Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 85407 |
|---|---|
| ensemblid | ENSG00000140807.7 |
| hgncid | 17045 |
| symbol | NKD1 |
| name | NKD inhibitor of WNT signaling pathway 1 |
| refseq_nuc | NM_033119.5 |
| refseq_prot | NP_149110.1 |
| ensembl_nuc | ENST00000268459.6 |
| ensembl_prot | ENSP00000268459.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 50548396 |
| end | 50649249 |
| strand | + |
| ver | v1.2 |
| region | chr16:50548396-50649249 |
| region5000 | chr16:50543396-50654249 |
| regionname0 | NKD1_chr16_50548396_50649249 |
| regionname5000 | NKD1_chr16_50543396_50654249 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1413 | 200 | 68 | 38 | 50 | 8 | 34 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| c0002 | 0/0 | 1413 | 6 | 6 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| c0003 | 0/0 | 1413 | 2 | 0 | 1 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| c0004 | 0/0 | 1413 | 2 | 0 | 0 | 2 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| c0005 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| c0006 | 0/0 | 1413 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 15627 | 31 | 3 | 10 | 8 | 1 | 8 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0002 | 0/0 | 15620 | 27 | 4 | 11 | 0 | 3 | 9 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0003 | 0/0 | 15627 | 25 | 8 | 5 | 9 | 0 | 3 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0004 | 0/0 | 15620 | 20 | 1 | 1 | 16 | 0 | 2 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0005 | 0/0 | 15627 | 8 | 0 | 4 | 3 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0006 | 0/0 | 15620 | 5 | 5 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0007 | 0/0 | 15620 | 5 | 5 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0008 | 0/0 | 15626 | 5 | 5 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0009 | 0/0 | 15627 | 5 | 5 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0010 | 0/0 | 15621 | 4 | 1 | 0 | 2 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0011 | 0/0 | 15620 | 4 | 4 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0012 | 0/0 | 15626 | 3 | 3 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0013 | 0/0 | 15620 | 3 | 0 | 1 | 0 | 1 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0014 | 0/0 | 15627 | 3 | 3 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0015 | 0/0 | 15627 | 3 | 0 | 0 | 3 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0016 | 0/0 | 15620 | 2 | 2 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0017 | 0/0 | 15620 | 2 | 2 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0018 | 0/0 | 15620 | 2 | 1 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0019 | 0/0 | 15627 | 2 | 0 | 0 | 1 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0020 | 0/0 | 15627 | 2 | 2 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0021 | 0/0 | 15627 | 2 | 0 | 0 | 2 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0022 | 0/0 | 15627 | 2 | 0 | 1 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0023 | 0/0 | 15627 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0024 | 0/0 | 15620 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0025 | 0/0 | 15620 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0026 | 0/0 | 15620 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0027 | 0/0 | 15620 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0028 | 0/0 | 15626 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0029 | 0/0 | 15620 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0030 | 0/0 | 15621 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0031 | 0/0 | 15620 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0032 | 0/0 | 15620 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0033 | 0/0 | 15620 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0034 | 0/0 | 15620 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0035 | 0/0 | 15620 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0036 | 0/0 | 15620 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0037 | 0/0 | 15620 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0038 | 0/0 | 15620 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0039 | 0/0 | 15621 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0040 | 0/0 | 15627 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0041 | 0/0 | 15620 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0042 | 0/0 | 15627 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0043 | 0/0 | 15627 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0044 | 0/0 | 15627 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0045 | 0/0 | 15627 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0046 | 0/0 | 15627 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0047 | 0/0 | 15627 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0048 | 0/0 | 15627 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0049 | 0/1 | 15627 | 1 | 0 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0050 | 0/0 | 15627 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0051 | 0/0 | 15627 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0052 | 0/0 | 15627 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0053 | 0/0 | 15627 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0054 | 0/0 | 15626 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0055 | 0/0 | 15627 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0056 | 0/0 | 15627 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0057 | 0/0 | 15627 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0058 | 0/0 | 15627 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0059 | 0/0 | 15627 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0060 | 0/0 | 15627 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0061 | 0/0 | 15627 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0062 | 0/0 | 15626 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0063 | 0/0 | 15627 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0064 | 0/0 | 15627 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0065 | 0/0 | 15627 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0066 | 0/0 | 15627 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0067 | 0/0 | 15627 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0068 | 0/0 | 15627 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| t0069 | 0/0 | 15627 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1413 | 200 | 68 | 38 | 50 | 8 | 34 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0002 | 0/0 | 1413 | 6 | 6 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0003 | 0/0 | 1413 | 2 | 0 | 1 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0004 | 0/0 | 1413 | 2 | 0 | 0 | 2 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0005 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0002c0006 | 0/0 | 1413 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 17039 | 28 | 3 | 9 | 7 | 1 | 7 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0002 | 0/0 | 17032 | 27 | 4 | 11 | 0 | 3 | 9 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0003 | 0/0 | 17039 | 25 | 8 | 5 | 9 | 0 | 3 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0004 | 0/0 | 17032 | 17 | 1 | 0 | 15 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0005 | 0/0 | 17039 | 8 | 0 | 4 | 3 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0006 | 0/0 | 17032 | 5 | 5 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0007 | 0/0 | 17032 | 5 | 5 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0009 | 0/0 | 17039 | 5 | 5 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0010 | 0/0 | 17033 | 4 | 1 | 0 | 2 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0011 | 0/0 | 17032 | 4 | 4 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0012 | 0/0 | 17038 | 3 | 3 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0013 | 0/0 | 17032 | 3 | 0 | 1 | 0 | 1 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0014 | 0/0 | 17039 | 3 | 3 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0015 | 0/0 | 17039 | 3 | 0 | 0 | 3 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0016 | 0/0 | 17032 | 2 | 2 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0017 | 0/0 | 17032 | 2 | 2 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0018 | 0/0 | 17032 | 2 | 1 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0019 | 0/0 | 17039 | 2 | 0 | 0 | 1 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0020 | 0/0 | 17039 | 2 | 2 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0021 | 0/0 | 17039 | 2 | 0 | 0 | 2 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0022 | 0/0 | 17039 | 2 | 0 | 1 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0023 | 0/0 | 17039 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0024 | 0/0 | 17032 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0025 | 0/0 | 17032 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0026 | 0/0 | 17032 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0027 | 0/0 | 17032 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0028 | 0/0 | 17038 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0029 | 0/0 | 17032 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0030 | 0/0 | 17033 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0031 | 0/0 | 17032 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0032 | 0/0 | 17032 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0033 | 0/0 | 17032 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0034 | 0/0 | 17032 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0035 | 0/0 | 17032 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0036 | 0/0 | 17032 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0037 | 0/0 | 17032 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0038 | 0/0 | 17032 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0039 | 0/0 | 17033 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0040 | 0/0 | 17039 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0041 | 0/0 | 17032 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0042 | 0/0 | 17039 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0043 | 0/0 | 17039 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0044 | 0/0 | 17039 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0045 | 0/0 | 17039 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0046 | 0/0 | 17039 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0047 | 0/0 | 17039 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0048 | 0/0 | 17039 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0049 | 0/1 | 17039 | 1 | 0 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0050 | 0/0 | 17039 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0051 | 0/0 | 17039 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0052 | 0/0 | 17039 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0053 | 0/0 | 17039 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0055 | 0/0 | 17039 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0056 | 0/0 | 17039 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0057 | 0/0 | 17039 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0058 | 0/0 | 17039 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0059 | 0/0 | 17039 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0060 | 0/0 | 17039 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0061 | 0/0 | 17039 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0062 | 0/0 | 17038 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0063 | 0/0 | 17039 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0064 | 0/0 | 17039 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0065 | 0/0 | 17039 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0066 | 0/0 | 17039 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0067 | 0/0 | 17039 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0068 | 0/0 | 17039 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0001t0069 | 0/0 | 17039 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0002t0008 | 0/0 | 17038 | 5 | 5 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0002t0054 | 0/0 | 17038 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0003t0004 | 0/0 | 17032 | 2 | 0 | 1 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0004t0001 | 0/0 | 17039 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0004t0004 | 0/0 | 17032 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0001c0005t0001 | 0/0 | 17039 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| a0002c0006t0001 | 0/0 | 17039 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | copy fasta | chr16 | 50543396 | 50654249 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0010g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0010g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0010g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0011g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0011g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0012g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0012g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0012g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0013g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0013g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0013g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0014g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0014g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0014g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0015g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0015g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0015g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0016g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0016g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0017g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0017g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0018g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0018g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0019g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0019g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0020g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0021g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0021g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0022g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0022g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0023g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0024g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0025g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0026g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0027g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0028g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0029g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0030g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0031g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0032g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0033g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0034g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0035g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0036g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0037g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0038g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0039g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0040g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0041g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0042g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0043g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0044g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0045g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0046g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0047g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0048g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0049g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0050g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0051g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0052g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0053g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0055g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0056g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0057g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0058g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0059g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0060g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0061g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0062g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0063g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0064g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0065g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0066g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0067g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0068g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0001t0069g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0002t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0002t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0002t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0002t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0002t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0002t0054g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0003t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0003t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0004t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0001c0005t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| a0002c0006t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0049 | EUR | FIN | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0166 | EUR | FIN | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0035 | EUR | FIN | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG00408 | hp1 | a0001 | c0001 | t0021 | g0165 | EAS | CHS | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG00408 | hp2 | a0001 | c0004 | t0001 | g0030 | EAS | CHS | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | CHS | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG00597 | hp1 | a0001 | c0001 | t0030 | g0150 | EAS | CHS | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG00639 | hp1 | a0001 | c0001 | t0018 | g0115 | AMR | PUR | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0146 | AMR | PUR | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0177 | AMR | PUR | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01071 | hp1 | a0001 | c0001 | t0059 | g0062 | AMR | PUR | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01109 | hp1 | a0001 | c0001 | t0069 | g0162 | AMR | PUR | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01109 | hp2 | a0002 | c0006 | t0001 | g0052 | AMR | PUR | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01175 | hp2 | a0001 | c0001 | t0040 | g0123 | AMR | PUR | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01192 | hp2 | a0001 | c0003 | t0004 | g0181 | AMR | PUR | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01255 | hp1 | a0001 | c0001 | t0013 | g0180 | AMR | CLM | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01255 | hp2 | a0001 | c0001 | t0023 | g0151 | AMR | CLM | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | CLM | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | CLM | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01346 | hp1 | a0001 | c0001 | t0022 | g0091 | AMR | CLM | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | CLM | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01358 | hp2 | a0001 | c0001 | t0031 | g0004 | AMR | CLM | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | CLM | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01516 | hp1 | a0001 | c0001 | t0013 | g0178 | EUR | IBS | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01516 | hp2 | a0001 | c0001 | t0026 | g0120 | EUR | IBS | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01884 | hp2 | a0001 | c0001 | t0028 | g0065 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01943 | hp2 | a0001 | c0001 | t0053 | g0160 | AMR | PEL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0167 | AMR | PEL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PEL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02055 | hp1 | a0001 | c0001 | t0035 | g0090 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02074 | hp1 | a0001 | c0004 | t0004 | g0144 | EAS | KHV | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02074 | hp2 | a0001 | c0001 | t0019 | g0201 | EAS | KHV | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0164 | AMR | PEL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0125 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02257 | hp2 | a0001 | c0001 | t0037 | g0081 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | PEL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02280 | hp2 | a0001 | c0001 | t0020 | g0001 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02451 | hp2 | a0001 | c0002 | t0008 | g0024 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02602 | hp1 | a0001 | c0001 | t0022 | g0128 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0036 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02615 | hp2 | a0001 | c0002 | t0054 | g0026 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0063 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0021 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02717 | hp2 | a0001 | c0001 | t0012 | g0207 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02723 | hp1 | a0001 | c0001 | t0048 | g0069 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0010 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02735 | hp1 | a0001 | c0001 | t0062 | g0038 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02735 | hp2 | a0001 | c0001 | t0063 | g0058 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02738 | hp2 | a0001 | c0001 | t0065 | g0071 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02809 | hp2 | a0001 | c0001 | t0046 | g0082 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0064 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02886 | hp1 | a0001 | c0001 | t0016 | g0116 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02886 | hp2 | a0001 | c0001 | t0032 | g0080 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02896 | hp2 | a0001 | c0001 | t0038 | g0034 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0012 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0100 | AFR | ESN | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02970 | hp2 | a0001 | c0001 | t0042 | g0205 | AFR | ESN | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03017 | hp1 | a0001 | c0001 | t0041 | g0070 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0059 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03098 | hp1 | a0001 | c0001 | t0047 | g0204 | AFR | MSL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | MSL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03130 | hp1 | a0001 | c0001 | t0056 | g0118 | AFR | ESN | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | ESN | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03139 | hp1 | a0001 | c0001 | t0052 | g0176 | AFR | ESN | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03139 | hp2 | a0001 | c0001 | t0055 | g0009 | AFR | ESN | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | ESN | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03195 | hp2 | a0001 | c0001 | t0068 | g0161 | AFR | ESN | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03209 | hp1 | a0001 | c0001 | t0066 | g0107 | AFR | MSL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | MSL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0011 | AFR | MSL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03225 | hp2 | a0001 | c0002 | t0008 | g0083 | AFR | MSL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0074 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03516 | hp1 | a0001 | c0001 | t0050 | g0028 | AFR | ESN | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03516 | hp2 | a0001 | c0001 | t0012 | g0209 | AFR | ESN | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0113 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03579 | hp1 | a0001 | c0002 | t0008 | g0101 | AFR | MSL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03579 | hp2 | a0001 | c0001 | t0017 | g0206 | AFR | MSL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03654 | hp1 | a0001 | c0001 | t0058 | g0153 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03688 | hp1 | a0001 | c0001 | t0027 | g0043 | SAS | STU | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03688 | hp2 | a0001 | c0001 | t0061 | g0210 | SAS | STU | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03710 | hp1 | a0001 | c0001 | t0067 | g0087 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03710 | hp2 | a0001 | c0005 | t0001 | g0149 | SAS | PJL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03831 | hp1 | a0001 | c0003 | t0004 | g0191 | SAS | BEB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03834 | hp1 | a0001 | c0001 | t0019 | g0197 | SAS | BEB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03834 | hp2 | a0001 | c0001 | t0013 | g0179 | SAS | BEB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | BEB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | BEB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG04184 | hp1 | a0001 | c0001 | t0010 | g0175 | SAS | BEB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG04199 | hp1 | a0001 | c0001 | t0034 | g0039 | SAS | STU | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | STU | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG04228 | hp1 | a0001 | c0001 | t0060 | g0137 | SAS | STU | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0092 | SAS | STU | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18522 | hp1 | a0001 | c0001 | t0016 | g0109 | AFR | YRI | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18522 | hp2 | a0001 | c0001 | t0017 | g0032 | AFR | YRI | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | CHB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | CHB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18952 | hp2 | a0001 | c0001 | t0015 | g0158 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18954 | hp1 | a0001 | c0001 | t0015 | g0131 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18960 | hp2 | a0001 | c0001 | t0029 | g0105 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18969 | hp1 | a0001 | c0001 | t0043 | g0199 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18970 | hp1 | a0001 | c0001 | t0010 | g0048 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18981 | hp2 | a0001 | c0001 | t0057 | g0060 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18988 | hp1 | a0001 | c0001 | t0025 | g0057 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18988 | hp2 | a0001 | c0001 | t0039 | g0046 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18992 | hp2 | a0001 | c0001 | t0015 | g0143 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18998 | hp1 | a0001 | c0001 | t0044 | g0200 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0171 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0168 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19011 | hp2 | a0001 | c0001 | t0021 | g0169 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19030 | hp1 | a0001 | c0002 | t0008 | g0102 | AFR | LWK | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0068 | AFR | LWK | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0094 | AFR | LWK | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0127 | AFR | LWK | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19060 | hp2 | a0001 | c0001 | t0010 | g0124 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19065 | hp2 | a0001 | c0001 | t0045 | g0192 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19240 | hp1 | a0001 | c0001 | t0033 | g0016 | AFR | YRI | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0013 | AFR | YRI | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | ASW | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA20129 | hp2 | a0001 | c0001 | t0018 | g0104 | AFR | ASW | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA20805 | hp1 | a0001 | c0001 | t0036 | g0157 | EUR | TSI | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0027 | EUR | TSI | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02109 | hp1 | a0001 | c0001 | t0051 | g0172 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0208 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02486 | hp2 | a0001 | c0001 | t0020 | g0001 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0015 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0159 | AFR | ACB | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0066 | AFR | MSL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0019 | AFR | MSL | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG06807 | hp1 | a0001 | c0002 | t0008 | g0025 | AFR | USA | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | USA | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA20300 | hp1 | a0001 | c0001 | t0014 | g0014 | AFR | USA | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA20300 | hp2 | a0001 | c0001 | t0064 | g0096 | AFR | USA | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA21309 | hp1 | a0001 | c0001 | t0024 | g0005 | AFR | LWK | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | LWK | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0049 | g0170 | REF | REF | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0079 | REF | REF | NKD1_chr16_50543396_50654249 | NKD1 | chr16 | 50543396 | 50654249 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:50630286
|
C | T | 1 | a0002 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.563C>T | p.Ala188Val | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 7/10 | 721/17039 | 563/1413 | 188/470 | chr16 | 50630286 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:50608344
|
C | T | 1 | a0001c0004 | 2 | HG00408.hp2 HG02074.hp1 |
synonymous_variant | LOW | c.243C>T | p.Asp81Asp | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/10 | 401/17039 | 243/1413 | 81/470 | chr16 | 50608344 | ||
| chr16:50630836
|
C | T | 1 | a0001c0005 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.621C>T | p.Ser207Ser | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 8/10 | 779/17039 | 621/1413 | 207/470 | chr16 | 50630836 | ||
| chr16:50633388
|
C | T | 1 | a0001c0003 | 2 | HG01192.hp2 HG03831.hp1 |
synonymous_variant | LOW | c.1020C>T | p.Asp340Asp | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 1178/17039 | 1020/1413 | 340/470 | chr16 | 50633388 | ||
| chr16:50633448
|
C | T | 1 | a0001c0002 | 6 | HG02451.hp2 HG02615.hp2 HG03225.hp2 others(3): Show |
synonymous_variant | LOW | c.1080C>T | p.His360His | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 1238/17039 | 1080/1413 | 360/470 | chr16 | 50633448 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:50634164
|
C | T | 3 | a0001c0001t0009a0001c0001t0068a0001c0001t0069 | 7 | HG01109.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*383C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 383 | chr16 | 50634164 | |||||
| chr16:50634166
|
G | T | 1 | a0001c0001t0022 | 2 | HG01346.hp1 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*385G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 385 | chr16 | 50634166 | |||||
| chr16:50634257
|
T | C | 1 | a0001c0001t0012 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*476T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 476 | chr16 | 50634257 | |||||
| chr16:50634258
|
A | G | 1 | a0001c0001t0067 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*477A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 477 | chr16 | 50634258 | |||||
| chr16:50634325
|
C | A | 1 | a0001c0001t0023 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*544C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 544 | chr16 | 50634325 | |||||
| chr16:50634515
|
T | C | 31 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(28): Show | 94 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*734T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 734 | chr16 | 50634515 | |||||
| chr16:50634620
|
C | G | 1 | a0001c0001t0066 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*839C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 839 | chr16 | 50634620 | |||||
| chr16:50634808
|
G | A | 1 | a0001c0001t0042 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1027G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 1027 | chr16 | 50634808 | |||||
| chr16:50634991
|
A | T | 1 | a0001c0001t0021 | 2 | HG00408.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1210A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 1210 | chr16 | 50634991 | |||||
| chr16:50635392
|
C | G | 1 | a0001c0001t0041 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1611C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 1611 | chr16 | 50635392 | |||||
| chr16:50635451
|
G | C | 1 | a0001c0001t0012 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1670G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 1670 | chr16 | 50635451 | |||||
| chr16:50635653
|
C | T | 1 | a0001c0001t0066 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1872C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 1872 | chr16 | 50635653 | |||||
| chr16:50635829
|
T | C | 3 | a0001c0001t0043a0001c0001t0044a0001c0001t0045 | 3 | NA18969.hp1 NA18998.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2048T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 2048 | chr16 | 50635829 | |||||
| chr16:50636183
|
A | G | 1 | a0001c0001t0065 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2402A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 2402 | chr16 | 50636183 | |||||
| chr16:50636271
|
G | C | 30 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(27): Show | 92 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2490G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 2490 | chr16 | 50636271 | |||||
| chr16:50636285
|
T | C | 1 | a0001c0001t0024 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2504T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 2504 | chr16 | 50636285 | |||||
| chr16:50636748
|
A | C | 1 | a0001c0001t0039 | 1 | NA18988.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2967A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 2967 | chr16 | 50636748 | |||||
| chr16:50637376
|
G | A | 1 | a0001c0001t0025 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3595G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 3595 | chr16 | 50637376 | |||||
| chr16:50637444
|
T | C | 1 | a0001c0001t0066 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3663T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 3663 | chr16 | 50637444 | |||||
| chr16:50637488
|
A | C | 1 | a0001c0001t0012 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3707A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 3707 | chr16 | 50637488 | |||||
| chr16:50637810
|
G | A | 48 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(45): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*4029G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 4029 | chr16 | 50637810 | |||||
| chr16:50637830
|
A | G | 1 | a0001c0001t0042 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4049A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 4049 | chr16 | 50637830 | |||||
| chr16:50638030
|
C | T | 1 | a0001c0001t0041 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4249C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 4249 | chr16 | 50638030 | |||||
| chr16:50638064
|
C | T | 1 | a0001c0001t0038 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4283C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 4283 | chr16 | 50638064 | |||||
| chr16:50638179
|
G | A | 2 | a0001c0001t0068a0001c0001t0069 | 2 | HG01109.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4398G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 4398 | chr16 | 50638179 | |||||
| chr16:50638254
|
A | T | 1 | a0001c0001t0012 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4473A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 4473 | chr16 | 50638254 | |||||
| chr16:50638423
|
C | T | 1 | a0001c0001t0066 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4642C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 4642 | chr16 | 50638423 | |||||
| chr16:50638451
|
A | C | 1 | a0001c0001t0037 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4670A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 4670 | chr16 | 50638451 | |||||
| chr16:50638522
|
G | A | 1 | a0001c0001t0026 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4741G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 4741 | chr16 | 50638522 | |||||
| chr16:50638571
|
G | A | 1 | a0001c0001t0066 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4790G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 4790 | chr16 | 50638571 | |||||
| chr16:50639067
|
A | T | 1 | a0001c0001t0064 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5286A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 5286 | chr16 | 50639067 | |||||
| chr16:50639319
|
C | T | 1 | a0001c0001t0066 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5538C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 5538 | chr16 | 50639319 | |||||
| chr16:50639375
|
T | A | 1 | a0001c0001t0016 | 2 | HG02886.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5594T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 5594 | chr16 | 50639375 | |||||
| chr16:50639401
|
T | C | 2 | a0001c0001t0014a0001c0001t0055 | 4 | HG02559.hp1 HG03139.hp2 NA19240.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5620T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 5620 | chr16 | 50639401 | |||||
| chr16:50639512
|
G | A | 1 | a0001c0001t0027 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5731G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 5731 | chr16 | 50639512 | |||||
| chr16:50639549
|
G | A | 1 | a0001c0001t0017 | 2 | HG03579.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5768G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 5768 | chr16 | 50639549 | |||||
| chr16:50639550
|
C | T | 31 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(28): Show | 97 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*5769C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 5769 | chr16 | 50639550 | |||||
| chr16:50639740
|
T | C | 34 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(31): Show | 102 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*5959T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 5959 | chr16 | 50639740 | |||||
| chr16:50640120
|
G | A | 3 | a0001c0001t0009a0001c0001t0068a0001c0001t0069 | 7 | HG01109.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6339G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 6339 | chr16 | 50640120 | |||||
| chr16:50640837
|
TAAAAAG | T | 28 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(25): Show | 90 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*7062_*7067delGAAA others(2): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 7062 | INFO_REALIGN_3_PRIME | chr16 | 50640837 | ||||
| chr16:50641028
|
T | C | 1 | a0001c0001t0056 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7247T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 7247 | chr16 | 50641028 | |||||
| chr16:50641049
|
G | A | 3 | a0001c0001t0009a0001c0001t0068a0001c0001t0069 | 7 | HG01109.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7268G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 7268 | chr16 | 50641049 | |||||
| chr16:50641092
|
G | C | 1 | a0001c0001t0043 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7311G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 7311 | chr16 | 50641092 | |||||
| chr16:50641153
|
T | C | 1 | a0001c0001t0009 | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7372T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 7372 | chr16 | 50641153 | |||||
| chr16:50641370
|
A | G | 2 | a0001c0002t0008a0001c0002t0054 | 6 | HG02451.hp2 HG02615.hp2 HG03225.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7589A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 7589 | chr16 | 50641370 | |||||
| chr16:50641437
|
A | G | 1 | a0001c0001t0053 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7656A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 7656 | chr16 | 50641437 | |||||
| chr16:50641441
|
T | G | 1 | a0001c0001t0009 | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7660T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 7660 | chr16 | 50641441 | |||||
| chr16:50642019
|
A | G | 1 | a0001c0001t0018 | 2 | HG00639.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8238A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 8238 | chr16 | 50642019 | |||||
| chr16:50642198
|
T | C | 1 | a0001c0001t0029 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8417T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 8417 | chr16 | 50642198 | |||||
| chr16:50642305
|
A | T | 1 | a0001c0001t0063 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8524A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 8524 | chr16 | 50642305 | |||||
| chr16:50642366
|
C | T | 1 | a0001c0001t0052 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8585C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 8585 | chr16 | 50642366 | |||||
| chr16:50642603
|
G | A | 30 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(27): Show | 92 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*8822G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 8822 | chr16 | 50642603 | |||||
| chr16:50642947
|
C | T | 3 | a0001c0001t0005a0001c0001t0021a0001c0001t0053 | 11 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*9166C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 9166 | chr16 | 50642947 | |||||
| chr16:50642958
|
T | C | 1 | a0001c0001t0066 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9177T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 9177 | chr16 | 50642958 | |||||
| chr16:50643065
|
C | A | 29 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(26): Show | 91 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*9284C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 9284 | chr16 | 50643065 | |||||
| chr16:50643603
|
G | A | 2 | a0001c0001t0068a0001c0001t0069 | 2 | HG01109.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9822G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 9822 | chr16 | 50643603 | |||||
| chr16:50643646
|
C | T | 1 | a0001c0001t0011 | 4 | HG02615.hp1 HG02723.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9865C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 9865 | chr16 | 50643646 | |||||
| chr16:50643660
|
C | T | 61 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(58): Show | 168 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*9879C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 9879 | chr16 | 50643660 | |||||
| chr16:50643835
|
T | C | 1 | a0001c0001t0012 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10054T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 10054 | chr16 | 50643835 | |||||
| chr16:50644001
|
T | C | 1 | a0001c0001t0068 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10220T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 10220 | chr16 | 50644001 | |||||
| chr16:50644085
|
T | C | 2 | a0001c0001t0006a0001c0001t0028 | 6 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*10304T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 10304 | chr16 | 50644085 | |||||
| chr16:50644243
|
A | G | 3 | a0001c0001t0020a0001c0001t0036a0001c0001t0051 | 4 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10462A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 10462 | chr16 | 50644243 | |||||
| chr16:50644259
|
G | C | 2 | a0001c0001t0068a0001c0001t0069 | 2 | HG01109.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10478G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 10478 | chr16 | 50644259 | |||||
| chr16:50644277
|
T | C | 31 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(28): Show | 93 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*10496T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 10496 | chr16 | 50644277 | |||||
| chr16:50644278
|
G | A | 8 | a0001c0001t0004a0001c0001t0018a0001c0001t0025others(5): Show | 26 | HG00597.hp1 HG00639.hp1 HG01175.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*10497G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 10497 | chr16 | 50644278 | |||||
| chr16:50644607
|
T | G | 1 | a0001c0001t0031 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10826T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 10826 | chr16 | 50644607 | |||||
| chr16:50644736
|
T | C | 1 | a0001c0001t0059 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10955T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 10955 | chr16 | 50644736 | |||||
| chr16:50644801
|
G | A | 1 | a0001c0001t0032 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11020G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 11020 | chr16 | 50644801 | |||||
| chr16:50644817
|
C | G | 1 | a0001c0001t0035 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11036C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 11036 | chr16 | 50644817 | |||||
| chr16:50644952
|
C | G | 1 | a0001c0001t0066 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11171C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 11171 | chr16 | 50644952 | |||||
| chr16:50645167
|
G | T | 1 | a0001c0001t0050 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11386G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 11386 | chr16 | 50645167 | |||||
| chr16:50645216
|
G | A | 1 | a0001c0001t0057 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11435G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 11435 | chr16 | 50645216 | |||||
| chr16:50645284
|
G | A | 3 | a0001c0001t0009a0001c0001t0068a0001c0001t0069 | 7 | HG01109.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11503G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 11503 | chr16 | 50645284 | |||||
| chr16:50645353
|
G | T | 1 | a0001c0001t0049 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11572G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 11572 | chr16 | 50645353 | |||||
| chr16:50645404
|
A | C | 29 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(26): Show | 88 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*11623A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 11623 | chr16 | 50645404 | |||||
| chr16:50645422
|
A | C | 1 | a0001c0001t0009 | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*11641A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 11641 | chr16 | 50645422 | |||||
| chr16:50645598
|
G | A | 1 | a0001c0001t0047 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11817G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 11817 | chr16 | 50645598 | |||||
| chr16:50646013
|
T | C | 1 | a0001c0001t0012 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12232T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 12232 | chr16 | 50646013 | |||||
| chr16:50646370
|
AG | A | 30 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(27): Show | 95 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*12599delG | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 12599 | INFO_REALIGN_3_PRIME | chr16 | 50646370 | ||||
| chr16:50646371
|
G | A | 1 | a0001c0001t0060 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12590G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 12590 | chr16 | 50646371 | |||||
| chr16:50646372
|
G | T | 1 | a0001c0001t0058 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12591G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 12591 | chr16 | 50646372 | |||||
| chr16:50646374
|
G | C | 2 | a0001c0001t0066a0001c0002t0008 | 6 | HG02451.hp2 HG03209.hp1 HG03225.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*12593G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 12593 | chr16 | 50646374 | |||||
| chr16:50646375
|
G | C | 1 | a0001c0001t0044 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12594G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 12594 | chr16 | 50646375 | |||||
| chr16:50646378
|
G | C | 1 | a0001c0001t0061 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12597G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 12597 | chr16 | 50646378 | |||||
| chr16:50646447
|
A | T | 1 | a0001c0001t0034 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12666A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 12666 | chr16 | 50646447 | |||||
| chr16:50646537
|
C | T | 2 | a0001c0001t0068a0001c0001t0069 | 2 | HG01109.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12756C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 12756 | chr16 | 50646537 | |||||
| chr16:50646567
|
C | T | 1 | a0001c0001t0024 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12786C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 12786 | chr16 | 50646567 | |||||
| chr16:50646629
|
C | T | 1 | a0001c0001t0047 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12848C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 12848 | chr16 | 50646629 | |||||
| chr16:50646756
|
A | G | 1 | a0001c0001t0013 | 3 | HG01255.hp1 HG01516.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12975A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 12975 | chr16 | 50646756 | |||||
| chr16:50646939
|
T | G | 1 | a0001c0001t0021 | 2 | HG00408.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13158T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 13158 | chr16 | 50646939 | |||||
| chr16:50647001
|
C | T | 2 | a0001c0001t0007a0001c0001t0035 | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*13220C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 13220 | chr16 | 50647001 | |||||
