001c0018t0001g0244a0001c0035t0001g0207 | 3 | HG01081.hp1 HG01884.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.681+10100_681+1011 others(19): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(9): Show |
9 | a0001c0003t0001g0242a0001c0003t0001g0243a0002c0001t0001g0096others(6): Show | 9 | HG01952.hp1 HG02055.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.681+10099_681+1011 others(20): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(10): Show |
3 | a0001c0003t0001g0313a0002c0001t0001g0095a0002c0040t0002g0162 | 3 | HG02647.hp1 HG03098.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.681+10098_681+1011 others(21): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(11): Show |
2 | a0001c0003t0001g0240a0001c0003t0001g0241 | 2 | HG00323.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.681+10097_681+1011 others(22): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(12): Show |
1 | a0001c0003t0001g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.681+10096_681+1011 others(23): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(14): Show |
1 | a0024c0060t0001g0254 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.681+10094_681+1011 others(25): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(16): Show |
3 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0089 | 3 | HG00438.hp1 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.681+10092_681+1011 others(27): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(18): Show |
2 | a0001c0003t0001g0314a0004c0006t0001g0088 | 2 | HG02523.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.681+10090_681+1011 others(29): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(20): Show |
1 | a0004c0006t0001g0087 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.681+10114_681+1011 others(31): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(21): Show |
1 | a0004c0006t0001g0086 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.681+10114_681+1011 others(32): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(23): Show |
1 | a0004c0006t0001g0081 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.681+10114_681+1011 others(34): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(26): Show |
2 | a0004c0006t0001g0080a0004c0006t0001g0085 | 2 | HG03486.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.681+10114_681+1011 others(37): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
C | CAAAAAAA others(27): Show |
2 | a0004c0006t0001g0083a0004c0006t0001g0084 | 2 | NA19011.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.681+10114_681+1011 others(38): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195699
|
CA | C | 9 | a0001c0002t0001g0067a0001c0014t0002g0255a0001c0018t0001g0005others(6): Show | 9 | HG02258.hp2 HG02965.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.681+10114delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93195699 | |||||
| chr9:93195794
|
G | T | 5 | a0002c0001t0001g0144a0006c0016t0001g0140a0006c0016t0001g0141others(2): Show | 5 | HG02071.hp2 NA18944.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+10184G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93195794 | ||||||
| chr9:93195813
|
G | A | 229 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.681+10203G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93195813 | ||||||
| chr9:93195859
|
G | A | 4 | a0001c0002t0001g0217a0001c0034t0001g0216a0001c0035t0001g0207others(1): Show | 4 | HG01081.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+10249G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93195859 | ||||||
| chr9:93196315
|
A | G | 36 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(33): Show | 37 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.681+10705A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93196315 | ||||||
| chr9:93196441
|
C | T | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.681+10831C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93196441 | ||||||
| chr9:93196478
|
C | T | 1 | a0001c0022t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.681+10868C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93196478 | ||||||
| chr9:93196775
|
G | A | 1 | a0001c0002t0001g0003 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.681+11165G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93196775 | ||||||
| chr9:93196861
|
C | T | 1 | a0001c0003t0001g0314 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.681+11251C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93196861 | ||||||
| chr9:93197007
|
G | A | 1 | a0001c0002t0001g0047 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.681+11397G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93197007 | ||||||
| chr9:93197259
|
C | T | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681+11649C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93197259 | ||||||
| chr9:93197425
|
A | T | 1 | a0011c0062t0001g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.681+11815A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93197425 | ||||||
| chr9:93197428
|
C | T | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681+11818C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93197428 | ||||||
| chr9:93197567
|
C | G | 157 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.681+11957C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93197567 | ||||||
| chr9:93197582
|
A | G | 4 | a0001c0003t0001g0245a0001c0003t0001g0246a0001c0003t0001g0253others(1): Show | 4 | NA18943.hp1 NA18964.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+11972A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93197582 | ||||||
| chr9:93197742
|
T | C | 157 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.681+12132T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93197742 | ||||||
| chr9:93197846
|
G | T | 1 | a0001c0002t0001g0066 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.681+12236G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93197846 | ||||||
| chr9:93198150
|
G | A | 105 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(102): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.681+12540G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93198150 | ||||||
| chr9:93198209
|
C | T | 1 | a0001c0022t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.681+12599C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93198209 | ||||||
| chr9:93198239
|
G | A | 12 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0011t0001g0210others(9): Show | 12 | HG01081.hp1 HG02647.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.681+12629G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93198239 | ||||||
| chr9:93198264
|
G | A | 52 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0004t0002g0002others(49): Show | 53 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.681+12654G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93198264 | ||||||
| chr9:93198412
|
G | A | 1 | a0002c0001t0001g0172 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.681+12802G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93198412 | ||||||
| chr9:93198455
|
C | T | 40 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(37): Show | 41 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.681+12845C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93198455 | ||||||
| chr9:93198457
|
G | A | 1 | a0001c0003t0001g0103 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.681+12847G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93198457 | ||||||
| chr9:93198480
|
G | T | 1 | a0001c0003t0001g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.681+12870G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93198480 | ||||||
| chr9:93198528
|
G | T | 36 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(33): Show | 37 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.681+12918G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93198528 | ||||||
| chr9:93198584
|
TG | T | 52 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0004t0002g0002others(49): Show | 53 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.681+12978delG | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93198584 | |||||
| chr9:93198586
|
G | A | 52 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0004t0002g0002others(49): Show | 53 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.681+12976G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93198586 | ||||||
| chr9:93198720
|
A | G | 1 | a0007c0020t0001g0287 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.681+13110A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93198720 | ||||||
| chr9:93198984
|
C | T | 1 | a0001c0002t0001g0047 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.681+13374C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93198984 | ||||||
| chr9:93198988
|
T | C | 1 | a0005c0012t0001g0192 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.681+13378T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93198988 | ||||||
| chr9:93199064
|
C | T | 40 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(37): Show | 41 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.681+13454C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93199064 | ||||||
| chr9:93199145
|
C | T | 2 | a0005c0012t0001g0196a0005c0012t0001g0197 | 2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.681+13535C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93199145 | ||||||
| chr9:93199146
|
G | A | 52 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0004t0002g0002others(49): Show | 53 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.681+13536G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93199146 | ||||||
| chr9:93199334
|
G | C | 8 | a0001c0003t0001g0209a0001c0011t0001g0210a0001c0011t0001g0211others(5): Show | 8 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.681+13724G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93199334 | ||||||
| chr9:93199381
|
T | C | 52 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0004t0002g0002others(49): Show | 53 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.681+13771T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93199381 | ||||||
| chr9:93199504
|
G | A | 8 | a0001c0003t0001g0209a0001c0011t0001g0210a0001c0011t0001g0211others(5): Show | 8 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.681+13894G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93199504 | ||||||
| chr9:93199624
|
T | C | 2 | a0008c0026t0001g0305a0008c0026t0001g0306 | 2 | HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.681+14014T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93199624 | ||||||
| chr9:93199715
|
G | A | 52 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0004t0002g0002others(49): Show | 53 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.681+14105G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93199715 | ||||||
| chr9:93199725
|
C | T | 105 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(102): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.681+14115C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93199725 | ||||||
| chr9:93199813
|
G | A | 52 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0004t0002g0002others(49): Show | 53 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.681+14203G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93199813 | ||||||
| chr9:93199899
|
C | CAAAAAAA | 35 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(32): Show | 36 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.681+14295_681+1430 others(11): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93199899 | |||||
| chr9:93199899
|
C | CAAAAAAA others(5): Show |
3 | a0001c0013t0001g0157a0001c0013t0001g0158a0001c0052t0001g0156 | 3 | NA18970.hp1 NA19011.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.681+14290_681+1430 others(16): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93199899 | |||||
| chr9:93199899
|
C | CAAAAAAA others(8): Show |
6 | a0001c0002t0001g0093a0002c0001t0001g0137a0002c0001t0001g0138others(3): Show | 6 | HG00280.hp2 HG01884.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.681+14301_681+1430 others(19): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93199899 | |||||
| chr9:93199899
|
C | CAAAAAAA others(9): Show |
79 | a0001c0002t0001g0124a0001c0002t0001g0166a0001c0003t0001g0170others(76): Show | 80 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.681+14301_681+1430 others(20): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93199899 | |||||
| chr9:93199899
|
C | CAAAAAAA others(10): Show |
17 | a0001c0003t0001g0103a0001c0013t0001g0145a0001c0017t0001g0161others(14): Show | 17 | HG00621.hp1 HG01106.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.681+14301_681+1430 others(21): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93199899 | |||||
| chr9:93199899
|
C | CAAAAAAA others(12): Show |
2 | a0001c0002t0001g0217a0001c0034t0001g0216 | 2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.681+14301_681+1430 others(23): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93199899 | |||||
| chr9:93199899
|
C | CAAAAAAA others(13): Show |
5 | a0001c0011t0001g0211a0001c0011t0001g0212a0001c0011t0001g0213others(2): Show | 5 | HG01081.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+14301_681+1430 others(24): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93199899 | |||||
| chr9:93199899
|
C | CAAAAAAA others(14): Show |
5 | a0001c0003t0001g0209a0001c0011t0001g0210a0001c0021t0002g0218others(2): Show | 5 | HG02818.hp2 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+14301_681+1430 others(25): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93199899 | |||||
| chr9:93200051
|
G | A | 8 | a0001c0003t0001g0209a0001c0011t0001g0210a0001c0011t0001g0211others(5): Show | 8 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.681+14441G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93200051 | ||||||
| chr9:93200112
|
C | G | 19 | a0001c0002t0001g0166a0001c0008t0001g0132a0001c0025t0001g0163others(16): Show | 19 | HG00544.hp2 HG00597.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.681+14502C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93200112 | ||||||
| chr9:93200132
|
G | A | 1 | a0023c0033t0001g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.681+14522G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93200132 | ||||||
| chr9:93200212
|
G | A | 2 | a0001c0025t0001g0163a0002c0001t0001g0164 | 2 | NA18955.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.681+14602G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93200212 | ||||||
| chr9:93200378
|
T | C | 5 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+14768T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93200378 | ||||||
| chr9:93200382
|
C | T | 1 | a0001c0002t0001g0022 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.681+14772C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93200382 | ||||||
| chr9:93200472
|
G | A | 157 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.681+14862G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93200472 | ||||||
| chr9:93200495
|
G | A | 5 | a0001c0015t0001g0293a0007c0020t0001g0312a0009c0023t0001g0291others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.681+14885G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93200495 | ||||||
| chr9:93200608
|
C | T | 105 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(102): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.681+14998C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93200608 | ||||||
| chr9:93200784
|
A | T | 3 | a0001c0003t0001g0077a0001c0003t0001g0250a0001c0003t0001g0251 | 3 | HG00642.hp1 HG01074.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.681+15174A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93200784 | ||||||
| chr9:93200832
|
G | A | 157 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.681+15222G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93200832 | ||||||
| chr9:93200866
|
T | G | 313 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(310): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.681+15256T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93200866 | ||||||
| chr9:93200875
|
G | T | 1 | a0001c0021t0002g0068 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.681+15265G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93200875 | ||||||
| chr9:93200894
|
C | T | 12 | a0001c0002t0001g0217a0001c0003t0001g0209a0001c0011t0001g0210others(9): Show | 12 | HG01081.hp1 HG02647.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.681+15284C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93200894 | ||||||
| chr9:93201034
|
T | C | 52 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0029others(49): Show | 52 | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.681+15424T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201034 | ||||||
| chr9:93201034
|
T | G | 1 | a0007c0020t0001g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.681+15424T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201034 | ||||||
| chr9:93201118
|
C | G | 152 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.681+15508C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201118 | ||||||
| chr9:93201128
|
A | G | 2 | a0004c0006t0001g0078a0004c0006t0001g0079 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.681+15518A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201128 | ||||||
| chr9:93201178
|
G | A | 3 | a0001c0003t0001g0077a0001c0003t0001g0250a0001c0003t0001g0251 | 3 | HG00642.hp1 HG01074.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.681+15568G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201178 | ||||||
| chr9:93201183
|
G | A | 2 | a0004c0006t0001g0086a0004c0006t0001g0088 | 2 | HG02523.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.681+15573G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201183 | ||||||
| chr9:93201205
|
C | G | 4 | a0001c0002t0001g0217a0001c0034t0001g0216a0001c0035t0001g0207others(1): Show | 4 | HG01081.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+15595C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201205 | ||||||
| chr9:93201214
|
C | T | 1 | a0001c0057t0003g0275 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.681+15604C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201214 | ||||||
| chr9:93201279
|
C | A | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.681+15669C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201279 | ||||||
| chr9:93201299
|
C | T | 1 | a0002c0001t0001g0109 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.681+15689C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201299 | ||||||
| chr9:93201311
|
T | C | 1 | a0002c0001t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.681+15701T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201311 | ||||||
| chr9:93201392
|
C | T | 17 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0003t0001g0239others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.681+15782C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201392 | ||||||
| chr9:93201426
|
T | C | 144 | a0001c0002t0001g0072a0001c0002t0001g0124a0001c0002t0001g0166others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.681+15816T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201426 | ||||||
| chr9:93201435
|
G | A | 8 | a0001c0003t0001g0209a0001c0011t0001g0210a0001c0011t0001g0211others(5): Show | 8 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.681+15825G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201435 | ||||||
| chr9:93201581
|
C | G | 141 | a0001c0002t0001g0124a0001c0002t0001g0166a0001c0003t0001g0103others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.681+15971C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201581 | ||||||
| chr9:93201695
|
C | T | 9 | a0004c0006t0001g0078a0004c0006t0001g0079a0005c0012t0001g0192others(6): Show | 9 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.681+16085C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201695 | ||||||
| chr9:93201795
|
A | G | 1 | a0001c0003t0001g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.681+16185A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201795 | ||||||
| chr9:93201851
|
G | A | 1 | a0001c0004t0002g0282 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.681+16241G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201851 | ||||||
| chr9:93201851
|
G | T | 5 | a0001c0002t0001g0166a0001c0025t0001g0163a0002c0001t0001g0164others(2): Show | 5 | HG00544.hp2 NA18939.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.681+16241G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93201851 | ||||||
| chr9:93202020
|
A | G | 1 | a0001c0002t0001g0032 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.681+16410A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202020 | ||||||
| chr9:93202034
|
C | T | 4 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(1): Show | 5 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+16424C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202034 | ||||||
| chr9:93202206
|
C | T | 1 | a0001c0002t0001g0006 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.681+16596C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202206 | ||||||
| chr9:93202210
|
A | G | 1 | a0004c0006t0001g0084 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.681+16600A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202210 | ||||||
| chr9:93202274
|
C | T | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681+16664C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202274 | ||||||
| chr9:93202282
|
G | A | 148 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.681+16672G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202282 | ||||||
| chr9:93202292
|
G | A | 1 | a0001c0003t0001g0253 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.681+16682G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202292 | ||||||
| chr9:93202325
|
C | CAT | 8 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.681+16715_681+1671 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202325 | ||||||
| chr9:93202325
|
C | CGT | 18 | a0001c0002t0001g0003a0001c0002t0001g0051a0001c0002t0001g0052others(15): Show | 18 | HG00140.hp1 HG00609.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.681+16756_681+1675 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202325 | |||||
| chr9:93202325
|
C | CGTGT | 67 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0029others(64): Show | 68 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.681+16754_681+1675 others(8): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202325 | |||||
| chr9:93202325
|
C | CGTGTGT | 28 | a0001c0002t0001g0006a0001c0002t0001g0065a0001c0002t0001g0075others(25): Show | 28 | HG00438.hp1 HG00544.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.681+16752_681+1675 others(10): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202325 | |||||
| chr9:93202325
|
C | CGTGTGTG others(1): Show |
18 | a0001c0003t0001g0221a0001c0003t0001g0233a0001c0003t0001g0251others(15): Show | 18 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.681+16750_681+1675 others(12): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202325 | |||||
| chr9:93202325
|
C | CGTGTGTG others(3): Show |
12 | a0001c0002t0001g0031a0001c0003t0001g0077a0001c0003t0001g0295others(9): Show | 12 | HG00621.hp2 HG01167.hp1 HG03486.hp2 others(9): Show |
intron_variant | MODIFIER | c.681+16748_681+1675 others(14): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202325 | |||||
| chr9:93202325
|
C | CGTGTGTG others(5): Show |
7 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0003t0001g0242others(4): Show | 7 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.681+16746_681+1675 others(16): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202325 | |||||
| chr9:93202325
|
C | CGTGTGTG others(7): Show |
1 | a0005c0012t0001g0197 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.681+16744_681+1675 others(18): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202325 | |||||
| chr9:93202325
|
C | CGTGTGTG others(9): Show |
2 | a0001c0003t0001g0243a0001c0003t0001g0245 | 2 | NA18943.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.681+16742_681+1675 others(20): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202325 | |||||
| chr9:93202325
|
C | CGTGTGTG others(11): Show |
2 | a0001c0003t0001g0246a0001c0003t0001g0253 | 2 | NA18964.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.681+16740_681+1675 others(22): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202325 | |||||
| chr9:93202325
|
C | CGTGTGTG others(13): Show |
1 | a0001c0003t0001g0247 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.681+16738_681+1675 others(24): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202325 | |||||
| chr9:93202325
|
CGTGTGTG others(1): Show |
C | 6 | a0001c0004t0002g0260a0001c0004t0002g0261a0001c0004t0002g0262others(3): Show | 6 | HG02145.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.681+16750_681+1675 others(12): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202325 | |||||
| chr9:93202325
|
CGTGTGTG others(3): Show |
C | 7 | a0001c0003t0001g0209a0001c0011t0001g0210a0001c0011t0001g0211others(4): Show | 7 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.681+16748_681+1675 others(14): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202325 | |||||
| chr9:93202325
|
CGTGTGTG others(9): Show |
C | 1 | a0008c0026t0001g0305 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.681+16742_681+1675 others(20): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202325 | |||||
| chr9:93202333
|
T | G | 8 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.681+16723T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202333 | ||||||
| chr9:93202334
|
G | A | 1 | a0001c0021t0002g0218 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.681+16724G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202334 | ||||||
| chr9:93202336
|
G | A | 7 | a0001c0003t0001g0209a0001c0011t0001g0210a0001c0011t0001g0211others(4): Show | 7 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.681+16726G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202336 | ||||||
| chr9:93202364
|
G | A | 10 | a0001c0002t0001g0217a0001c0004t0002g0260a0001c0004t0002g0261others(7): Show | 10 | HG01081.hp1 HG01358.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.681+16754G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202364 | ||||||
| chr9:93202364
|
G | GTA | 5 | a0001c0003t0001g0170a0002c0001t0001g0168a0002c0001t0001g0296others(2): Show | 5 | HG00099.hp1 HG01074.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+16755_681+1675 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202364 | |||||
| chr9:93202364
|
G | GTGTA | 86 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(83): Show | 87 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.681+16758_681+1676 others(8): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202364 | |||||
| chr9:93202364
|
G | GTGTGTA | 6 | a0001c0013t0001g0145a0001c0013t0001g0148a0001c0013t0001g0157others(3): Show | 6 | HG03130.hp2 NA18962.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+16757_681+1675 others(10): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202364 | |||||
| chr9:93202364
|
G | GTGTGTGT others(1): Show |
3 | a0001c0013t0001g0158a0002c0001t0001g0153a0002c0001t0001g0167 | 3 | HG02055.hp2 HG02523.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.681+16757_681+1675 others(12): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202364 | |||||
| chr9:93202364
|
G | GTGTGTGT others(3): Show |
2 | a0001c0028t0001g0310a0002c0001t0001g0091 | 2 | HG02451.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.681+16757_681+1675 others(14): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202364 | |||||
| chr9:93202364
|
G | GTGTGTGT others(5): Show |
1 | a0001c0028t0001g0311 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.681+16757_681+1675 others(16): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202364 | |||||
| chr9:93202364
|
G | GTGTGTGT others(9): Show |
1 | a0007c0020t0001g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.681+16757_681+1675 others(20): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202364 | |||||
| chr9:93202364
|
G | GTGTGTGT others(11): Show |
1 | a0007c0020t0001g0287 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.681+16757_681+1675 others(22): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93202364 | |||||
| chr9:93202412
|
C | T | 1 | a0001c0048t0001g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.681+16802C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202412 | ||||||
| chr9:93202487
|
C | T | 1 | a0020c0051t0001g0308 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.681+16877C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202487 | ||||||
| chr9:93202501
|
G | A | 1 | a0005c0030t0001g0208 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.681+16891G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202501 | ||||||
| chr9:93202529
|
G | A | 7 | a0001c0003t0001g0209a0001c0011t0001g0210a0001c0011t0001g0211others(4): Show | 7 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.681+16919G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202529 | ||||||
| chr9:93202625
|
G | C | 3 | a0001c0002t0001g0072a0001c0049t0001g0073a0010c0054t0001g0071 | 3 | HG03239.hp2 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.681+17015G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202625 | ||||||
| chr9:93202754
|
TC | T | 6 | a0001c0024t0001g0054a0004c0006t0001g0080a0004c0006t0001g0081others(3): Show | 6 | HG01255.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.681+17145delC | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93202754 | ||||||
| chr9:93203026
|
G | A | 2 | a0005c0012t0001g0192a0005c0012t0001g0194 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.681+17416G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203026 | ||||||
| chr9:93203029
|
A | G | 1 | a0001c0048t0001g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.681+17419A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203029 | ||||||
| chr9:93203094
|
T | C | 151 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0166others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.681+17484T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203094 | ||||||
| chr9:93203137
|
G | A | 4 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(1): Show | 4 | HG01884.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+17527G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203137 | ||||||
| chr9:93203227
|
A | G | 1 | a0002c0001t0001g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.681+17617A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203227 | ||||||
| chr9:93203368
|
C | G | 5 | a0001c0028t0001g0310a0001c0028t0001g0311a0009c0023t0001g0291others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.681+17758C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203368 | ||||||
| chr9:93203414
|
C | T | 293 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0020others(290): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.681+17804C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203414 | ||||||
| chr9:93203449
|
T | C | 18 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(15): Show | 18 | HG01081.hp1 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.681+17839T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203449 | ||||||
| chr9:93203543
|
G | A | 1 | a0002c0001t0001g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.681+17933G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203543 | ||||||
| chr9:93203557
|
C | T | 4 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(1): Show | 5 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+17947C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203557 | ||||||
| chr9:93203767
|
A | G | 1 | a0002c0001t0001g0100 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.681+18157A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203767 | ||||||
| chr9:93203812
|
C | A | 4 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(1): Show | 5 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+18202C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203812 | ||||||
| chr9:93203940
|
C | T | 1 | a0001c0007t0001g0274 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.681+18330C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203940 | ||||||
| chr9:93203987
|
A | T | 4 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(1): Show | 5 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+18377A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203987 | ||||||
| chr9:93203995
|
G | A | 2 | a0002c0001t0001g0171a0002c0001t0001g0174 | 2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.681+18385G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93203995 | ||||||
| chr9:93204159
|
G | A | 1 | a0002c0001t0001g0178 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.681+18549G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93204159 | ||||||
| chr9:93204174
|
C | T | 14 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(11): Show | 14 | HG01081.hp1 HG01109.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.681+18564C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93204174 | ||||||
| chr9:93204211
|
T | C | 1 | a0001c0003t0001g0314 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.681+18601T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93204211 | ||||||
| chr9:93204237
|
C | T | 3 | a0001c0059t0001g0304a0008c0026t0001g0305a0008c0026t0001g0306 | 3 | HG01255.hp1 HG02970.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.681+18627C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93204237 | ||||||
| chr9:93204338
|
C | T | 11 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(8): Show | 11 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.681+18728C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93204338 | ||||||
| chr9:93204797
|
G | A | 14 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(11): Show | 14 | HG01081.hp1 HG01109.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.681+19187G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93204797 | ||||||
| chr9:93204865
|
T | C | 293 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0020others(290): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.681+19255T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93204865 | ||||||
| chr9:93205176
|
C | T | 20 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(17): Show | 20 | HG01081.hp1 HG01109.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.681+19566C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93205176 | ||||||
| chr9:93205451
|
G | T | 7 | a0001c0002t0001g0093a0001c0011t0001g0210a0001c0011t0001g0211others(4): Show | 7 | HG01884.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.681+19841G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93205451 | ||||||
| chr9:93205518
|
C | T | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.681+19908C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93205518 | ||||||
| chr9:93205565
|
C | G | 1 | a0003c0005t0001g0127 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.681+19955C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93205565 | ||||||
| chr9:93205568
|
C | CG | 14 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(11): Show | 14 | HG01081.hp1 HG01109.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.681+19960dupG | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93205568 | |||||
| chr9:93205573
|
G | T | 3 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0032 | 3 | HG00621.hp2 NA19064.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.681+19963G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93205573 | ||||||
| chr9:93205722
|
C | T | 2 | a0001c0004t0002g0263a0001c0004t0002g0264 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.681+20112C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93205722 | ||||||
| chr9:93205786
|
G | A | 11 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(8): Show | 11 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.681+20176G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93205786 | ||||||
| chr9:93205819
|
TTGC | T | 11 | a0004c0006t0001g0080a0004c0006t0001g0081a0004c0006t0001g0082others(8): Show | 11 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.681+20215_681+2021 others(7): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93205819 | |||||
| chr9:93205843
|
T | G | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.681+20233T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93205843 | ||||||
| chr9:93205848
|
C | T | 4 | a0007c0020t0001g0312a0009c0023t0001g0291a0009c0023t0001g0292others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+20238C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93205848 | ||||||
| chr9:93205990
|
ATTG | A | 51 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0020others(48): Show | 51 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.681+20387_681+2038 others(7): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93205990 | |||||
| chr9:93206024
|
G | A | 11 | a0004c0006t0001g0080a0004c0006t0001g0081a0004c0006t0001g0082others(8): Show | 11 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.681+20414G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93206024 | ||||||
| chr9:93206128
|
G | A | 14 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(11): Show | 14 | HG01081.hp1 HG01109.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.681+20518G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93206128 | ||||||
| chr9:93206134
|
G | A | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681+20524G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93206134 | ||||||
| chr9:93206227
|
C | T | 205 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0020others(202): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.681+20617C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93206227 | ||||||
| chr9:93206335
|
C | T | 3 | a0001c0059t0001g0304a0008c0026t0001g0305a0008c0026t0001g0306 | 3 | HG01255.hp1 HG02970.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.681+20725C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93206335 | ||||||
| chr9:93206446
|
A | G | 15 | a0001c0003t0001g0077a0001c0003t0001g0239a0001c0003t0001g0240others(12): Show | 15 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.681+20836A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93206446 | ||||||
| chr9:93206486
|
A | T | 1 | a0001c0003t0001g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.681+20876A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93206486 | ||||||
| chr9:93206493
|
G | A | 1 | a0002c0001t0001g0179 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.681+20883G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93206493 | ||||||
| chr9:93206689
|
A | G | 4 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(1): Show | 5 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+21079A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93206689 | ||||||
| chr9:93206758
|
G | A | 20 | a0001c0002t0001g0238a0001c0003t0001g0103a0001c0003t0001g0220others(17): Show | 20 | HG00544.hp1 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.681+21148G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93206758 | ||||||
| chr9:93206978
|
G | A | 11 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(8): Show | 11 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.681+21368G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93206978 | ||||||
| chr9:93207070
|
G | A | 2 | a0001c0002t0001g0055a0001c0002t0001g0067 | 2 | NA19079.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.681+21460G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93207070 | ||||||
| chr9:93207078
|
A | G | 4 | a0007c0020t0001g0312a0009c0023t0001g0291a0009c0023t0001g0292others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+21468A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93207078 | ||||||
| chr9:93207279
|
A | G | 1 | a0007c0020t0001g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.681+21669A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93207279 | ||||||
| chr9:93207316
|
C | A | 1 | a0001c0007t0001g0274 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.681+21706C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93207316 | ||||||
| chr9:93207346
|
G | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.681+21736G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93207346 | ||||||
| chr9:93207441
|
G | T | 14 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(11): Show | 14 | HG01081.hp1 HG01109.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.681+21831G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93207441 | ||||||
| chr9:93207626
|
G | C | 1 | a0004c0006t0001g0090 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.681+22016G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93207626 | ||||||
| chr9:93207751
|
G | A | 11 | a0004c0006t0001g0080a0004c0006t0001g0081a0004c0006t0001g0082others(8): Show | 11 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.682-21945G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93207751 | ||||||
| chr9:93207850
|
AG | A | 8 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(5): Show | 8 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.682-21845delG | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93207850 | ||||||
| chr9:93207903
|
G | A | 14 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(11): Show | 14 | HG01081.hp1 HG01109.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.682-21793G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93207903 | ||||||
| chr9:93208042
|
C | A | 1 | a0001c0008t0001g0063 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.682-21654C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208042 | ||||||
| chr9:93208088
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-21608C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208088 | ||||||
| chr9:93208111
|
A | G | 18 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(15): Show | 18 | HG01081.hp1 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.682-21585A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208111 | ||||||
| chr9:93208467
|
C | T | 3 | a0004c0006t0001g0078a0004c0006t0001g0079a0008c0061t0001g0290 | 3 | HG02818.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.682-21229C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208467 | ||||||
| chr9:93208509
|
G | A | 8 | a0004c0006t0001g0083a0004c0006t0001g0084a0004c0006t0001g0085others(5): Show | 8 | HG00438.hp1 HG02523.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.682-21187G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208509 | ||||||
| chr9:93208545
|
G | T | 13 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(10): Show | 13 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.682-21151G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208545 | ||||||
| chr9:93208604
|
C | CTG | 13 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(10): Show | 13 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.682-21086_682-2108 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208604 | |||||
| chr9:93208624
|
C | T | 6 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(3): Show | 6 | HG01884.hp2 HG01952.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-21072C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208624 | ||||||
| chr9:93208667
|
T | C | 1 | a0001c0002t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.682-21029T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208667 | ||||||
| chr9:93208703
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-20993C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208703 | ||||||
| chr9:93208727
|
C | T | 1 | a0018c0036t0001g0019 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.682-20969C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208727 | ||||||
| chr9:93208741
|
G | GTTC | 13 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(10): Show | 13 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.682-20954_682-2095 others(7): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208741 | |||||
| chr9:93208745
|
A | G | 4 | a0001c0002t0001g0015a0001c0002t0001g0022a0001c0002t0001g0248others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-20951A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208745 | ||||||
| chr9:93208749
|
G | GTGTTTTG others(470): Show |
135 | a0001c0002t0001g0124a0001c0002t0001g0166a0001c0002t0001g0217others(132): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.682-20944_682-2094 others(481): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208749 | |||||
| chr9:93208749
|
G | GTGTTTTG others(468): Show |
1 | a0002c0001t0001g0136 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.682-20944_682-2094 others(479): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208749 | |||||
| chr9:93208749
|
G | GTGTTTTG others(470): Show |
6 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(3): Show | 7 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.682-20944_682-2094 others(481): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208749 | |||||
| chr9:93208749
|
G | GTGTTTTG others(471): Show |
1 | a0001c0002t0001g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.682-20944_682-2094 others(482): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208749 | |||||
| chr9:93208749
|
G | GTGTTTTG others(473): Show |
3 | a0007c0020t0001g0312a0009c0023t0001g0291a0009c0023t0001g0292 | 3 | HG02258.hp2 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.682-20944_682-2094 others(484): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208749 | |||||
| chr9:93208749
|
G | GTGTTTTG others(471): Show |
1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.682-20944_682-2094 others(482): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208749 | |||||
| chr9:93208749
|
G | GTGTTTTG others(471): Show |
1 | a0001c0003t0001g0103 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.682-20944_682-2094 others(482): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208749 | |||||
| chr9:93208749
|
G | GTGTTTTG others(471): Show |
73 | a0001c0002t0001g0238a0001c0003t0001g0077a0001c0003t0001g0209others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.682-20944_682-2094 others(482): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208749 | |||||
| chr9:93208749
|
G | GTGTTTTG others(471): Show |
1 | a0001c0002t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.682-20944_682-2094 others(482): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208749 | |||||
| chr9:93208749
|
G | GTGTTTTG others(470): Show |
3 | a0001c0024t0001g0054a0001c0024t0001g0056a0027c0056t0001g0298 | 3 | HG01081.hp2 HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.682-20944_682-2094 others(481): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208749 | |||||
| chr9:93208749
|
G | GTGTTTTG others(471): Show |
1 | a0001c0002t0001g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.682-20944_682-2094 others(482): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208749 | |||||
| chr9:93208749
|
G | GTGTTTTG others(471): Show |
77 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(74): Show | 77 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.682-20944_682-2094 others(482): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208749 | |||||
| chr9:93208749
|
G | GTGTTTTG others(469): Show |
1 | a0001c0002t0001g0037 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.682-20944_682-2094 others(480): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208749 | |||||
| chr9:93208749
|
G | GTGTTTTG others(469): Show |
9 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(6): Show | 9 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-20944_682-2094 others(480): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93208749 | |||||
| chr9:93208781
|
G | A | 8 | a0001c0002t0001g0093a0001c0011t0001g0210a0001c0011t0001g0211others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.682-20915G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208781 | ||||||
| chr9:93208828
|
G | A | 1 | a0009c0023t0001g0291 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.682-20868G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208828 | ||||||
| chr9:93208857
|
C | T | 1 | a0001c0034t0001g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.682-20839C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208857 | ||||||
| chr9:93208950
|
G | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-20746G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208950 | ||||||
| chr9:93208971
|
C | T | 9 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(6): Show | 9 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-20725C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93208971 | ||||||
| chr9:93209140
|
T | C | 1 | a0002c0001t0001g0152 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.682-20556T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93209140 | ||||||
| chr9:93209192
|
G | T | 1 | a0021c0050t0001g0070 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.682-20504G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93209192 | ||||||
| chr9:93209202
|
C | T | 7 | a0002c0001t0001g0095a0002c0001t0001g0096a0002c0001t0001g0099others(4): Show | 7 | HG02109.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.682-20494C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93209202 | ||||||
| chr9:93209232
|
G | A | 2 | a0007c0020t0001g0312a0026c0045t0001g0294 | 2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.682-20464G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93209232 | ||||||
| chr9:93209253
|
G | A | 1 | a0002c0001t0001g0172 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.682-20443G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93209253 | ||||||
| chr9:93209433
|
C | T | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-20263C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93209433 | ||||||
| chr9:93209435
|
G | C | 266 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0020others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.682-20261G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93209435 | ||||||
| chr9:93209540
|
G | C | 1 | a0001c0011t0001g0215 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.682-20156G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93209540 | ||||||
| chr9:93209594
|
G | A | 266 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0020others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.682-20102G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93209594 | ||||||
| chr9:93209722
|
G | C | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.682-19974G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93209722 | ||||||
| chr9:93209940
|
G | A | 9 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(6): Show | 9 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-19756G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93209940 | ||||||
| chr9:93209974
|
C | T | 1 | a0002c0001t0001g0092 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.682-19722C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93209974 | ||||||
| chr9:93210078
|
A | G | 9 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(6): Show | 9 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-19618A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93210078 | ||||||
| chr9:93210127
|
G | T | 7 | a0001c0002t0001g0093a0001c0011t0001g0210a0001c0011t0001g0211others(4): Show | 7 | HG01884.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.682-19569G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93210127 | ||||||
| chr9:93210140
|
C | A | 12 | a0001c0002t0001g0093a0001c0011t0001g0210a0001c0011t0001g0211others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.682-19556C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93210140 | ||||||
| chr9:93210158
|
C | T | 3 | a0004c0006t0001g0080a0004c0006t0001g0081a0004c0006t0001g0082 | 3 | HG01255.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.682-19538C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93210158 | ||||||
| chr9:93210278
|
A | T | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.682-19418A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93210278 | ||||||
| chr9:93210362
|
A | G | 27 | a0001c0002t0001g0093a0001c0011t0001g0210a0001c0011t0001g0211others(24): Show | 27 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.682-19334A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93210362 | ||||||
| chr9:93210519
|
G | A | 15 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.682-19177G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93210519 | ||||||
| chr9:93210546
|
G | A | 9 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(6): Show | 9 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-19150G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93210546 | ||||||
| chr9:93210649
|
T | C | 2 | a0001c0008t0001g0010a0001c0008t0001g0011 | 2 | HG01106.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.682-19047T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93210649 | ||||||
| chr9:93211000
|
CTCACTCA others(3): Show |
C | 6 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(3): Show | 6 | HG01884.hp2 HG01952.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-18688_682-1867 others(14): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93211000 | |||||
| chr9:93211108
|
A | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-18588A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211108 | ||||||
| chr9:93211115
|
C | CACTCATC others(9): Show |
1 | a0001c0003t0001g0314 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.682-18567_682-1856 others(20): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93211115 | |||||
| chr9:93211124
|
C | A | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-18572C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211124 | ||||||
| chr9:93211131
|
T | C | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-18565T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211131 | ||||||
| chr9:93211159
|
G | C | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-18537G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211159 | ||||||
| chr9:93211178
|
C | T | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-18518C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211178 | ||||||
| chr9:93211196
|
A | G | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-18500A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211196 | ||||||
| chr9:93211213
|
A | C | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-18483A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211213 | ||||||
| chr9:93211215
|
C | T | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-18481C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211215 | ||||||
| chr9:93211216
|
A | G | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-18480A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211216 | ||||||
| chr9:93211226
|
T | TCACTCAC others(265): Show |
3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-18460_682-1845 others(276): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93211226 | |||||
| chr9:93211226
|
T | TCACTCAC others(261): Show |
4 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(1): Show | 4 | HG01884.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-18460_682-1845 others(272): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93211226 | |||||
| chr9:93211234
|
T | TCATCCAC others(217): Show |
2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.682-18460_682-1845 others(228): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93211234 | |||||
| chr9:93211238
|
T | TCACTCAT others(149): Show |
6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-18456_682-1845 others(160): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93211238 | |||||
| chr9:93211239
|
C | T | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.682-18457C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211239 | ||||||
| chr9:93211241
|
T | C | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-18455T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211241 | ||||||
| chr9:93211242
|
T | C | 305 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.682-18454T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211242 | ||||||
| chr9:93211249
|
C | G | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.682-18447C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211249 | ||||||
| chr9:93211249
|
C | T | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-18447C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211249 | ||||||
| chr9:93211250
|
T | A | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-18446T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211250 | ||||||
| chr9:93211250
|
T | TCATA | 7 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(4): Show | 7 | HG01081.hp1 HG01884.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.682-18444_682-1844 others(8): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93211250 | |||||
| chr9:93211257
|
T | G | 13 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(10): Show | 13 | HG01081.hp1 HG01884.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.682-18439T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211257 | ||||||
| chr9:93211257
|
T | TCCACTCA others(273): Show |
295 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(292): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.682-18439_682-1843 others(284): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211257 | ||||||
| chr9:93211257
|
T | TCCACTCA others(269): Show |
3 | a0001c0002t0001g0061a0001c0002t0001g0062a0004c0006t0001g0079 | 3 | HG02818.hp1 NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.682-18439_682-1843 others(280): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211257 | ||||||
| chr9:93211262
|
T | C | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.682-18434T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211262 | ||||||
| chr9:93211265
|
T | C | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.682-18431T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211265 | ||||||
| chr9:93211278
|
C | A | 2 | a0008c0026t0001g0305a0008c0026t0001g0306 | 2 | HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.682-18418C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211278 | ||||||
| chr9:93211278
|
C | CCACTCAC others(21): Show |
2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.682-18406_682-1837 others(32): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93211278 | |||||
| chr9:93211345
|
T | TTCAC | 15 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.682-18347_682-1834 others(8): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93211345 | |||||
| chr9:93211437
|
C | A | 12 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0032others(9): Show | 12 | HG00621.hp2 HG02040.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.682-18259C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211437 | ||||||
| chr9:93211598
|
CCACT | C | 3 | a0001c0003t0001g0219a0001c0003t0001g0233a0008c0026t0001g0305 | 3 | HG00733.hp2 HG02622.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.682-18090_682-1808 others(8): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93211598 | |||||
| chr9:93211626
|
C | T | 12 | a0001c0002t0001g0093a0001c0011t0001g0210a0001c0011t0001g0211others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.682-18070C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211626 | ||||||
| chr9:93211650
|
CCACTCAT others(5): Show |
C | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-18032_682-1802 others(16): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93211650 | |||||
| chr9:93211652
|
A | G | 2 | a0001c0008t0001g0010a0001c0008t0001g0011 | 2 | HG01106.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.682-18044A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211652 | ||||||
| chr9:93211765
|
G | A | 9 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(6): Show | 9 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-17931G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211765 | ||||||
| chr9:93211838
|
G | A | 15 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.682-17858G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211838 | ||||||
| chr9:93211854
|
C | A | 15 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.682-17842C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211854 | ||||||
| chr9:93211864
|
A | T | 15 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.682-17832A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211864 | ||||||
| chr9:93211867
|
T | C | 15 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.682-17829T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211867 | ||||||
| chr9:93211876
|
T | C | 15 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.682-17820T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211876 | ||||||
| chr9:93211877
|
C | T | 15 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.682-17819C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211877 | ||||||
| chr9:93211880
|
A | T | 15 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.682-17816A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211880 | ||||||
| chr9:93211883
|
C | T | 15 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.682-17813C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211883 | ||||||
| chr9:93211887
|
CACAT | C | 15 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.682-17808_682-1780 others(8): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211887 | ||||||
| chr9:93211892
|
T | C | 1 | a0001c0002t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.682-17804T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211892 | ||||||
| chr9:93211893
|
T | C | 15 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.682-17803T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211893 | ||||||
| chr9:93211999
|
G | T | 9 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(6): Show | 9 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-17697G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93211999 | ||||||
| chr9:93212005
|
AT | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-17689delT | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93212005 | |||||
| chr9:93212293
|
T | C | 1 | a0007c0020t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.682-17403T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93212293 | ||||||
| chr9:93212500
|
T | A | 9 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(6): Show | 9 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-17196T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93212500 | ||||||
| chr9:93212547
|
T | C | 2 | a0001c0004t0002g0265a0001c0004t0002g0266 | 2 | HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.682-17149T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93212547 | ||||||
| chr9:93212548
|
C | T | 1 | a0001c0002t0001g0015 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.682-17148C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93212548 | ||||||
| chr9:93212586
|
C | T | 6 | a0001c0028t0001g0310a0001c0028t0001g0311a0007c0020t0001g0312others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-17110C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93212586 | ||||||
| chr9:93212605
|
G | A | 1 | a0005c0019t0001g0139 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.682-17091G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93212605 | ||||||
| chr9:93212606
|
G | T | 9 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(6): Show | 9 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-17090G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93212606 | ||||||
| chr9:93212785
|
G | A | 9 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(6): Show | 9 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-16911G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93212785 | ||||||
| chr9:93213052
|
C | A | 1 | a0001c0003t0001g0221 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.682-16644C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213052 | ||||||
| chr9:93213061
|
A | AG | 143 | a0001c0002t0001g0124a0001c0002t0001g0166a0001c0002t0001g0217others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.682-16632dupG | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93213061 | |||||
| chr9:93213064
|
G | A | 1 | a0001c0028t0001g0311 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.682-16632G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213064 | ||||||
| chr9:93213077
|
T | C | 9 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(6): Show | 9 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-16619T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213077 | ||||||
| chr9:93213168
|
A | G | 4 | a0007c0020t0001g0312a0009c0023t0001g0291a0009c0023t0001g0292others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-16528A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213168 | ||||||
| chr9:93213253
|
G | A | 9 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(6): Show | 9 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-16443G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213253 | ||||||
| chr9:93213282
|
G | A | 6 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(3): Show | 6 | HG01884.hp2 HG01952.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-16414G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213282 | ||||||
| chr9:93213483
|
G | T | 1 | a0001c0003t0001g0314 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.682-16213G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213483 | ||||||
| chr9:93213511
|
C | T | 2 | a0001c0024t0001g0054a0001c0024t0001g0056 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.682-16185C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213511 | ||||||
| chr9:93213581
|
G | A | 1 | a0001c0002t0001g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.682-16115G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213581 | ||||||
| chr9:93213624
|
G | A | 1 | a0021c0050t0001g0070 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.682-16072G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213624 | ||||||
| chr9:93213714
|
A | G | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-15982A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213714 | ||||||
| chr9:93213721
|
A | G | 1 | a0001c0048t0001g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.682-15975A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213721 | ||||||
| chr9:93213730
|
A | T | 1 | a0001c0022t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.682-15966A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213730 | ||||||
| chr9:93213737
|
C | T | 69 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0020others(66): Show | 69 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.682-15959C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213737 | ||||||
| chr9:93213790
|
AAAAAC | A | 18 | a0001c0002t0001g0093a0001c0011t0001g0210a0001c0011t0001g0211others(15): Show | 18 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.682-15886_682-1588 others(9): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93213790 | |||||
| chr9:93213833
|
AGATTACA others(4): Show |
A | 1 | a0001c0002t0001g0059 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.682-15861_682-1585 others(15): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93213833 | |||||
| chr9:93213971
|
A | G | 2 | a0007c0020t0001g0312a0027c0056t0001g0298 | 2 | HG01081.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.682-15725A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213971 | ||||||
| chr9:93213981
|
G | A | 76 | a0001c0002t0001g0047a0001c0002t0001g0093a0001c0003t0001g0077others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.682-15715G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93213981 | ||||||
| chr9:93214212
|
C | T | 1 | a0005c0027t0001g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.682-15484C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214212 | ||||||
| chr9:93214266
|
C | A | 1 | a0001c0002t0001g0238 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.682-15430C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214266 | ||||||
| chr9:93214292
|
T | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-15404T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214292 | ||||||
| chr9:93214303
|
T | A | 103 | a0001c0003t0001g0170a0001c0004t0002g0260a0001c0004t0002g0261others(100): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.682-15393T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214303 | ||||||
| chr9:93214313
|
A | T | 77 | a0001c0002t0001g0093a0001c0003t0001g0077a0001c0003t0001g0103others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.682-15383A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214313 | ||||||
| chr9:93214326
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-15370C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214326 | ||||||
| chr9:93214327
|
G | A | 2 | a0002c0001t0001g0176a0002c0001t0001g0178 | 2 | HG01175.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.682-15369G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214327 | ||||||
| chr9:93214462
|
C | G | 1 | a0001c0003t0001g0241 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.682-15234C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214462 | ||||||
| chr9:93214492
|
C | T | 4 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0032others(1): Show | 4 | HG00621.hp2 NA19064.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-15204C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214492 | ||||||
| chr9:93214667
|
C | T | 21 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(18): Show | 21 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.682-15029C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214667 | ||||||
| chr9:93214696
|
T | G | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.682-15000T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214696 | ||||||
| chr9:93214697
|
G | GC | 17 | a0001c0003t0001g0236a0001c0003t0001g0243a0001c0003t0001g0251others(14): Show | 18 | HG01071.hp1 HG01071.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.682-14985dupC | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93214697 | |||||
| chr9:93214697
|
GC | G | 47 | a0001c0003t0001g0077a0001c0003t0001g0221a0001c0003t0001g0222others(44): Show | 47 | HG00140.hp2 HG00673.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.682-14985delC | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93214697 | |||||
| chr9:93214697
|
GCC | G | 21 | a0001c0003t0001g0233a0001c0003t0001g0237a0001c0009t0001g0199others(18): Show | 21 | HG00280.hp1 HG00544.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.682-14986_682-1498 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93214697 | |||||
| chr9:93214697
|
GCCC | G | 56 | a0001c0003t0001g0314a0001c0004t0002g0002a0001c0004t0002g0206others(53): Show | 57 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.682-14987_682-1498 others(7): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93214697 | |||||
| chr9:93214705
|
C | CCCCCG | 30 | a0001c0002t0001g0003a0001c0002t0001g0020a0001c0002t0001g0031others(27): Show | 30 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.682-14987_682-1498 others(9): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93214705 | |||||
| chr9:93214705
|
C | CCCCG | 37 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0018others(34): Show | 37 | HG00735.hp2 HG01256.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.682-14988_682-1498 others(8): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93214705 | |||||
| chr9:93214705
|
C | G | 3 | a0001c0003t0001g0239a0001c0003t0001g0240a0001c0003t0001g0241 | 3 | HG00323.hp2 HG02559.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.682-14991C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214705 | ||||||
| chr9:93214706
|
C | G | 1 | a0002c0001t0001g0150 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.682-14990C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214706 | ||||||
| chr9:93214707
|
C | G | 54 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(51): Show | 55 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.682-14989C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214707 | ||||||
| chr9:93214711
|
C | CT | 23 | a0001c0025t0001g0163a0002c0001t0001g0012a0002c0001t0001g0095others(20): Show | 23 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.682-14985_682-1498 others(5): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214711 | ||||||
| chr9:93214711
|
C | T | 37 | a0001c0003t0001g0170a0001c0014t0002g0255a0001c0014t0002g0300others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.682-14985C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214711 | ||||||
| chr9:93214716
|
T | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-14980T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93214716 | ||||||
| chr9:93214876
|
CATTATT | C | 13 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(10): Show | 13 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.682-14804_682-1479 others(10): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93214876 | |||||
| chr9:93215110
|
T | A | 1 | a0001c0059t0001g0304 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.682-14586T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215110 | ||||||
| chr9:93215184
|
C | T | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.682-14512C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215184 | ||||||
| chr9:93215191
|
G | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-14505G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215191 | ||||||
| chr9:93215212
|
C | T | 1 | a0001c0004t0002g0264 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.682-14484C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215212 | ||||||
| chr9:93215310
|
A | G | 54 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(51): Show | 55 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.682-14386A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215310 | ||||||
| chr9:93215392
|
A | G | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-14304A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215392 | ||||||
| chr9:93215441
|
T | C | 1 | a0001c0003t0001g0243 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.682-14255T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215441 | ||||||
| chr9:93215553
|
G | A | 1 | a0004c0006t0001g0090 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.682-14143G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215553 | ||||||
| chr9:93215660
|
T | C | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-14036T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215660 | ||||||
| chr9:93215758
|
A | G | 54 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(51): Show | 55 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.682-13938A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215758 | ||||||
| chr9:93215818
|
C | T | 1 | a0001c0003t0001g0242 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.682-13878C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215818 | ||||||
| chr9:93215824
|
G | A | 4 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(1): Show | 5 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-13872G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215824 | ||||||
| chr9:93215844
|
A | G | 1 | a0001c0007t0001g0273 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.682-13852A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215844 | ||||||
| chr9:93215867
|
C | G | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-13829C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215867 | ||||||
| chr9:93215882
|
G | A | 1 | a0007c0020t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.682-13814G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215882 | ||||||
| chr9:93215896
|
C | A | 230 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(227): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.682-13800C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215896 | ||||||
| chr9:93215941
|
G | A | 1 | a0004c0006t0001g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.682-13755G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215941 | ||||||
| chr9:93215968
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-13728C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215968 | ||||||
| chr9:93215983
|
G | A | 39 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(36): Show | 40 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.682-13713G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93215983 | ||||||
| chr9:93216086
|
A | C | 38 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0209others(35): Show | 38 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.682-13610A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93216086 | ||||||
| chr9:93216090
|
C | A | 2 | a0001c0025t0001g0163a0002c0001t0001g0164 | 2 | NA18955.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.682-13606C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93216090 | ||||||
| chr9:93216217
|
T | C | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-13479T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93216217 | ||||||
| chr9:93216324
|
G | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.682-13372G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93216324 | ||||||
| chr9:93216558
|
C | T | 1 | a0008c0061t0001g0290 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.682-13138C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93216558 | ||||||
| chr9:93216658
|
G | A | 5 | a0001c0003t0001g0170a0002c0001t0001g0168a0002c0001t0001g0169others(2): Show | 5 | HG00099.hp1 HG01074.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-13038G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93216658 | ||||||
| chr9:93216699
|
C | G | 13 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(10): Show | 13 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.682-12997C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93216699 | ||||||
| chr9:93216725
|
C | A | 1 | a0001c0002t0001g0035 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.682-12971C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93216725 | ||||||
| chr9:93216756
|
T | C | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.682-12940T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93216756 | ||||||
| chr9:93216826
|
CA | C | 296 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(293): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.682-12867delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93216826 | |||||
| chr9:93216827
|
A | AAC | 7 | a0001c0003t0001g0237a0004c0006t0001g0083a0004c0006t0001g0084others(4): Show | 7 | HG00544.hp1 HG02523.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.682-12868_682-1286 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93216827 | |||||
| chr9:93216966
|
C | CTT | 55 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(52): Show | 56 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.682-12720_682-1271 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93216966 | |||||
| chr9:93216972
|
T | C | 1 | a0001c0002t0001g0166 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.682-12724T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93216972 | ||||||
| chr9:93217012
|
G | C | 4 | a0001c0008t0001g0023a0001c0008t0001g0024a0001c0008t0001g0025others(1): Show | 4 | HG03490.hp1 HG03492.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-12684G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93217012 | ||||||
| chr9:93217173
|
G | C | 13 | a0002c0001t0001g0012a0002c0001t0001g0138a0002c0001t0001g0150others(10): Show | 13 | HG00438.hp2 HG02523.hp2 NA18944.hp2 others(10): Show |
intron_variant | MODIFIER | c.682-12523G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93217173 | ||||||
| chr9:93217269
|
T | G | 2 | a0001c0003t0001g0219a0001c0003t0001g0233 | 2 | HG00733.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.682-12427T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93217269 | ||||||