| chr16:50647034
|
C | T | 1 | a0001c0001t0048 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13253C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 13253 | chr16 | 50647034 | |||||
| chr16:50647066
|
T | C | 2 | a0001c0002t0008a0001c0002t0054 | 6 | HG02451.hp2 HG02615.hp2 HG03225.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*13285T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 13285 | chr16 | 50647066 | |||||
| chr16:50647622
|
G | C | 2 | a0001c0002t0008a0001c0002t0054 | 6 | HG02451.hp2 HG02615.hp2 HG03225.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*13841G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 13841 | chr16 | 50647622 | |||||
| chr16:50647854
|
A | T | 1 | a0001c0001t0020 | 2 | HG02280.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*14073A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 14073 | chr16 | 50647854 | |||||
| chr16:50648504
|
A | G | 1 | a0001c0002t0008 | 5 | HG02451.hp2 HG03225.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*14723A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 14723 | chr16 | 50648504 | |||||
| chr16:50648685
|
C | T | 1 | a0001c0001t0033 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14904C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 14904 | chr16 | 50648685 | |||||
| chr16:50649206
|
C | G | 2 | a0001c0001t0015a0001c0001t0057 | 4 | NA18952.hp2 NA18954.hp1 NA18981.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*15425C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 10/10 | 15425 | chr16 | 50649206 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:50548794
|
C | A | 1 | a0001c0001t0002g0003 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.58+45C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 2/9 | chr16 | 50548794 | ||||||
| chr16:50549344
|
G | A | 1 | a0001c0001t0031g0004 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.59-78G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 2/9 | chr16 | 50549344 | ||||||
| chr16:50549360
|
C | T | 1 | a0001c0001t0061g0210 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.59-62C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 2/9 | chr16 | 50549360 | ||||||
| chr16:50549778
|
C | G | 6 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209others(3): Show | 6 | HG02486.hp1 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+223C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50549778 | ||||||
| chr16:50549858
|
C | A | 2 | a0001c0001t0003g0006a0001c0001t0024g0005 | 2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.192+303C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50549858 | ||||||
| chr16:50549876
|
C | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.192+321C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50549876 | ||||||
| chr16:50550003
|
T | C | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+448T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50550003 | ||||||
| chr16:50550077
|
G | C | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+522G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50550077 | ||||||
| chr16:50550128
|
G | C | 3 | a0001c0001t0014g0013a0001c0001t0014g0014a0001c0001t0014g0015 | 3 | HG02559.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.192+573G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50550128 | ||||||
| chr16:50550146
|
A | T | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+591A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50550146 | ||||||
| chr16:50550151
|
G | A | 2 | a0001c0001t0017g0206a0001c0001t0042g0205 | 2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.192+596G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50550151 | ||||||
| chr16:50550354
|
A | AT | 18 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0202others(15): Show | 19 | HG01358.hp1 HG01952.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.192+816dupT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50550354 | |||||
| chr16:50550660
|
C | CT | 5 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0003g0185others(2): Show | 5 | NA18951.hp2 NA18970.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+1106dupT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50550660 | |||||
| chr16:50550724
|
G | C | 17 | a0001c0001t0003g0023a0001c0001t0007g0020a0001c0001t0009g0017others(14): Show | 17 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.192+1169G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50550724 | ||||||
| chr16:50550801
|
C | T | 27 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0173others(24): Show | 27 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.192+1246C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50550801 | ||||||
| chr16:50550948
|
CCTTTTT | C | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.192+1405_192+1410d others(8): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50550948 | |||||
| chr16:50550966
|
C | CT | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+1419dupT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50550966 | |||||
| chr16:50551027
|
G | A | 1 | a0001c0001t0002g0027 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.192+1472G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50551027 | ||||||
| chr16:50551351
|
T | C | 49 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0023others(46): Show | 49 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.192+1796T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50551351 | ||||||
| chr16:50551719
|
A | C | 2 | a0001c0001t0001g0202a0001c0001t0004g0203 | 2 | NA19011.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.192+2164A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50551719 | ||||||
| chr16:50551721
|
C | CT | 5 | a0001c0001t0007g0159a0001c0001t0011g0010a0001c0001t0011g0011others(2): Show | 5 | HG02559.hp2 HG02723.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+2177dupT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50551721 | |||||
| chr16:50552029
|
G | A | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+2474G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50552029 | ||||||
| chr16:50552446
|
G | A | 6 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209others(3): Show | 6 | HG02486.hp1 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+2891G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50552446 | ||||||
| chr16:50552468
|
T | A | 1 | a0001c0001t0002g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.192+2913T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50552468 | ||||||
| chr16:50552854
|
C | T | 1 | a0001c0001t0015g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.192+3299C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50552854 | ||||||
| chr16:50552855
|
C | T | 1 | a0001c0001t0015g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.192+3300C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50552855 | ||||||
| chr16:50553030
|
C | G | 31 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0173others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.192+3475C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50553030 | ||||||
| chr16:50553190
|
AATAG | A | 5 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(2): Show | 5 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+3642_192+3645d others(6): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50553190 | |||||
| chr16:50553218
|
T | C | 1 | a0001c0004t0001g0030 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.192+3663T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50553218 | ||||||
| chr16:50553489
|
G | T | 6 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209others(3): Show | 6 | HG02486.hp1 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+3934G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50553489 | ||||||
| chr16:50553589
|
C | T | 3 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156 | 3 | HG02717.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.192+4034C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50553589 | ||||||
| chr16:50553637
|
A | G | 3 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0054g0026 | 3 | HG02451.hp2 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.192+4082A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50553637 | ||||||
| chr16:50553682
|
A | C | 48 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0023others(45): Show | 48 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.192+4127A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50553682 | ||||||
| chr16:50553870
|
C | T | 1 | a0001c0001t0003g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192+4315C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50553870 | ||||||
| chr16:50554065
|
C | T | 26 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(23): Show | 26 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.192+4510C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50554065 | ||||||
| chr16:50554105
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.192+4550G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50554105 | ||||||
| chr16:50555165
|
C | T | 2 | a0001c0001t0002g0129a0001c0001t0047g0204 | 2 | HG02602.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.192+5610C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50555165 | ||||||
| chr16:50555166
|
G | A | 1 | a0001c0001t0017g0032 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.192+5611G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50555166 | ||||||
| chr16:50555223
|
C | G | 1 | a0001c0001t0019g0201 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.192+5668C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50555223 | ||||||
| chr16:50555332
|
A | G | 48 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0023others(45): Show | 48 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.192+5777A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50555332 | ||||||
| chr16:50555536
|
G | A | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+5981G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50555536 | ||||||
| chr16:50555639
|
A | G | 5 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(2): Show | 5 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+6084A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50555639 | ||||||
| chr16:50555675
|
G | A | 48 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0023others(45): Show | 48 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.192+6120G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50555675 | ||||||
| chr16:50555710
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0042g0205 | 2 | HG02970.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.192+6155G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50555710 | ||||||
| chr16:50555856
|
C | T | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.192+6301C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50555856 | ||||||
| chr16:50555900
|
C | T | 1 | a0001c0001t0002g0027 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.192+6345C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50555900 | ||||||
| chr16:50555960
|
C | T | 1 | a0001c0001t0003g0156 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.192+6405C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50555960 | ||||||
| chr16:50555964
|
C | G | 1 | a0001c0001t0003g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192+6409C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50555964 | ||||||
| chr16:50556145
|
A | G | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+6590A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50556145 | ||||||
| chr16:50556146
|
G | A | 3 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156 | 3 | HG02717.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.192+6591G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50556146 | ||||||
| chr16:50556360
|
A | G | 7 | a0001c0001t0007g0020a0001c0001t0009g0017a0001c0001t0009g0018others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+6805A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50556360 | ||||||
| chr16:50556378
|
C | T | 4 | a0001c0001t0013g0178a0001c0001t0013g0179a0001c0001t0013g0180others(1): Show | 4 | HG01192.hp2 HG01255.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+6823C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50556378 | ||||||
| chr16:50556410
|
C | T | 46 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0023others(43): Show | 46 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.192+6855C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50556410 | ||||||
| chr16:50556445
|
G | A | 1 | a0001c0001t0003g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192+6890G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50556445 | ||||||
| chr16:50556461
|
G | T | 2 | a0001c0001t0002g0126a0001c0001t0006g0127 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.192+6906G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50556461 | ||||||
| chr16:50556688
|
A | G | 7 | a0001c0001t0007g0020a0001c0001t0009g0017a0001c0001t0009g0018others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+7133A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50556688 | ||||||
| chr16:50556695
|
A | G | 1 | a0001c0001t0043g0199 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.192+7140A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50556695 | ||||||
| chr16:50556728
|
G | GT | 11 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0003g0023others(8): Show | 11 | HG00741.hp1 HG01175.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.192+7195dupT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50556728 | |||||
| chr16:50556728
|
G | GTT | 6 | a0001c0001t0007g0020a0001c0001t0009g0018a0001c0001t0009g0019others(3): Show | 6 | HG01884.hp1 HG02647.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+7194_192+7195d others(4): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50556728 | |||||
| chr16:50556728
|
GT | G | 10 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0130others(7): Show | 10 | HG00323.hp2 HG01943.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.192+7195delT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50556728 | |||||
| chr16:50556751
|
A | T | 2 | a0001c0001t0007g0125a0001c0001t0058g0153 | 2 | HG02257.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.192+7196A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50556751 | ||||||
| chr16:50556810
|
A | G | 1 | a0001c0001t0003g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.192+7255A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50556810 | ||||||
| chr16:50556825
|
T | C | 2 | a0001c0001t0009g0018a0001c0001t0009g0019 | 2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.192+7270T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50556825 | ||||||
| chr16:50556936
|
T | A | 28 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0173others(25): Show | 28 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.192+7381T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50556936 | ||||||
| chr16:50557318
|
G | A | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+7763G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50557318 | ||||||
| chr16:50557320
|
G | T | 1 | a0001c0001t0004g0152 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.192+7765G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50557320 | ||||||
| chr16:50557728
|
G | A | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+8173G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50557728 | ||||||
| chr16:50558024
|
C | T | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+8469C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50558024 | ||||||
| chr16:50558092
|
A | G | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+8537A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50558092 | ||||||
| chr16:50558137
|
T | A | 3 | a0001c0001t0009g0017a0001c0001t0009g0021a0001c0001t0009g0022 | 3 | HG02451.hp1 HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.192+8582T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50558137 | ||||||
| chr16:50558324
|
G | A | 1 | a0001c0001t0052g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.192+8769G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50558324 | ||||||
| chr16:50558702
|
C | T | 2 | a0001c0001t0017g0032a0001c0001t0047g0204 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.192+9147C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50558702 | ||||||
| chr16:50558719
|
C | CA | 15 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(12): Show | 15 | HG01109.hp1 HG01943.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.192+9181dupA | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50558719 | |||||
| chr16:50558733
|
A | G | 1 | a0001c0001t0003g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192+9178A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50558733 | ||||||
| chr16:50558750
|
G | GA | 9 | a0001c0001t0001g0007a0001c0001t0002g0033a0001c0001t0002g0040others(6): Show | 9 | HG01175.hp1 HG01175.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.192+9205dupA | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50558750 | |||||
| chr16:50558765
|
C | T | 11 | a0001c0001t0003g0023a0001c0001t0007g0020a0001c0001t0009g0017others(8): Show | 11 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.192+9210C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50558765 | ||||||
| chr16:50558832
|
C | T | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+9277C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50558832 | ||||||
| chr16:50558908
|
T | TCAAA | 11 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0002g0029others(8): Show | 11 | HG00280.hp1 HG00741.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.192+9377_192+9380d others(6): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50558908 | |||||
| chr16:50558908
|
T | TCAAACAA others(1): Show |
8 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0044others(5): Show | 8 | HG01175.hp1 HG01433.hp1 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+9373_192+9380d others(10): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50558908 | |||||
| chr16:50558908
|
T | TCAAACAA others(5): Show |
2 | a0001c0001t0001g0007a0001c0001t0002g0033 | 2 | HG03491.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.192+9369_192+9380d others(14): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50558908 | |||||
| chr16:50558908
|
TCAAA | T | 5 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0002g0126others(2): Show | 5 | HG01099.hp2 HG01433.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+9377_192+9380d others(6): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50558908 | |||||
| chr16:50559067
|
C | T | 1 | a0001c0001t0023g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.192+9512C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50559067 | ||||||
| chr16:50559173
|
G | A | 23 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0202others(20): Show | 24 | HG01071.hp1 HG01261.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.192+9618G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50559173 | ||||||
| chr16:50559838
|
G | A | 5 | a0001c0001t0006g0063a0001c0001t0006g0064a0001c0001t0006g0066others(2): Show | 5 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+10283G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50559838 | ||||||
| chr16:50560326
|
C | A | 1 | a0001c0001t0001g0136 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.192+10771C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50560326 | ||||||
| chr16:50560452
|
T | C | 1 | a0001c0001t0010g0068 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.192+10897T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50560452 | ||||||
| chr16:50560582
|
A | G | 7 | a0001c0001t0007g0020a0001c0001t0009g0017a0001c0001t0009g0018others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+11027A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50560582 | ||||||
| chr16:50560629
|
G | GT | 12 | a0001c0001t0003g0182a0001c0001t0007g0020a0001c0001t0009g0017others(9): Show | 12 | HG01884.hp1 HG02451.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.192+11089dupT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50560629 | |||||
| chr16:50560630
|
T | G | 37 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0002g0003others(34): Show | 37 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.192+11075T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50560630 | ||||||
| chr16:50560661
|
C | T | 1 | a0001c0001t0010g0175 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.192+11106C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50560661 | ||||||
| chr16:50560823
|
C | CATCT | 20 | a0001c0001t0001g0050a0001c0001t0001g0139a0001c0001t0002g0027others(17): Show | 20 | HG01346.hp2 HG01516.hp1 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.192+11306_192+1130 others(8): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50560823 | |||||
| chr16:50560823
|
C | CATCTATC others(1): Show |
50 | a0001c0001t0001g0051a0001c0001t0001g0084a0001c0001t0001g0086others(47): Show | 50 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.192+11302_192+1130 others(12): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50560823 | |||||
| chr16:50560823
|
C | CATCTATC others(5): Show |
89 | a0001c0001t0001g0037a0001c0001t0001g0089a0001c0001t0001g0098others(86): Show | 90 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.192+11298_192+1130 others(16): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50560823 | |||||
| chr16:50560823
|
C | CATCTATC others(9): Show |
45 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0031others(42): Show | 46 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.192+11294_192+1130 others(20): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50560823 | |||||
| chr16:50560823
|
C | CATCTATC others(13): Show |
2 | a0001c0001t0001g0117a0001c0001t0030g0150 | 2 | HG00597.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.192+11290_192+1130 others(24): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50560823 | |||||
| chr16:50560823
|
C | T | 2 | a0001c0001t0068g0161a0001c0001t0069g0162 | 2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.192+11268C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50560823 | ||||||
| chr16:50561322
|
C | T | 1 | a0001c0001t0011g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.192+11767C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50561322 | ||||||
| chr16:50561393
|
T | TA | 41 | a0001c0001t0002g0126a0001c0001t0002g0163a0001c0001t0003g0006others(38): Show | 41 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.192+11853dupA | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50561393 | |||||
| chr16:50561393
|
T | TAAA | 9 | a0001c0001t0007g0020a0001c0001t0009g0017a0001c0001t0009g0018others(6): Show | 9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+11851_192+1185 others(7): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50561393 | |||||
| chr16:50561435
|
T | G | 1 | a0001c0001t0002g0047 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.192+11880T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50561435 | ||||||
| chr16:50561444
|
G | T | 4 | a0001c0001t0014g0013a0001c0001t0014g0014a0001c0001t0014g0015others(1): Show | 4 | HG02559.hp1 HG03516.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+11889G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50561444 | ||||||
| chr16:50561485
|
C | G | 1 | a0001c0001t0003g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192+11930C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50561485 | ||||||
| chr16:50561486
|
T | A | 3 | a0001c0001t0010g0048a0001c0001t0010g0124a0001c0001t0039g0046 | 3 | NA18970.hp1 NA18988.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.192+11931T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50561486 | ||||||
| chr16:50561490
|
C | G | 4 | a0001c0001t0013g0178a0001c0001t0013g0179a0001c0001t0013g0180others(1): Show | 4 | HG01192.hp2 HG01255.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+11935C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50561490 | ||||||
| chr16:50562237
|
A | T | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+12682A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562237 | ||||||
| chr16:50562361
|
A | G | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.192+12806A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562361 | ||||||
| chr16:50562647
|
C | G | 45 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0023others(42): Show | 45 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.192+13092C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562647 | ||||||
| chr16:50562760
|