| chr9:93217279
|
C | T | 1 | a0001c0032t0001g0017 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.682-12417C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93217279 | ||||||
| chr9:93217296
|
A | T | 16 | a0001c0003t0001g0077a0001c0003t0001g0239a0001c0003t0001g0240others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.682-12400A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93217296 | ||||||
| chr9:93217428
|
T | C | 1 | a0001c0003t0001g0077 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.682-12268T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93217428 | ||||||
| chr9:93217506
|
C | T | 1 | a0001c0015t0001g0293 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.682-12190C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93217506 | ||||||
| chr9:93217536
|
C | T | 1 | a0001c0004t0002g0285 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.682-12160C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93217536 | ||||||
| chr9:93217779
|
T | C | 1 | a0008c0061t0001g0290 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.682-11917T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93217779 | ||||||
| chr9:93217804
|
G | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.682-11892G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93217804 | ||||||
| chr9:93217862
|
C | G | 1 | a0001c0003t0001g0307 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.682-11834C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93217862 | ||||||
| chr9:93217871
|
CT | C | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.682-11824delT | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93217871 | ||||||
| chr9:93218050
|
C | T | 68 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(65): Show | 68 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.682-11646C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93218050 | ||||||
| chr9:93218297
|
G | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.682-11399G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93218297 | ||||||
| chr9:93218346
|
C | T | 1 | a0001c0059t0001g0304 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.682-11350C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93218346 | ||||||
| chr9:93218386
|
C | T | 1 | a0001c0009t0001g0203 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.682-11310C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93218386 | ||||||
| chr9:93218435
|
C | T | 18 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(15): Show | 18 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.682-11261C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93218435 | ||||||
| chr9:93218624
|
C | T | 2 | a0001c0024t0001g0054a0001c0024t0001g0056 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.682-11072C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93218624 | ||||||
| chr9:93218666
|
G | A | 1 | a0001c0022t0001g0008 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.682-11030G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93218666 | ||||||
| chr9:93218733
|
A | C | 1 | a0004c0006t0001g0087 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.682-10963A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93218733 | ||||||
| chr9:93218861
|
G | T | 2 | a0002c0001t0001g0171a0002c0001t0001g0174 | 2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.682-10835G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93218861 | ||||||
| chr9:93218870
|
C | T | 1 | a0001c0003t0001g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.682-10826C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93218870 | ||||||
| chr9:93218885
|
G | A | 18 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(15): Show | 18 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.682-10811G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93218885 | ||||||
| chr9:93218903
|
G | A | 3 | a0001c0003t0001g0239a0001c0003t0001g0240a0001c0003t0001g0241 | 3 | HG00323.hp2 HG02559.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.682-10793G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93218903 | ||||||
| chr9:93218932
|
C | G | 4 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(1): Show | 4 | HG01884.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-10764C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93218932 | ||||||
| chr9:93218944
|
G | A | 1 | a0001c0032t0001g0017 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.682-10752G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93218944 | ||||||
| chr9:93219068
|
G | A | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.682-10628G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93219068 | ||||||
| chr9:93219096
|
G | T | 23 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0029others(20): Show | 23 | HG00140.hp1 HG00621.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.682-10600G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93219096 | ||||||
| chr9:93219214
|
C | T | 54 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(51): Show | 55 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.682-10482C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93219214 | ||||||
| chr9:93219256
|
C | T | 1 | a0001c0004t0002g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.682-10440C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93219256 | ||||||
| chr9:93219277
|
C | T | 54 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(51): Show | 55 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.682-10419C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93219277 | ||||||
| chr9:93219457
|
C | A | 1 | a0005c0030t0001g0208 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.682-10239C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93219457 | ||||||
| chr9:93219546
|
T | G | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-10150T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93219546 | ||||||
| chr9:93219637
|
A | T | 1 | a0004c0006t0001g0090 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.682-10059A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93219637 | ||||||
| chr9:93219777
|
G | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-9919G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93219777 | ||||||
| chr9:93219778
|
C | T | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.682-9918C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93219778 | ||||||
| chr9:93219864
|
A | T | 2 | a0001c0003t0001g0247a0001c0003t0001g0295 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.682-9832A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93219864 | ||||||
| chr9:93219940
|
G | A | 1 | a0001c0007t0001g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.682-9756G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93219940 | ||||||
| chr9:93219979
|
G | C | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-9717G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93219979 | ||||||
| chr9:93220033
|
C | T | 1 | a0005c0027t0001g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.682-9663C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220033 | ||||||
| chr9:93220042
|
T | C | 2 | a0001c0004t0002g0257a0001c0004t0002g0258 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.682-9654T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220042 | ||||||
| chr9:93220043
|
G | T | 1 | a0001c0059t0001g0304 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.682-9653G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220043 | ||||||
| chr9:93220047
|
A | G | 1 | a0001c0007t0001g0028 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.682-9649A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220047 | ||||||
| chr9:93220146
|
T | C | 1 | a0001c0009t0001g0204 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.682-9550T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220146 | ||||||
| chr9:93220165
|
G | A | 2 | a0002c0001t0001g0106a0002c0001t0001g0128 | 2 | HG02738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.682-9531G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220165 | ||||||
| chr9:93220173
|
A | G | 1 | a0001c0007t0001g0281 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.682-9523A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220173 | ||||||
| chr9:93220229
|
A | G | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-9467A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220229 | ||||||
| chr9:93220283
|
G | A | 68 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(65): Show | 68 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.682-9413G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220283 | ||||||
| chr9:93220298
|
C | T | 1 | a0001c0003t0001g0242 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.682-9398C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220298 | ||||||
| chr9:93220359
|
C | T | 1 | a0001c0002t0001g0029 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.682-9337C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220359 | ||||||
| chr9:93220734
|
G | T | 4 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-8962G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220734 | ||||||
| chr9:93220763
|
G | A | 98 | a0001c0003t0001g0170a0001c0014t0002g0255a0001c0014t0002g0299others(95): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.682-8933G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220763 | ||||||
| chr9:93220768
|
G | A | 1 | a0002c0001t0001g0174 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.682-8928G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220768 | ||||||
| chr9:93220799
|
G | A | 2 | a0009c0023t0001g0291a0009c0023t0001g0292 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.682-8897G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220799 | ||||||
| chr9:93220858
|
G | A | 3 | a0001c0003t0001g0239a0001c0003t0001g0240a0001c0003t0001g0241 | 3 | HG00323.hp2 HG02559.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.682-8838G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220858 | ||||||
| chr9:93220983
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-8713C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93220983 | ||||||
| chr9:93221100
|
C | T | 2 | a0001c0004t0002g0206a0001c0004t0002g0282 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.682-8596C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221100 | ||||||
| chr9:93221118
|
C | G | 1 | a0001c0008t0001g0023 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.682-8578C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221118 | ||||||
| chr9:93221181
|
A | G | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-8515A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221181 | ||||||
| chr9:93221328
|
T | C | 299 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.682-8368T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221328 | ||||||
| chr9:93221349
|
G | A | 1 | a0002c0001t0001g0169 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.682-8347G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221349 | ||||||
| chr9:93221396
|
T | C | 299 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.682-8300T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221396 | ||||||
| chr9:93221489
|
C | G | 5 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-8207C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221489 | ||||||
| chr9:93221554
|
A | G | 1 | a0001c0003t0001g0314 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.682-8142A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221554 | ||||||
| chr9:93221586
|
G | A | 1 | a0002c0010t0001g0181 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.682-8110G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221586 | ||||||
| chr9:93221704
|
G | A | 54 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(51): Show | 55 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.682-7992G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221704 | ||||||
| chr9:93221789
|
G | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-7907G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221789 | ||||||
| chr9:93221799
|
G | A | 1 | a0010c0054t0001g0071 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.682-7897G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221799 | ||||||
| chr9:93221901
|
G | A | 1 | a0001c0017t0001g0122 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.682-7795G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221901 | ||||||
| chr9:93221917
|
G | A | 8 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(5): Show | 8 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.682-7779G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221917 | ||||||
| chr9:93221973
|
G | C | 1 | a0011c0062t0001g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.682-7723G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93221973 | ||||||
| chr9:93222035
|
G | A | 39 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(36): Show | 40 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.682-7661G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93222035 | ||||||
| chr9:93222113
|
GGT | G | 98 | a0001c0003t0001g0170a0001c0014t0002g0255a0001c0014t0002g0299others(95): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.682-7581_682-7580d others(4): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93222113 | |||||
| chr9:93222159
|
C | T | 66 | a0001c0003t0001g0170a0001c0025t0001g0027a0001c0025t0001g0163others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.682-7537C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93222159 | ||||||
| chr9:93222325
|
C | T | 1 | a0002c0001t0001g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.682-7371C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93222325 | ||||||
| chr9:93222455
|
G | T | 4 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(1): Show | 4 | HG01884.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-7241G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93222455 | ||||||
| chr9:93222472
|
A | G | 68 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(65): Show | 68 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.682-7224A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93222472 | ||||||
| chr9:93222478
|
C | T | 54 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(51): Show | 55 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.682-7218C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93222478 | ||||||
| chr9:93222650
|
T | C | 1 | a0005c0012t0001g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.682-7046T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93222650 | ||||||
| chr9:93222724
|
C | T | 1 | a0002c0043t0001g0121 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.682-6972C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93222724 | ||||||
| chr9:93222884
|
A | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-6812A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93222884 | ||||||
| chr9:93222962
|
G | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-6734G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93222962 | ||||||
| chr9:93222999
|
A | G | 98 | a0001c0003t0001g0170a0001c0014t0002g0255a0001c0014t0002g0299others(95): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.682-6697A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93222999 | ||||||
| chr9:93223106
|
T | C | 1 | a0001c0007t0001g0269 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.682-6590T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93223106 | ||||||
| chr9:93223281
|
G | A | 3 | a0001c0002t0001g0072a0001c0049t0001g0073a0010c0054t0001g0071 | 3 | HG03239.hp2 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.682-6415G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93223281 | ||||||
| chr9:93223310
|
C | T | 41 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0209others(38): Show | 41 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.682-6386C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93223310 | ||||||
| chr9:93223371
|
C | T | 155 | a0001c0003t0001g0170a0001c0004t0002g0002a0001c0004t0002g0206others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.682-6325C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93223371 | ||||||
| chr9:93223432
|
T | C | 303 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.682-6264T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93223432 | ||||||
| chr9:93223662
|
C | T | 2 | a0002c0001t0001g0118a0002c0001t0001g0119 | 2 | HG02135.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.682-6034C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93223662 | ||||||
| chr9:93223847
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.682-5849G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93223847 | ||||||
| chr9:93223901
|
TC | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-5792delC | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93223901 | |||||
| chr9:93224186
|
C | T | 1 | a0003c0005t0001g0117 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.682-5510C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93224186 | ||||||
| chr9:93224195
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.682-5501C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93224195 | ||||||
| chr9:93224315
|
C | T | 1 | a0018c0036t0001g0019 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.682-5381C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93224315 | ||||||
| chr9:93224468
|
T | A | 1 | a0002c0010t0001g0181 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.682-5228T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93224468 | ||||||
| chr9:93224515
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-5181C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93224515 | ||||||
| chr9:93224557
|
C | T | 2 | a0001c0003t0001g0314a0002c0001t0001g0107 | 2 | NA18990.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.682-5139C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93224557 | ||||||
| chr9:93224715
|
C | T | 38 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0209others(35): Show | 38 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.682-4981C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93224715 | ||||||
| chr9:93224733
|
A | G | 1 | a0001c0003t0001g0230 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.682-4963A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93224733 | ||||||
| chr9:93225230
|
A | G | 7 | a0005c0012t0001g0192a0005c0012t0001g0193a0005c0012t0001g0194others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.682-4466A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93225230 | ||||||
| chr9:93225233
|
T | G | 1 | a0023c0033t0001g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.682-4463T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93225233 | ||||||
| chr9:93225261
|
T | C | 19 | a0002c0001t0001g0106a0002c0001t0001g0120a0002c0001t0001g0128others(16): Show | 20 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.682-4435T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93225261 | ||||||
| chr9:93225339
|
T | C | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-4357T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93225339 | ||||||
| chr9:93225612
|
C | T | 1 | a0001c0059t0001g0304 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.682-4084C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93225612 | ||||||
| chr9:93225914
|
A | ATGTTG | 14 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(11): Show | 15 | HG00639.hp2 HG00642.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.682-3750_682-3746d others(7): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93225914 | |||||
| chr9:93225914
|
A | ATGTTGTG others(3): Show |
12 | a0001c0007t0001g0028a0001c0007t0001g0256a0001c0007t0001g0269others(9): Show | 12 | HG00673.hp2 HG01081.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.682-3755_682-3746d others(12): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93225914 | |||||
| chr9:93225914
|
A | ATGTTGTG others(8): Show |
10 | a0001c0004t0002g0260a0001c0004t0002g0261a0001c0004t0002g0262others(7): Show | 10 | HG01993.hp1 HG02135.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.682-3760_682-3746d others(17): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93225914 | |||||
| chr9:93225914
|
A | G | 3 | a0004c0006t0001g0080a0004c0006t0001g0081a0004c0006t0001g0082 | 3 | HG01255.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.682-3782A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93225914 | ||||||
| chr9:93225914
|
ATGTTG | A | 176 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0209others(173): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.682-3750_682-3746d others(7): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93225914 | |||||
| chr9:93225914
|
ATGTTGTG others(3): Show |
A | 71 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.682-3755_682-3746d others(12): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93225914 | |||||
| chr9:93225914
|
ATGTTGTG others(8): Show |
A | 1 | a0002c0001t0001g0153 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.682-3760_682-3746d others(17): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93225914 | |||||
| chr9:93225951
|
A | G | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.682-3745A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93225951 | ||||||
| chr9:93226164
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-3532C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93226164 | ||||||
| chr9:93226189
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-3507C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93226189 | ||||||
| chr9:93226283
|
C | G | 3 | a0001c0059t0001g0304a0008c0026t0001g0305a0008c0026t0001g0306 | 3 | HG01255.hp1 HG02970.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.682-3413C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93226283 | ||||||
| chr9:93226472
|
A | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-3224A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93226472 | ||||||
| chr9:93226686
|
C | T | 230 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(227): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.682-3010C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93226686 | ||||||
| chr9:93226697
|
G | C | 1 | a0002c0001t0001g0007 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.682-2999G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93226697 | ||||||
| chr9:93226900
|
A | G | 68 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(65): Show | 68 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.682-2796A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93226900 | ||||||
| chr9:93226950
|
T | C | 1 | a0009c0023t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.682-2746T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93226950 | ||||||
| chr9:93227039
|
C | T | 4 | a0002c0010t0001g0173a0002c0010t0001g0185a0002c0010t0001g0191others(1): Show | 4 | HG00099.hp2 HG00733.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-2657C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93227039 | ||||||
| chr9:93227117
|
C | CT | 56 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(53): Show | 57 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.682-2563dupT | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93227117 | |||||
| chr9:93227117
|
CT | C | 18 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(15): Show | 18 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.682-2563delT | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93227117 | |||||
| chr9:93227228
|
C | T | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.682-2468C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93227228 | ||||||
| chr9:93227262
|
C | T | 1 | a0001c0002t0001g0309 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.682-2434C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93227262 | ||||||
| chr9:93227270
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-2426C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93227270 | ||||||
| chr9:93227315
|
A | G | 188 | a0001c0003t0001g0170a0001c0004t0002g0002a0001c0004t0002g0206others(185): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.682-2381A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93227315 | ||||||
| chr9:93227409
|
G | A | 1 | a0001c0002t0001g0046 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.682-2287G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93227409 | ||||||
| chr9:93227759
|
C | T | 4 | a0001c0004t0002g0206a0001c0004t0002g0282a0001c0004t0002g0285others(1): Show | 4 | HG01515.hp1 HG02280.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-1937C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93227759 | ||||||
| chr9:93227818
|
G | A | 1 | a0001c0015t0001g0293 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.682-1878G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93227818 | ||||||
| chr9:93227875
|
A | G | 13 | a0001c0002t0001g0006a0001c0002t0001g0020a0001c0002t0001g0044others(10): Show | 13 | HG00597.hp1 HG00609.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.682-1821A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93227875 | ||||||
| chr9:93228219
|
C | T | 74 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0209others(71): Show | 74 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1477C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93228219 | ||||||
| chr9:93228220
|
G | A | 1 | a0001c0004t0002g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.682-1476G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93228220 | ||||||
| chr9:93228234
|
A | C | 3 | a0001c0059t0001g0304a0004c0006t0001g0078a0004c0006t0001g0079 | 3 | HG02818.hp1 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.682-1462A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93228234 | ||||||
| chr9:93228271
|
A | AT | 5 | a0001c0003t0001g0224a0005c0012t0001g0192a0005c0012t0001g0193others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.682-1417dupT | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93228271 | |||||
| chr9:93228327
|
C | T | 1 | a0001c0002t0001g0049 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.682-1369C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93228327 | ||||||
| chr9:93228454
|
G | T | 58 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(55): Show | 59 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.682-1242G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93228454 | ||||||
| chr9:93228504
|
G | A | 8 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(5): Show | 8 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.682-1192G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93228504 | ||||||
| chr9:93228740
|
G | C | 1 | a0001c0002t0001g0309 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.682-956G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93228740 | ||||||
| chr9:93228935
|
C | T | 3 | a0001c0059t0001g0304a0004c0006t0001g0078a0004c0006t0001g0079 | 3 | HG02818.hp1 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.682-761C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93228935 | ||||||
| chr9:93228957
|
G | A | 1 | a0001c0018t0001g0004 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.682-739G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93228957 | ||||||
| chr9:93229176
|
TGC | T | 4 | a0001c0008t0001g0023a0001c0008t0001g0024a0001c0008t0001g0025others(1): Show | 4 | HG03490.hp1 HG03492.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-519_682-518del others(2): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93229176 | ||||||
| chr9:93229265
|
C | T | 55 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(52): Show | 56 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.682-431C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93229265 | ||||||
| chr9:93229307
|
T | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-389T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93229307 | ||||||
| chr9:93229522
|
AAGG | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.682-171_682-169del others(3): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr9 | 93229522 | |||||
| chr9:93229613
|
T | C | 58 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(55): Show | 59 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.682-83T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 2/29 | chr9 | 93229613 | ||||||
| chr9:93229931
|
A | G | 299 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.854+63A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93229931 | ||||||
| chr9:93229958
|
G | T | 55 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(52): Show | 56 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.854+90G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93229958 | ||||||
| chr9:93230012
|
G | T | 5 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.854+144G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230012 | ||||||
| chr9:93230037
|
G | A | 68 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(65): Show | 68 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.854+169G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230037 | ||||||
| chr9:93230121
|
C | A | 15 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.854+253C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230121 | ||||||
| chr9:93230143
|
C | T | 2 | a0001c0049t0001g0073a0010c0054t0001g0071 | 2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.854+275C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230143 | ||||||
| chr9:93230289
|
C | A | 68 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(65): Show | 68 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.854+421C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230289 | ||||||
| chr9:93230362
|
G | A | 1 | a0001c0003t0001g0237 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.854+494G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230362 | ||||||
| chr9:93230456
|
A | G | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.855-432A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230456 | ||||||
| chr9:93230491
|
C | T | 1 | a0001c0002t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.855-397C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230491 | ||||||
| chr9:93230520
|
C | T | 74 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0209others(71): Show | 74 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.855-368C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230520 | ||||||
| chr9:93230540
|
C | G | 2 | a0001c0002t0001g0058a0001c0002t0001g0059 | 2 | NA18953.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.855-348C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230540 | ||||||
| chr9:93230550
|
GCT | G | 6 | a0001c0013t0001g0125a0001c0013t0001g0145a0001c0013t0001g0148others(3): Show | 6 | NA18944.hp1 NA18962.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.855-337_855-336del others(2): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230550 | ||||||
| chr9:93230621
|
A | T | 1 | a0001c0002t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.855-267A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230621 | ||||||
| chr9:93230733
|
G | A | 53 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(50): Show | 54 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.855-155G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230733 | ||||||
| chr9:93230752
|
C | A | 2 | a0001c0002t0001g0003a0001c0002t0001g0053 | 2 | HG00140.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.855-136C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230752 | ||||||
| chr9:93230759
|
T | C | 4 | a0005c0012t0001g0192a0005c0012t0001g0193a0005c0012t0001g0194others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.855-129T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230759 | ||||||
| chr9:93230764
|
C | T | 1 | a0021c0050t0001g0070 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.855-124C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230764 | ||||||
| chr9:93230783
|
C | T | 2 | a0001c0003t0001g0230a0001c0008t0001g0016 | 2 | HG01981.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.855-105C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230783 | ||||||
| chr9:93230841
|
C | G | 2 | a0002c0001t0001g0179a0002c0001t0001g0186 | 2 | HG01192.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.855-47C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230841 | ||||||
| chr9:93230872
|
C | A | 1 | a0001c0002t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.855-16C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 3/29 | chr9 | 93230872 | ||||||
| chr9:93231147
|
G | C | 68 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(65): Show | 68 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1075+39G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93231147 | ||||||
| chr9:93231305
|
C | T | 1 | a0002c0001t0001g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1075+197C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93231305 | ||||||
| chr9:93231321
|
A | G | 312 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(309): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1075+213A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93231321 | ||||||
| chr9:93231337
|
T | C | 126 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(123): Show | 127 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.1075+229T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93231337 | ||||||
| chr9:93231475
|
G | A | 68 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(65): Show | 68 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1075+367G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93231475 | ||||||
| chr9:93231650
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1075+542C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93231650 | ||||||
| chr9:93231779
|
C | T | 1 | a0001c0021t0002g0068 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1075+671C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93231779 | ||||||
| chr9:93231802
|
C | T | 7 | a0002c0001t0001g0095a0002c0001t0001g0096a0002c0001t0001g0099others(4): Show | 7 | HG02109.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075+694C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93231802 | ||||||
| chr9:93231842
|
G | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1075+734G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93231842 | ||||||
| chr9:93231873
|
C | T | 55 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(52): Show | 56 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1075+765C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93231873 | ||||||
| chr9:93231880
|
C | G | 14 | a0003c0005t0001g0001a0003c0005t0001g0094a0003c0005t0001g0101others(11): Show | 15 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.1075+772C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93231880 | ||||||
| chr9:93231891
|
A | C | 1 | a0002c0001t0001g0007 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1075+783A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93231891 | ||||||
| chr9:93231910
|
G | A | 1 | a0005c0030t0001g0208 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1075+802G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93231910 | ||||||
| chr9:93232002
|
C | G | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1075+894C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232002 | ||||||
| chr9:93232015
|
G | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1075+907G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232015 | ||||||
| chr9:93232040
|
A | G | 1 | a0001c0004t0002g0266 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1075+932A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232040 | ||||||
| chr9:93232052
|
C | T | 1 | a0001c0004t0002g0259 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1075+944C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232052 | ||||||
| chr9:93232069
|
G | T | 2 | a0002c0001t0001g0175a0002c0001t0001g0184 | 2 | HG00735.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1075+961G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232069 | ||||||
| chr9:93232120
|
C | T | 55 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(52): Show | 56 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1075+1012C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232120 | ||||||
| chr9:93232272
|
C | T | 42 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0209others(39): Show | 42 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1075+1164C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232272 | ||||||
| chr9:93232288
|
T | G | 68 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(65): Show | 68 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1075+1180T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232288 | ||||||
| chr9:93232312
|
G | A | 68 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(65): Show | 68 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1075+1204G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232312 | ||||||
| chr9:93232417
|
G | A | 55 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(52): Show | 56 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1075+1309G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232417 | ||||||
| chr9:93232461
|
C | T | 1 | a0001c0003t0001g0219 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1075+1353C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232461 | ||||||
| chr9:93232466
|
T | C | 299 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1075+1358T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232466 | ||||||
| chr9:93232536
|
G | A | 1 | a0008c0061t0001g0290 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1075+1428G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232536 | ||||||
| chr9:93232542
|
A | G | 298 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(295): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1075+1434A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232542 | ||||||
| chr9:93232586
|
A | G | 68 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(65): Show | 68 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1075+1478A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232586 | ||||||
| chr9:93232874
|
T | G | 68 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(65): Show | 68 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1075+1766T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232874 | ||||||
| chr9:93232877
|
C | T | 68 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(65): Show | 68 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1075+1769C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232877 | ||||||
| chr9:93232924
|
C | T | 2 | a0001c0009t0001g0198a0001c0009t0001g0201 | 2 | HG02300.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1075+1816C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93232924 | ||||||
| chr9:93232964
|
C | CA | 73 | a0001c0003t0001g0077a0001c0003t0001g0222a0001c0003t0001g0223others(70): Show | 74 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1076-1823dupA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr9 | 93232964 | |||||
| chr9:93232964
|
C | CAA | 80 | a0001c0003t0001g0103a0001c0003t0001g0170a0001c0003t0001g0220others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1076-1824_1076-182 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr9 | 93232964 | |||||
| chr9:93232964
|
C | CAAA | 76 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(73): Show | 76 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.1076-1825_1076-182 others(7): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr9 | 93232964 | |||||
| chr9:93232964
|
C | CAAAA | 7 | a0001c0002t0001g0022a0001c0002t0001g0032a0001c0002t0001g0035others(4): Show | 7 | HG01361.hp2 HG02080.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.1076-1826_1076-182 others(8): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr9 | 93232964 | |||||
| chr9:93232964
|
CA | C | 13 | a0001c0004t0002g0263a0001c0004t0002g0264a0001c0007t0001g0272others(10): Show | 13 | HG01081.hp1 HG02630.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.1076-1823delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr9 | 93232964 | |||||
| chr9:93233131
|
G | A | 126 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(123): Show | 127 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.1076-1677G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93233131 | ||||||
| chr9:93233146
|
T | C | 55 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(52): Show | 56 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1076-1662T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93233146 | ||||||
| chr9:93233197
|
C | CA | 66 | a0001c0002t0001g0003a0001c0002t0001g0015a0001c0002t0001g0018others(63): Show | 66 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1076-1591dupA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr9 | 93233197 | |||||
| chr9:93233197
|
C | CAA | 8 | a0001c0002t0001g0020a0001c0002t0001g0030a0001c0002t0001g0036others(5): Show | 8 | HG00597.hp1 HG02056.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.1076-1592_1076-159 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr9 | 93233197 | |||||
| chr9:93233197
|
CA | C | 42 | a0001c0003t0001g0245a0001c0004t0002g0278a0001c0007t0001g0268others(39): Show | 42 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.1076-1591delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr9 | 93233197 | |||||
| chr9:93233197
|
CAA | C | 88 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0209others(85): Show | 89 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1076-1592_1076-159 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr9 | 93233197 | |||||
| chr9:93233286
|
G | T | 1 | a0001c0002t0001g0047 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1076-1522G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93233286 | ||||||
| chr9:93233292
|
C | A | 1 | a0007c0020t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1076-1516C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93233292 | ||||||
| chr9:93233378
|
C | T | 2 | a0001c0011t0001g0211a0001c0011t0001g0213 | 2 | HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1076-1430C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93233378 | ||||||
| chr9:93233467
|
G | A | 1 | a0009c0023t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1076-1341G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93233467 | ||||||
| chr9:93233701
|
C | CA | 212 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1076-1087dupA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr9 | 93233701 | |||||
| chr9:93233701
|
C | CAA | 10 | a0001c0002t0001g0053a0001c0002t0001g0166a0001c0003t0001g0225others(7): Show | 10 | HG00609.hp1 HG01175.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1076-1088_1076-108 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr9 | 93233701 | |||||
| chr9:93233701
|
CA | C | 10 | a0001c0004t0002g0285a0001c0007t0001g0267a0001c0007t0001g0277others(7): Show | 10 | HG01081.hp1 HG01515.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.1076-1087delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr9 | 93233701 | |||||
| chr9:93233703
|
A | T | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1076-1105A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93233703 | ||||||
| chr9:93233756
|
A | G | 1 | a0002c0001t0001g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1076-1052A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93233756 | ||||||
| chr9:93233869
|
G | A | 1 | a0002c0001t0001g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1076-939G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93233869 | ||||||
| chr9:93233943
|
A | G | 1 | a0007c0020t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1076-865A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93233943 | ||||||
| chr9:93233946
|
G | A | 2 | a0001c0002t0001g0055a0001c0002t0001g0067 | 2 | NA19079.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1076-862G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93233946 | ||||||
| chr9:93234259
|
A | C | 1 | a0001c0002t0001g0060 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1076-549A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93234259 | ||||||
| chr9:93234291
|
G | A | 154 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(151): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1076-517G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93234291 | ||||||
| chr9:93234305
|
G | T | 1 | a0002c0001t0001g0092 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1076-503G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93234305 | ||||||
| chr9:93234799
|
C | T | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1076-9C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 4/29 | chr9 | 93234799 | ||||||
| chr9:93235261
|
T | C | 62 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(59): Show | 62 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1233+296T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93235261 | ||||||
| chr9:93235353
|
A | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1233+388A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93235353 | ||||||
| chr9:93235392
|
T | C | 1 | a0015c0039t0001g0097 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1233+427T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93235392 | ||||||
| chr9:93235455
|
T | C | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1233+490T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93235455 | ||||||
| chr9:93235548
|
G | T | 2 | a0005c0012t0001g0196a0005c0012t0001g0197 | 2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1233+583G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93235548 | ||||||
| chr9:93235663
|
G | A | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1233+698G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93235663 | ||||||
| chr9:93235784
|
G | A | 1 | a0007c0020t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1233+819G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93235784 | ||||||
| chr9:93235858
|
G | C | 1 | a0001c0035t0001g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1233+893G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93235858 | ||||||
| chr9:93235947
|
C | T | 1 | a0001c0003t0001g0219 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1233+982C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93235947 | ||||||
| chr9:93236067
|
C | T | 1 | a0001c0057t0003g0275 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1233+1102C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93236067 | ||||||
| chr9:93236147
|
A | T | 2 | a0008c0026t0001g0305a0008c0026t0001g0306 | 2 | HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1233+1182A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93236147 | ||||||
| chr9:93236158
|
C | T | 3 | a0001c0007t0001g0256a0001c0007t0001g0271a0001c0007t0001g0281 | 3 | HG00673.hp2 HG02129.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1233+1193C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93236158 | ||||||
| chr9:93236162
|
C | T | 2 | a0001c0007t0001g0268a0001c0007t0001g0277 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1233+1197C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93236162 | ||||||
| chr9:93236264
|
T | C | 1 | a0004c0006t0001g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1233+1299T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93236264 | ||||||
| chr9:93236286
|
C | T | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1233+1321C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93236286 | ||||||
| chr9:93236367
|
C | T | 4 | a0001c0008t0001g0023a0001c0008t0001g0024a0001c0008t0001g0025others(1): Show | 4 | HG03490.hp1 HG03492.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+1402C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93236367 | ||||||
| chr9:93236423
|
G | C | 1 | a0005c0027t0001g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1233+1458G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93236423 | ||||||
| chr9:93236708
|
C | T | 130 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1234-1525C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93236708 | ||||||
| chr9:93236858
|
C | T | 1 | a0001c0002t0001g0062 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1234-1375C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93236858 | ||||||
| chr9:93236869
|
G | A | 5 | a0001c0034t0001g0216a0001c0035t0001g0207a0007c0020t0001g0286others(2): Show | 5 | HG01081.hp1 HG01952.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-1364G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93236869 | ||||||
| chr9:93237449
|
G | A | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1234-784G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93237449 | ||||||
| chr9:93237506
|
T | A | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1234-727T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93237506 | ||||||
| chr9:93237602
|
G | A | 2 | a0002c0001t0001g0118a0002c0001t0001g0119 | 2 | HG02135.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1234-631G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93237602 | ||||||
| chr9:93237857
|
CT | C | 79 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(76): Show | 79 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1234-362delT | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr9 | 93237857 | |||||
| chr9:93237981
|
G | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1234-252G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93237981 | ||||||
| chr9:93238051
|
C | T | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1234-182C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93238051 | ||||||
| chr9:93238156
|
G | A | 2 | a0002c0001t0001g0118a0002c0001t0001g0119 | 2 | HG02135.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1234-77G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93238156 | ||||||
| chr9:93238198
|
G | A | 5 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-35G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 5/29 | chr9 | 93238198 | ||||||
| chr9:93238340
|
C | T | 297 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1322+19C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93238340 | ||||||
| chr9:93238342
|
G | T | 2 | a0009c0023t0001g0291a0009c0023t0001g0292 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1322+21G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93238342 | ||||||
| chr9:93238410
|
G | T | 1 | a0001c0008t0001g0132 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1322+89G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93238410 | ||||||
| chr9:93238418
|
G | A | 1 | a0001c0004t0002g0284 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1322+97G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93238418 | ||||||
| chr9:93238540
|
T | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1322+219T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93238540 | ||||||
| chr9:93238576
|
C | A | 1 | a0003c0005t0001g0117 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1322+255C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93238576 | ||||||
| chr9:93238576
|
C | T | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1322+255C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93238576 | ||||||
| chr9:93238591
|
G | A | 2 | a0001c0003t0001g0170a0001c0003t0001g0252 | 2 | HG00099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1322+270G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93238591 | ||||||
| chr9:93238639
|
A | C | 62 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(59): Show | 62 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1322+318A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93238639 | ||||||
| chr9:93238787
|
T | A | 8 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1322+466T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93238787 | ||||||
| chr9:93238795
|
A | C | 1 | a0009c0023t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1322+474A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93238795 | ||||||
| chr9:93238813
|
G | A | 1 | a0001c0004t0002g0279 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1322+492G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93238813 | ||||||
| chr9:93239117
|
C | T | 2 | a0001c0004t0002g0206a0001c0004t0002g0282 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1323-640C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93239117 | ||||||
| chr9:93239191
|
C | T | 140 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(137): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1323-566C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93239191 | ||||||
| chr9:93239233
|
C | T | 2 | a0009c0023t0001g0291a0009c0023t0001g0292 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1323-524C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93239233 | ||||||
| chr9:93239316
|
T | C | 1 | a0001c0004t0002g0285 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1323-441T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93239316 | ||||||
| chr9:93239467
|
G | A | 1 | a0002c0001t0001g0119 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1323-290G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 6/29 | chr9 | 93239467 | ||||||
| chr9:93239997
|
G | A | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1542+21G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93239997 | ||||||
| chr9:93240024
|
C | T | 3 | a0001c0002t0001g0049a0001c0002t0001g0050a0001c0003t0001g0295 | 3 | HG01167.hp1 HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1542+48C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93240024 | ||||||
| chr9:93240345
|
G | T | 8 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542+369G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93240345 | ||||||
| chr9:93240446
|
G | A | 2 | a0008c0026t0001g0305a0008c0026t0001g0306 | 2 | HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1542+470G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93240446 | ||||||
| chr9:93240476
|
G | T | 2 | a0004c0006t0001g0078a0004c0006t0001g0079 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1542+500G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93240476 | ||||||
| chr9:93240538
|
C | T | 1 | a0009c0023t0001g0291 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1542+562C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93240538 | ||||||
| chr9:93240642
|
G | A | 1 | a0001c0002t0001g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1542+666G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93240642 | ||||||
| chr9:93240701
|
C | T | 36 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(33): Show | 37 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1542+725C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93240701 | ||||||
| chr9:93240795
|
A | G | 1 | a0002c0001t0001g0152 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1542+819A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93240795 | ||||||
| chr9:93240980
|
C | T | 10 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(7): Show | 10 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1542+1004C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93240980 | ||||||
| chr9:93241153
|
A | G | 97 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(94): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1542+1177A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93241153 | ||||||
| chr9:93241201
|
T | C | 1 | a0001c0003t0001g0170 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1542+1225T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93241201 | ||||||
| chr9:93241250
|
G | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1542+1274G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93241250 | ||||||
| chr9:93241342
|
G | A | 1 | a0001c0032t0001g0017 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1542+1366G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93241342 | ||||||
| chr9:93241499
|
C | G | 1 | a0002c0001t0001g0176 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1542+1523C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93241499 | ||||||
| chr9:93241544
|
C | T | 97 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(94): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1542+1568C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93241544 | ||||||
| chr9:93241545
|
G | C | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1542+1569G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93241545 | ||||||
| chr9:93241622
|
G | A | 24 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(21): Show | 24 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.1542+1646G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93241622 | ||||||
| chr9:93241713
|
C | G | 5 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1542+1737C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93241713 | ||||||
| chr9:93241860
|
TC | T | 13 | a0005c0012t0001g0192a0005c0012t0001g0193a0005c0012t0001g0194others(10): Show | 13 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1542+1886delC | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr9 | 93241860 | |||||
| chr9:93242006
|
C | T | 1 | a0001c0008t0001g0016 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1542+2030C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93242006 | ||||||
| chr9:93242156
|
G | A | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1542+2180G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93242156 | ||||||
| chr9:93242245
|
C | T | 4 | a0001c0008t0001g0023a0001c0008t0001g0024a0001c0008t0001g0025others(1): Show | 4 | HG03490.hp1 HG03492.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1542+2269C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93242245 | ||||||
| chr9:93242246
|
G | A | 7 | a0001c0004t0002g0260a0001c0004t0002g0261a0001c0004t0002g0262others(4): Show | 7 | HG02145.hp1 HG02970.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542+2270G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93242246 | ||||||
| chr9:93242546
|
C | T | 1 | a0001c0002t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1542+2570C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93242546 | ||||||
| chr9:93242593
|
T | C | 1 | a0001c0017t0001g0122 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1542+2617T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93242593 | ||||||
| chr9:93242629
|
G | A | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1542+2653G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93242629 | ||||||
| chr9:93242705
|
A | C | 3 | a0001c0004t0002g0265a0001c0004t0002g0266a0001c0004t0002g0284 | 3 | HG00639.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1542+2729A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93242705 | ||||||
| chr9:93242966
|
G | A | 3 | a0006c0016t0001g0141a0006c0016t0001g0142a0006c0016t0001g0143 | 3 | NA18944.hp2 NA18950.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1542+2990G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93242966 | ||||||
| chr9:93243022
|
G | A | 1 | a0008c0061t0001g0290 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1542+3046G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243022 | ||||||
| chr9:93243025
|
G | T | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1542+3049G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243025 | ||||||
| chr9:93243074
|
A | G | 2 | a0001c0024t0001g0054a0001c0024t0001g0056 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1542+3098A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243074 | ||||||
| chr9:93243261
|
C | T | 2 | a0002c0001t0001g0189a0002c0001t0001g0190 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.1542+3285C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243261 | ||||||
| chr9:93243350
|
A | G | 1 | a0001c0009t0001g0200 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1542+3374A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243350 | ||||||
| chr9:93243392
|
C | T | 1 | a0007c0020t0001g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542+3416C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243392 | ||||||
| chr9:93243443
|
C | G | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1542+3467C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243443 | ||||||
| chr9:93243456
|
C | T | 24 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(21): Show | 24 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.1542+3480C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243456 | ||||||
| chr9:93243584
|
G | A | 1 | a0001c0022t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1542+3608G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243584 | ||||||
| chr9:93243589
|
A | G | 2 | a0026c0045t0001g0294a0027c0056t0001g0298 | 2 | HG01081.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1542+3613A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243589 | ||||||
| chr9:93243627
|
G | A | 2 | a0002c0001t0001g0133a0002c0001t0001g0146 | 2 | HG01106.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1542+3651G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243627 | ||||||
| chr9:93243652
|
A | G | 17 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(14): Show | 17 | HG01081.hp2 HG01884.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.1542+3676A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243652 | ||||||
| chr9:93243763
|
C | T | 2 | a0008c0026t0001g0305a0008c0026t0001g0306 | 2 | HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1543-3780C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243763 | ||||||
| chr9:93243810
|
A | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1543-3733A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243810 | ||||||
| chr9:93243843
|
T | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1543-3700T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243843 | ||||||
| chr9:93243908
|
A | G | 1 | a0002c0042t0001g0147 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1543-3635A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243908 | ||||||
| chr9:93243965
|
C | T | 1 | a0005c0027t0001g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1543-3578C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93243965 | ||||||
| chr9:93244042
|
T | C | 1 | a0002c0001t0001g0172 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1543-3501T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244042 | ||||||
| chr9:93244080
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1543-3463C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244080 | ||||||
| chr9:93244222
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1543-3321C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244222 | ||||||
| chr9:93244235
|
C | T | 14 | a0001c0059t0001g0304a0004c0006t0001g0078a0004c0006t0001g0079others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1543-3308C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244235 | ||||||
| chr9:93244256
|
G | A | 1 | a0001c0003t0001g0222 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1543-3287G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244256 | ||||||
| chr9:93244394
|
A | G | 1 | a0001c0002t0001g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1543-3149A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244394 | ||||||
| chr9:93244445
|
C | T | 1 | a0001c0032t0001g0017 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1543-3098C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244445 | ||||||
| chr9:93244588
|
G | A | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1543-2955G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244588 | ||||||
| chr9:93244595
|
G | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1543-2948G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244595 | ||||||
| chr9:93244614
|
C | G | 1 | a0002c0001t0001g0100 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1543-2929C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244614 | ||||||
| chr9:93244643
|
C | T | 1 | a0001c0009t0001g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1543-2900C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244643 | ||||||
| chr9:93244657
|
C | T | 4 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(1): Show | 4 | HG01884.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1543-2886C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244657 | ||||||
| chr9:93244660
|
C | T | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1543-2883C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244660 | ||||||
| chr9:93244661
|
G | A | 1 | a0002c0001t0001g0107 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1543-2882G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244661 | ||||||
| chr9:93244754
|
C | T | 4 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(1): Show | 4 | HG01884.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1543-2789C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244754 | ||||||
| chr9:93244805
|
C | G | 4 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(1): Show | 4 | HG01884.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1543-2738C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244805 | ||||||
| chr9:93244971
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1543-2572C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93244971 | ||||||
| chr9:93245193
|
C | T | 1 | a0001c0007t0001g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1543-2350C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93245193 | ||||||
| chr9:93245293
|
A | G | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1543-2250A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93245293 | ||||||
| chr9:93245320
|
A | G | 128 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1543-2223A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93245320 | ||||||
| chr9:93245413
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1543-2130C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93245413 | ||||||
| chr9:93245511
|
C | T | 2 | a0001c0004t0002g0284a0026c0045t0001g0294 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1543-2032C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93245511 | ||||||
| chr9:93245901
|
C | T | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1543-1642C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93245901 | ||||||
| chr9:93245934
|
A | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1543-1609A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93245934 | ||||||
| chr9:93246085
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1543-1458C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93246085 | ||||||
| chr9:93246095
|
C | T | 1 | a0001c0003t0001g0219 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1543-1448C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93246095 | ||||||
| chr9:93246147
|
A | G | 3 | a0007c0020t0001g0286a0007c0020t0001g0287a0007c0020t0001g0312 | 3 | HG01952.hp1 HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1543-1396A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93246147 | ||||||
| chr9:93246184
|
A | T | 1 | a0001c0048t0001g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1543-1359A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93246184 | ||||||
| chr9:93246324
|
G | A | 2 | a0002c0001t0001g0189a0002c0001t0001g0190 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.1543-1219G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93246324 | ||||||
| chr9:93246447
|
G | C | 2 | a0026c0045t0001g0294a0027c0056t0001g0298 | 2 | HG01081.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1543-1096G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93246447 | ||||||
| chr9:93246493
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1543-1050C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93246493 | ||||||
| chr9:93246496
|
T | G | 1 | a0001c0055t0001g0064 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1543-1047T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93246496 | ||||||
| chr9:93246980
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1543-563C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93246980 | ||||||
| chr9:93246987
|
T | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1543-556T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93246987 | ||||||
| chr9:93246989
|
T | C | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1543-554T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93246989 | ||||||
| chr9:93247003
|
A | G | 1 | a0013c0041t0001g0154 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1543-540A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93247003 | ||||||
| chr9:93247012
|
C | T | 1 | a0002c0001t0001g0164 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1543-531C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93247012 | ||||||
| chr9:93247079
|
G | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1543-464G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93247079 | ||||||
| chr9:93247223
|
C | A | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1543-320C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93247223 | ||||||
| chr9:93247338
|
G | A | 1 | a0001c0004t0002g0282 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1543-205G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93247338 | ||||||
| chr9:93247342
|
T | C | 1 | a0001c0004t0002g0285 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1543-201T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93247342 | ||||||
| chr9:93247402
|
G | A | 1 | a0001c0007t0001g0271 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1543-141G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93247402 | ||||||
| chr9:93247494
|
C | T | 18 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(15): Show | 19 | HG00438.hp1 HG00639.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1543-49C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93247494 | ||||||
| chr9:93247495
|
G | A | 2 | a0008c0026t0001g0305a0008c0026t0001g0306 | 2 | HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1543-48G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 7/29 | chr9 | 93247495 | ||||||
| chr9:93247958
|
C | A | 299 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1834+124C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93247958 | ||||||
| chr9:93248002
|
T | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1834+168T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93248002 | ||||||
| chr9:93248018
|
G | A | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1834+184G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93248018 | ||||||
| chr9:93248019
|
T | C | 1 | a0001c0002t0001g0309 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1834+185T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93248019 | ||||||
| chr9:93248074
|
G | A | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1834+240G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93248074 | ||||||
| chr9:93248085
|
G | A | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1834+251G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93248085 | ||||||
| chr9:93248239
|
G | T | 24 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(21): Show | 24 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.1834+405G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93248239 | ||||||
| chr9:93248600
|
C | T | 2 | a0009c0023t0001g0291a0009c0023t0001g0292 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1834+766C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93248600 | ||||||
| chr9:93248654
|
A | G | 1 | a0001c0009t0001g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1834+820A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93248654 | ||||||
| chr9:93248790
|
G | A | 1 | a0023c0033t0001g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1834+956G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93248790 | ||||||
| chr9:93248946
|
C | G | 1 | a0001c0008t0001g0151 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1834+1112C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93248946 | ||||||
| chr9:93249038
|
C | T | 2 | a0002c0001t0001g0133a0002c0001t0001g0146 | 2 | HG01106.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1834+1204C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93249038 | ||||||
| chr9:93249059
|
G | A | 1 | a0024c0060t0001g0254 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1834+1225G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93249059 | ||||||
| chr9:93249353
|
G | A | 19 | a0001c0003t0001g0103a0001c0003t0001g0220a0001c0003t0001g0221others(16): Show | 19 | HG00544.hp1 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1834+1519G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93249353 | ||||||
| chr9:93249464
|
CA | C | 6 | a0005c0019t0001g0040a0005c0019t0001g0041a0005c0019t0001g0139others(3): Show | 6 | HG02145.hp2 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1834+1635delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr9 | 93249464 | |||||
| chr9:93249536
|
C | T | 2 | a0002c0001t0001g0176a0002c0001t0001g0178 | 2 | HG01175.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1834+1702C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93249536 | ||||||
| chr9:93249601
|
G | A | 4 | a0005c0012t0001g0192a0005c0012t0001g0193a0005c0012t0001g0194others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1834+1767G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93249601 | ||||||
| chr9:93249685
|
A | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1834+1851A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93249685 | ||||||
| chr9:93249716
|
C | T | 1 | a0001c0009t0001g0201 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1834+1882C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93249716 | ||||||
| chr9:93249720
|
C | T | 2 | a0004c0006t0001g0089a0026c0045t0001g0294 | 2 | HG00438.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1834+1886C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93249720 | ||||||
| chr9:93249803
|
G | A | 122 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1834+1969G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93249803 | ||||||
| chr9:93249804
|
G | C | 1 | a0002c0001t0001g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1834+1970G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93249804 | ||||||
| chr9:93249808
|
C | T | 8 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1834+1974C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93249808 | ||||||
| chr9:93249854
|
C | T | 1 | a0002c0001t0001g0146 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1834+2020C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93249854 | ||||||
| chr9:93249863
|
G | T | 41 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(38): Show | 41 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1834+2029G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93249863 | ||||||
| chr9:93249907
|
A | AT | 6 | a0001c0011t0001g0210a0002c0001t0001g0153a0002c0001t0001g0179others(3): Show | 6 | HG01192.hp1 HG01261.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1834+2099dupT | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr9 | 93249907 | |||||
| chr9:93249907
|
A | ATT | 74 | a0001c0002t0001g0050a0001c0011t0001g0211a0001c0011t0001g0212others(71): Show | 74 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1834+2098_1834+209 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr9 | 93249907 | |||||
| chr9:93249907
|
A | ATTT | 39 | a0001c0002t0001g0048a0001c0002t0001g0053a0001c0002t0001g0066others(36): Show | 40 | HG00544.hp2 HG00597.hp2 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.1834+2097_1834+209 others(7): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr9 | 93249907 | |||||
| chr9:93249907
|
A | ATTTT | 106 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(103): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.1834+2096_1834+209 others(8): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr9 | 93249907 | |||||
| chr9:93249907
|
A | ATTTTT | 48 | a0001c0002t0001g0022a0001c0003t0001g0077a0001c0003t0001g0209others(45): Show | 48 | HG00323.hp2 HG00544.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1834+2095_1834+209 others(9): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr9 | 93249907 | |||||
| chr9:93249907
|
A | ATTTTTT | 15 | a0001c0002t0001g0072a0001c0003t0001g0103a0001c0003t0001g0220others(12): Show | 15 | HG00621.hp1 HG00673.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.1834+2094_1834+209 others(10): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr9 | 93249907 | |||||
| chr9:93249907
|
A | ATTTTTTT others(1): Show |
7 | a0001c0003t0001g0219a0004c0006t0001g0083a0004c0006t0001g0084others(4): Show | 7 | HG00733.hp2 HG02523.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1834+2092_1834+209 others(12): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr9 | 93249907 | |||||
| chr9:93250073
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1834+2239C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93250073 | ||||||
| chr9:93250100
|
AAAT | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1834+2274_1834+227 others(7): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr9 | 93250100 | |||||
| chr9:93250240
|
C | T | 90 | a0002c0001t0001g0007a0002c0001t0001g0012a0002c0001t0001g0091others(87): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1834+2406C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93250240 | ||||||
| chr9:93250282
|
C | A | 2 | a0001c0009t0001g0198a0001c0009t0001g0201 | 2 | HG02300.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1834+2448C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93250282 | ||||||
| chr9:93250304
|
CAT | C | 3 | a0001c0004t0002g0260a0001c0004t0002g0261a0001c0004t0002g0262 | 3 | HG02145.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1834+2473_1834+247 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr9 | 93250304 | |||||
| chr9:93250359
|
A | G | 1 | a0001c0025t0001g0027 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1835-2524A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93250359 | ||||||
| chr9:93250417
|
G | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1835-2466G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93250417 | ||||||
| chr9:93250728
|
A | G | 122 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1835-2155A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93250728 | ||||||
| chr9:93250782
|
C | CT | 160 | a0001c0002t0001g0003a0001c0002t0001g0015a0001c0002t0001g0018others(157): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1835-2081dupT | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr9 | 93250782 | |||||
| chr9:93250782
|
C | CTT | 40 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(37): Show | 40 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.1835-2082_1835-208 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr9 | 93250782 | |||||
| chr9:93250854
|
G | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1835-2029G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93250854 | ||||||
| chr9:93250995
|
AG | A | 299 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1835-1885delG | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr9 | 93250995 | |||||
| chr9:93251034
|
G | A | 128 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1835-1849G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93251034 | ||||||
| chr9:93251085
|
C | T | 1 | a0001c0002t0001g0058 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1835-1798C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93251085 | ||||||
| chr9:93251116
|
A | T | 41 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(38): Show | 41 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1835-1767A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93251116 | ||||||
| chr9:93251179
|