G | T | 28 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0202others(25): Show | 29 | HG01071.hp1 HG01261.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.192+13205G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562760 | ||||||
| chr16:50562893
|
A | ACTGTGG | 6 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209others(3): Show | 6 | HG02486.hp1 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+13342_192+1334 others(10): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50562893 | |||||
| chr16:50562927
|
G | A | 28 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0173others(25): Show | 28 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.192+13372G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562927 | ||||||
| chr16:50562980
|
A | ACCCCCCC others(7): Show |
1 | a0001c0001t0052g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.192+13427_192+1342 others(18): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50562980 | |||||
| chr16:50562980
|
A | C | 1 | a0001c0002t0008g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.192+13425A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562980 | ||||||
| chr16:50562983
|
A | ACCCCCCA others(3): Show |
2 | a0001c0001t0003g0023a0001c0001t0003g0173 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.192+13430_192+1343 others(14): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50562983 | |||||
| chr16:50562983
|
A | ACCCCCCA others(4): Show |
1 | a0001c0001t0051g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.192+13430_192+1343 others(15): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50562983 | |||||
| chr16:50562983
|
A | ACCCCCCA others(6): Show |
1 | a0001c0001t0014g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.192+13430_192+1343 others(17): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50562983 | |||||
| chr16:50562983
|
A | ACCCCCCA others(7): Show |
2 | a0001c0001t0014g0015a0001c0001t0050g0028 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.192+13430_192+1343 others(18): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50562983 | |||||
| chr16:50562983
|
A | ACCCCCCA others(8): Show |
1 | a0001c0001t0014g0013 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.192+13430_192+1343 others(19): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50562983 | |||||
| chr16:50562983
|
A | C | 8 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(5): Show | 8 | HG02451.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+13428A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562983 | ||||||
| chr16:50562986
|
A | AC | 43 | a0001c0001t0001g0050a0001c0001t0001g0089a0001c0001t0001g0108others(40): Show | 43 | HG00408.hp2 HG00741.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.192+13443dupC | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50562986 | |||||
| chr16:50562986
|
A | ACCACCAC others(4): Show |
3 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012 | 3 | HG02723.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.192+13433_192+1343 others(15): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50562986 | |||||
| chr16:50562986
|
A | ACCACCAC others(5): Show |
1 | a0001c0001t0055g0009 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.192+13433_192+1343 others(16): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50562986 | |||||
| chr16:50562986
|
A | C | 39 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0023others(36): Show | 39 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.192+13431A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562986 | ||||||
| chr16:50562986
|
AC | A | 17 | a0001c0001t0002g0045a0001c0001t0002g0047a0001c0001t0002g0106others(14): Show | 19 | HG00639.hp1 HG01071.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.192+13443delC | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50562986 | |||||
| chr16:50562987
|
C | CCCACCCC others(4): Show |
1 | a0001c0001t0005g0171 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.192+13434_192+1343 others(15): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50562987 | |||||
| chr16:50562988
|
C | CCACCCCC others(3): Show |
15 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0005g0166others(12): Show | 15 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.192+13434_192+1343 others(14): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50562988 | |||||
| chr16:50562989
|
C | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0026g0120 | 3 | HG01099.hp2 HG01433.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.192+13434C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562989 | ||||||
| chr16:50562989
|
C | CACCCCCC others(3): Show |
1 | a0001c0001t0005g0164 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.192+13434_192+1343 others(14): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562989 | ||||||
| chr16:50562989
|
C | CACCCCCC others(2): Show |
4 | a0001c0001t0021g0169a0001c0001t0024g0005a0001c0001t0049g0170others(1): Show | 4 | HG01943.hp2 NA19011.hp2 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+13434_192+1343 others(13): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562989 | ||||||
| chr16:50562990
|
C | G | 1 | a0001c0001t0018g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.192+13435C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562990 | ||||||
| chr16:50562992
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.192+13437C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562992 | ||||||
| chr16:50562994
|
C | A | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+13439C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562994 | ||||||
| chr16:50562994
|
C | G | 1 | a0001c0001t0002g0003 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.192+13439C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562994 | ||||||
| chr16:50562995
|
C | A | 1 | a0001c0001t0006g0066 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.192+13440C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50562995 | ||||||
| chr16:50563028
|
A | G | 44 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0023others(41): Show | 44 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.192+13473A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50563028 | ||||||
| chr16:50563033
|
T | C | 44 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0023others(41): Show | 44 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.192+13478T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50563033 | ||||||
| chr16:50563042
|
G | T | 6 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209others(3): Show | 6 | HG02486.hp1 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+13487G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50563042 | ||||||
| chr16:50563132
|
C | A | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+13577C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50563132 | ||||||
| chr16:50563148
|
G | A | 1 | a0001c0001t0021g0165 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.192+13593G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50563148 | ||||||
| chr16:50563173
|
T | C | 1 | a0001c0001t0009g0021 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.192+13618T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50563173 | ||||||
| chr16:50563261
|
TCCTGTGT others(173): Show |
T | 1 | a0001c0001t0004g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.192+13742_192+1392 others(4): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50563261 | |||||
| chr16:50563301
|
T | C | 48 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0023others(45): Show | 48 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.192+13746T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50563301 | ||||||
| chr16:50563347
|
C | G | 1 | a0001c0005t0001g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.192+13792C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50563347 | ||||||
| chr16:50563417
|
A | ACAGCCCT others(53): Show |
2 | a0001c0001t0001g0110a0001c0001t0067g0087 | 2 | HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.192+13888_192+1394 others(64): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50563417 | |||||
| chr16:50563428
|
C | T | 3 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0054g0026 | 3 | HG02451.hp2 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.192+13873C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50563428 | ||||||
| chr16:50563429
|
C | G | 3 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0054g0026 | 3 | HG02451.hp2 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.192+13874C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50563429 | ||||||
| chr16:50563433
|
G | A | 2 | a0001c0001t0017g0206a0001c0001t0042g0205 | 2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.192+13878G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50563433 | ||||||
| chr16:50563549
|
CCATGGAG others(112): Show |
C | 1 | a0001c0001t0020g0001 | 2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.192+14084_192+1420 others(4): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50563549 | |||||
| chr16:50563595
|
G | A | 3 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0054g0026 | 3 | HG02451.hp2 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.192+14040G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50563595 | ||||||
| chr16:50563728
|
GCATGGAG others(113): Show |
G | 3 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0054g0026 | 3 | HG02451.hp2 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.192+14203_192+1432 others(4): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50563728 | |||||
| chr16:50563848
|
T | TCATGGAG others(53): Show |
1 | a0001c0001t0012g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.192+14402_192+1446 others(64): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50563848 | |||||
| chr16:50563848
|
TCATGGAG others(53): Show |
T | 22 | a0001c0001t0001g0084a0001c0001t0002g0163a0001c0001t0003g0006others(19): Show | 22 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.192+14402_192+1446 others(64): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50563848 | |||||
| chr16:50564024
|
G | A | 2 | a0001c0001t0017g0206a0001c0001t0042g0205 | 2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.192+14469G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50564024 | ||||||
| chr16:50564170
|
G | C | 1 | a0001c0001t0015g0143 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.192+14615G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50564170 | ||||||
| chr16:50564177
|
G | A | 4 | a0001c0001t0014g0013a0001c0001t0014g0014a0001c0001t0014g0015others(1): Show | 4 | HG02559.hp1 HG03516.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+14622G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50564177 | ||||||
| chr16:50564393
|
G | A | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+14838G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50564393 | ||||||
| chr16:50564511
|
T | A | 10 | a0001c0001t0007g0020a0001c0001t0009g0017a0001c0001t0009g0018others(7): Show | 10 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.192+14956T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50564511 | ||||||
| chr16:50564627
|
A | G | 1 | a0001c0001t0011g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.192+15072A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50564627 | ||||||
| chr16:50564664
|
A | G | 2 | a0001c0001t0003g0185a0001c0001t0003g0186 | 2 | NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.192+15109A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50564664 | ||||||
| chr16:50564887
|
G | T | 45 | a0001c0001t0002g0163a0001c0001t0003g0006a0001c0001t0003g0173others(42): Show | 45 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.192+15332G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50564887 | ||||||
| chr16:50565131
|
T | G | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+15576T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50565131 | ||||||
| chr16:50565172
|
G | A | 1 | a0001c0001t0009g0022 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.192+15617G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50565172 | ||||||
| chr16:50565191
|
T | C | 25 | a0001c0001t0003g0006a0001c0001t0003g0023a0001c0001t0003g0173others(22): Show | 25 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.192+15636T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50565191 | ||||||
| chr16:50565296
|
C | T | 1 | a0001c0001t0048g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.192+15741C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50565296 | ||||||
| chr16:50565297
|
G | A | 1 | a0001c0001t0010g0175 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.192+15742G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50565297 | ||||||
| chr16:50565371
|
CA | C | 7 | a0001c0001t0003g0023a0001c0001t0007g0020a0001c0001t0009g0017others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+15830delA | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50565371 | |||||
| chr16:50565595
|
G | A | 1 | a0001c0001t0053g0160 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.192+16040G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50565595 | ||||||
| chr16:50565671
|
A | G | 7 | a0001c0001t0007g0020a0001c0001t0012g0207a0001c0001t0012g0208others(4): Show | 7 | HG01884.hp1 HG02486.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+16116A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50565671 | ||||||
| chr16:50565745
|
A | C | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+16190A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50565745 | ||||||
| chr16:50565994
|
G | C | 1 | a0001c0001t0023g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.192+16439G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50565994 | ||||||
| chr16:50566089
|
C | T | 26 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(23): Show | 26 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.192+16534C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50566089 | ||||||
| chr16:50566475
|
C | T | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+16920C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50566475 | ||||||
| chr16:50566513
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.192+16958T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50566513 | ||||||
| chr16:50566537
|
C | T | 6 | a0001c0001t0007g0100a0001c0001t0007g0113a0001c0001t0035g0090others(3): Show | 6 | HG02055.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+16982C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50566537 | ||||||
| chr16:50566758
|
A | G | 41 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(38): Show | 41 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.192+17203A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50566758 | ||||||
| chr16:50566916
|
C | G | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+17361C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50566916 | ||||||
| chr16:50566966
|
T | C | 29 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(26): Show | 29 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.192+17411T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50566966 | ||||||
| chr16:50567005
|
G | GC | 27 | a0001c0001t0002g0029a0001c0001t0002g0044a0001c0001t0002g0045others(24): Show | 27 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(24): Show |
intron_variant | MODIFIER | c.192+17459dupC | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50567005 | |||||
| chr16:50567015
|
T | C | 26 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(23): Show | 26 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.192+17460T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50567015 | ||||||
| chr16:50567041
|
C | T | 4 | a0001c0001t0014g0013a0001c0001t0014g0014a0001c0001t0014g0015others(1): Show | 4 | HG02559.hp1 HG03516.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+17486C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50567041 | ||||||
| chr16:50567059
|
A | G | 2 | a0001c0001t0068g0161a0001c0001t0069g0162 | 2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.192+17504A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50567059 | ||||||
| chr16:50567076
|
G | C | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.192+17521G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50567076 | ||||||
| chr16:50567080
|
G | A | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.192+17525G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50567080 | ||||||
| chr16:50567119
|
A | C | 2 | a0001c0001t0003g0173a0001c0001t0051g0172 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.192+17564A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50567119 | ||||||
| chr16:50567122
|
C | T | 2 | a0001c0001t0011g0036a0001c0001t0066g0107 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.192+17567C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50567122 | ||||||
| chr16:50567582
|
T | C | 3 | a0001c0001t0003g0173a0001c0001t0051g0172a0001c0001t0052g0176 | 3 | HG02109.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.192+18027T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50567582 | ||||||
| chr16:50567712
|
C | T | 4 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+18157C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50567712 | ||||||
| chr16:50568271
|
G | A | 4 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+18716G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50568271 | ||||||
| chr16:50568484
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.192+18929G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50568484 | ||||||
| chr16:50568511
|
C | T | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.192+18956C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50568511 | ||||||
| chr16:50568542
|
A | G | 1 | a0001c0001t0003g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.192+18987A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50568542 | ||||||
| chr16:50568559
|
C | T | 1 | a0001c0001t0062g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.192+19004C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50568559 | ||||||
| chr16:50568853
|
T | C | 1 | a0001c0001t0003g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192+19298T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50568853 | ||||||
| chr16:50568964
|
G | T | 1 | a0001c0001t0004g0059 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.192+19409G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50568964 | ||||||
| chr16:50569157
|
T | C | 2 | a0001c0001t0032g0080a0001c0001t0033g0016 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.192+19602T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50569157 | ||||||
| chr16:50569262
|
C | T | 1 | a0001c0001t0037g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.192+19707C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50569262 | ||||||
| chr16:50569263
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.192+19708G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50569263 | ||||||
| chr16:50569279
|
T | C | 2 | a0001c0001t0003g0185a0001c0001t0003g0186 | 2 | NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.192+19724T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50569279 | ||||||
| chr16:50569818
|
C | T | 1 | a0001c0001t0011g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.192+20263C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50569818 | ||||||
| chr16:50569993
|
A | G | 37 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(34): Show | 37 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.192+20438A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50569993 | ||||||
| chr16:50570093
|
T | A | 1 | a0001c0001t0004g0056 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.192+20538T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50570093 | ||||||
| chr16:50570094
|
A | T | 3 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0054g0026 | 3 | HG02451.hp2 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.192+20539A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50570094 | ||||||
| chr16:50570301
|
G | A | 1 | a0001c0001t0058g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.192+20746G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50570301 | ||||||
| chr16:50570302
|
C | T | 2 | a0001c0001t0011g0036a0001c0001t0066g0107 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.192+20747C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50570302 | ||||||
| chr16:50570345
|
A | C | 1 | a0001c0001t0002g0040 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.192+20790A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50570345 | ||||||
| chr16:50570468
|
G | C | 2 | a0001c0001t0002g0033a0001c0001t0002g0040 | 2 | HG03491.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.192+20913G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50570468 | ||||||
| chr16:50570513
|
G | T | 1 | a0001c0001t0006g0066 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.192+20958G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50570513 | ||||||
| chr16:50570539
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.192+20984G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50570539 | ||||||
| chr16:50570563
|
T | C | 209 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0031others(206): Show | 211 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.192+21008T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50570563 | ||||||
| chr16:50570799
|
C | T | 1 | a0001c0001t0027g0043 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.192+21244C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50570799 | ||||||
| chr16:50570804
|
G | A | 1 | a0001c0001t0023g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.192+21249G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50570804 | ||||||
| chr16:50571003
|
C | T | 2 | a0001c0001t0011g0036a0001c0001t0066g0107 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.192+21448C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50571003 | ||||||
| chr16:50571015
|
C | A | 36 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.192+21460C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50571015 | ||||||
| chr16:50571292
|
G | T | 2 | a0001c0001t0016g0109a0001c0001t0016g0116 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.192+21737G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50571292 | ||||||
| chr16:50571471
|
A | T | 1 | a0001c0001t0028g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.192+21916A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50571471 | ||||||
| chr16:50571593
|
G | C | 1 | a0001c0001t0057g0060 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.192+22038G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50571593 | ||||||
| chr16:50571598
|
G | T | 1 | a0001c0001t0004g0148 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.192+22043G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50571598 | ||||||
| chr16:50571842
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.192+22287C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50571842 | ||||||
| chr16:50571847
|
T | C | 15 | a0001c0001t0003g0085a0001c0001t0003g0092a0001c0001t0003g0114others(12): Show | 15 | HG00639.hp1 HG01175.hp2 HG02735.hp1 others(12): Show |
intron_variant | MODIFIER | c.192+22292T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50571847 | ||||||
| chr16:50571945
|
A | C | 32 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(29): Show | 32 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.192+22390A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50571945 | ||||||
| chr16:50571996
|
T | C | 3 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0054g0026 | 3 | HG02451.hp2 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.192+22441T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50571996 | ||||||
| chr16:50572005
|
C | T | 3 | a0001c0001t0014g0013a0001c0001t0014g0014a0001c0001t0014g0015 | 3 | HG02559.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.192+22450C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572005 | ||||||
| chr16:50572101
|
G | C | 1 | a0001c0001t0007g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.192+22546G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572101 | ||||||
| chr16:50572315
|
C | A | 1 | a0001c0001t0011g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.192+22760C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572315 | ||||||
| chr16:50572345
|
A | G | 26 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(23): Show | 26 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.192+22790A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572345 | ||||||
| chr16:50572391
|
G | A | 4 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+22836G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572391 | ||||||
| chr16:50572502
|