G | A | 1 | a0001c0002t0001g0036 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1835-1704G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93251179 | ||||||
| chr9:93251239
|
C | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1835-1644C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93251239 | ||||||
| chr9:93251290
|
C | T | 9 | a0001c0003t0001g0314a0001c0009t0001g0198a0001c0009t0001g0199others(6): Show | 9 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1835-1593C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93251290 | ||||||
| chr9:93251329
|
G | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1835-1554G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93251329 | ||||||
| chr9:93251359
|
T | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1835-1524T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93251359 | ||||||
| chr9:93251428
|
T | A | 1 | a0001c0002t0001g0037 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1835-1455T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93251428 | ||||||
| chr9:93251512
|
C | T | 1 | a0005c0027t0001g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1835-1371C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93251512 | ||||||
| chr9:93251645
|
G | A | 17 | a0001c0002t0001g0018a0001c0002t0001g0029a0001c0002t0001g0030others(14): Show | 17 | HG00621.hp2 HG02040.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1835-1238G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93251645 | ||||||
| chr9:93251729
|
G | C | 1 | a0006c0016t0001g0142 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1835-1154G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93251729 | ||||||
| chr9:93251780
|
C | T | 1 | a0001c0003t0001g0295 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1835-1103C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93251780 | ||||||
| chr9:93251959
|
C | T | 3 | a0004c0006t0001g0080a0004c0006t0001g0081a0004c0006t0001g0082 | 3 | HG01255.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1835-924C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93251959 | ||||||
| chr9:93252071
|
TC | T | 5 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1835-811delC | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93252071 | ||||||
| chr9:93252130
|
G | A | 1 | a0007c0020t0001g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1835-753G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93252130 | ||||||
| chr9:93252199
|
C | T | 1 | a0018c0036t0001g0019 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1835-684C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93252199 | ||||||
| chr9:93252261
|
G | T | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1835-622G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93252261 | ||||||
| chr9:93252358
|
G | T | 1 | a0004c0006t0001g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1835-525G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93252358 | ||||||
| chr9:93252388
|
G | A | 1 | a0001c0002t0001g0015 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1835-495G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93252388 | ||||||
| chr9:93252389
|
C | T | 2 | a0001c0002t0001g0018a0001c0002t0001g0029 | 2 | NA18943.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1835-494C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93252389 | ||||||
| chr9:93252468
|
G | A | 3 | a0007c0020t0001g0286a0007c0020t0001g0287a0007c0020t0001g0312 | 3 | HG01952.hp1 HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1835-415G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93252468 | ||||||
| chr9:93252484
|
A | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1835-399A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93252484 | ||||||
| chr9:93252635
|
G | T | 1 | a0003c0005t0001g0111 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1835-248G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93252635 | ||||||
| chr9:93252697
|
G | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1835-186G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 8/29 | chr9 | 93252697 | ||||||
| chr9:93253095
|
A | G | 299 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2034+13A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93253095 | ||||||
| chr9:93253108
|
C | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2034+26C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93253108 | ||||||
| chr9:93253116
|
A | T | 158 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(155): Show | 160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.2034+34A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93253116 | ||||||
| chr9:93253207
|
G | A | 13 | a0005c0012t0001g0192a0005c0012t0001g0193a0005c0012t0001g0194others(10): Show | 13 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2034+125G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93253207 | ||||||
| chr9:93253356
|
C | A | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.2034+274C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93253356 | ||||||
| chr9:93253430
|
C | T | 1 | a0001c0017t0001g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2034+348C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93253430 | ||||||
| chr9:93253686
|
G | T | 1 | a0001c0017t0001g0122 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2034+604G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93253686 | ||||||
| chr9:93253725
|
A | G | 312 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(309): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2034+643A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93253725 | ||||||
| chr9:93253841
|
G | A | 1 | a0001c0017t0001g0161 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2034+759G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93253841 | ||||||
| chr9:93253845
|
C | T | 27 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(24): Show | 27 | HG00140.hp2 HG00280.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.2034+763C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93253845 | ||||||
| chr9:93253939
|
T | C | 299 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2034+857T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93253939 | ||||||
| chr9:93254063
|
C | T | 1 | a0001c0014t0002g0255 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2034+981C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93254063 | ||||||
| chr9:93254118
|
T | C | 1 | a0001c0003t0001g0234 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2034+1036T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93254118 | ||||||
| chr9:93254267
|
A | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2034+1185A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93254267 | ||||||
| chr9:93254396
|
G | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2034+1314G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93254396 | ||||||
| chr9:93254401
|
C | T | 1 | a0001c0004t0002g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2034+1319C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93254401 | ||||||
| chr9:93254666
|
A | G | 1 | a0001c0003t0001g0221 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2034+1584A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93254666 | ||||||
| chr9:93254699
|
C | A | 1 | a0009c0023t0001g0291 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2035-1600C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93254699 | ||||||
| chr9:93254715
|
G | C | 1 | a0002c0001t0001g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2035-1584G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93254715 | ||||||
| chr9:93254849
|
G | C | 3 | a0002c0001t0001g0164a0012c0044t0001g0165a0013c0041t0001g0154 | 3 | HG00544.hp2 NA18939.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2035-1450G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93254849 | ||||||
| chr9:93254990
|
T | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2035-1309T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93254990 | ||||||
| chr9:93254995
|
C | A | 1 | a0001c0013t0001g0145 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2035-1304C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93254995 | ||||||
| chr9:93255136
|
G | A | 1 | a0001c0007t0001g0271 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2035-1163G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93255136 | ||||||
| chr9:93255219
|
G | A | 2 | a0001c0003t0001g0170a0001c0003t0001g0252 | 2 | HG00099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.2035-1080G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93255219 | ||||||
| chr9:93255230
|
A | G | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.2035-1069A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93255230 | ||||||
| chr9:93255407
|
G | A | 1 | a0001c0002t0001g0015 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2035-892G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93255407 | ||||||
| chr9:93255469
|
T | C | 141 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(138): Show | 141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.2035-830T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93255469 | ||||||
| chr9:93255470
|
G | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2035-829G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93255470 | ||||||
| chr9:93255481
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2035-818C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93255481 | ||||||
| chr9:93255793
|
T | A | 2 | a0001c0008t0001g0025a0001c0008t0001g0026 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2035-506T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93255793 | ||||||
| chr9:93255897
|
T | C | 1 | a0008c0026t0001g0305 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2035-402T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93255897 | ||||||
| chr9:93256077
|
T | C | 299 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2035-222T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93256077 | ||||||
| chr9:93256167
|
G | A | 1 | a0001c0011t0001g0212 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2035-132G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93256167 | ||||||
| chr9:93256217
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2035-82C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 9/29 | chr9 | 93256217 | ||||||
| chr9:93256461
|
G | A | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.2190+7G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 10/29 | chr9 | 93256461 | ||||||
| chr9:93256488
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2190+34C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 10/29 | chr9 | 93256488 | ||||||
| chr9:93256512
|
G | A | 1 | a0002c0001t0001g0119 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2190+58G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 10/29 | chr9 | 93256512 | ||||||
| chr9:93256615
|
G | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2190+161G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 10/29 | chr9 | 93256615 | ||||||
| chr9:93256836
|
A | G | 299 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2191-112A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 10/29 | chr9 | 93256836 | ||||||
| chr9:93256850
|
G | C | 1 | a0001c0008t0001g0016 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2191-98G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 10/29 | chr9 | 93256850 | ||||||
| chr9:93256895
|
C | T | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.2191-53C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 10/29 | chr9 | 93256895 | ||||||
| chr9:93256896
|
G | T | 1 | a0001c0002t0001g0035 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2191-52G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 10/29 | chr9 | 93256896 | ||||||
| chr9:93256897
|
C | T | 1 | a0001c0002t0001g0035 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2191-51C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 10/29 | chr9 | 93256897 | ||||||
| chr9:93257283
|
C | T | 27 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(24): Show | 27 | HG00140.hp2 HG00280.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.2382+144C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/29 | chr9 | 93257283 | ||||||
| chr9:93257519
|
A | G | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.2382+380A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/29 | chr9 | 93257519 | ||||||
| chr9:93257560
|
C | T | 1 | a0001c0003t0001g0314 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2382+421C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/29 | chr9 | 93257560 | ||||||
| chr9:93257589
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2382+450C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/29 | chr9 | 93257589 | ||||||
| chr9:93257688
|
C | T | 89 | a0002c0001t0001g0007a0002c0001t0001g0012a0002c0001t0001g0091others(86): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2382+549C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/29 | chr9 | 93257688 | ||||||
| chr9:93257710
|
A | G | 1 | a0002c0001t0001g0152 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2382+571A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/29 | chr9 | 93257710 | ||||||
| chr9:93257839
|
G | A | 122 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.2382+700G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/29 | chr9 | 93257839 | ||||||
| chr9:93257882
|
G | A | 14 | a0001c0059t0001g0304a0004c0006t0001g0078a0004c0006t0001g0079others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.2382+743G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/29 | chr9 | 93257882 | ||||||
| chr9:93257927
|
C | G | 1 | a0001c0002t0001g0031 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2382+788C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/29 | chr9 | 93257927 | ||||||
| chr9:93258075
|
G | A | 2 | a0001c0002t0001g0051a0001c0002t0001g0052 | 2 | HG00609.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2383-856G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/29 | chr9 | 93258075 | ||||||
| chr9:93258159
|
C | T | 39 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(36): Show | 39 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.2383-772C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/29 | chr9 | 93258159 | ||||||
| chr9:93258384
|
C | T | 4 | a0001c0008t0001g0023a0001c0008t0001g0024a0001c0008t0001g0025others(1): Show | 4 | HG03490.hp1 HG03492.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.2383-547C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/29 | chr9 | 93258384 | ||||||
| chr9:93258544
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2383-387C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/29 | chr9 | 93258544 | ||||||
| chr9:93258767
|
C | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2383-164C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 11/29 | chr9 | 93258767 | ||||||
| chr9:93259781
|
C | T | 1 | a0002c0001t0001g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3066+167C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93259781 | ||||||
| chr9:93259826
|
C | T | 14 | a0001c0059t0001g0304a0004c0006t0001g0078a0004c0006t0001g0079others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.3066+212C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93259826 | ||||||
| chr9:93259834
|
C | T | 124 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.3066+220C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93259834 | ||||||
| chr9:93259962
|
T | C | 1 | a0008c0026t0001g0306 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3066+348T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93259962 | ||||||
| chr9:93260013
|
G | A | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.3066+399G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93260013 | ||||||
| chr9:93260099
|
G | C | 1 | a0001c0009t0001g0202 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3066+485G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93260099 | ||||||
| chr9:93260123
|
C | G | 1 | a0018c0036t0001g0019 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3066+509C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93260123 | ||||||
| chr9:93260148
|
A | T | 6 | a0004c0006t0001g0083a0004c0006t0001g0084a0004c0006t0001g0085others(3): Show | 6 | HG02523.hp1 NA18963.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.3066+534A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93260148 | ||||||
| chr9:93260185
|
C | T | 1 | a0003c0005t0001g0112 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3066+571C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93260185 | ||||||
| chr9:93260195
|
C | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3066+581C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93260195 | ||||||
| chr9:93260306
|
T | G | 299 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.3066+692T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93260306 | ||||||
| chr9:93260500
|
C | T | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.3066+886C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93260500 | ||||||
| chr9:93260583
|
A | G | 128 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.3066+969A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93260583 | ||||||
| chr9:93260617
|
C | T | 2 | a0002c0001t0001g0164a0013c0041t0001g0154 | 2 | NA18939.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.3066+1003C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93260617 | ||||||
| chr9:93260656
|
A | C | 1 | a0002c0001t0001g0153 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3066+1042A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93260656 | ||||||
| chr9:93260942
|
G | A | 1 | a0007c0020t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3067-872G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93260942 | ||||||
| chr9:93261107
|
C | T | 1 | a0002c0001t0001g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3067-707C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93261107 | ||||||
| chr9:93261288
|
C | G | 14 | a0001c0059t0001g0304a0004c0006t0001g0078a0004c0006t0001g0079others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.3067-526C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93261288 | ||||||
| chr9:93261339
|
G | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3067-475G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93261339 | ||||||
| chr9:93261404
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3067-410G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93261404 | ||||||
| chr9:93261561
|
G | A | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.3067-253G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93261561 | ||||||
| chr9:93261612
|
G | A | 1 | a0001c0011t0001g0213 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3067-202G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93261612 | ||||||
| chr9:93261703
|
G | C | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.3067-111G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93261703 | ||||||
| chr9:93261752
|
C | T | 4 | a0001c0008t0001g0023a0001c0008t0001g0024a0001c0008t0001g0025others(1): Show | 4 | HG03490.hp1 HG03492.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.3067-62C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 12/29 | chr9 | 93261752 | ||||||
| chr9:93262158
|
C | T | 13 | a0005c0012t0001g0192a0005c0012t0001g0193a0005c0012t0001g0194others(10): Show | 13 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.3360+51C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/29 | chr9 | 93262158 | ||||||
| chr9:93262166
|
T | C | 13 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(10): Show | 13 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.3360+59T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/29 | chr9 | 93262166 | ||||||
| chr9:93262320
|
A | T | 1 | a0002c0001t0001g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3360+213A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/29 | chr9 | 93262320 | ||||||
| chr9:93262339
|
A | G | 1 | a0002c0001t0001g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3360+232A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/29 | chr9 | 93262339 | ||||||
| chr9:93262463
|
G | A | 1 | a0002c0001t0001g0172 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3361-207G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/29 | chr9 | 93262463 | ||||||
| chr9:93262512
|
T | C | 299 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.3361-158T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/29 | chr9 | 93262512 | ||||||
| chr9:93262553
|
C | T | 4 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(1): Show | 5 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.3361-117C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/29 | chr9 | 93262553 | ||||||
| chr9:93262557
|
G | A | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3361-113G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/29 | chr9 | 93262557 | ||||||
| chr9:93262577
|
A | G | 303 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.3361-93A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/29 | chr9 | 93262577 | ||||||
| chr9:93262601
|
C | T | 27 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(24): Show | 28 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.3361-69C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/29 | chr9 | 93262601 | ||||||
| chr9:93262632
|
G | A | 2 | a0009c0023t0001g0291a0009c0023t0001g0292 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3361-38G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 13/29 | chr9 | 93262632 | ||||||
| chr9:93262744
|
G | A | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.3410+25G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 14/29 | chr9 | 93262744 | ||||||
| chr9:93262770
|
T | C | 40 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(37): Show | 41 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.3410+51T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 14/29 | chr9 | 93262770 | ||||||
| chr9:93262965
|
G | A | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3410+246G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 14/29 | chr9 | 93262965 | ||||||
| chr9:93263075
|
G | A | 125 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.3410+356G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 14/29 | chr9 | 93263075 | ||||||
| chr9:93263090
|
G | T | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02080.hp1 HG02129.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3410+371G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 14/29 | chr9 | 93263090 | ||||||
| chr9:93263091
|
G | C | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02080.hp1 HG02129.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3410+372G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 14/29 | chr9 | 93263091 | ||||||
| chr9:93263218
|
C | T | 7 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0055others(4): Show | 7 | HG02056.hp2 NA18950.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.3411-348C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 14/29 | chr9 | 93263218 | ||||||
| chr9:93263337
|
G | A | 14 | a0001c0059t0001g0304a0004c0006t0001g0078a0004c0006t0001g0079others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.3411-229G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 14/29 | chr9 | 93263337 | ||||||
| chr9:93263435
|
C | CAG | 299 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.3411-131_3411-130i others(4): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 14/29 | chr9 | 93263435 | ||||||
| chr9:93263489
|
G | A | 299 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.3411-77G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 14/29 | chr9 | 93263489 | ||||||
| chr9:93263555
|
G | T | 1 | a0001c0007t0001g0280 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3411-11G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 14/29 | chr9 | 93263555 | ||||||
| chr9:93263776
|
GCATGGTG others(21): Show |
G | 27 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(24): Show | 28 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.3579+44_3579+71del others(28): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr9 | 93263776 | |||||
| chr9:93263777
|
CATGGTGG others(4): Show |
C | 1 | a0004c0006t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3579+44_3579+54del others(11): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 15/29 | chr9 | 93263777 | ||||||
| chr9:93263804
|
C | G | 286 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(283): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.3579+70C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 15/29 | chr9 | 93263804 | ||||||
| chr9:93263815
|
G | T | 3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3579+81G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 15/29 | chr9 | 93263815 | ||||||
| chr9:93263827
|
T | TG | 18 | a0001c0002t0001g0035a0001c0002t0001g0093a0001c0003t0001g0077others(15): Show | 18 | HG00544.hp2 HG00642.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.3580-83dupG | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr9 | 93263827 | |||||
| chr9:93263840
|
T | TG | 313 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(310): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.3580-77_3580-76ins others(1): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 15/29 | chr9 | 93263840 | ||||||
| chr9:93263854
|
T | TG | 6 | a0001c0002t0001g0032a0001c0007t0001g0028a0001c0007t0001g0256others(3): Show | 6 | HG00544.hp2 HG01978.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.3580-58dupG | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr9 | 93263854 | |||||
| chr9:93263861
|
G | A | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.3580-56G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 15/29 | chr9 | 93263861 | ||||||
| chr9:93264063
|
C | T | 1 | a0001c0002t0001g0048 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3696+30C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93264063 | ||||||
| chr9:93264079
|
C | T | 14 | a0001c0059t0001g0304a0004c0006t0001g0078a0004c0006t0001g0079others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.3696+46C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93264079 | ||||||
| chr9:93264111
|
A | G | 14 | a0001c0059t0001g0304a0004c0006t0001g0078a0004c0006t0001g0079others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.3696+78A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93264111 | ||||||
| chr9:93264146
|
G | C | 2 | a0001c0024t0001g0054a0001c0024t0001g0056 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3696+113G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93264146 | ||||||
| chr9:93264345
|
G | C | 90 | a0002c0001t0001g0007a0002c0001t0001g0012a0002c0001t0001g0091others(87): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.3696+312G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93264345 | ||||||
| chr9:93264392
|
A | G | 1 | a0001c0002t0001g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3696+359A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93264392 | ||||||
| chr9:93264420
|
G | A | 38 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(35): Show | 38 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.3696+387G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93264420 | ||||||
| chr9:93264532
|
T | TA | 15 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(12): Show | 15 | HG01255.hp1 HG01884.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.3696+499_3696+500i others(3): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93264532 | ||||||
| chr9:93264533
|
G | T | 15 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(12): Show | 15 | HG01255.hp1 HG01884.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.3696+500G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93264533 | ||||||
| chr9:93264646
|
T | C | 2 | a0009c0023t0001g0291a0009c0023t0001g0292 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3696+613T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93264646 | ||||||
| chr9:93264654
|
A | G | 1 | a0001c0003t0001g0228 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3696+621A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93264654 | ||||||
| chr9:93264798
|
G | A | 28 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(25): Show | 29 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.3696+765G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93264798 | ||||||
| chr9:93264977
|
G | A | 1 | a0001c0003t0001g0250 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3696+944G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93264977 | ||||||
| chr9:93265042
|
C | G | 104 | a0001c0059t0001g0304a0002c0001t0001g0007a0002c0001t0001g0012others(101): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.3696+1009C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93265042 | ||||||
| chr9:93265347
|
G | T | 9 | a0001c0003t0001g0077a0001c0003t0001g0170a0001c0003t0001g0239others(6): Show | 9 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.3696+1314G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93265347 | ||||||
| chr9:93265485
|
T | C | 67 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(64): Show | 68 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.3696+1452T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93265485 | ||||||
| chr9:93265493
|
G | A | 4 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(1): Show | 4 | HG01884.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3696+1460G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93265493 | ||||||
| chr9:93265498
|
G | T | 1 | a0002c0001t0001g0159 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3696+1465G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93265498 | ||||||
| chr9:93265531
|
C | G | 128 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.3696+1498C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93265531 | ||||||
| chr9:93265889
|
G | A | 13 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(10): Show | 13 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.3696+1856G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93265889 | ||||||
| chr9:93265970
|
A | G | 91 | a0001c0059t0001g0304a0002c0001t0001g0007a0002c0001t0001g0012others(88): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.3697-1776A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93265970 | ||||||
| chr9:93266082
|
C | T | 13 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(10): Show | 13 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.3697-1664C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93266082 | ||||||
| chr9:93266202
|
G | A | 1 | a0012c0044t0001g0165 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3697-1544G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93266202 | ||||||
| chr9:93266277
|
A | G | 2 | a0003c0005t0001g0112a0003c0005t0001g0127 | 2 | HG02056.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.3697-1469A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93266277 | ||||||
| chr9:93266361
|
G | A | 1 | a0002c0001t0001g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3697-1385G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93266361 | ||||||
| chr9:93266403
|
G | A | 122 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.3697-1343G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93266403 | ||||||
| chr9:93266439
|
A | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3697-1307A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93266439 | ||||||
| chr9:93266516
|
A | G | 288 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.3697-1230A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93266516 | ||||||
| chr9:93266538
|
C | A | 1 | a0002c0046t0001g0187 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3697-1208C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93266538 | ||||||
| chr9:93266790
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3697-956C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93266790 | ||||||
| chr9:93266995
|
A | G | 1 | a0011c0062t0001g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3697-751A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93266995 | ||||||
| chr9:93267069
|
A | G | 276 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(273): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.3697-677A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93267069 | ||||||
| chr9:93267164
|
G | A | 1 | a0001c0002t0001g0018 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3697-582G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93267164 | ||||||
| chr9:93267167
|
A | G | 2 | a0001c0003t0001g0224a0025c0031t0001g0235 | 2 | NA18747.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.3697-579A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93267167 | ||||||
| chr9:93267168
|
C | T | 8 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3697-578C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93267168 | ||||||
| chr9:93267252
|
A | G | 276 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(273): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.3697-494A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93267252 | ||||||
| chr9:93267357
|
T | C | 81 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(78): Show | 81 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.3697-389T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 16/29 | chr9 | 93267357 | ||||||
| chr9:93267948
|
T | C | 276 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(273): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.3867+32T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 17/29 | chr9 | 93267948 | ||||||
| chr9:93267976
|
G | A | 13 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(10): Show | 13 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.3868-44G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 17/29 | chr9 | 93267976 | ||||||
| chr9:93268014
|
A | G | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
splice_region_variant&intron_variant | LOW | c.3868-6A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 17/29 | chr9 | 93268014 | ||||||
| chr9:93268110
|
G | T | 128 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.3913+45G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 18/29 | chr9 | 93268110 | ||||||
| chr9:93268236
|
G | A | 3 | a0001c0002t0001g0072a0001c0049t0001g0073a0010c0054t0001g0071 | 3 | HG03239.hp2 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3913+171G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 18/29 | chr9 | 93268236 | ||||||
| chr9:93268313
|
G | A | 3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3913+248G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 18/29 | chr9 | 93268313 | ||||||
| chr9:93268466
|
T | C | 13 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(10): Show | 13 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.3914-161T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 18/29 | chr9 | 93268466 | ||||||
| chr9:93268587
|
G | A | 1 | a0001c0002t0001g0037 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3914-40G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 18/29 | chr9 | 93268587 | ||||||
| chr9:93268753
|
G | T | 2 | a0001c0017t0001g0122a0001c0017t0001g0123 | 2 | NA18995.hp1 NA19070.hp2 |
splice_region_variant&intron_variant | LOW | c.4033+7G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93268753 | ||||||
| chr9:93268761
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4033+15C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93268761 | ||||||
| chr9:93268845
|
T | C | 3 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038 | 3 | HG01884.hp2 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4033+99T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93268845 | ||||||
| chr9:93268878
|
C | T | 2 | a0001c0002t0001g0018a0001c0002t0001g0029 | 2 | NA18943.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.4033+132C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93268878 | ||||||
| chr9:93268907
|
A | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4033+161A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93268907 | ||||||
| chr9:93268941
|
C | A | 1 | a0001c0004t0002g0284 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4033+195C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93268941 | ||||||
| chr9:93268971
|
C | T | 2 | a0002c0001t0001g0189a0002c0001t0001g0190 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.4033+225C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93268971 | ||||||
| chr9:93268980
|
T | C | 276 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(273): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.4033+234T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93268980 | ||||||
| chr9:93269103
|
C | T | 4 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038others(1): Show | 4 | HG01884.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.4033+357C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93269103 | ||||||
| chr9:93269133
|
G | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4033+387G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93269133 | ||||||
| chr9:93269211
|
T | TCTGCAC | 245 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.4033+476_4033+481d others(8): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93269211 | |||||
| chr9:93269335
|
C | A | 2 | a0001c0007t0001g0272a0001c0022t0001g0074 | 2 | HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.4033+589C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93269335 | ||||||
| chr9:93269336
|
C | A | 2 | a0002c0001t0001g0175a0002c0001t0001g0184 | 2 | HG00735.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.4033+590C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93269336 | ||||||
| chr9:93269364
|
A | G | 11 | a0001c0004t0002g0206a0001c0004t0002g0265a0001c0004t0002g0266others(8): Show | 11 | HG00639.hp1 HG00642.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.4033+618A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93269364 | ||||||
| chr9:93269467
|
C | T | 1 | a0003c0005t0001g0117 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.4033+721C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93269467 | ||||||
| chr9:93269468
|
G | A | 1 | a0004c0006t0001g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4033+722G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93269468 | ||||||
| chr9:93269539
|
A | G | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4033+793A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93269539 | ||||||
| chr9:93269552
|
G | C | 1 | a0002c0001t0001g0159 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4033+806G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93269552 | ||||||
| chr9:93269628
|
G | A | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+882G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93269628 | ||||||
| chr9:93269794
|
C | G | 1 | a0022c0029t0001g0009 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4033+1048C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93269794 | ||||||
| chr9:93269878
|
G | A | 1 | a0001c0007t0001g0270 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4033+1132G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93269878 | ||||||
| chr9:93269884
|
C | T | 1 | a0001c0034t0001g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4033+1138C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93269884 | ||||||
| chr9:93269997
|
G | C | 28 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(25): Show | 29 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.4033+1251G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93269997 | ||||||
| chr9:93270049
|
G | A | 128 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.4033+1303G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93270049 | ||||||
| chr9:93270147
|
C | T | 13 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(10): Show | 13 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.4033+1401C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93270147 | ||||||
| chr9:93270217
|
A | C | 1 | a0012c0044t0001g0165 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4033+1471A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93270217 | ||||||
| chr9:93270237
|
C | T | 41 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(38): Show | 41 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.4033+1491C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93270237 | ||||||
| chr9:93270333
|
T | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4033+1587T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93270333 | ||||||
| chr9:93270437
|
G | A | 245 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.4033+1691G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93270437 | ||||||
| chr9:93270557
|
A | T | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+1811A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93270557 | ||||||
| chr9:93270617
|
T | G | 2 | a0001c0002t0001g0036a0001c0002t0001g0037 | 2 | HG02129.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.4033+1871T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93270617 | ||||||
| chr9:93270619
|
G | T | 3 | a0001c0002t0001g0072a0001c0049t0001g0073a0010c0054t0001g0071 | 3 | HG03239.hp2 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.4033+1873G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93270619 | ||||||
| chr9:93270646
|
G | T | 1 | a0002c0001t0001g0095 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4033+1900G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93270646 | ||||||
| chr9:93270745
|
A | G | 22 | a0001c0003t0001g0103a0001c0003t0001g0209a0001c0003t0001g0219others(19): Show | 22 | HG00544.hp1 HG00621.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.4033+1999A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93270745 | ||||||
| chr9:93270755
|
C | A | 1 | a0001c0009t0001g0013 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4033+2009C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93270755 | ||||||
| chr9:93270820
|
A | G | 1 | a0002c0010t0001g0173 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.4033+2074A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93270820 | ||||||
| chr9:93270926
|
C | T | 1 | a0001c0002t0001g0065 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4033+2180C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93270926 | ||||||
| chr9:93271135
|
C | T | 2 | a0001c0008t0001g0010a0001c0008t0001g0011 | 2 | HG01106.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.4033+2389C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93271135 | ||||||
| chr9:93271521
|
CAA | C | 4 | a0001c0007t0001g0256a0001c0007t0001g0271a0001c0007t0001g0281others(1): Show | 4 | HG00673.hp2 HG02129.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.4033+2777_4033+277 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93271521 | |||||
| chr9:93271588
|
T | C | 1 | a0001c0003t0001g0243 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4033+2842T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93271588 | ||||||
| chr9:93271646
|
A | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4033+2900A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93271646 | ||||||
| chr9:93271672
|
G | A | 1 | a0001c0034t0001g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4033+2926G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93271672 | ||||||
| chr9:93271915
|
T | C | 266 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.4033+3169T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93271915 | ||||||
| chr9:93271924
|
A | G | 1 | a0001c0011t0001g0215 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4033+3178A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93271924 | ||||||
| chr9:93271943
|
G | A | 3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4033+3197G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93271943 | ||||||
| chr9:93272105
|
A | G | 1 | a0002c0001t0001g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4033+3359A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93272105 | ||||||
| chr9:93272272
|
A | T | 7 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0055others(4): Show | 7 | HG02056.hp2 NA18950.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.4033+3526A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93272272 | ||||||
| chr9:93272292
|
C | T | 3 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0238 | 3 | HG00621.hp2 NA19064.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.4033+3546C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93272292 | ||||||
| chr9:93272559
|
A | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4033+3813A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93272559 | ||||||
| chr9:93272733
|
C | A | 245 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.4033+3987C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93272733 | ||||||
| chr9:93272738
|
C | CA | 19 | a0001c0004t0002g0284a0001c0008t0001g0023a0001c0008t0001g0024others(16): Show | 19 | HG00438.hp1 HG00639.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.4033+4010dupA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAA | 40 | a0001c0002t0001g0058a0001c0002t0001g0124a0001c0003t0001g0170others(37): Show | 40 | HG00099.hp1 HG00642.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.4033+4009_4033+401 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAA | 117 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(114): Show | 118 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.4033+4008_4033+401 others(7): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAAA | 14 | a0001c0002t0001g0047a0001c0002t0001g0049a0001c0002t0001g0055others(11): Show | 14 | HG00735.hp1 HG00735.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.4033+4007_4033+401 others(8): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAAAA | 79 | a0001c0059t0001g0304a0002c0001t0001g0007a0002c0001t0001g0012others(76): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.4033+4006_4033+401 others(9): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAAAAAA others(4): Show |
3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4033+4000_4033+401 others(15): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAAAAAA others(12): Show |
3 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038 | 3 | HG01884.hp2 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4033+4010_4033+401 others(23): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAAAAAA others(13): Show |
6 | a0001c0009t0001g0202a0001c0009t0001g0203a0001c0009t0001g0205others(3): Show | 6 | HG01168.hp1 HG02895.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.4033+4010_4033+401 others(24): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAAAAAA others(14): Show |
6 | a0001c0009t0001g0200a0001c0009t0001g0204a0001c0011t0001g0210others(3): Show | 6 | HG00140.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.4033+4010_4033+401 others(25): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAAAAAA others(15): Show |
3 | a0001c0009t0001g0198a0005c0030t0001g0208a0009c0023t0001g0292 | 3 | HG02258.hp2 HG02895.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.4033+4010_4033+401 others(26): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAAAAAA others(16): Show |
1 | a0001c0009t0001g0201 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.4033+4010_4033+401 others(27): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAAAAAA others(17): Show |
5 | a0005c0012t0001g0197a0005c0019t0001g0041a0005c0027t0001g0043others(2): Show | 5 | HG02280.hp2 HG02886.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4033+4010_4033+401 others(28): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAAAAAA others(18): Show |
4 | a0005c0012t0001g0196a0005c0019t0001g0040a0005c0019t0001g0139others(1): Show | 4 | HG01243.hp1 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.4033+4010_4033+401 others(29): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAAAAAA others(19): Show |
1 | a0001c0009t0001g0013 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4033+4010_4033+401 others(30): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAAAAAA others(20): Show |
1 | a0005c0012t0001g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4033+4010_4033+401 others(31): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAAAAAA others(21): Show |
2 | a0001c0009t0001g0199a0005c0012t0001g0192 | 2 | HG00280.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.4033+4010_4033+401 others(32): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272738
|
C | CAAAAAAA others(22): Show |
2 | a0005c0012t0001g0194a0016c0037t0001g0195 | 2 | HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4033+4010_4033+401 others(33): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93272738 | |||||
| chr9:93272995
|
A | G | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+4249A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93272995 | ||||||
| chr9:93273020
|
A | G | 13 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(10): Show | 13 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.4033+4274A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93273020 | ||||||
| chr9:93273221
|
G | A | 1 | a0002c0001t0001g0174 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4033+4475G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93273221 | ||||||
| chr9:93273332
|
T | C | 245 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.4033+4586T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93273332 | ||||||
| chr9:93273376
|
C | T | 1 | a0001c0009t0001g0199 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4033+4630C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93273376 | ||||||
| chr9:93273726
|
G | A | 28 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(25): Show | 29 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.4033+4980G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93273726 | ||||||
| chr9:93273795
|
T | A | 1 | a0013c0041t0001g0154 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4033+5049T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93273795 | ||||||
| chr9:93273803
|
G | A | 26 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(23): Show | 26 | HG00438.hp1 HG01071.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.4033+5057G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93273803 | ||||||
| chr9:93273809
|
C | T | 2 | a0003c0005t0001g0101a0003c0005t0001g0105 | 2 | NA19000.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.4033+5063C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93273809 | ||||||
| chr9:93274233
|
G | A | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+5487G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274233 | ||||||
| chr9:93274265
|
G | A | 1 | a0001c0002t0001g0059 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.4033+5519G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274265 | ||||||
| chr9:93274283
|
C | T | 1 | a0001c0011t0001g0215 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4033+5537C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274283 | ||||||
| chr9:93274292
|
C | T | 28 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(25): Show | 29 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.4033+5546C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274292 | ||||||
| chr9:93274304
|
A | G | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+5558A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274304 | ||||||
| chr9:93274339
|
C | T | 1 | a0001c0002t0001g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4033+5593C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274339 | ||||||
| chr9:93274380
|
C | T | 14 | a0001c0003t0001g0077a0001c0003t0001g0170a0001c0003t0001g0239others(11): Show | 14 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.4033+5634C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274380 | ||||||
| chr9:93274383
|
G | A | 1 | a0001c0008t0001g0151 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4033+5637G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274383 | ||||||
| chr9:93274514
|
C | T | 1 | a0001c0007t0001g0028 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4033+5768C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274514 | ||||||
| chr9:93274515
|
C | CA | 21 | a0001c0009t0001g0205a0001c0011t0001g0210a0001c0011t0001g0211others(18): Show | 21 | HG01081.hp2 HG01243.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.4033+5792dupA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93274515 | |||||
| chr9:93274515
|
C | CAA | 6 | a0001c0011t0001g0212a0005c0027t0001g0039a0008c0026t0001g0305others(3): Show | 6 | HG01255.hp1 HG02145.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4033+5791_4033+579 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93274515 | |||||
| chr9:93274515
|
CA | C | 213 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.4033+5792delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93274515 | |||||
| chr9:93274515
|
CAAAAAAA others(9): Show |
C | 28 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(25): Show | 28 | HG00438.hp1 HG01071.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.4033+5777_4033+579 others(20): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93274515 | |||||
| chr9:93274523
|
A | G | 30 | a0001c0002t0001g0032a0001c0003t0001g0245a0001c0004t0002g0002others(27): Show | 31 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.4033+5777A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274523 | ||||||
| chr9:93274524
|
A | G | 213 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.4033+5778A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274524 | ||||||
| chr9:93274525
|
A | G | 1 | a0001c0002t0001g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4033+5779A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274525 | ||||||
| chr9:93274537
|
A | G | 2 | a0001c0002t0001g0032a0001c0003t0001g0245 | 2 | NA18943.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.4033+5791A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274537 | ||||||
| chr9:93274538
|
A | G | 128 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.4033+5792A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274538 | ||||||
| chr9:93274539
|
G | A | 2 | a0001c0002t0001g0032a0001c0003t0001g0245 | 2 | NA18943.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.4033+5793G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274539 | ||||||
| chr9:93274679
|
T | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4033+5933T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274679 | ||||||
| chr9:93274730
|
C | A | 1 | a0024c0060t0001g0254 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4033+5984C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93274730 | ||||||
| chr9:93275060
|
TA | T | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+6318delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93275060 | |||||
| chr9:93275063
|
A | T | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+6317A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275063 | ||||||
| chr9:93275064
|
A | G | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+6318A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275064 | ||||||
| chr9:93275066
|
G | C | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+6320G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275066 | ||||||
| chr9:93275068
|
C | CTA | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+6322_4033+632 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275068 | ||||||
| chr9:93275069
|
A | T | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+6323A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275069 | ||||||
| chr9:93275070
|
G | A | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+6324G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275070 | ||||||
| chr9:93275110
|
T | C | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4033+6364T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275110 | ||||||
| chr9:93275145
|
A | G | 1 | a0001c0009t0001g0013 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4033+6399A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275145 | ||||||
| chr9:93275179
|
G | A | 4 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(1): Show | 5 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.4033+6433G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275179 | ||||||
| chr9:93275396
|
A | T | 13 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(10): Show | 13 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.4033+6650A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275396 | ||||||
| chr9:93275408
|
T | G | 122 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.4033+6662T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275408 | ||||||
| chr9:93275425
|
C | G | 3 | a0001c0003t0001g0245a0001c0003t0001g0246a0001c0003t0001g0253 | 3 | NA18943.hp1 NA18964.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.4033+6679C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275425 | ||||||
| chr9:93275476
|
A | C | 3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4033+6730A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275476 | ||||||
| chr9:93275486
|
C | G | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+6740C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275486 | ||||||
| chr9:93275658
|
T | G | 1 | a0007c0020t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4033+6912T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275658 | ||||||
| chr9:93275879
|
A | G | 41 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(38): Show | 41 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.4033+7133A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275879 | ||||||
| chr9:93275980
|
T | C | 91 | a0001c0059t0001g0304a0002c0001t0001g0007a0002c0001t0001g0012others(88): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.4033+7234T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93275980 | ||||||
| chr9:93276242
|
G | T | 245 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.4033+7496G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93276242 | ||||||
| chr9:93276252
|
C | A | 1 | a0001c0015t0001g0293 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4033+7506C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93276252 | ||||||
| chr9:93276520
|
G | A | 1 | a0001c0002t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4033+7774G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93276520 | ||||||
| chr9:93276705
|
A | G | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+7959A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93276705 | ||||||
| chr9:93277034
|
C | CA | 15 | a0001c0002t0001g0032a0002c0001t0001g0164a0004c0006t0001g0078others(12): Show | 15 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.4033+8302dupA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93277034 | |||||
| chr9:93277158
|
A | T | 26 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(23): Show | 26 | HG00438.hp1 HG01071.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.4033+8412A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93277158 | ||||||
| chr9:93277460
|
A | C | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+8714A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93277460 | ||||||
| chr9:93277550
|
C | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4033+8804C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93277550 | ||||||
| chr9:93277775
|
T | C | 1 | a0001c0017t0001g0161 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.4033+9029T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93277775 | ||||||
| chr9:93277800
|
A | G | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4033+9054A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93277800 | ||||||
| chr9:93277928
|
G | A | 1 | a0001c0008t0001g0014 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.4033+9182G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93277928 | ||||||
| chr9:93278101
|
A | G | 2 | a0008c0026t0001g0305a0008c0026t0001g0306 | 2 | HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.4033+9355A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93278101 | ||||||
| chr9:93278302
|
C | T | 1 | a0002c0001t0001g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4033+9556C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93278302 | ||||||
| chr9:93278311
|
C | T | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.4033+9565C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93278311 | ||||||
| chr9:93278492
|
C | T | 3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4033+9746C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93278492 | ||||||
| chr9:93278820
|
T | C | 2 | a0002c0001t0001g0153a0002c0001t0001g0159 | 2 | HG02523.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4034-9968T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93278820 | ||||||
| chr9:93278955
|
A | G | 3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4034-9833A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93278955 | ||||||
| chr9:93279431
|
T | C | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4034-9357T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93279431 | ||||||
| chr9:93279473
|
C | T | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4034-9315C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93279473 | ||||||
| chr9:93279617
|
CAG | C | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4034-9169_4034-916 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93279617 | |||||
| chr9:93279736
|
C | G | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.4034-9052C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93279736 | ||||||
| chr9:93279779
|
A | G | 245 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.4034-9009A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93279779 | ||||||
| chr9:93279857
|
C | A | 1 | a0001c0008t0001g0151 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4034-8931C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93279857 | ||||||
| chr9:93280160
|
G | T | 1 | a0001c0007t0001g0270 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4034-8628G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93280160 | ||||||
| chr9:93280382
|
A | G | 91 | a0001c0059t0001g0304a0002c0001t0001g0007a0002c0001t0001g0012others(88): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.4034-8406A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93280382 | ||||||
| chr9:93280642
|
C | G | 288 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.4034-8146C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93280642 | ||||||
| chr9:93280687
|
T | C | 1 | a0002c0001t0001g0092 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4034-8101T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93280687 | ||||||
| chr9:93280767
|
G | T | 4 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4034-8021G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93280767 | ||||||
| chr9:93280869
|
C | T | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4034-7919C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93280869 | ||||||
| chr9:93281373
|
CA | C | 245 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.4034-7406delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93281373 | |||||
| chr9:93281469
|
G | A | 2 | a0001c0007t0001g0268a0001c0007t0001g0277 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.4034-7319G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93281469 | ||||||
| chr9:93281512
|
C | T | 1 | a0001c0003t0001g0253 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4034-7276C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93281512 | ||||||
| chr9:93281580
|
T | C | 1 | a0001c0003t0001g0077 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4034-7208T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93281580 | ||||||
| chr9:93281730
|
A | C | 12 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.4034-7058A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93281730 | ||||||
| chr9:93281744
|
A | G | 1 | a0001c0002t0001g0309 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4034-7044A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93281744 | ||||||
| chr9:93281801
|
C | T | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4034-6987C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93281801 | ||||||
| chr9:93281971
|
A | T | 1 | a0002c0042t0001g0147 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.4034-6817A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93281971 | ||||||
| chr9:93282116
|
A | G | 11 | a0001c0004t0002g0206a0001c0004t0002g0265a0001c0004t0002g0266others(8): Show | 11 | HG00639.hp1 HG00642.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.4034-6672A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93282116 | ||||||
| chr9:93282136
|
G | T | 28 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(25): Show | 29 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.4034-6652G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93282136 | ||||||
| chr9:93282293
|
T | TGTG | 274 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(271): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.4034-6493_4034-649 others(7): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93282293 | |||||
| chr9:93282298
|
A | T | 1 | a0006c0016t0001g0140 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4034-6490A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93282298 | ||||||
| chr9:93282463
|
GA | G | 8 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(5): Show | 8 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.4034-6313delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93282463 | |||||
| chr9:93282484
|
A | G | 1 | a0001c0009t0001g0199 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4034-6304A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93282484 | ||||||
| chr9:93282487
|
C | T | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4034-6301C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93282487 | ||||||
| chr9:93282488
|
A | G | 272 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(269): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.4034-6300A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93282488 | ||||||
| chr9:93282488
|
A | T | 3 | a0001c0002t0001g0055a0001c0002t0001g0067a0001c0025t0001g0163 | 3 | NA18955.hp2 NA19079.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.4034-6300A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93282488 | ||||||
| chr9:93282499
|
A | G | 1 | a0001c0002t0001g0020 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4034-6289A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93282499 | ||||||
| chr9:93282677
|
C | T | 1 | a0001c0017t0001g0161 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.4034-6111C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93282677 | ||||||
| chr9:93282761
|
G | T | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4034-6027G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93282761 | ||||||
| chr9:93282891
|
C | T | 27 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(24): Show | 28 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.4034-5897C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93282891 | ||||||
| chr9:93283050
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4034-5738C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93283050 | ||||||
| chr9:93283341
|
G | A | 1 | a0001c0048t0001g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4034-5447G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93283341 | ||||||
| chr9:93283405
|
T | C | 41 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(38): Show | 41 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.4034-5383T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93283405 | ||||||
| chr9:93283465
|
A | G | 272 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(269): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.4034-5323A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93283465 | ||||||
| chr9:93283712
|
A | C | 1 | a0001c0002t0001g0020 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4034-5076A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93283712 | ||||||
| chr9:93283754
|
A | G | 13 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(10): Show | 13 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.4034-5034A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93283754 | ||||||
| chr9:93283805
|
T | A | 7 | a0001c0003t0001g0220a0001c0003t0001g0223a0001c0003t0001g0225others(4): Show | 7 | HG01261.hp1 HG01346.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.4034-4983T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93283805 | ||||||
| chr9:93284212
|
G | A | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4034-4576G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93284212 | ||||||
| chr9:93284215
|
A | G | 1 | a0001c0035t0001g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4034-4573A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93284215 | ||||||
| chr9:93284347
|
A | G | 91 | a0001c0059t0001g0304a0002c0001t0001g0007a0002c0001t0001g0012others(88): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.4034-4441A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93284347 | ||||||
| chr9:93284426
|
C | A | 1 | a0002c0001t0001g0091 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.4034-4362C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93284426 | ||||||
| chr9:93284558
|
G | A | 9 | a0001c0002t0001g0018a0001c0002t0001g0029a0001c0002t0001g0045others(6): Show | 9 | HG02056.hp2 NA18943.hp2 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.4034-4230G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93284558 | ||||||
| chr9:93284786
|
G | A | 26 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(23): Show | 26 | HG00438.hp1 HG01071.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.4034-4002G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93284786 | ||||||
| chr9:93284807
|
G | C | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4034-3981G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93284807 | ||||||
| chr9:93284818
|
A | G | 5 | a0001c0024t0001g0054a0001c0024t0001g0056a0007c0020t0001g0286others(2): Show | 5 | HG01952.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.4034-3970A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93284818 | ||||||
| chr9:93284840
|
A | G | 1 | a0002c0001t0001g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4034-3948A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93284840 | ||||||
| chr9:93284845
|
C | T | 272 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(269): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.4034-3943C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93284845 | ||||||
| chr9:93284958
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4034-3830G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93284958 | ||||||
| chr9:93285011
|
T | A | 39 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(36): Show | 39 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.4034-3777T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93285011 | ||||||
| chr9:93285170
|
T | C | 245 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.4034-3618T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93285170 | ||||||
| chr9:93285260
|
A | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4034-3528A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93285260 | ||||||
| chr9:93285429
|
A | G | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4034-3359A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93285429 | ||||||
| chr9:93285430
|
T | C | 1 | a0025c0031t0001g0235 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4034-3358T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93285430 | ||||||
| chr9:93285563
|
G | T | 1 | a0001c0003t0001g0224 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4034-3225G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93285563 | ||||||
| chr9:93285932
|
C | T | 6 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(3): Show | 6 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.4034-2856C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93285932 | ||||||
| chr9:93286088
|
A | G | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4034-2700A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93286088 | ||||||
| chr9:93286167
|
ATTTGACT others(27): Show |
A | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4034-2620_4034-258 others(38): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93286167 | ||||||
| chr9:93286185
|
A | C | 302 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(299): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.4034-2603A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93286185 | ||||||
| chr9:93286231
|
C | T | 3 | a0003c0005t0001g0094a0003c0005t0001g0104a0003c0005t0001g0111 | 3 | NA18966.hp1 NA19066.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.4034-2557C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93286231 | ||||||
| chr9:93286232
|
G | A | 27 | a0001c0002t0001g0124a0001c0004t0002g0002a0001c0004t0002g0206others(24): Show | 28 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.4034-2556G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93286232 | ||||||
| chr9:93286263
|
A | T | 3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4034-2525A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93286263 | ||||||
| chr9:93286380
|
A | G | 1 | a0001c0003t0001g0230 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4034-2408A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93286380 | ||||||
| chr9:93286488
|
T | A | 123 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.4034-2300T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93286488 | ||||||
| chr9:93286603
|
A | G | 2 | a0001c0004t0002g0265a0001c0004t0002g0266 | 2 | HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4034-2185A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93286603 | ||||||
| chr9:93286939
|
C | T | 91 | a0001c0059t0001g0304a0002c0001t0001g0007a0002c0001t0001g0012others(88): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.4034-1849C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93286939 | ||||||
| chr9:93286997
|
CCAG | C | 4 | a0001c0007t0001g0256a0001c0007t0001g0271a0001c0007t0001g0281others(1): Show | 4 | HG00673.hp2 HG02129.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.4034-1786_4034-178 others(7): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr9 | 93286997 | |||||
| chr9:93287097
|
G | A | 13 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(10): Show | 13 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.4034-1691G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287097 | ||||||
| chr9:93287218
|
G | A | 1 | a0021c0050t0001g0070 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4034-1570G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287218 | ||||||
| chr9:93287355
|
G | T | 13 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(10): Show | 13 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.4034-1433G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287355 | ||||||
| chr9:93287360
|
C | T | 91 | a0001c0059t0001g0304a0002c0001t0001g0007a0002c0001t0001g0012others(88): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.4034-1428C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287360 | ||||||
| chr9:93287362
|
C | T | 1 | a0007c0020t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4034-1426C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287362 | ||||||
| chr9:93287365
|
A | C | 5 | a0001c0002t0001g0020a0001c0002t0001g0051a0001c0002t0001g0052others(2): Show | 5 | HG00597.hp1 HG00609.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.4034-1423A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287365 | ||||||
| chr9:93287385
|
G | A | 1 | a0002c0001t0001g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4034-1403G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287385 | ||||||
| chr9:93287425
|
A | G | 1 | a0014c0047t0001g0183 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4034-1363A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287425 | ||||||
| chr9:93287438
|
A | C | 1 | a0001c0022t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4034-1350A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287438 | ||||||
| chr9:93287517
|
G | A | 1 | a0016c0037t0001g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4034-1271G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287517 | ||||||
| chr9:93287580
|
C | A | 4 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(1): Show | 5 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.4034-1208C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287580 | ||||||
| chr9:93287801
|
C | T | 6 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(3): Show | 6 | HG01891.hp1 HG02717.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.4034-987C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287801 | ||||||
| chr9:93287824
|
G | A | 90 | a0001c0059t0001g0304a0002c0001t0001g0007a0002c0001t0001g0012others(87): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.4034-964G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287824 | ||||||
| chr9:93287854
|
A | T | 2 | a0001c0002t0001g0045a0001c0002t0001g0046 | 2 | HG02056.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.4034-934A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287854 | ||||||
| chr9:93287873
|
C | T | 5 | a0001c0024t0001g0054a0001c0024t0001g0056a0007c0020t0001g0286others(2): Show | 5 | HG01952.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.4034-915C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93287873 | ||||||
| chr9:93288074
|
C | T | 30 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(27): Show | 30 | HG00438.hp1 HG01071.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.4034-714C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93288074 | ||||||
| chr9:93288193
|
G | T | 288 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.4034-595G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93288193 | ||||||
| chr9:93288333
|
C | G | 167 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(164): Show | 167 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.4034-455C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93288333 | ||||||
| chr9:93288338
|
C | T | 1 | a0001c0002t0001g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4034-450C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93288338 | ||||||
| chr9:93288462
|
C | G | 164 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(161): Show | 164 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.4034-326C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93288462 | ||||||
| chr9:93288690
|
C | T | 17 | a0001c0003t0001g0077a0001c0003t0001g0170a0001c0003t0001g0239others(14): Show | 17 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.4034-98C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 19/29 | chr9 | 93288690 | ||||||
| chr9:93289648
|
C | T | 9 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(6): Show | 9 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.4866+28C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/29 | chr9 | 93289648 | ||||||
| chr9:93289693
|
G | A | 1 | a0002c0001t0001g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4866+73G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/29 | chr9 | 93289693 | ||||||
| chr9:93289719
|
G | A | 10 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(7): Show | 10 | HG01884.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.4866+99G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/29 | chr9 | 93289719 | ||||||
| chr9:93289752
|
C | T | 3 | a0004c0006t0001g0080a0004c0006t0001g0081a0004c0006t0001g0082 | 3 | HG01255.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4866+132C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/29 | chr9 | 93289752 | ||||||
| chr9:93289859
|