T | A | 1 | a0001c0001t0006g0063 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.192+22947T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572502 | ||||||
| chr16:50572579
|
G | A | 3 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0054g0026 | 3 | HG02451.hp2 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.192+23024G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572579 | ||||||
| chr16:50572606
|
C | T | 4 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+23051C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572606 | ||||||
| chr16:50572721
|
T | C | 2 | a0001c0001t0004g0196a0001c0001t0043g0199 | 2 | NA18969.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.192+23166T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572721 | ||||||
| chr16:50572758
|
C | T | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+23203C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572758 | ||||||
| chr16:50572773
|
C | T | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+23218C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572773 | ||||||
| chr16:50572782
|
C | T | 1 | a0001c0001t0030g0150 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.192+23227C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572782 | ||||||
| chr16:50572805
|
G | A | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+23250G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572805 | ||||||
| chr16:50572825
|
AT | A | 2 | a0001c0001t0011g0036a0001c0001t0066g0107 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.192+23271delT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572825 | ||||||
| chr16:50572940
|
G | T | 1 | a0001c0001t0017g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.192+23385G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50572940 | ||||||
| chr16:50573089
|
A | G | 36 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.192+23534A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50573089 | ||||||
| chr16:50573273
|
C | A | 2 | a0001c0001t0011g0036a0001c0001t0066g0107 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.192+23718C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50573273 | ||||||
| chr16:50573287
|
G | GGTCTCCA others(11): Show |
3 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0054g0026 | 3 | HG02451.hp2 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.192+23734_192+2375 others(22): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50573287 | |||||
| chr16:50573434
|
T | C | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+23879T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50573434 | ||||||
| chr16:50573477
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.192+23922G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50573477 | ||||||
| chr16:50573546
|
C | T | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+23991C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50573546 | ||||||
| chr16:50574051
|
T | TAGAC | 36 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.192+24498_192+2449 others(8): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50574051 | |||||
| chr16:50574105
|
T | C | 95 | a0001c0001t0001g0108a0001c0001t0002g0003a0001c0001t0002g0027others(92): Show | 95 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.192+24550T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50574105 | ||||||
| chr16:50574323
|
G | A | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+24768G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50574323 | ||||||
| chr16:50574483
|
ACT | A | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+24932_192+2493 others(6): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50574483 | |||||
| chr16:50574521
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0004g0142 | 2 | NA19000.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.192+24966C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50574521 | ||||||
| chr16:50574554
|
C | G | 1 | a0001c0001t0045g0192 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.192+24999C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50574554 | ||||||
| chr16:50574557
|
G | A | 2 | a0001c0001t0011g0036a0001c0001t0066g0107 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.192+25002G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50574557 | ||||||
| chr16:50574671
|
C | A | 5 | a0001c0001t0006g0063a0001c0001t0006g0064a0001c0001t0006g0066others(2): Show | 5 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+25116C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50574671 | ||||||
| chr16:50574942
|
AAACATCA others(1): Show |
A | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+25390_192+2539 others(12): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50574942 | |||||
| chr16:50574999
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.192+25444G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50574999 | ||||||
| chr16:50575043
|
A | G | 46 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(43): Show | 46 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.192+25488A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50575043 | ||||||
| chr16:50575052
|
C | G | 1 | a0001c0001t0017g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.192+25497C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50575052 | ||||||
| chr16:50575066
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.192+25511A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50575066 | ||||||
| chr16:50575095
|
G | GT | 6 | a0001c0001t0001g0089a0001c0001t0007g0159a0001c0001t0014g0015others(3): Show | 6 | HG00597.hp1 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+25554dupT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50575095 | |||||
| chr16:50575112
|
T | C | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.192+25557T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50575112 | ||||||
| chr16:50575274
|
A | T | 26 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(23): Show | 26 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.192+25719A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50575274 | ||||||
| chr16:50575308
|
A | T | 2 | a0001c0001t0015g0131a0001c0001t0015g0143 | 2 | NA18954.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.192+25753A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50575308 | ||||||
| chr16:50575344
|
C | CAG | 2 | a0001c0001t0011g0036a0001c0001t0066g0107 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.192+25792_192+2579 others(6): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50575344 | |||||
| chr16:50575381
|
G | A | 28 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(25): Show | 28 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.192+25826G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50575381 | ||||||
| chr16:50575382
|
C | T | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192+25827C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50575382 | ||||||
| chr16:50575420
|
G | T | 1 | a0001c0001t0051g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.192+25865G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50575420 | ||||||
| chr16:50575421
|
G | T | 1 | a0001c0001t0051g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.192+25866G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50575421 | ||||||
| chr16:50575483
|
T | C | 2 | a0001c0001t0003g0097a0001c0001t0003g0198 | 2 | HG00558.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.192+25928T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50575483 | ||||||
| chr16:50575809
|
C | T | 1 | a0001c0001t0002g0003 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.192+26254C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50575809 | ||||||
| chr16:50575851
|
C | T | 1 | a0001c0001t0009g0021 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.192+26296C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50575851 | ||||||
| chr16:50576642
|
C | A | 4 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+27087C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50576642 | ||||||
| chr16:50576693
|
T | A | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.192+27138T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50576693 | ||||||
| chr16:50576746
|
C | CT | 157 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0031others(154): Show | 159 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.192+27206dupT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50576746 | |||||
| chr16:50576746
|
C | CTT | 10 | a0001c0001t0001g0089a0001c0001t0001g0110a0001c0001t0001g0135others(7): Show | 10 | HG01175.hp2 HG02273.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.192+27205_192+2720 others(6): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50576746 | |||||
| chr16:50576746
|
C | CTTT | 25 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0173others(22): Show | 25 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.192+27204_192+2720 others(7): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50576746 | |||||
| chr16:50576869
|
C | T | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.192+27314C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50576869 | ||||||
| chr16:50577006
|
G | A | 1 | a0001c0001t0003g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192+27451G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50577006 | ||||||
| chr16:50577284
|
T | G | 1 | a0001c0001t0066g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.192+27729T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50577284 | ||||||
| chr16:50577327
|
A | G | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.192+27772A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50577327 | ||||||
| chr16:50577349
|
G | A | 5 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG01943.hp1 HG01952.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+27794G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50577349 | ||||||
| chr16:50577420
|
A | G | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+27865A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50577420 | ||||||
| chr16:50577496
|
T | C | 1 | a0001c0001t0007g0100 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.192+27941T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50577496 | ||||||
| chr16:50577547
|
T | A | 1 | a0001c0004t0001g0030 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.192+27992T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50577547 | ||||||
| chr16:50577556
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.192+28001T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50577556 | ||||||
| chr16:50577651
|
A | G | 1 | a0001c0001t0004g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.192+28096A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50577651 | ||||||
| chr16:50577755
|
G | A | 2 | a0001c0001t0005g0171a0001c0001t0042g0205 | 2 | HG02970.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.192+28200G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50577755 | ||||||
| chr16:50577938
|
C | T | 1 | a0001c0001t0022g0128 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.192+28383C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50577938 | ||||||
| chr16:50578323
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.192+28768A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50578323 | ||||||
| chr16:50578675
|
C | G | 28 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(25): Show | 28 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.192+29120C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50578675 | ||||||
| chr16:50578735
|
C | T | 1 | a0001c0001t0011g0011 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.192+29180C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50578735 | ||||||
| chr16:50579019
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.193-29275C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579019 | ||||||
| chr16:50579183
|
C | G | 3 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0054g0026 | 3 | HG02451.hp2 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.193-29111C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579183 | ||||||
| chr16:50579190
|
A | G | 3 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0054g0026 | 3 | HG02451.hp2 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.193-29104A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579190 | ||||||
| chr16:50579199
|
G | A | 1 | a0001c0001t0026g0120 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.193-29095G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579199 | ||||||
| chr16:50579228
|
T | C | 3 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0054g0026 | 3 | HG02451.hp2 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.193-29066T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579228 | ||||||
| chr16:50579247
|
G | T | 41 | a0001c0001t0002g0003a0001c0001t0002g0027a0001c0001t0002g0029others(38): Show | 41 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.193-29047G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579247 | ||||||
| chr16:50579345
|
A | C | 1 | a0001c0001t0052g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.193-28949A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579345 | ||||||
| chr16:50579390
|
A | C | 1 | a0001c0001t0052g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.193-28904A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579390 | ||||||
| chr16:50579391
|
G | A | 1 | a0001c0001t0052g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.193-28903G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579391 | ||||||
| chr16:50579396
|
A | ACATGCAC others(50): Show |
1 | a0001c0001t0002g0049 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.193-28826_193-2877 others(61): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50579396 | |||||
| chr16:50579396
|
A | G | 1 | a0001c0001t0052g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.193-28898A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579396 | ||||||
| chr16:50579411
|
G | C | 1 | a0001c0001t0052g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.193-28883G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579411 | ||||||
| chr16:50579427
|
GCTACACA others(107): Show |
G | 26 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(23): Show | 26 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.193-28753_193-2864 others(4): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50579427 | |||||
| chr16:50579447
|
C | A | 1 | a0001c0001t0052g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.193-28847C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579447 | ||||||
| chr16:50579453
|
G | A | 1 | a0001c0001t0052g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.193-28841G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579453 | ||||||
| chr16:50579484
|
GCTACACA others(50): Show |
G | 2 | a0001c0001t0047g0204a0001c0001t0052g0176 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.193-28769_193-2871 others(61): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50579484 | |||||
| chr16:50579525
|
C | G | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-28769C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579525 | ||||||
| chr16:50579535
|
G | C | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-28759G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579535 | ||||||
| chr16:50579535
|
G | GTACCCGC others(50): Show |
5 | a0001c0001t0011g0036a0001c0001t0066g0107a0001c0002t0008g0024others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-28754_193-2875 others(61): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50579535 | |||||
| chr16:50579541
|
A | G | 13 | a0001c0001t0003g0023a0001c0001t0011g0010a0001c0001t0011g0011others(10): Show | 13 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.193-28753A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579541 | ||||||
| chr16:50579598
|
G | A | 1 | a0001c0001t0003g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193-28696G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579598 | ||||||
| chr16:50579649
|
G | C | 1 | a0001c0001t0003g0061 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.193-28645G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579649 | ||||||
| chr16:50579663
|
C | T | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.193-28631C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579663 | ||||||
| chr16:50579689
|
T | C | 1 | a0001c0001t0010g0068 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.193-28605T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579689 | ||||||
| chr16:50579696
|
C | G | 28 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(25): Show | 28 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.193-28598C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579696 | ||||||
| chr16:50579738
|
GCATGCAC others(50): Show |
G | 1 | a0001c0001t0003g0042 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.193-28535_193-2847 others(61): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50579738 | |||||
| chr16:50579795
|
A | G | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-28499A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50579795 | ||||||
| chr16:50580042
|
C | T | 3 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0054g0026 | 3 | HG02451.hp2 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.193-28252C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50580042 | ||||||
| chr16:50580062
|
G | A | 1 | a0001c0001t0003g0055 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.193-28232G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50580062 | ||||||
| chr16:50580112
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.193-28182G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50580112 | ||||||
| chr16:50580193
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.193-28101G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50580193 | ||||||
| chr16:50580295
|
G | T | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193-27999G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50580295 | ||||||
| chr16:50580361
|
G | A | 1 | a0001c0001t0006g0066 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.193-27933G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50580361 | ||||||
| chr16:50580683
|
G | C | 1 | a0001c0001t0003g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193-27611G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50580683 | ||||||
| chr16:50580835
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.193-27459G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50580835 | ||||||
| chr16:50580865
|
C | G | 1 | a0001c0001t0005g0168 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.193-27429C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50580865 | ||||||
| chr16:50581232
|
G | C | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-27062G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50581232 | ||||||
| chr16:50581405
|
C | A | 1 | a0001c0001t0017g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.193-26889C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50581405 | ||||||
| chr16:50581521
|
T | A | 5 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG01943.hp1 HG01952.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-26773T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50581521 | ||||||
| chr16:50581525
|
A | G | 1 | a0001c0001t0024g0005 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.193-26769A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50581525 | ||||||
| chr16:50581538
|
G | T | 1 | a0001c0001t0050g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.193-26756G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50581538 | ||||||
| chr16:50581711
|
C | A | 1 | a0001c0001t0002g0003 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.193-26583C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50581711 | ||||||
| chr16:50582531
|
GGAATGGC others(4): Show |
G | 1 | a0001c0001t0005g0174 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.193-25762_193-2575 others(15): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50582531 | ||||||
| chr16:50582597
|
G | A | 2 | a0001c0001t0022g0091a0001c0001t0022g0128 | 2 | HG01346.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.193-25697G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50582597 | ||||||
| chr16:50583088
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.193-25206G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50583088 | ||||||
| chr16:50583206
|
G | T | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-25088G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50583206 | ||||||
| chr16:50583223
|
T | C | 1 | a0001c0001t0033g0016 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.193-25071T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50583223 | ||||||
| chr16:50583235
|
G | A | 26 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(23): Show | 26 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.193-25059G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50583235 | ||||||
| chr16:50583333
|
G | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG01943.hp1 HG01952.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-24961G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50583333 | ||||||
| chr16:50583773
|
T | C | 15 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0005g0164others(12): Show | 15 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.193-24521T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50583773 | ||||||
| chr16:50584014
|
T | C | 2 | a0001c0001t0002g0126a0001c0001t0006g0127 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.193-24280T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50584014 | ||||||
| chr16:50584044
|
C | T | 1 | a0001c0001t0003g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193-24250C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50584044 | ||||||
| chr16:50584278
|
C | T | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-24016C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50584278 | ||||||
| chr16:50584316
|
G | A | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-23978G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50584316 | ||||||
| chr16:50584351
|
C | T | 1 | a0001c0001t0011g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.193-23943C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50584351 | ||||||
| chr16:50584489
|
G | A | 1 | a0001c0005t0001g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.193-23805G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50584489 | ||||||
| chr16:50584496
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.193-23798C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50584496 | ||||||
| chr16:50584530
|
A | T | 2 | a0001c0001t0003g0097a0001c0001t0003g0198 | 2 | HG00558.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.193-23764A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50584530 | ||||||
| chr16:50584697
|
A | T | 3 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0054g0026 | 3 | HG02451.hp2 HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.193-23597A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50584697 | ||||||
| chr16:50584771
|
A | G | 3 | a0001c0001t0005g0171a0001c0001t0005g0174a0001c0001t0005g0177 | 3 | HG00741.hp1 NA18992.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.193-23523A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50584771 | ||||||
| chr16:50584909
|
C | T | 1 | a0001c0001t0063g0058 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.193-23385C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50584909 | ||||||
| chr16:50584910
|
G | A | 1 | a0001c0002t0008g0024 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.193-23384G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50584910 | ||||||
| chr16:50584913
|
A | G | 1 | a0001c0001t0003g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193-23381A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50584913 | ||||||
| chr16:50585145
|
G | A | 1 | a0001c0001t0007g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-23149G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50585145 | ||||||
| chr16:50585277
|
G | A | 1 | a0001c0001t0003g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.193-23017G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50585277 | ||||||
| chr16:50585390
|
C | T | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.193-22904C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50585390 | ||||||
| chr16:50585418
|
A | T | 6 | a0001c0001t0003g0173a0001c0001t0014g0013a0001c0001t0014g0014others(3): Show | 6 | HG02109.hp1 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-22876A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50585418 | ||||||
| chr16:50585456
|