C | T | 1 | a0001c0014t0002g0302 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4867-119C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/29 | chr9 | 93289859 | ||||||
| chr9:93289859
|
CAG | C | 12 | a0003c0005t0001g0001a0003c0005t0001g0094a0003c0005t0001g0101others(9): Show | 13 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.4867-118_4867-117d others(4): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/29 | chr9 | 93289859 | ||||||
| chr9:93289897
|
G | A | 90 | a0001c0059t0001g0304a0002c0001t0001g0007a0002c0001t0001g0012others(87): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.4867-81G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/29 | chr9 | 93289897 | ||||||
| chr9:93289897
|
G | T | 1 | a0001c0002t0001g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4867-81G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 20/29 | chr9 | 93289897 | ||||||
| chr9:93290332
|
C | CT | 24 | a0001c0003t0001g0103a0001c0003t0001g0220a0001c0003t0001g0221others(21): Show | 24 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.4936+299dupT | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr9 | 93290332 | |||||
| chr9:93290332
|
CT | C | 9 | a0001c0002t0001g0238a0002c0001t0001g0095a0002c0001t0001g0096others(6): Show | 9 | HG02109.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.4936+299delT | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr9 | 93290332 | |||||
| chr9:93290390
|
G | A | 12 | a0001c0002t0001g0006a0001c0002t0001g0020a0001c0002t0001g0051others(9): Show | 12 | HG00597.hp1 HG00609.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.4936+343G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93290390 | ||||||
| chr9:93290402
|
A | T | 26 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(23): Show | 27 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.4936+355A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93290402 | ||||||
| chr9:93290614
|
C | G | 128 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.4936+567C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93290614 | ||||||
| chr9:93290638
|
C | G | 1 | a0003c0005t0001g0101 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4936+591C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93290638 | ||||||
| chr9:93290718
|
G | A | 1 | a0001c0007t0001g0281 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.4936+671G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93290718 | ||||||
| chr9:93290724
|
C | T | 17 | a0001c0003t0001g0077a0001c0003t0001g0170a0001c0003t0001g0239others(14): Show | 17 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.4936+677C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93290724 | ||||||
| chr9:93290811
|
C | T | 3 | a0001c0003t0001g0239a0001c0003t0001g0240a0001c0003t0001g0241 | 3 | HG00323.hp2 HG02559.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.4936+764C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93290811 | ||||||
| chr9:93291100
|
G | A | 1 | a0001c0025t0001g0027 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4936+1053G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93291100 | ||||||
| chr9:93291139
|
A | G | 16 | a0001c0003t0001g0077a0001c0003t0001g0170a0001c0003t0001g0239others(13): Show | 16 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.4936+1092A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93291139 | ||||||
| chr9:93291158
|
A | G | 305 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.4936+1111A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93291158 | ||||||
| chr9:93291335
|
C | A | 41 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(38): Show | 41 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.4937-973C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93291335 | ||||||
| chr9:93291586
|
T | G | 91 | a0001c0059t0001g0304a0002c0001t0001g0007a0002c0001t0001g0012others(88): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.4937-722T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93291586 | ||||||
| chr9:93291646
|
G | A | 214 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.4937-662G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93291646 | ||||||
| chr9:93291657
|
C | T | 1 | a0002c0001t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4937-651C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93291657 | ||||||
| chr9:93292001
|
T | G | 167 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(164): Show | 167 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.4937-307T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93292001 | ||||||
| chr9:93292057
|
G | A | 2 | a0004c0006t0001g0078a0004c0006t0001g0079 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4937-251G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93292057 | ||||||
| chr9:93292155
|
A | G | 2 | a0002c0001t0001g0120a0002c0001t0001g0149 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4937-153A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93292155 | ||||||
| chr9:93292235
|
T | C | 1 | a0001c0007t0001g0269 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4937-73T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 21/29 | chr9 | 93292235 | ||||||
| chr9:93292477
|
G | A | 19 | a0001c0003t0001g0103a0001c0003t0001g0220a0001c0003t0001g0221others(16): Show | 19 | HG00544.hp1 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.5026-14G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 22/29 | chr9 | 93292477 | ||||||
| chr9:93293322
|
C | CT | 12 | a0001c0002t0001g0045a0001c0002t0001g0072a0001c0003t0001g0230others(9): Show | 12 | HG00438.hp2 HG00673.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.5708+166dupT | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93293322 | |||||
| chr9:93293389
|
C | T | 155 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(152): Show | 155 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.5708+216C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93293389 | ||||||
| chr9:93293642
|
G | A | 288 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.5708+469G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93293642 | ||||||
| chr9:93293662
|
T | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5708+489T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93293662 | ||||||
| chr9:93293662
|
T | C | 287 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(284): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.5708+489T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93293662 | ||||||
| chr9:93293673
|
G | A | 155 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(152): Show | 155 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.5708+500G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93293673 | ||||||
| chr9:93293807
|
C | T | 4 | a0005c0012t0001g0192a0005c0012t0001g0193a0005c0012t0001g0194others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.5708+634C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93293807 | ||||||
| chr9:93294017
|
TTTA | T | 10 | a0001c0004t0002g0206a0001c0004t0002g0265a0001c0004t0002g0266others(7): Show | 10 | HG00639.hp1 HG00642.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.5708+847_5708+849d others(5): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93294017 | |||||
| chr9:93294117
|
G | A | 2 | a0002c0001t0001g0102a0002c0001t0001g0134 | 2 | NA18955.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.5708+944G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93294117 | ||||||
| chr9:93294153
|
G | A | 7 | a0002c0010t0001g0177a0002c0010t0001g0180a0002c0010t0001g0181others(4): Show | 7 | HG01167.hp2 HG01928.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.5708+980G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93294153 | ||||||
| chr9:93294155
|
C | T | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.5708+982C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93294155 | ||||||
| chr9:93294179
|
C | T | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.5708+1006C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93294179 | ||||||
| chr9:93294301
|
G | A | 2 | a0008c0026t0001g0305a0008c0026t0001g0306 | 2 | HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.5708+1128G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93294301 | ||||||
| chr9:93294482
|
C | A | 3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.5708+1309C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93294482 | ||||||
| chr9:93294600
|
G | A | 1 | a0001c0002t0001g0309 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5708+1427G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93294600 | ||||||
| chr9:93294720
|
A | C | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5708+1547A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93294720 | ||||||
| chr9:93295177
|
C | T | 1 | a0008c0026t0001g0305 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.5708+2004C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93295177 | ||||||
| chr9:93295231
|
C | T | 4 | a0001c0002t0001g0124a0001c0003t0001g0239a0001c0003t0001g0240others(1): Show | 4 | HG00323.hp2 HG02165.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.5708+2058C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93295231 | ||||||
| chr9:93295295
|
G | A | 13 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(10): Show | 13 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.5708+2122G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93295295 | ||||||
| chr9:93295304
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5708+2131C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93295304 | ||||||
| chr9:93295629
|
A | G | 39 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(36): Show | 39 | HG00438.hp1 HG01071.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.5709-2224A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93295629 | ||||||
| chr9:93295708
|
C | T | 2 | a0001c0035t0001g0207a0024c0060t0001g0254 | 2 | HG01081.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-2145C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93295708 | ||||||
| chr9:93295740
|
C | G | 26 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(23): Show | 27 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.5709-2113C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93295740 | ||||||
| chr9:93295823
|
T | A | 1 | a0001c0003t0001g0231 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.5709-2030T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93295823 | ||||||
| chr9:93295829
|
C | CTCAACTC others(143): Show |
2 | a0001c0034t0001g0216a0024c0060t0001g0254 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1977_5709-197 others(154): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93295829 | |||||
| chr9:93295829
|
C | CTCAACTC others(199): Show |
1 | a0001c0035t0001g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5709-1943_5709-194 others(210): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93295829 | |||||
| chr9:93295863
|
T | A | 1 | a0001c0003t0001g0231 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.5709-1990T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93295863 | ||||||
| chr9:93295877
|
T | G | 1 | a0002c0001t0001g0136 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.5709-1976T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93295877 | ||||||
| chr9:93295907
|
T | A | 1 | a0001c0003t0001g0231 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.5709-1946T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93295907 | ||||||
| chr9:93295941
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5709-1912C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93295941 | ||||||
| chr9:93296009
|
T | G | 1 | a0002c0001t0001g0136 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.5709-1844T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296009 | ||||||
| chr9:93296024
|
C | T | 1 | a0002c0001t0001g0136 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.5709-1829C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296024 | ||||||
| chr9:93296047
|
C | CATCCTCC others(20): Show |
4 | a0001c0003t0001g0239a0002c0001t0001g0189a0002c0001t0001g0190others(1): Show | 4 | HG00280.hp2 HG00323.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.5709-1755_5709-172 others(31): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93296047 | |||||
| chr9:93296097
|
C | CT | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1756_5709-175 others(5): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296097 | ||||||
| chr9:93296099
|
T | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1754T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296099 | ||||||
| chr9:93296101
|
T | C | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1752T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296101 | ||||||
| chr9:93296102
|
A | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1751A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296102 | ||||||
| chr9:93296113
|
A | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1740A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296113 | ||||||
| chr9:93296116
|
T | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1737T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296116 | ||||||
| chr9:93296118
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1735C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296118 | ||||||
| chr9:93296119
|
C | G | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1734C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296119 | ||||||
| chr9:93296130
|
A | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1723A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296130 | ||||||
| chr9:93296132
|
T | C | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1721T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296132 | ||||||
| chr9:93296133
|
G | C | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1720G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296133 | ||||||
| chr9:93296141
|
T | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1712T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296141 | ||||||
| chr9:93296144
|
T | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1709T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296144 | ||||||
| chr9:93296145
|
T | C | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1708T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296145 | ||||||
| chr9:93296159
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1694C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296159 | ||||||
| chr9:93296173
|
TCCTCCCC others(7): Show |
T | 1 | a0002c0001t0001g0107 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.5709-1666_5709-165 others(18): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93296173 | |||||
| chr9:93296260
|
T | TCCCCTCC others(225): Show |
1 | a0001c0002t0001g0309 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5709-1561_5709-156 others(236): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93296260 | |||||
| chr9:93296268
|
ATCCTCCC others(7): Show |
A | 1 | a0008c0061t0001g0290 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5709-1562_5709-154 others(18): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93296268 | |||||
| chr9:93296293
|
A | G | 26 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(23): Show | 27 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.5709-1560A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296293 | ||||||
| chr9:93296355
|
T | TCCCCTCA others(64): Show |
3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02080.hp1 HG02129.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.5709-1480_5709-147 others(75): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93296355 | |||||
| chr9:93296362
|
A | ACCATCCT others(20): Show |
1 | a0002c0001t0001g0118 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5709-1440_5709-141 others(31): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93296362 | |||||
| chr9:93296362
|
ACCATCCT others(20): Show |
A | 1 | a0002c0001t0001g0092 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.5709-1440_5709-141 others(31): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93296362 | |||||
| chr9:93296429
|
C | CACCTTCC others(20): Show |
79 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(76): Show | 79 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.5709-1409_5709-138 others(31): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93296429 | |||||
| chr9:93296429
|
C | T | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02080.hp1 HG02129.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.5709-1424C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296429 | ||||||
| chr9:93296436
|
C | G | 1 | a0001c0008t0001g0063 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.5709-1417C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296436 | ||||||
| chr9:93296449
|
C | T | 4 | a0001c0008t0001g0023a0001c0008t0001g0024a0001c0008t0001g0025others(1): Show | 4 | HG03490.hp1 HG03492.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.5709-1404C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296449 | ||||||
| chr9:93296500
|
A | T | 1 | a0001c0003t0001g0246 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.5709-1353A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296500 | ||||||
| chr9:93296500
|
ATCCTCCC others(7): Show |
A | 9 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(6): Show | 9 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.5709-1343_5709-133 others(18): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93296500 | |||||
| chr9:93296501
|
T | C | 1 | a0001c0003t0001g0246 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.5709-1352T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296501 | ||||||
| chr9:93296583
|
A | G | 1 | a0007c0020t0001g0287 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.5709-1270A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296583 | ||||||
| chr9:93296607
|
CTCCATCC others(20): Show |
C | 1 | a0001c0003t0001g0221 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.5709-1226_5709-120 others(31): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93296607 | |||||
| chr9:93296654
|
T | C | 1 | a0001c0003t0001g0231 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.5709-1199T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296654 | ||||||
| chr9:93296690
|
C | A | 1 | a0001c0002t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5709-1163C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296690 | ||||||
| chr9:93296719
|
C | G | 35 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(32): Show | 35 | HG00438.hp1 HG01071.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.5709-1134C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296719 | ||||||
| chr9:93296735
|
T | C | 1 | a0022c0029t0001g0009 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5709-1118T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296735 | ||||||
| chr9:93296767
|
CCTCCCCT others(48): Show |
C | 14 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.5709-1076_5709-102 others(59): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93296767 | |||||
| chr9:93296812
|
T | C | 25 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(22): Show | 25 | HG01071.hp1 HG01071.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.5709-1041T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296812 | ||||||
| chr9:93296830
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5709-1023C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296830 | ||||||
| chr9:93296872
|
C | T | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.5709-981C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296872 | ||||||
| chr9:93296876
|
C | CCCTCCCC others(106): Show |
12 | a0005c0012t0001g0192a0005c0012t0001g0194a0005c0012t0001g0196others(9): Show | 12 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.5709-956_5709-844d others(115): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93296876 | |||||
| chr9:93296887
|
G | T | 2 | a0004c0006t0001g0089a0013c0041t0001g0154 | 2 | HG00438.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.5709-966G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296887 | ||||||
| chr9:93296906
|
C | T | 5 | a0001c0014t0002g0255a0001c0014t0002g0299a0001c0014t0002g0300others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.5709-947C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296906 | ||||||
| chr9:93296971
|
G | A | 2 | a0001c0002t0001g0048a0001c0059t0001g0304 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5709-882G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93296971 | ||||||
| chr9:93297033
|
C | T | 1 | a0001c0003t0001g0313 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5709-820C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93297033 | ||||||
| chr9:93297100
|
TTCCTCCC others(7): Show |
T | 3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.5709-743_5709-730d others(16): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93297100 | |||||
| chr9:93297107
|
C | A | 1 | a0001c0003t0001g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5709-746C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93297107 | ||||||
| chr9:93297110
|
T | C | 3 | a0001c0003t0001g0239a0001c0003t0001g0240a0001c0003t0001g0241 | 3 | HG00323.hp2 HG02559.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.5709-743T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93297110 | ||||||
| chr9:93297110
|
T | TGGCGTCC others(7): Show |
1 | a0001c0003t0001g0243 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.5709-722_5709-709d others(16): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93297110 | |||||
| chr9:93297110
|
TGGCGTCC others(7): Show |
T | 1 | a0001c0002t0001g0124 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.5709-722_5709-709d others(16): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93297110 | |||||
| chr9:93297127
|
C | T | 1 | a0012c0044t0001g0165 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.5709-726C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93297127 | ||||||
| chr9:93297131
|
CTCCCCTC others(7): Show |
C | 1 | a0002c0001t0001g0129 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.5709-714_5709-701d others(16): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr9 | 93297131 | |||||
| chr9:93297139
|
G | A | 1 | a0001c0002t0001g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5709-714G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93297139 | ||||||
| chr9:93297232
|
C | T | 1 | a0001c0002t0001g0006 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.5709-621C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93297232 | ||||||
| chr9:93297387
|
C | T | 1 | a0001c0004t0002g0284 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5709-466C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93297387 | ||||||
| chr9:93297430
|
A | G | 3 | a0001c0003t0001g0239a0001c0003t0001g0240a0001c0003t0001g0241 | 3 | HG00323.hp2 HG02559.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.5709-423A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93297430 | ||||||
| chr9:93297654
|
G | C | 39 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(36): Show | 39 | HG00438.hp1 HG01071.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.5709-199G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93297654 | ||||||
| chr9:93297668
|
G | C | 1 | a0007c0020t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5709-185G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93297668 | ||||||
| chr9:93297761
|
T | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5709-92T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 23/29 | chr9 | 93297761 | ||||||
| chr9:93298100
|
C | T | 2 | a0001c0003t0001g0246a0001c0003t0001g0253 | 2 | NA18964.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.5923+33C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298100 | ||||||
| chr9:93298140
|
C | T | 1 | a0002c0001t0001g0152 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.5923+73C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298140 | ||||||
| chr9:93298141
|
G | A | 1 | a0002c0001t0001g0172 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.5923+74G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298141 | ||||||
| chr9:93298192
|
A | G | 1 | a0002c0001t0001g0102 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.5923+125A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298192 | ||||||
| chr9:93298243
|
C | G | 1 | a0002c0001t0001g0119 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.5923+176C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298243 | ||||||
| chr9:93298302
|
C | T | 1 | a0001c0007t0001g0273 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5923+235C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298302 | ||||||
| chr9:93298477
|
C | T | 122 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.5923+410C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298477 | ||||||
| chr9:93298595
|
G | A | 1 | a0001c0007t0001g0273 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5924-475G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298595 | ||||||
| chr9:93298604
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5924-466C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298604 | ||||||
| chr9:93298636
|
C | G | 1 | a0001c0017t0001g0122 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.5924-434C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298636 | ||||||
| chr9:93298636
|
C | T | 1 | a0001c0007t0001g0028 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5924-434C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298636 | ||||||
| chr9:93298652
|
G | T | 2 | a0007c0020t0001g0286a0007c0020t0001g0287 | 2 | HG01952.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.5924-418G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298652 | ||||||
| chr9:93298850
|
A | G | 1 | a0002c0001t0001g0131 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.5924-220A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298850 | ||||||
| chr9:93298918
|
C | T | 5 | a0001c0024t0001g0054a0001c0024t0001g0056a0007c0020t0001g0286others(2): Show | 5 | HG01952.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.5924-152C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298918 | ||||||
| chr9:93298958
|
C | T | 10 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(7): Show | 10 | HG01884.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.5924-112C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298958 | ||||||
| chr9:93298987
|
A | G | 288 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.5924-83A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 24/29 | chr9 | 93298987 | ||||||
| chr9:93299399
|
TA | T | 25 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(22): Show | 25 | HG01071.hp1 HG01071.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.6115+149delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr9 | 93299399 | |||||
| chr9:93299424
|
G | T | 25 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(22): Show | 25 | HG01071.hp1 HG01071.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.6115+163G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 25/29 | chr9 | 93299424 | ||||||
| chr9:93299724
|
C | T | 1 | a0001c0004t0002g0285 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.6116-327C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 25/29 | chr9 | 93299724 | ||||||
| chr9:93299996
|
C | A | 1 | a0001c0002t0001g0006 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.6116-55C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 25/29 | chr9 | 93299996 | ||||||
| chr9:93300180
|
C | T | 2 | a0001c0004t0002g0206a0001c0004t0002g0282 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.6214+31C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93300180 | ||||||
| chr9:93300210
|
C | T | 14 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.6214+61C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93300210 | ||||||
| chr9:93300318
|
C | T | 2 | a0001c0002t0001g0003a0001c0002t0001g0053 | 2 | HG00140.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.6214+169C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93300318 | ||||||
| chr9:93300319
|
G | A | 1 | a0001c0002t0001g0047 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.6214+170G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93300319 | ||||||
| chr9:93300426
|
G | A | 10 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(7): Show | 10 | HG01884.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.6214+277G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93300426 | ||||||
| chr9:93300498
|
T | A | 1 | a0001c0007t0001g0271 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.6214+349T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93300498 | ||||||
| chr9:93300569
|
G | A | 13 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(10): Show | 13 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.6214+420G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93300569 | ||||||
| chr9:93300689
|
T | G | 14 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.6214+540T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93300689 | ||||||
| chr9:93300736
|
C | T | 1 | a0023c0033t0001g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6214+587C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93300736 | ||||||
| chr9:93300746
|
C | T | 1 | a0002c0001t0001g0091 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.6214+597C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93300746 | ||||||
| chr9:93300792
|
C | T | 1 | a0001c0002t0001g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.6214+643C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93300792 | ||||||
| chr9:93300877
|
G | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6214+728G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93300877 | ||||||
| chr9:93300927
|
G | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6214+778G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93300927 | ||||||
| chr9:93301057
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6214+908C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301057 | ||||||
| chr9:93301174
|
G | A | 38 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(35): Show | 38 | HG00438.hp1 HG01071.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.6214+1025G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301174 | ||||||
| chr9:93301198
|
A | AT | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6214+1054dupT | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr9 | 93301198 | |||||
| chr9:93301213
|
TC | T | 39 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(36): Show | 39 | HG00438.hp1 HG01071.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.6214+1065delC | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301213 | ||||||
| chr9:93301248
|
T | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6214+1099T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301248 | ||||||
| chr9:93301309
|
G | A | 3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.6214+1160G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301309 | ||||||
| chr9:93301371
|
A | G | 14 | a0002c0001t0001g0095a0005c0012t0001g0192a0005c0012t0001g0193others(11): Show | 14 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.6214+1222A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301371 | ||||||
| chr9:93301408
|
T | G | 39 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(36): Show | 39 | HG00438.hp1 HG01071.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.6214+1259T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301408 | ||||||
| chr9:93301441
|
G | C | 1 | a0001c0003t0001g0313 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.6214+1292G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301441 | ||||||
| chr9:93301514
|
G | A | 1 | a0001c0022t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6214+1365G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301514 | ||||||
| chr9:93301582
|
T | C | 2 | a0008c0026t0001g0305a0008c0026t0001g0306 | 2 | HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.6214+1433T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301582 | ||||||
| chr9:93301590
|
C | G | 1 | a0001c0003t0001g0242 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.6214+1441C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301590 | ||||||
| chr9:93301647
|
C | T | 1 | a0027c0056t0001g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6214+1498C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301647 | ||||||
| chr9:93301655
|
G | A | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6214+1506G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301655 | ||||||
| chr9:93301714
|
C | T | 5 | a0001c0024t0001g0054a0001c0024t0001g0056a0007c0020t0001g0286others(2): Show | 5 | HG01952.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.6214+1565C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301714 | ||||||
| chr9:93301844
|
G | A | 61 | a0002c0001t0001g0007a0002c0001t0001g0012a0002c0001t0001g0091others(58): Show | 61 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.6214+1695G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301844 | ||||||
| chr9:93301932
|
C | T | 1 | a0002c0001t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6214+1783C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93301932 | ||||||
| chr9:93302019
|
C | A | 289 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.6214+1870C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93302019 | ||||||
| chr9:93302198
|
A | C | 1 | a0001c0002t0001g0036 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.6214+2049A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93302198 | ||||||
| chr9:93302250
|
G | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6214+2101G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93302250 | ||||||
| chr9:93302368
|
G | A | 4 | a0001c0008t0001g0023a0001c0008t0001g0024a0001c0008t0001g0025others(1): Show | 4 | HG03490.hp1 HG03492.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.6214+2219G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93302368 | ||||||
| chr9:93302470
|
G | A | 4 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254others(1): Show | 4 | HG01081.hp1 HG01081.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.6214+2321G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93302470 | ||||||
| chr9:93302897
|
C | T | 9 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(6): Show | 9 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.6214+2748C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93302897 | ||||||
| chr9:93302911
|
C | T | 1 | a0002c0001t0001g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.6214+2762C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93302911 | ||||||
| chr9:93302925
|
C | CT | 222 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.6214+2787dupT | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr9 | 93302925 | |||||
| chr9:93302925
|
C | T | 1 | a0001c0002t0001g0035 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.6214+2776C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93302925 | ||||||
| chr9:93302942
|
A | G | 2 | a0001c0003t0001g0247a0001c0003t0001g0295 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.6214+2793A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93302942 | ||||||
| chr9:93303001
|
C | G | 1 | a0001c0034t0001g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6214+2852C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93303001 | ||||||
| chr9:93303226
|
A | G | 10 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(7): Show | 10 | HG01884.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.6214+3077A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93303226 | ||||||
| chr9:93303268
|
G | A | 1 | a0007c0020t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6214+3119G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93303268 | ||||||
| chr9:93303296
|
C | T | 13 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(10): Show | 13 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.6214+3147C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93303296 | ||||||
| chr9:93303322
|
G | C | 1 | a0001c0002t0001g0022 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6214+3173G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93303322 | ||||||
| chr9:93303501
|
C | T | 20 | a0001c0003t0001g0103a0001c0003t0001g0220a0001c0003t0001g0221others(17): Show | 20 | HG00544.hp1 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.6215-3276C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93303501 | ||||||
| chr9:93303625
|
C | T | 2 | a0001c0003t0001g0247a0001c0003t0001g0295 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.6215-3152C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93303625 | ||||||
| chr9:93303644
|
T | A | 2 | a0001c0028t0001g0310a0001c0028t0001g0311 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.6215-3133T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93303644 | ||||||
| chr9:93303788
|
G | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6215-2989G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93303788 | ||||||
| chr9:93303837
|
A | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6215-2940A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93303837 | ||||||
| chr9:93303975
|
G | T | 1 | a0001c0008t0001g0063 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.6215-2802G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93303975 | ||||||
| chr9:93303983
|
G | A | 1 | a0002c0001t0001g0136 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.6215-2794G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93303983 | ||||||
| chr9:93304000
|
C | T | 4 | a0001c0024t0001g0054a0001c0024t0001g0056a0007c0020t0001g0286others(1): Show | 4 | HG01952.hp1 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.6215-2777C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93304000 | ||||||
| chr9:93304075
|
G | A | 1 | a0001c0003t0001g0241 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.6215-2702G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93304075 | ||||||
| chr9:93304343
|
C | G | 3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.6215-2434C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93304343 | ||||||
| chr9:93304443
|
C | T | 2 | a0001c0004t0002g0265a0001c0004t0002g0266 | 2 | HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.6215-2334C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93304443 | ||||||
| chr9:93304509
|
A | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6215-2268A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93304509 | ||||||
| chr9:93304526
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6215-2251C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93304526 | ||||||
| chr9:93304557
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6215-2220C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93304557 | ||||||
| chr9:93304690
|
G | A | 2 | a0002c0001t0001g0168a0002c0001t0001g0169 | 2 | HG01074.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.6215-2087G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93304690 | ||||||
| chr9:93304705
|
G | A | 1 | a0005c0030t0001g0208 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.6215-2072G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93304705 | ||||||
| chr9:93304932
|
G | A | 27 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(24): Show | 28 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.6215-1845G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93304932 | ||||||
| chr9:93305241
|
G | C | 288 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.6215-1536G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93305241 | ||||||
| chr9:93305494
|
G | A | 1 | a0001c0022t0001g0008 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.6215-1283G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93305494 | ||||||
| chr9:93305621
|
A | T | 3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.6215-1156A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93305621 | ||||||