G | A | 1 | a0001c0001t0007g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-22838G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50585456 | ||||||
| chr16:50585561
|
C | T | 1 | a0001c0001t0005g0177 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.193-22733C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50585561 | ||||||
| chr16:50585562
|
G | A | 3 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012 | 3 | HG02723.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.193-22732G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50585562 | ||||||
| chr16:50585571
|
G | C | 1 | a0001c0001t0059g0062 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.193-22723G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50585571 | ||||||
| chr16:50585606
|
C | T | 1 | a0001c0001t0003g0114 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.193-22688C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50585606 | ||||||
| chr16:50585639
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.193-22655C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50585639 | ||||||
| chr16:50585805
|
A | G | 2 | a0001c0001t0011g0036a0001c0001t0066g0107 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.193-22489A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50585805 | ||||||
| chr16:50585881
|
CT | C | 2 | a0001c0001t0004g0111a0001c0001t0015g0158 | 2 | NA18952.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.193-22412delT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50585881 | ||||||
| chr16:50585965
|
T | C | 1 | a0001c0004t0004g0144 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.193-22329T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50585965 | ||||||
| chr16:50586022
|
C | T | 3 | a0001c0001t0013g0178a0001c0001t0013g0179a0001c0001t0013g0180 | 3 | HG01255.hp1 HG01516.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.193-22272C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50586022 | ||||||
| chr16:50586137
|
C | T | 1 | a0001c0001t0003g0092 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.193-22157C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50586137 | ||||||
| chr16:50586211
|
C | T | 7 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-22083C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50586211 | ||||||
| chr16:50586292
|
A | G | 1 | a0001c0001t0066g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.193-22002A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50586292 | ||||||
| chr16:50586342
|
G | T | 1 | a0001c0001t0003g0042 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.193-21952G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50586342 | ||||||
| chr16:50586402
|
C | G | 6 | a0001c0001t0003g0023a0001c0001t0003g0094a0001c0001t0003g0095others(3): Show | 6 | HG02818.hp1 HG03130.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-21892C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50586402 | ||||||
| chr16:50586466
|
G | A | 1 | a0001c0001t0050g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.193-21828G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50586466 | ||||||
| chr16:50586475
|
G | A | 1 | a0001c0001t0004g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.193-21819G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50586475 | ||||||
| chr16:50586527
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.193-21767G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50586527 | ||||||
| chr16:50586530
|
C | T | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-21764C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50586530 | ||||||
| chr16:50586556
|
C | T | 2 | a0001c0001t0016g0109a0001c0001t0016g0116 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.193-21738C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50586556 | ||||||
| chr16:50587212
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.193-21082T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50587212 | ||||||
| chr16:50587383
|
T | G | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-20911T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50587383 | ||||||
| chr16:50587498
|
C | T | 5 | a0001c0001t0006g0063a0001c0001t0006g0064a0001c0001t0006g0067others(2): Show | 5 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-20796C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50587498 | ||||||
| chr16:50587554
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.193-20740G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50587554 | ||||||
| chr16:50587733
|
T | C | 39 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0006others(36): Show | 39 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.193-20561T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50587733 | ||||||
| chr16:50587893
|
A | G | 1 | a0001c0001t0029g0105 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.193-20401A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50587893 | ||||||
| chr16:50588006
|
C | T | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193-20288C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50588006 | ||||||
| chr16:50588080
|
G | T | 1 | a0001c0001t0004g0059 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.193-20214G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50588080 | ||||||
| chr16:50588534
|
T | C | 3 | a0001c0001t0013g0178a0001c0001t0013g0179a0001c0001t0013g0180 | 3 | HG01255.hp1 HG01516.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.193-19760T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50588534 | ||||||
| chr16:50588540
|
C | A | 1 | a0001c0001t0048g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.193-19754C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50588540 | ||||||
| chr16:50588598
|
C | CT | 35 | a0001c0001t0001g0037a0001c0001t0001g0108a0001c0001t0001g0119others(32): Show | 35 | HG00323.hp2 HG01175.hp1 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.193-19672dupT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50588598 | |||||
| chr16:50588598
|
CT | C | 14 | a0001c0001t0001g0031a0001c0001t0001g0136a0001c0001t0001g0140others(11): Show | 14 | HG00558.hp2 HG01109.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.193-19672delT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50588598 | |||||
| chr16:50588684
|
C | T | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.193-19610C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50588684 | ||||||
| chr16:50588835
|
G | A | 6 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0008g0083others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-19459G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50588835 | ||||||
| chr16:50588944
|
G | A | 1 | a0001c0001t0007g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.193-19350G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50588944 | ||||||
| chr16:50589580
|
C | T | 1 | a0001c0001t0050g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.193-18714C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50589580 | ||||||
| chr16:50589682
|
G | T | 1 | a0001c0001t0003g0085 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.193-18612G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50589682 | ||||||
| chr16:50589684
|
T | TTTTCTTT others(4): Show |
1 | a0001c0001t0003g0085 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.193-18608_193-1860 others(15): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589684 | |||||
| chr16:50589689
|
T | C | 1 | a0001c0001t0003g0085 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.193-18605T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50589689 | ||||||
| chr16:50589689
|
TTTCTTTT others(8): Show |
T | 2 | a0001c0001t0004g0056a0001c0001t0044g0200 | 2 | NA18747.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.193-18600_193-1858 others(19): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589689 | |||||
| chr16:50589694
|
T | C | 2 | a0001c0001t0003g0085a0001c0001t0037g0081 | 2 | HG02257.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.193-18600T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50589694 | ||||||
| chr16:50589694
|
T | TTTCTC | 17 | a0001c0001t0001g0135a0001c0001t0002g0112a0001c0001t0002g0126others(14): Show | 17 | HG01884.hp1 HG01884.hp2 HG02273.hp1 others(14): Show |
intron_variant | MODIFIER | c.193-18533_193-1852 others(9): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589694 | |||||
| chr16:50589694
|
T | TTTCTCTT others(3): Show |
9 | a0001c0001t0001g0089a0001c0001t0001g0098a0001c0001t0002g0106others(6): Show | 9 | HG01109.hp1 HG02647.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-18538_193-1852 others(14): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589694 | |||||
| chr16:50589694
|
T | TTTCTCTT others(13): Show |
1 | a0001c0001t0029g0105 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.193-18548_193-1852 others(24): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589694 | |||||
| chr16:50589694
|
T | TTTCTCTT others(18): Show |
1 | a0001c0001t0003g0155 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.193-18553_193-1852 others(29): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589694 | |||||
| chr16:50589694
|
T | TTTCTCTT others(23): Show |
1 | a0001c0001t0003g0154 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.193-18558_193-1852 others(34): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589694 | |||||
| chr16:50589694
|
TTTCTC | T | 41 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0121others(38): Show | 42 | HG00597.hp2 HG01071.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.193-18533_193-1852 others(9): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589694 | |||||
| chr16:50589694
|
TTTCTCTT others(3): Show |
T | 38 | a0001c0001t0001g0031a0001c0001t0001g0051a0001c0001t0001g0084others(35): Show | 39 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.193-18538_193-1852 others(14): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589694 | |||||
| chr16:50589694
|
TTTCTCTT others(8): Show |
T | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0050others(19): Show | 22 | HG00323.hp1 HG00408.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.193-18543_193-1852 others(19): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589694 | |||||
| chr16:50589694
|
TTTCTCTT others(13): Show |
T | 7 | a0001c0001t0002g0035a0001c0001t0002g0077a0001c0001t0002g0099others(4): Show | 7 | HG00323.hp2 HG00408.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.193-18548_193-1852 others(24): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589694 | |||||
| chr16:50589694
|
TTTCTCTT others(18): Show |
T | 11 | a0001c0001t0001g0037a0001c0001t0011g0010a0001c0001t0011g0011others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-18553_193-1852 others(29): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589694 | |||||
| chr16:50589694
|
TTTCTCTT others(23): Show |
T | 1 | a0001c0002t0054g0026 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.193-18558_193-1852 others(34): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589694 | |||||
| chr16:50589699
|
C | T | 1 | a0001c0003t0004g0181 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.193-18595C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50589699 | ||||||
| chr16:50589736
|
TCTCTTCT others(23): Show |
T | 1 | a0001c0001t0014g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.193-18553_193-1852 others(34): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589736 | |||||
| chr16:50589736
|
TCTCTTCT others(33): Show |
T | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193-18553_193-1851 others(44): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589736 | |||||
| chr16:50589736
|
TCTCTTCT others(38): Show |
T | 1 | a0001c0001t0049g0170 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.193-18553_193-1850 others(49): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589736 | |||||
| chr16:50589736
|
TCTCTTCT others(43): Show |
T | 1 | a0001c0001t0002g0193 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.193-18553_193-1850 others(54): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589736 | |||||
| chr16:50589741
|
T | C | 4 | a0001c0002t0008g0025a0001c0002t0008g0083a0001c0002t0008g0101others(1): Show | 4 | HG03225.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-18553T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50589741 | ||||||
| chr16:50589741
|
TCTCTTCT others(28): Show |
T | 1 | a0001c0001t0005g0166 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.193-18548_193-1851 others(39): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589741 | |||||
| chr16:50589741
|
TCTCTTCT others(33): Show |
T | 4 | a0001c0001t0002g0163a0001c0001t0005g0167a0001c0001t0010g0175others(1): Show | 4 | HG01943.hp2 HG01975.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-18548_193-1850 others(44): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589741 | |||||
| chr16:50589746
|
T | C | 4 | a0001c0002t0008g0025a0001c0002t0008g0083a0001c0002t0008g0101others(1): Show | 4 | HG03225.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-18548T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50589746 | ||||||
| chr16:50589746
|
TCTCTTCT others(18): Show |
T | 3 | a0001c0001t0005g0171a0001c0001t0005g0177a0001c0003t0004g0181 | 3 | HG00741.hp1 HG01192.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.193-18543_193-1851 others(29): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589746 | |||||
| chr16:50589746
|
TCTCTTCT others(23): Show |
T | 1 | a0001c0001t0021g0169 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.193-18543_193-1851 others(34): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589746 | |||||
| chr16:50589746
|
TCTCTTCT others(28): Show |
T | 1 | a0001c0001t0005g0164 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.193-18543_193-1850 others(39): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589746 | |||||
| chr16:50589751
|
T | C | 5 | a0001c0001t0050g0028a0001c0002t0008g0025a0001c0002t0008g0083others(2): Show | 5 | HG03225.hp2 HG03516.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-18543T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50589751 | ||||||
| chr16:50589751
|
TCTCTTCT others(8): Show |
T | 2 | a0001c0001t0003g0006a0001c0001t0052g0176 | 2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.193-18538_193-1852 others(19): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589751 | |||||
| chr16:50589751
|
TCTCTTCT others(13): Show |
T | 1 | a0001c0001t0015g0143 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.193-18538_193-1851 others(24): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589751 | |||||
| chr16:50589751
|
TCTCTTCT others(18): Show |
T | 1 | a0001c0001t0005g0168 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.193-18538_193-1851 others(29): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589751 | |||||
| chr16:50589756
|
T | C | 6 | a0001c0001t0020g0001a0001c0001t0050g0028a0001c0002t0008g0025others(3): Show | 7 | HG02280.hp2 HG02486.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-18538T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50589756 | ||||||
| chr16:50589756
|
TCTCTTCT others(3): Show |
T | 3 | a0001c0001t0003g0189a0001c0001t0017g0032a0001c0001t0026g0120 | 3 | HG01358.hp1 HG01516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.193-18533_193-1852 others(14): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589756 | |||||
| chr16:50589756
|
TCTCTTCT others(8): Show |
T | 1 | a0001c0001t0005g0174 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.193-18533_193-1851 others(19): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589756 | |||||
| chr16:50589756
|
TCTCTTCT others(13): Show |
T | 1 | a0001c0001t0001g0132 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.193-18533_193-1851 others(24): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589756 | |||||
| chr16:50589761
|
T | C | 10 | a0001c0001t0003g0173a0001c0001t0015g0158a0001c0001t0020g0001others(7): Show | 11 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.193-18533T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50589761 | ||||||
| chr16:50589761
|
T | TCTCTC | 26 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0084others(23): Show | 26 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.193-18467_193-1846 others(9): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589761 | |||||
| chr16:50589761
|
T | TCTCTCCT others(3): Show |
7 | a0001c0001t0001g0051a0001c0001t0002g0112a0001c0001t0003g0023others(4): Show | 7 | HG01496.hp2 HG02738.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.193-18472_193-1846 others(14): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589761 | |||||
| chr16:50589761
|
T | TCTCTCCT others(8): Show |
6 | a0001c0001t0003g0092a0001c0001t0004g0111a0001c0001t0007g0100others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-18477_193-1846 others(19): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589761 | |||||
| chr16:50589761
|
T | TCTCTCCT others(13): Show |
2 | a0001c0001t0033g0016a0001c0001t0037g0081 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.193-18482_193-1846 others(24): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589761 | |||||
| chr16:50589761
|
T | TCTCTCCT others(18): Show |
2 | a0001c0001t0004g0196a0001c0001t0045g0192 | 2 | NA19065.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.193-18487_193-1846 others(29): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589761 | |||||
| chr16:50589761
|
TCTCTC | T | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0031others(52): Show | 56 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.193-18467_193-1846 others(9): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589761 | |||||
| chr16:50589761
|
TCTCTCCT others(3): Show |
T | 31 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0130others(28): Show | 31 | HG00408.hp2 HG01099.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.193-18472_193-1846 others(14): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589761 | |||||
| chr16:50589761
|
TCTCTCCT others(8): Show |
T | 11 | a0001c0001t0001g0110a0001c0001t0002g0106a0001c0001t0003g0156others(8): Show | 11 | HG00408.hp1 HG00639.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-18477_193-1846 others(19): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589761 | |||||
| chr16:50589761
|
TCTCTCCT others(13): Show |
T | 4 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-18482_193-1846 others(24): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50589761 | |||||
| chr16:50590178
|
A | T | 22 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0173others(19): Show | 22 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.193-18116A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50590178 | ||||||
| chr16:50590223
|
C | A | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-18071C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50590223 | ||||||
| chr16:50590358
|
A | G | 3 | a0001c0001t0009g0017a0001c0001t0009g0021a0001c0001t0009g0022 | 3 | HG02451.hp1 HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.193-17936A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50590358 | ||||||
| chr16:50590600
|
CA | C | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-17692delA | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50590600 | |||||
| chr16:50590726
|
G | C | 1 | a0001c0001t0002g0027 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.193-17568G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50590726 | ||||||
| chr16:50590821
|
G | T | 3 | a0001c0001t0004g0194a0001c0001t0009g0019a0001c0001t0021g0169 | 3 | HG02809.hp1 HG03471.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.193-17473G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50590821 | ||||||
| chr16:50590906
|
C | T | 1 | a0001c0002t0054g0026 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.193-17388C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50590906 | ||||||
| chr16:50590991
|
T | A | 1 | a0001c0001t0002g0088 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.193-17303T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50590991 | ||||||
| chr16:50591242
|
T | C | 1 | a0001c0001t0015g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.193-17052T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50591242 | ||||||
| chr16:50591317
|
G | A | 1 | a0001c0002t0008g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.193-16977G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50591317 | ||||||
| chr16:50591597
|
T | C | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-16697T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50591597 | ||||||
| chr16:50591726
|
T | C | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193-16568T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50591726 | ||||||
| chr16:50591739
|
C | T | 1 | a0001c0001t0036g0157 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.193-16555C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50591739 | ||||||
| chr16:50591790
|
T | C | 4 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0056g0118others(1): Show | 4 | HG02818.hp1 HG03130.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-16504T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50591790 | ||||||
| chr16:50591931
|
C | T | 1 | a0001c0001t0003g0183 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.193-16363C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50591931 | ||||||
| chr16:50592074
|
C | T | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-16220C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50592074 | ||||||
| chr16:50592181
|
A | G | 39 | a0001c0001t0002g0003a0001c0001t0002g0027a0001c0001t0002g0029others(36): Show | 39 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.193-16113A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50592181 | ||||||
| chr16:50592182
|
T | C | 1 | a0001c0001t0003g0114 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.193-16112T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50592182 | ||||||
| chr16:50592236
|
G | A | 1 | a0001c0001t0002g0047 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.193-16058G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50592236 | ||||||
| chr16:50592284
|
A | G | 92 | a0001c0001t0002g0003a0001c0001t0002g0027a0001c0001t0002g0029others(89): Show | 92 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.193-16010A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50592284 | ||||||
| chr16:50592731
|
G | A | 5 | a0001c0001t0003g0023a0001c0001t0066g0107a0001c0002t0008g0024others(2): Show | 5 | HG02451.hp2 HG02615.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-15563G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50592731 | ||||||
| chr16:50592786
|
G | A | 8 | a0001c0001t0003g0023a0001c0001t0066g0107a0001c0002t0008g0024others(5): Show | 8 | HG02451.hp2 HG02615.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-15508G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50592786 | ||||||
| chr16:50592838
|
T | C | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-15456T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50592838 | ||||||
| chr16:50592910
|
A | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0119a0001c0001t0001g0121 | 3 | HG00323.hp1 HG01099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.193-15384A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50592910 | ||||||
| chr16:50593063
|
C | T | 1 | a0001c0001t0003g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.193-15231C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50593063 | ||||||
| chr16:50593338
|
A | G | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-14956A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50593338 | ||||||
| chr16:50593393
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.193-14901C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50593393 | ||||||
| chr16:50593415
|
T | G | 3 | a0001c0001t0013g0178a0001c0001t0013g0179a0001c0001t0013g0180 | 3 | HG01255.hp1 HG01516.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.193-14879T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50593415 | ||||||
| chr16:50593467
|
T | C | 170 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0003others(167): Show | 172 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.193-14827T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50593467 | ||||||
| chr16:50593474
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01496.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.193-14820A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50593474 | ||||||
| chr16:50593560
|
T | A | 7 | a0001c0001t0002g0035a0001c0001t0002g0073a0001c0001t0002g0075others(4): Show | 7 | HG00323.hp2 HG01192.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.193-14734T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50593560 | ||||||
| chr16:50593646
|