| chr9:93305636
|
C | T | 4 | a0001c0034t0001g0216a0001c0035t0001g0207a0005c0030t0001g0208others(1): Show | 4 | HG01081.hp1 HG02895.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.6215-1141C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93305636 | ||||||
| chr9:93305817
|
A | G | 18 | a0001c0034t0001g0216a0001c0035t0001g0207a0004c0006t0001g0078others(15): Show | 18 | HG00438.hp1 HG01081.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.6215-960A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93305817 | ||||||
| chr9:93305884
|
C | T | 13 | a0005c0012t0001g0192a0005c0012t0001g0193a0005c0012t0001g0194others(10): Show | 13 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.6215-893C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93305884 | ||||||
| chr9:93305920
|
C | CGTCCCAG others(12): Show |
2 | a0004c0006t0001g0078a0004c0006t0001g0079 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.6215-856_6215-838d others(21): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr9 | 93305920 | |||||
| chr9:93305952
|
G | T | 82 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(79): Show | 82 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.6215-825G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93305952 | ||||||
| chr9:93305960
|
C | T | 2 | a0001c0003t0001g0247a0001c0003t0001g0295 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.6215-817C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93305960 | ||||||
| chr9:93306000
|
A | AGG | 10 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(7): Show | 10 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.6215-777_6215-776i others(4): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93306000 | ||||||
| chr9:93306001
|
C | G | 10 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(7): Show | 10 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.6215-776C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93306001 | ||||||
| chr9:93306046
|
C | T | 13 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(10): Show | 13 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.6215-731C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93306046 | ||||||
| chr9:93306168
|
C | T | 1 | a0001c0007t0001g0280 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.6215-609C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93306168 | ||||||
| chr9:93306211
|
C | T | 1 | a0001c0002t0001g0047 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.6215-566C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93306211 | ||||||
| chr9:93306231
|
A | T | 1 | a0001c0008t0001g0024 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.6215-546A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93306231 | ||||||
| chr9:93306339
|
G | A | 1 | a0003c0005t0001g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.6215-438G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93306339 | ||||||
| chr9:93306468
|
C | CT | 11 | a0002c0001t0001g0106a0002c0001t0001g0134a0004c0006t0001g0083others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.6215-303dupT | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr9 | 93306468 | |||||
| chr9:93306475
|
C | T | 308 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(305): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.6215-302C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 26/29 | chr9 | 93306475 | ||||||
| chr9:93306874
|
C | T | 1 | a0001c0048t0001g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.6259+53C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93306874 | ||||||
| chr9:93306881
|
A | C | 1 | a0001c0011t0001g0212 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.6259+60A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93306881 | ||||||
| chr9:93306905
|
C | T | 1 | a0003c0005t0001g0127 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.6259+84C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93306905 | ||||||
| chr9:93307002
|
G | A | 6 | a0004c0006t0001g0083a0004c0006t0001g0084a0004c0006t0001g0085others(3): Show | 6 | HG02523.hp1 NA18963.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.6259+181G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307002 | ||||||
| chr9:93307231
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6259+410C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307231 | ||||||
| chr9:93307447
|
A | G | 4 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(1): Show | 5 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.6259+626A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307447 | ||||||
| chr9:93307617
|
G | C | 14 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.6260-711G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307617 | ||||||
| chr9:93307659
|
C | T | 6 | a0005c0019t0001g0040a0005c0019t0001g0041a0005c0019t0001g0139others(3): Show | 6 | HG02145.hp2 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.6260-669C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307659 | ||||||
| chr9:93307682
|
G | C | 122 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.6260-646G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307682 | ||||||
| chr9:93307718
|
C | T | 1 | a0002c0010t0001g0181 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.6260-610C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307718 | ||||||
| chr9:93307803
|
A | C | 2 | a0002c0001t0001g0152a0002c0001t0001g0155 | 2 | NA19082.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.6260-525A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307803 | ||||||
| chr9:93307815
|
G | A | 1 | a0007c0020t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6260-513G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307815 | ||||||
| chr9:93307846
|
G | A | 1 | a0002c0001t0001g0160 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.6260-482G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307846 | ||||||
| chr9:93307889
|
G | A | 1 | a0001c0008t0001g0024 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.6260-439G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307889 | ||||||
| chr9:93307897
|
A | G | 1 | a0002c0010t0001g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6260-431A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307897 | ||||||
| chr9:93307898
|
T | C | 5 | a0001c0024t0001g0054a0001c0024t0001g0056a0007c0020t0001g0286others(2): Show | 5 | HG01952.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.6260-430T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307898 | ||||||
| chr9:93307933
|
C | T | 1 | a0008c0061t0001g0290 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6260-395C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307933 | ||||||
| chr9:93307948
|
T | C | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6260-380T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93307948 | ||||||
| chr9:93308069
|
C | T | 1 | a0001c0015t0001g0293 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6260-259C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93308069 | ||||||
| chr9:93308189
|
C | T | 1 | a0001c0002t0001g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.6260-139C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 27/29 | chr9 | 93308189 | ||||||
| chr9:93308607
|
G | C | 14 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.6516+23G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93308607 | ||||||
| chr9:93308617
|
G | A | 2 | a0002c0001t0001g0118a0002c0001t0001g0119 | 2 | HG02135.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.6516+33G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93308617 | ||||||
| chr9:93308812
|
C | A | 19 | a0001c0003t0001g0103a0001c0003t0001g0220a0001c0003t0001g0221others(16): Show | 19 | HG00544.hp1 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.6516+228C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93308812 | ||||||
| chr9:93309016
|
C | T | 1 | a0001c0002t0001g0062 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.6516+432C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93309016 | ||||||
| chr9:93309037
|
C | T | 1 | a0001c0004t0002g0282 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6516+453C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93309037 | ||||||
| chr9:93309093
|
C | T | 1 | a0001c0008t0001g0024 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.6516+509C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93309093 | ||||||
| chr9:93309126
|
TC | T | 39 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(36): Show | 39 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.6516+543delC | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93309126 | ||||||
| chr9:93309155
|
A | G | 39 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(36): Show | 39 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.6516+571A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93309155 | ||||||
| chr9:93309318
|
CTAAT | C | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6516+736_6516+739d others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93309318 | |||||
| chr9:93309444
|
T | C | 4 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(1): Show | 5 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.6516+860T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93309444 | ||||||
| chr9:93309562
|
C | T | 13 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(10): Show | 13 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.6516+978C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93309562 | ||||||
| chr9:93310170
|
T | C | 288 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.6516+1586T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93310170 | ||||||
| chr9:93310442
|
C | CA | 139 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.6516+1865dupA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93310442 | |||||
| chr9:93310448
|
A | T | 1 | a0001c0008t0001g0151 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.6516+1864A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93310448 | ||||||
| chr9:93310450
|
T | A | 125 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.6516+1866T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93310450 | ||||||
| chr9:93310452
|
T | A | 1 | a0001c0002t0001g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6516+1868T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93310452 | ||||||
| chr9:93310464
|
T | A | 1 | a0002c0001t0001g0119 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.6516+1880T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93310464 | ||||||
| chr9:93310579
|
C | G | 90 | a0001c0028t0001g0311a0001c0059t0001g0304a0002c0001t0001g0007others(87): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.6516+1995C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93310579 | ||||||
| chr9:93310681
|
T | C | 39 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(36): Show | 39 | HG00438.hp1 HG01071.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.6516+2097T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93310681 | ||||||
| chr9:93310724
|
A | C | 13 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(10): Show | 13 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.6516+2140A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93310724 | ||||||
| chr9:93310765
|
A | G | 1 | a0001c0004t0002g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.6516+2181A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93310765 | ||||||
| chr9:93310825
|
G | A | 1 | a0001c0034t0001g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6516+2241G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93310825 | ||||||
| chr9:93311292
|
C | T | 14 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.6516+2708C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93311292 | ||||||
| chr9:93311320
|
C | T | 2 | a0001c0004t0002g0288a0001c0004t0002g0289 | 2 | HG00642.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.6516+2736C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93311320 | ||||||
| chr9:93311513
|
G | A | 288 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.6516+2929G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93311513 | ||||||
| chr9:93311609
|
T | TTGTGTGT others(9): Show |
1 | a0001c0003t0001g0246 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.6516+3028_6516+302 others(20): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93311609 | |||||
| chr9:93311611
|
G | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6516+3027G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93311611 | ||||||
| chr9:93311613
|
T | G | 1 | a0001c0003t0001g0246 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.6516+3029T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93311613 | ||||||
| chr9:93311613
|
T | TGTGTGTG others(6): Show |
2 | a0001c0002t0001g0046a0008c0026t0001g0306 | 2 | HG01255.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.6516+3029_6516+303 others(17): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93311613 | ||||||
| chr9:93311613
|
T | TTG | 19 | a0001c0009t0001g0198a0001c0009t0001g0199a0001c0009t0001g0200others(16): Show | 19 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.6516+3055_6516+305 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93311613 | |||||
| chr9:93311613
|
T | TTGTGTG | 4 | a0001c0008t0001g0023a0001c0008t0001g0024a0001c0008t0001g0025others(1): Show | 4 | HG03490.hp1 HG03492.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.6516+3051_6516+305 others(10): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93311613 | |||||
| chr9:93311613
|
T | TTGTGTGT others(3): Show |
86 | a0001c0002t0001g0020a0001c0002t0001g0053a0001c0008t0001g0011others(83): Show | 86 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.6516+3047_6516+305 others(14): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93311613 | |||||
| chr9:93311613
|
T | TTGTGTGT others(5): Show |
126 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.6516+3045_6516+305 others(16): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93311613 | |||||
| chr9:93311613
|
T | TTGTGTGT others(7): Show |
45 | a0001c0002t0001g0076a0001c0003t0001g0103a0001c0003t0001g0222others(42): Show | 47 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.6516+3043_6516+305 others(18): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93311613 | |||||
| chr9:93311613
|
T | TTGTGTGT others(9): Show |
11 | a0001c0003t0001g0243a0001c0003t0001g0313a0001c0008t0001g0014others(8): Show | 11 | HG01071.hp1 HG02056.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.6516+3041_6516+305 others(20): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93311613 | |||||
| chr9:93311613
|
T | TTGTGTGT others(11): Show |
1 | a0001c0008t0001g0151 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.6516+3039_6516+305 others(22): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93311613 | |||||
| chr9:93311613
|
T | TTGTTTGT others(5): Show |
3 | a0001c0002t0001g0072a0001c0049t0001g0073a0010c0054t0001g0071 | 3 | HG03239.hp2 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.6516+3032_6516+303 others(16): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93311613 | |||||
| chr9:93311640
|
T | TGTGTGTG others(6): Show |
1 | a0001c0002t0001g0052 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.6516+3056_6516+305 others(17): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93311640 | ||||||
| chr9:93311681
|
A | C | 5 | a0001c0024t0001g0054a0001c0024t0001g0056a0007c0020t0001g0286others(2): Show | 5 | HG01952.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.6516+3097A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93311681 | ||||||
| chr9:93311744
|
C | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6516+3160C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93311744 | ||||||
| chr9:93311894
|
ACAGGCGT others(1): Show |
A | 90 | a0001c0028t0001g0311a0001c0059t0001g0304a0002c0001t0001g0007others(87): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.6516+3311_6516+331 others(12): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93311894 | ||||||
| chr9:93311920
|
G | A | 3 | a0001c0003t0001g0170a0001c0003t0001g0252a0005c0012t0001g0193 | 3 | HG00099.hp1 HG01168.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.6516+3336G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93311920 | ||||||
| chr9:93312142
|
TC | T | 14 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.6516+3559delC | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93312142 | ||||||
| chr9:93312258
|
G | A | 1 | a0001c0002t0001g0020 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.6516+3674G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93312258 | ||||||
| chr9:93312450
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6516+3866C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93312450 | ||||||
| chr9:93312452
|
G | A | 21 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(18): Show | 21 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.6516+3868G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93312452 | ||||||
| chr9:93312491
|
C | T | 1 | a0004c0006t0001g0086 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.6516+3907C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93312491 | ||||||
| chr9:93312561
|
G | A | 2 | a0002c0001t0001g0118a0002c0001t0001g0119 | 2 | HG02135.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.6516+3977G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93312561 | ||||||
| chr9:93312706
|
A | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6516+4122A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93312706 | ||||||
| chr9:93313048
|
A | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6516+4464A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93313048 | ||||||
| chr9:93313050
|
C | T | 1 | a0001c0009t0001g0199 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.6516+4466C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93313050 | ||||||
| chr9:93313105
|
C | T | 2 | a0001c0003t0001g0170a0001c0003t0001g0252 | 2 | HG00099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.6517-4415C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93313105 | ||||||
| chr9:93313163
|
C | T | 1 | a0020c0051t0001g0308 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.6517-4357C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93313163 | ||||||
| chr9:93313397
|
T | TA | 44 | a0001c0003t0001g0077a0001c0003t0001g0103a0001c0003t0001g0170others(41): Show | 44 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.6517-4109dupA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93313397 | |||||
| chr9:93313397
|
TA | T | 13 | a0001c0008t0001g0023a0001c0008t0001g0024a0001c0008t0001g0025others(10): Show | 13 | HG00609.hp1 HG01943.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.6517-4109delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93313397 | |||||
| chr9:93313524
|
T | C | 1 | a0002c0001t0001g0164 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.6517-3996T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93313524 | ||||||
| chr9:93313656
|
A | G | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6517-3864A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93313656 | ||||||
| chr9:93313735
|
A | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6517-3785A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93313735 | ||||||
| chr9:93313860
|
G | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6517-3660G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93313860 | ||||||
| chr9:93313964
|
C | G | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6517-3556C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93313964 | ||||||
| chr9:93313973
|
T | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6517-3547T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93313973 | ||||||
| chr9:93314036
|
T | C | 290 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(287): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.6517-3484T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93314036 | ||||||
| chr9:93314037
|
G | A | 5 | a0001c0024t0001g0054a0001c0024t0001g0056a0007c0020t0001g0286others(2): Show | 5 | HG01952.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.6517-3483G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93314037 | ||||||
| chr9:93314047
|
G | A | 22 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(19): Show | 22 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.6517-3473G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93314047 | ||||||
| chr9:93314116
|
C | CA | 9 | a0001c0007t0001g0268a0001c0007t0001g0269a0001c0007t0001g0277others(6): Show | 9 | HG01074.hp2 HG01175.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.6517-3388dupA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93314116 | |||||
| chr9:93314116
|
CA | C | 29 | a0001c0003t0001g0236a0001c0003t0001g0245a0001c0004t0002g0266others(26): Show | 29 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.6517-3388delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93314116 | |||||
| chr9:93314231
|
G | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6517-3289G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93314231 | ||||||
| chr9:93314261
|
G | A | 22 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(19): Show | 22 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.6517-3259G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93314261 | ||||||
| chr9:93314428
|
CAGAGCA | C | 3 | a0002c0001t0001g0095a0002c0001t0001g0099a0002c0038t0001g0098 | 3 | HG02622.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6517-3088_6517-308 others(10): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93314428 | |||||
| chr9:93314439
|
C | A | 3 | a0002c0001t0001g0095a0002c0001t0001g0099a0002c0038t0001g0098 | 3 | HG02622.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6517-3081C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93314439 | ||||||
| chr9:93314446
|
GA | G | 125 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.6517-3062delA | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93314446 | |||||
| chr9:93314513
|
C | T | 14 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.6517-3007C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93314513 | ||||||
| chr9:93314552
|
CTTATAAG others(16): Show |
C | 1 | a0001c0008t0001g0016 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.6517-2918_6517-289 others(27): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93314552 | |||||
| chr9:93314829
|
G | A | 1 | a0001c0003t0001g0232 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.6517-2691G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93314829 | ||||||
| chr9:93314930
|
A | G | 5 | a0001c0024t0001g0054a0001c0024t0001g0056a0007c0020t0001g0286others(2): Show | 5 | HG01952.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.6517-2590A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93314930 | ||||||
| chr9:93314954
|
A | G | 21 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(18): Show | 22 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.6517-2566A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93314954 | ||||||
| chr9:93315003
|
A | G | 5 | a0001c0024t0001g0054a0001c0024t0001g0056a0007c0020t0001g0286others(2): Show | 5 | HG01952.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.6517-2517A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93315003 | ||||||
| chr9:93315183
|
A | C | 126 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.6517-2337A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93315183 | ||||||
| chr9:93315228
|
C | T | 2 | a0004c0006t0001g0078a0004c0006t0001g0079 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.6517-2292C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93315228 | ||||||
| chr9:93315244
|
C | T | 1 | a0002c0001t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6517-2276C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93315244 | ||||||
| chr9:93315418
|
C | T | 14 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.6517-2102C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93315418 | ||||||
| chr9:93315606
|
T | C | 83 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(80): Show | 83 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.6517-1914T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93315606 | ||||||
| chr9:93315710
|
A | G | 40 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(37): Show | 40 | HG00438.hp1 HG01071.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.6517-1810A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93315710 | ||||||
| chr9:93315782
|
CTTGTGT | C | 14 | a0002c0001t0001g0007a0002c0001t0001g0102a0002c0001t0001g0107others(11): Show | 14 | HG00544.hp2 HG00597.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.6517-1737_6517-173 others(10): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93315782 | ||||||
| chr9:93315782
|
CTTGTGTG others(1): Show |
C | 17 | a0001c0059t0001g0304a0002c0001t0001g0174a0002c0001t0001g0175others(14): Show | 17 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.6517-1737_6517-173 others(12): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93315782 | ||||||
| chr9:93315782
|
CTTGTGTG others(3): Show |
C | 55 | a0001c0009t0001g0198a0001c0009t0001g0201a0001c0028t0001g0311others(52): Show | 56 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.6517-1737_6517-172 others(14): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93315782 | ||||||
| chr9:93315782
|
CTTGTGTG others(5): Show |
C | 1 | a0003c0005t0001g0104 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.6517-1737_6517-172 others(16): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93315782 | ||||||
| chr9:93315783
|
TTG | T | 3 | a0009c0023t0001g0291a0009c0023t0001g0292a0018c0036t0001g0019 | 3 | HG02258.hp2 HG02738.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.6517-1697_6517-169 others(6): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93315783 | |||||
| chr9:93315783
|
TTGTG | T | 8 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(5): Show | 8 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.6517-1699_6517-169 others(8): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93315783 | |||||
| chr9:93315783
|
TTGTGTG | T | 8 | a0001c0003t0001g0077a0001c0008t0001g0023a0001c0008t0001g0024others(5): Show | 8 | HG01081.hp1 HG02630.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.6517-1701_6517-169 others(10): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93315783 | |||||
| chr9:93315783
|
TTGTGTGT others(1): Show |
T | 13 | a0001c0004t0002g0002a0001c0004t0002g0257a0001c0004t0002g0258others(10): Show | 14 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.6517-1703_6517-169 others(12): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93315783 | |||||
| chr9:93315783
|
TTGTGTGT others(3): Show |
T | 153 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.6517-1705_6517-169 others(14): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93315783 | |||||
| chr9:93315783
|
TTGTGTGT others(5): Show |
T | 13 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0081others(10): Show | 13 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.6517-1707_6517-169 others(16): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93315783 | |||||
| chr9:93315783
|
TTGTGTGT others(7): Show |
T | 1 | a0004c0006t0001g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6517-1709_6517-169 others(18): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93315783 | |||||
| chr9:93315783
|
TTGTGTGT others(11): Show |
T | 3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.6517-1713_6517-169 others(22): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93315783 | |||||
| chr9:93315815
|
GTGTGTGT others(3): Show |
G | 1 | a0001c0022t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6517-1703_6517-169 others(14): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93315815 | |||||
| chr9:93315823
|
G | A | 62 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(59): Show | 62 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.6517-1697G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93315823 | ||||||
| chr9:93315823
|
G | GTGTGTA | 9 | a0001c0009t0001g0205a0005c0012t0001g0192a0005c0012t0001g0193others(6): Show | 9 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.6517-1696_6517-169 others(10): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93315823 | |||||
| chr9:93315823
|
G | GTGTGTGT others(1): Show |
4 | a0005c0019t0001g0040a0005c0019t0001g0041a0005c0019t0001g0139others(1): Show | 4 | HG02486.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.6517-1696_6517-169 others(12): Show |
WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93315823 | |||||
| chr9:93315825
|
A | G | 1 | a0002c0001t0001g0169 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.6517-1695A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93315825 | ||||||
| chr9:93315840
|
T | C | 1 | a0002c0001t0001g0119 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.6517-1680T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93315840 | ||||||
| chr9:93316075
|
G | A | 1 | a0001c0008t0001g0014 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.6517-1445G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316075 | ||||||
| chr9:93316174
|
T | G | 2 | a0001c0003t0001g0077a0001c0003t0001g0251 | 2 | HG01074.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.6517-1346T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316174 | ||||||
| chr9:93316322
|
G | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6517-1198G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316322 | ||||||
| chr9:93316378
|
T | G | 3 | a0002c0001t0001g0007a0002c0001t0001g0296a0002c0001t0001g0297 | 3 | HG01261.hp2 HG01346.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.6517-1142T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316378 | ||||||
| chr9:93316394
|
A | T | 1 | a0007c0020t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6517-1126A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316394 | ||||||
| chr9:93316417
|
G | A | 4 | a0002c0010t0001g0173a0002c0010t0001g0185a0002c0010t0001g0191others(1): Show | 4 | HG00099.hp2 HG00733.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.6517-1103G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316417 | ||||||
| chr9:93316421
|
G | A | 1 | a0001c0049t0001g0073 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6517-1099G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316421 | ||||||
| chr9:93316560
|
T | TG | 9 | a0001c0011t0001g0210a0001c0011t0001g0211a0001c0011t0001g0212others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6517-959dupG | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr9 | 93316560 | |||||
| chr9:93316579
|
G | C | 1 | a0001c0021t0002g0218 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6517-941G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316579 | ||||||
| chr9:93316588
|
T | G | 21 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(18): Show | 22 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.6517-932T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316588 | ||||||
| chr9:93316628
|
G | A | 1 | a0018c0036t0001g0019 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.6517-892G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316628 | ||||||
| chr9:93316757
|
C | A | 5 | a0002c0001t0001g0102a0002c0001t0001g0129a0002c0001t0001g0130others(2): Show | 5 | HG00597.hp2 NA18955.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.6517-763C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316757 | ||||||
| chr9:93316833
|
G | C | 1 | a0001c0034t0001g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6517-687G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316833 | ||||||
| chr9:93316888
|
G | A | 1 | a0001c0003t0001g0224 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.6517-632G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316888 | ||||||
| chr9:93316896
|
T | C | 1 | a0001c0009t0001g0199 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.6517-624T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316896 | ||||||
| chr9:93316897
|
T | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6517-623T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93316897 | ||||||
| chr9:93317027
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6517-493C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93317027 | ||||||
| chr9:93317061
|
A | G | 2 | a0002c0001t0001g0171a0002c0043t0001g0121 | 2 | NA20805.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.6517-459A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93317061 | ||||||
| chr9:93317088
|
A | G | 126 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.6517-432A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93317088 | ||||||
| chr9:93317180
|
G | C | 290 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(287): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.6517-340G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93317180 | ||||||
| chr9:93317207
|
T | C | 14 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.6517-313T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93317207 | ||||||
| chr9:93317228
|
A | G | 290 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(287): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.6517-292A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93317228 | ||||||
| chr9:93317251
|
C | T | 1 | a0001c0032t0001g0017 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.6517-269C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93317251 | ||||||
| chr9:93317259
|
T | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6517-261T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 28/29 | chr9 | 93317259 | ||||||
| chr9:93317668
|
C | T | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6628+37C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93317668 | ||||||
| chr9:93317669
|
G | A | 4 | a0002c0010t0001g0173a0002c0010t0001g0185a0002c0010t0001g0191others(1): Show | 4 | HG00099.hp2 HG00733.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.6628+38G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93317669 | ||||||
| chr9:93317849
|
G | T | 1 | a0001c0052t0001g0156 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.6628+218G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93317849 | ||||||
| chr9:93317894
|
G | A | 1 | a0008c0026t0001g0305 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.6628+263G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93317894 | ||||||
| chr9:93318048
|
G | A | 1 | a0002c0001t0001g0164 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.6628+417G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93318048 | ||||||
| chr9:93318256
|
A | T | 2 | a0001c0003t0001g0219a0001c0003t0001g0233 | 2 | HG00733.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.6628+625A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93318256 | ||||||
| chr9:93318417
|
C | T | 27 | a0001c0004t0002g0002a0001c0004t0002g0206a0001c0004t0002g0257others(24): Show | 28 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.6628+786C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93318417 | ||||||
| chr9:93318447
|
G | A | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6628+816G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93318447 | ||||||
| chr9:93318481
|
G | A | 1 | a0007c0020t0001g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6628+850G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93318481 | ||||||
| chr9:93318501
|
C | T | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6628+870C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93318501 | ||||||
| chr9:93318644
|
G | T | 2 | a0004c0006t0001g0078a0004c0006t0001g0079 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.6628+1013G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93318644 | ||||||
| chr9:93318797
|
C | G | 3 | a0001c0034t0001g0216a0001c0035t0001g0207a0024c0060t0001g0254 | 3 | HG01081.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6628+1166C>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93318797 | ||||||
| chr9:93318901
|
T | C | 14 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.6628+1270T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93318901 | ||||||
| chr9:93319163
|
T | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6629-1204T>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93319163 | ||||||
| chr9:93319268
|
C | A | 5 | a0001c0024t0001g0054a0001c0024t0001g0056a0007c0020t0001g0286others(2): Show | 5 | HG01952.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.6629-1099C>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93319268 | ||||||
| chr9:93319333
|
G | A | 1 | a0001c0008t0001g0132 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.6629-1034G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93319333 | ||||||
| chr9:93319371
|
C | T | 1 | a0002c0010t0001g0181 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.6629-996C>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93319371 | ||||||
| chr9:93319430
|
G | A | 1 | a0005c0012t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6629-937G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93319430 | ||||||
| chr9:93319570
|
G | T | 3 | a0008c0026t0001g0305a0008c0026t0001g0306a0008c0061t0001g0290 | 3 | HG01255.hp1 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.6629-797G>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93319570 | ||||||
| chr9:93319653
|
A | T | 1 | a0002c0001t0001g0108 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.6629-714A>T | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93319653 | ||||||
| chr9:93319726
|
G | C | 5 | a0001c0013t0001g0125a0001c0013t0001g0145a0001c0013t0001g0148others(2): Show | 5 | NA18944.hp1 NA18962.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.6629-641G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93319726 | ||||||
| chr9:93319856
|
A | C | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6629-511A>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93319856 | ||||||
| chr9:93319886
|
T | C | 290 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0015others(287): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.6629-481T>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93319886 | ||||||
| chr9:93319954
|
G | A | 3 | a0001c0015t0001g0033a0001c0015t0001g0034a0001c0015t0001g0038 | 3 | HG01884.hp2 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.6629-413G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93319954 | ||||||
| chr9:93320029
|
A | G | 1 | a0026c0045t0001g0294 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6629-338A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93320029 | ||||||
| chr9:93320046
|
A | G | 1 | a0002c0001t0001g0012 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.6629-321A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93320046 | ||||||
| chr9:93320058
|
G | C | 14 | a0004c0006t0001g0078a0004c0006t0001g0079a0004c0006t0001g0080others(11): Show | 14 | HG00438.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.6629-309G>C | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93320058 | ||||||
| chr9:93320061
|
T | A | 9 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(6): Show | 9 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.6629-306T>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93320061 | ||||||
| chr9:93320089
|
A | G | 23 | a0001c0008t0001g0010a0001c0008t0001g0011a0001c0008t0001g0014others(20): Show | 23 | HG01071.hp1 HG01071.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.6629-278A>G | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93320089 | ||||||
| chr9:93320240
|
G | A | 1 | a0001c0002t0001g0003 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.6629-127G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93320240 | ||||||
| chr9:93320350
|
G | A | 2 | a0003c0005t0001g0114a0003c0005t0001g0115 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.6629-17G>A | WNK2 | ENSG00000165238.17 | transcript | ENST00000427277.7 | protein_coding | 29/29 | chr9 | 93320350 |