C | T | 1 | a0001c0001t0052g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.193-14648C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50593646 | ||||||
| chr16:50593941
|
G | A | 4 | a0001c0001t0014g0013a0001c0001t0014g0014a0001c0001t0014g0015others(1): Show | 4 | HG02559.hp1 HG03516.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-14353G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50593941 | ||||||
| chr16:50594206
|
T | G | 1 | a0001c0001t0048g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.193-14088T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50594206 | ||||||
| chr16:50594400
|
G | A | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-13894G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50594400 | ||||||
| chr16:50594493
|
C | G | 1 | a0001c0001t0007g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.193-13801C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50594493 | ||||||
| chr16:50594547
|
A | T | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193-13747A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50594547 | ||||||
| chr16:50594913
|
G | A | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193-13381G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50594913 | ||||||
| chr16:50595140
|
C | T | 6 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0008g0083others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-13154C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50595140 | ||||||
| chr16:50595173
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.193-13121C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50595173 | ||||||
| chr16:50595257
|
C | T | 1 | a0001c0001t0011g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.193-13037C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50595257 | ||||||
| chr16:50595333
|
T | C | 2 | a0001c0001t0003g0097a0001c0001t0003g0198 | 2 | HG00558.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.193-12961T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50595333 | ||||||
| chr16:50595644
|
C | T | 2 | a0001c0001t0004g0002a0001c0001t0004g0148 | 3 | NA18960.hp1 NA18981.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.193-12650C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50595644 | ||||||
| chr16:50595730
|
A | G | 1 | a0001c0001t0037g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.193-12564A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50595730 | ||||||
| chr16:50595761
|
C | T | 2 | a0001c0001t0068g0161a0001c0001t0069g0162 | 2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.193-12533C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50595761 | ||||||
| chr16:50595811
|
T | A | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-12483T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50595811 | ||||||
| chr16:50596132
|
T | G | 47 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0023others(44): Show | 48 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.193-12162T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50596132 | ||||||
| chr16:50596257
|
C | T | 4 | a0001c0001t0004g0196a0001c0001t0043g0199a0001c0001t0045g0192others(1): Show | 4 | HG04228.hp1 NA18969.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-12037C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50596257 | ||||||
| chr16:50596374
|
AT | A | 48 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0023others(45): Show | 49 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.193-11910delT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50596374 | |||||
| chr16:50596546
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.193-11748C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50596546 | ||||||
| chr16:50596695
|
G | A | 1 | a0001c0005t0001g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.193-11599G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50596695 | ||||||
| chr16:50596888
|
G | A | 1 | a0001c0001t0004g0111 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-11406G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50596888 | ||||||
| chr16:50596903
|
T | C | 36 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0023others(33): Show | 37 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.193-11391T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50596903 | ||||||
| chr16:50596981
|
G | A | 1 | a0001c0001t0023g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.193-11313G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50596981 | ||||||
| chr16:50597074
|
T | G | 1 | a0001c0001t0010g0175 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.193-11220T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50597074 | ||||||
| chr16:50597266
|
A | G | 2 | a0001c0001t0042g0205a0001c0001t0047g0204 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.193-11028A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50597266 | ||||||
| chr16:50597295
|
G | C | 1 | a0001c0001t0064g0096 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.193-10999G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50597295 | ||||||
| chr16:50597317
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.193-10977G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50597317 | ||||||
| chr16:50597396
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.193-10898C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50597396 | ||||||
| chr16:50597427
|
G | A | 47 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0023others(44): Show | 48 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.193-10867G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50597427 | ||||||
| chr16:50597462
|
G | T | 1 | a0001c0001t0003g0114 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.193-10832G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50597462 | ||||||
| chr16:50597543
|
G | A | 1 | a0001c0001t0065g0071 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.193-10751G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50597543 | ||||||
| chr16:50597572
|
C | T | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-10722C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50597572 | ||||||
| chr16:50597631
|
C | T | 23 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0173others(20): Show | 24 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.193-10663C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50597631 | ||||||
| chr16:50597662
|
C | T | 23 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0173others(20): Show | 24 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.193-10632C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50597662 | ||||||
| chr16:50597733
|
A | C | 1 | a0001c0001t0002g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.193-10561A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50597733 | ||||||
| chr16:50597814
|
G | A | 2 | a0001c0001t0042g0205a0001c0001t0047g0204 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.193-10480G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50597814 | ||||||
| chr16:50597866
|
C | T | 5 | a0001c0001t0006g0063a0001c0001t0006g0064a0001c0001t0006g0067others(2): Show | 5 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-10428C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50597866 | ||||||
| chr16:50598101
|
G | A | 2 | a0001c0001t0015g0131a0001c0001t0015g0143 | 2 | NA18954.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.193-10193G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50598101 | ||||||
| chr16:50598229
|
C | CTG | 64 | a0001c0001t0001g0089a0001c0001t0001g0187a0001c0001t0001g0188others(61): Show | 65 | HG00323.hp2 HG00597.hp1 HG01071.hp1 others(62): Show |
intron_variant | MODIFIER | c.193-10032_193-1003 others(6): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50598229 | |||||
| chr16:50598229
|
C | CTGTG | 27 | a0001c0001t0002g0072a0001c0001t0002g0078a0001c0001t0002g0093others(24): Show | 27 | HG01099.hp1 HG01496.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.193-10034_193-1003 others(8): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50598229 | |||||
| chr16:50598229
|
C | CTGTGTGT others(1): Show |
2 | a0001c0001t0002g0027a0001c0001t0003g0055 | 2 | HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.193-10038_193-1003 others(12): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50598229 | |||||
| chr16:50598229
|
CTG | C | 5 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0036others(2): Show | 5 | HG01516.hp2 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-10032_193-1003 others(6): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50598229 | |||||
| chr16:50598229
|
CTGTG | C | 7 | a0001c0001t0002g0112a0001c0002t0008g0024a0001c0002t0008g0025others(4): Show | 7 | HG02451.hp2 HG02615.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.193-10034_193-1003 others(8): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50598229 | |||||
| chr16:50598262
|
T | C | 9 | a0001c0001t0001g0108a0001c0001t0002g0045a0001c0002t0008g0024others(6): Show | 9 | HG01346.hp2 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-10032T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50598262 | ||||||
| chr16:50598262
|
T | TGTGCGCG others(3): Show |
6 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0010g0175others(3): Show | 6 | HG01192.hp2 HG01952.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-10031_193-1003 others(14): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50598262 | |||||
| chr16:50598262
|
T | TGTGTGCG others(5): Show |
4 | a0001c0001t0005g0164a0001c0001t0005g0166a0001c0001t0021g0165others(1): Show | 4 | HG00280.hp2 HG00408.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-10031_193-1003 others(16): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50598262 | |||||
| chr16:50598262
|
T | TGTGTGTG others(5): Show |
4 | a0001c0001t0003g0173a0001c0001t0020g0001a0001c0001t0042g0205others(1): Show | 5 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-10031_193-1003 others(16): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50598262 | |||||
| chr16:50598262
|
T | TGTGTGTG others(7): Show |
6 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0171others(3): Show | 6 | HG01943.hp2 HG01975.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-10031_193-1003 others(18): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50598262 | |||||
| chr16:50598262
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0050g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.193-10031_193-1003 others(18): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50598262 | |||||
| chr16:50598262
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0069g0162 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.193-10031_193-1003 others(20): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50598262 | |||||
| chr16:50598262
|
T | TGTGTGTG others(9): Show |
3 | a0001c0001t0014g0013a0001c0001t0014g0014a0001c0001t0014g0015 | 3 | HG02559.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.193-10031_193-1003 others(20): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50598262 | |||||
| chr16:50598262
|
T | TGTGTGTG others(17): Show |
1 | a0001c0001t0012g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.193-10031_193-1003 others(28): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50598262 | |||||
| chr16:50598262
|
T | TGTGTGTG others(23): Show |
2 | a0001c0001t0012g0208a0001c0001t0012g0209 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.193-10031_193-1003 others(34): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50598262 | |||||
| chr16:50598298
|
G | A | 8 | a0001c0001t0003g0023a0001c0001t0066g0107a0001c0002t0008g0024others(5): Show | 8 | HG02451.hp2 HG02615.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-9996G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50598298 | ||||||
| chr16:50598359
|
T | A | 1 | a0001c0001t0003g0074 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.193-9935T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50598359 | ||||||
| chr16:50598560
|
C | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0119a0001c0001t0001g0121 | 3 | HG00323.hp1 HG01099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.193-9734C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50598560 | ||||||
| chr16:50598601
|
C | G | 5 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209others(2): Show | 5 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-9693C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50598601 | ||||||
| chr16:50598663
|
A | G | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-9631A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50598663 | ||||||
| chr16:50598669
|
G | A | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-9625G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50598669 | ||||||
| chr16:50598681
|
C | T | 1 | a0001c0004t0001g0030 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.193-9613C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50598681 | ||||||
| chr16:50598715
|
G | T | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.193-9579G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50598715 | ||||||
| chr16:50598736
|
G | T | 4 | a0001c0001t0002g0035a0001c0001t0002g0073a0001c0001t0002g0075others(1): Show | 4 | HG00323.hp2 HG01261.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-9558G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50598736 | ||||||
| chr16:50598789
|
C | T | 2 | a0001c0001t0042g0205a0001c0001t0047g0204 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.193-9505C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50598789 | ||||||
| chr16:50598803
|
G | A | 2 | a0001c0001t0042g0205a0001c0001t0047g0204 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.193-9491G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50598803 | ||||||
| chr16:50598941
|
G | A | 1 | a0001c0001t0002g0027 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.193-9353G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50598941 | ||||||
| chr16:50599087
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.193-9207G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50599087 | ||||||
| chr16:50599147
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.193-9147C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50599147 | ||||||
| chr16:50599255
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.193-9039C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50599255 | ||||||
| chr16:50599272
|
C | T | 2 | a0001c0001t0042g0205a0001c0001t0047g0204 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.193-9022C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50599272 | ||||||
| chr16:50599300
|
C | T | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.193-8994C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50599300 | ||||||
| chr16:50599457
|
T | G | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-8837T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50599457 | ||||||
| chr16:50599566
|
C | T | 2 | a0001c0001t0068g0161a0001c0001t0069g0162 | 2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.193-8728C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50599566 | ||||||
| chr16:50599726
|
G | A | 2 | a0001c0001t0003g0006a0001c0001t0042g0205 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.193-8568G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50599726 | ||||||
| chr16:50599915
|
T | C | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.193-8379T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50599915 | ||||||
| chr16:50599928
|
A | AT | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-8360dupT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50599928 | |||||
| chr16:50600121
|
C | T | 5 | a0001c0001t0007g0100a0001c0001t0007g0113a0001c0001t0007g0125others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-8173C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50600121 | ||||||
| chr16:50600240
|
AAAAC | A | 8 | a0001c0001t0003g0173a0001c0001t0014g0013a0001c0001t0014g0014others(5): Show | 9 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-8035_193-8032d others(6): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 50600240 | |||||
| chr16:50600243
|
A | C | 3 | a0001c0001t0004g0196a0001c0001t0043g0199a0001c0001t0045g0192 | 3 | NA18969.hp1 NA19065.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.193-8051A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50600243 | ||||||
| chr16:50600333
|
T | C | 49 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0023others(46): Show | 50 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.193-7961T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50600333 | ||||||
| chr16:50600496
|
C | A | 15 | a0001c0001t0003g0085a0001c0001t0003g0092a0001c0001t0003g0114others(12): Show | 15 | HG00639.hp1 HG02735.hp1 HG03688.hp2 others(12): Show |
intron_variant | MODIFIER | c.193-7798C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50600496 | ||||||
| chr16:50600620
|
C | T | 1 | a0001c0001t0048g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.193-7674C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50600620 | ||||||
| chr16:50600622
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.193-7672C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50600622 | ||||||
| chr16:50600632
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.193-7662A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50600632 | ||||||
| chr16:50600663
|
G | A | 2 | a0001c0001t0068g0161a0001c0001t0069g0162 | 2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.193-7631G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50600663 | ||||||
| chr16:50600744
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.193-7550A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50600744 | ||||||
| chr16:50600751
|
C | A | 2 | a0001c0001t0022g0091a0001c0001t0022g0128 | 2 | HG01346.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.193-7543C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50600751 | ||||||
| chr16:50600757
|
C | T | 23 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0173others(20): Show | 24 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.193-7537C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50600757 | ||||||
| chr16:50601191
|
G | A | 1 | a0001c0001t0007g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-7103G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50601191 | ||||||
| chr16:50601306
|
A | G | 1 | a0001c0001t0004g0148 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.193-6988A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50601306 | ||||||
| chr16:50601311
|
C | T | 3 | a0001c0001t0009g0017a0001c0001t0009g0021a0001c0001t0009g0022 | 3 | HG02451.hp1 HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.193-6983C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50601311 | ||||||
| chr16:50601445
|
C | T | 1 | a0001c0001t0013g0180 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.193-6849C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50601445 | ||||||
| chr16:50601642
|
C | T | 51 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0023others(48): Show | 52 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.193-6652C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50601642 | ||||||
| chr16:50601876
|
C | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0072 | 2 | HG01099.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.193-6418C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50601876 | ||||||
| chr16:50601892
|
G | A | 1 | a0001c0001t0043g0199 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.193-6402G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50601892 | ||||||
| chr16:50602160
|
G | A | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-6134G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50602160 | ||||||
| chr16:50602322
|
C | T | 15 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0005g0164others(12): Show | 15 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.193-5972C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50602322 | ||||||
| chr16:50602336
|
C | G | 2 | a0001c0001t0003g0154a0001c0001t0003g0155 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.193-5958C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50602336 | ||||||
| chr16:50602340
|
A | G | 4 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0056g0118others(1): Show | 4 | HG02818.hp1 HG03130.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-5954A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50602340 | ||||||
| chr16:50602581
|
T | C | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-5713T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50602581 | ||||||
| chr16:50602899
|
A | G | 42 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0003g0023others(39): Show | 43 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.193-5395A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50602899 | ||||||
| chr16:50602936
|
A | G | 1 | a0001c0001t0004g0053 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.193-5358A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50602936 | ||||||
| chr16:50603085
|
C | T | 2 | a0001c0001t0042g0205a0001c0001t0047g0204 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.193-5209C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50603085 | ||||||
| chr16:50603360
|
C | T | 9 | a0001c0001t0001g0188a0001c0001t0004g0053a0001c0001t0004g0054others(6): Show | 9 | HG00597.hp1 HG02074.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-4934C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50603360 | ||||||
| chr16:50603484
|
C | T | 2 | a0001c0001t0016g0109a0001c0001t0016g0116 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.193-4810C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50603484 | ||||||
| chr16:50603539
|
C | T | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-4755C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50603539 | ||||||
| chr16:50603565
|
C | A | 1 | a0001c0001t0068g0161 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.193-4729C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50603565 | ||||||
| chr16:50603658
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.193-4636A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50603658 | ||||||
| chr16:50604159
|
G | A | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-4135G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50604159 | ||||||
| chr16:50604175
|
G | A | 8 | a0001c0001t0003g0023a0001c0001t0066g0107a0001c0002t0008g0024others(5): Show | 8 | HG02451.hp2 HG02615.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-4119G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50604175 | ||||||
| chr16:50604368
|
A | T | 5 | a0001c0001t0002g0033a0001c0001t0002g0040a0001c0001t0002g0041others(2): Show | 5 | HG01175.hp1 HG03491.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-3926A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50604368 | ||||||
| chr16:50604742
|
G | A | 1 | a0001c0001t0065g0071 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.193-3552G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50604742 | ||||||
| chr16:50605326
|
C | A | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.193-2968C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50605326 | ||||||
| chr16:50605341
|
C | T | 1 | a0001c0001t0067g0087 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.193-2953C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50605341 | ||||||
| chr16:50605361
|
G | A | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-2933G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50605361 | ||||||
| chr16:50605396
|
A | G | 2 | a0001c0001t0003g0023a0001c0001t0066g0107 | 2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.193-2898A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50605396 | ||||||
| chr16:50605687
|
G | A | 8 | a0001c0001t0003g0173a0001c0001t0014g0013a0001c0001t0014g0014others(5): Show | 9 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-2607G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50605687 | ||||||
| chr16:50605734
|
A | G | 5 | a0001c0001t0007g0100a0001c0001t0007g0113a0001c0001t0007g0125others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-2560A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50605734 | ||||||
| chr16:50605798
|
A | G | 3 | a0001c0001t0013g0178a0001c0001t0013g0179a0001c0001t0013g0180 | 3 | HG01255.hp1 HG01516.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.193-2496A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50605798 | ||||||
| chr16:50605856
|
A | C | 1 | a0001c0001t0010g0048 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.193-2438A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50605856 | ||||||
| chr16:50605916
|
C | T | 2 | a0001c0001t0068g0161a0001c0001t0069g0162 | 2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.193-2378C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50605916 | ||||||
| chr16:50606034
|
C | T | 1 | a0001c0002t0008g0024 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.193-2260C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50606034 | ||||||
| chr16:50606201
|
T | G | 33 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(30): Show | 34 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.193-2093T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50606201 | ||||||
| chr16:50606204
|
C | A | 8 | a0001c0001t0003g0173a0001c0001t0014g0013a0001c0001t0014g0014others(5): Show | 9 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-2090C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50606204 | ||||||
| chr16:50606212
|
T | C | 40 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(37): Show | 41 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.193-2082T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50606212 | ||||||
| chr16:50606215
|
G | A | 1 | a0001c0001t0003g0198 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.193-2079G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50606215 | ||||||
| chr16:50606306
|
C | G | 13 | a0001c0001t0002g0088a0001c0001t0002g0099a0001c0001t0006g0063others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.193-1988C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50606306 | ||||||
| chr16:50606620
|
C | A | 2 | a0001c0001t0017g0032a0001c0001t0017g0206 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.193-1674C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50606620 | ||||||
| chr16:50606699
|
C | T | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-1595C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50606699 | ||||||
| chr16:50606777
|
T | G | 1 | a0001c0001t0003g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193-1517T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50606777 | ||||||
| chr16:50606874
|
T | C | 8 | a0001c0001t0003g0173a0001c0001t0014g0013a0001c0001t0014g0014others(5): Show | 9 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-1420T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50606874 | ||||||
| chr16:50606878
|
A | G | 8 | a0001c0001t0003g0023a0001c0001t0066g0107a0001c0002t0008g0024others(5): Show | 8 | HG02451.hp2 HG02615.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-1416A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50606878 | ||||||
| chr16:50606894
|
T | G | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.193-1400T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50606894 | ||||||
| chr16:50607000
|
C | G | 1 | a0001c0001t0033g0016 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.193-1294C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50607000 | ||||||
| chr16:50607282
|
C | T | 1 | a0001c0001t0057g0060 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.193-1012C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50607282 | ||||||
| chr16:50607352
|
T | C | 1 | a0002c0006t0001g0052 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.193-942T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50607352 | ||||||
| chr16:50607362
|
A | G | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-932A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50607362 | ||||||
| chr16:50607508
|
C | T | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193-786C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50607508 | ||||||
| chr16:50607753
|
G | A | 1 | a0001c0001t0016g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.193-541G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50607753 | ||||||
| chr16:50607754
|
G | T | 1 | a0001c0001t0065g0071 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.193-540G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50607754 | ||||||
| chr16:50607797
|
T | C | 5 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209others(2): Show | 5 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-497T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50607797 | ||||||
| chr16:50608077
|
T | C | 41 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(38): Show | 42 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.193-217T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50608077 | ||||||
| chr16:50608119
|
A | C | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193-175A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50608119 | ||||||
| chr16:50608226
|
T | C | 41 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(38): Show | 42 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.193-68T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50608226 | ||||||
| chr16:50608235
|
C | T | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193-59C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50608235 | ||||||
| chr16:50608290
|
G | C | 163 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0031others(160): Show | 165 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(162): Show |
splice_region_variant&intron_variant | LOW | c.193-4G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | chr16 | 50608290 | ||||||
| chr16:50608409
|
C | T | 1 | a0001c0001t0066g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.259+49C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50608409 | ||||||
| chr16:50608453
|
G | T | 22 | a0001c0001t0003g0173a0001c0001t0005g0146a0001c0001t0005g0164others(19): Show | 23 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.259+93G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50608453 | ||||||
| chr16:50608543
|
T | C | 27 | a0001c0001t0003g0173a0001c0001t0005g0146a0001c0001t0005g0164others(24): Show | 28 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.259+183T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50608543 | ||||||
| chr16:50608561
|
C | G | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.259+201C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50608561 | ||||||
| chr16:50608575
|
G | A | 1 | a0001c0001t0018g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259+215G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50608575 | ||||||
| chr16:50608819
|
C | G | 1 | a0001c0001t0002g0099 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.259+459C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50608819 | ||||||
| chr16:50609041
|
T | C | 22 | a0001c0001t0003g0173a0001c0001t0005g0146a0001c0001t0005g0164others(19): Show | 23 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.259+681T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50609041 | ||||||
| chr16:50609105
|
G | A | 3 | a0001c0001t0010g0048a0001c0001t0010g0124a0001c0001t0039g0046 | 3 | NA18970.hp1 NA18988.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.259+745G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50609105 | ||||||
| chr16:50609175
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.259+815C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50609175 | ||||||
| chr16:50609207
|
T | G | 1 | a0001c0001t0029g0105 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.259+847T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50609207 | ||||||
| chr16:50609742
|
G | A | 1 | a0001c0001t0010g0068 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.259+1382G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50609742 | ||||||
| chr16:50610195
|
T | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | HG01943.hp1 HG01975.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+1835T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50610195 | ||||||
| chr16:50610275
|
T | A | 2 | a0001c0001t0068g0161a0001c0001t0069g0162 | 2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.259+1915T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50610275 | ||||||
| chr16:50610568
|
G | A | 1 | a0001c0001t0015g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.259+2208G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50610568 | ||||||
| chr16:50610631
|
T | C | 2 | a0001c0001t0003g0092a0001c0001t0061g0210 | 2 | HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.259+2271T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50610631 | ||||||
| chr16:50610662
|
A | C | 1 | a0001c0001t0002g0027 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.259+2302A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50610662 | ||||||
| chr16:50610700
|
T | C | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.259+2340T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50610700 | ||||||
| chr16:50611077
|
C | T | 8 | a0001c0001t0003g0023a0001c0001t0066g0107a0001c0002t0008g0024others(5): Show | 8 | HG02451.hp2 HG02615.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+2717C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50611077 | ||||||
| chr16:50611295
|
G | A | 1 | a0001c0001t0007g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.259+2935G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50611295 | ||||||
| chr16:50611335
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.259+2975C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50611335 | ||||||
| chr16:50611370
|
G | GGGCGTGG others(17): Show |
46 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(43): Show | 47 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.259+3010_259+3011i others(26): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50611370 | ||||||
| chr16:50611372
|
T | TGC | 46 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(43): Show | 47 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.259+3012_259+3013i others(4): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50611372 | ||||||
| chr16:50611499
|
C | T | 23 | a0001c0001t0003g0173a0001c0001t0004g0142a0001c0001t0005g0146others(20): Show | 24 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.259+3139C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50611499 | ||||||
| chr16:50611546
|
A | T | 1 | a0001c0001t0048g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.259+3186A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50611546 | ||||||
| chr16:50611633
|
G | A | 2 | a0001c0001t0068g0161a0001c0001t0069g0162 | 2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.259+3273G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50611633 | ||||||
| chr16:50611757
|
C | CA | 2 | a0001c0001t0002g0027a0001c0001t0002g0072 | 2 | HG01099.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.259+3398dupA | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 50611757 | |||||
| chr16:50611797
|
C | T | 40 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(37): Show | 41 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.259+3437C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50611797 | ||||||
| chr16:50611871
|
G | C | 36 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(33): Show | 37 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.259+3511G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50611871 | ||||||
| chr16:50611891
|
G | A | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+3531G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50611891 | ||||||
| chr16:50612412
|
A | G | 2 | a0001c0001t0025g0057a0001c0001t0044g0200 | 2 | NA18988.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.259+4052A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50612412 | ||||||
| chr16:50612704
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.259+4344G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50612704 | ||||||
| chr16:50612750
|
A | G | 36 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(33): Show | 37 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.259+4390A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50612750 | ||||||
| chr16:50612884
|
T | G | 47 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(44): Show | 48 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.259+4524T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50612884 | ||||||
| chr16:50612975
|
A | G | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+4615A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50612975 | ||||||
| chr16:50612997
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.259+4637G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50612997 | ||||||
| chr16:50613014
|
G | C | 1 | a0001c0001t0057g0060 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.259+4654G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50613014 | ||||||
| chr16:50613117
|
C | T | 4 | a0001c0001t0011g0010a0001c0001t0011g0011a0001c0001t0011g0012others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+4757C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50613117 | ||||||
| chr16:50613229
|
C | T | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.259+4869C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50613229 | ||||||
| chr16:50613681
|
T | C | 4 | a0001c0001t0002g0035a0001c0001t0002g0073a0001c0001t0002g0075others(1): Show | 4 | HG00323.hp2 HG01261.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+5321T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50613681 | ||||||
| chr16:50613750
|
C | T | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.259+5390C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50613750 | ||||||
| chr16:50613774
|
G | A | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.259+5414G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50613774 | ||||||
| chr16:50613906
|
T | A | 1 | a0001c0001t0061g0210 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259+5546T>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50613906 | ||||||
| chr16:50614141
|
G | T | 2 | a0001c0001t0068g0161a0001c0001t0069g0162 | 2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.259+5781G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50614141 | ||||||
| chr16:50614363
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.259+6003C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50614363 | ||||||
| chr16:50614419
|
G | A | 1 | a0001c0001t0005g0168 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.259+6059G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50614419 | ||||||
| chr16:50614619
|
C | A | 2 | a0001c0001t0046g0082a0002c0006t0001g0052 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.259+6259C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50614619 | ||||||
| chr16:50614977
|
G | T | 2 | a0001c0001t0003g0156a0001c0001t0055g0009 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.259+6617G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50614977 | ||||||
| chr16:50615254
|
A | G | 1 | a0001c0001t0004g0141 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.260-6348A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50615254 | ||||||
| chr16:50615274
|
C | T | 40 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(37): Show | 41 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.260-6328C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50615274 | ||||||
| chr16:50615375
|
T | C | 36 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(33): Show | 37 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.260-6227T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50615375 | ||||||
| chr16:50615807
|
G | C | 1 | a0001c0001t0062g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.260-5795G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50615807 | ||||||
| chr16:50615967
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.260-5635C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50615967 | ||||||
| chr16:50616159
|
C | T | 2 | a0001c0001t0003g0097a0001c0001t0003g0198 | 2 | HG00558.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.260-5443C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50616159 | ||||||
| chr16:50616273
|
A | G | 2 | a0001c0001t0068g0161a0001c0001t0069g0162 | 2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.260-5329A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50616273 | ||||||
| chr16:50616468
|
C | A | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.260-5134C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50616468 | ||||||
| chr16:50617209
|
G | A | 2 | a0001c0001t0004g0152a0001c0001t0004g0203 | 2 | NA19011.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.260-4393G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50617209 | ||||||
| chr16:50617275
|
C | G | 2 | a0001c0001t0068g0161a0001c0001t0069g0162 | 2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.260-4327C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50617275 | ||||||
| chr16:50617315
|
G | A | 1 | a0001c0001t0060g0137 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.260-4287G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50617315 | ||||||
| chr16:50617346
|
G | A | 1 | a0001c0001t0005g0168 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.260-4256G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50617346 | ||||||
| chr16:50617357
|
G | GTCTGT | 40 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(37): Show | 41 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.260-4242_260-4238d others(7): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 50617357 | |||||
| chr16:50617660
|
G | A | 15 | a0001c0001t0003g0023a0001c0001t0011g0010a0001c0001t0011g0011others(12): Show | 15 | HG01109.hp1 HG02451.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.260-3942G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50617660 | ||||||
| chr16:50617702
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.260-3900G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50617702 | ||||||
| chr16:50618110
|
C | T | 2 | a0001c0001t0005g0171a0001c0001t0005g0174 | 2 | NA18992.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.260-3492C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50618110 | ||||||
| chr16:50618147
|
C | T | 1 | a0001c0001t0050g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.260-3455C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50618147 | ||||||
| chr16:50618367
|
T | C | 1 | a0001c0001t0004g0184 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.260-3235T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50618367 | ||||||
| chr16:50618404
|
C | T | 22 | a0001c0001t0003g0173a0001c0001t0005g0146a0001c0001t0005g0164others(19): Show | 23 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.260-3198C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50618404 | ||||||
| chr16:50618581
|
A | G | 40 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(37): Show | 41 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.260-3021A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50618581 | ||||||
| chr16:50618801
|
G | A | 1 | a0001c0001t0067g0087 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.260-2801G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50618801 | ||||||
| chr16:50618831
|
C | T | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.260-2771C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50618831 | ||||||
| chr16:50618986
|
C | T | 2 | a0001c0001t0003g0097a0001c0001t0003g0198 | 2 | HG00558.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.260-2616C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50618986 | ||||||
| chr16:50619247
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.260-2355C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50619247 | ||||||
| chr16:50619365
|
C | T | 1 | a0001c0001t0004g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.260-2237C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50619365 | ||||||
| chr16:50619445
|
C | G | 1 | a0001c0001t0002g0041 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.260-2157C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50619445 | ||||||
| chr16:50619515
|
G | A | 1 | a0001c0001t0028g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.260-2087G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50619515 | ||||||
| chr16:50619602
|
C | T | 2 | a0001c0001t0068g0161a0001c0001t0069g0162 | 2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.260-2000C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50619602 | ||||||
| chr16:50619776
|
A | G | 1 | a0001c0001t0005g0168 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.260-1826A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50619776 | ||||||
| chr16:50619832
|
G | A | 25 | a0001c0001t0003g0173a0001c0001t0005g0146a0001c0001t0005g0164others(22): Show | 26 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.260-1770G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50619832 | ||||||
| chr16:50619871
|
G | C | 40 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0005g0146others(37): Show | 41 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.260-1731G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50619871 | ||||||
| chr16:50619908
|
G | T | 1 | a0001c0002t0008g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.260-1694G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50619908 | ||||||
| chr16:50620081
|
G | A | 1 | a0001c0001t0003g0074 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.260-1521G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50620081 | ||||||
| chr16:50620464
|
A | T | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0031others(82): Show | 86 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.260-1138A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50620464 | ||||||
| chr16:50620522
|
C | T | 1 | a0001c0001t0004g0196 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.260-1080C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50620522 | ||||||
| chr16:50620737
|
C | T | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.260-865C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50620737 | ||||||
| chr16:50620819
|
A | G | 2 | a0001c0001t0033g0016a0001c0001t0066g0107 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.260-783A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50620819 | ||||||
| chr16:50620926
|
G | A | 1 | a0001c0001t0048g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.260-676G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50620926 | ||||||
| chr16:50621056
|
C | T | 40 | a0001c0001t0005g0146a0001c0001t0005g0164a0001c0001t0005g0166others(37): Show | 41 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.260-546C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50621056 | ||||||
| chr16:50621329
|
G | A | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.260-273G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50621329 | ||||||
| chr16:50621395
|
G | A | 1 | a0001c0001t0002g0027 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.260-207G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50621395 | ||||||
| chr16:50621492
|
C | A | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.260-110C>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50621492 | ||||||
| chr16:50621492
|
C | G | 1 | a0001c0001t0005g0164 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.260-110C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50621492 | ||||||
| chr16:50621501
|
G | A | 1 | a0001c0001t0003g0092 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.260-101G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 4/9 | chr16 | 50621501 | ||||||
| chr16:50621779
|
G | C | 1 | a0001c0001t0024g0005 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.366+71G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50621779 | ||||||
| chr16:50621820
|
C | T | 2 | a0001c0001t0016g0109a0001c0001t0016g0116 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.366+112C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50621820 | ||||||
| chr16:50621852
|
T | G | 2 | a0001c0001t0014g0013a0001c0001t0014g0014 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.366+144T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50621852 | ||||||
| chr16:50621867
|
C | T | 1 | a0001c0001t0047g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.366+159C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50621867 | ||||||
| chr16:50622135
|
T | C | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.366+427T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50622135 | ||||||
| chr16:50622139
|
G | T | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.366+431G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50622139 | ||||||
| chr16:50622159
|
C | T | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.366+451C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50622159 | ||||||
| chr16:50622482
|
G | C | 2 | a0001c0001t0068g0161a0001c0001t0069g0162 | 2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.366+774G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50622482 | ||||||
| chr16:50622808
|
G | A | 1 | a0001c0001t0006g0063 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.366+1100G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50622808 | ||||||
| chr16:50622980
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0022g0091a0001c0001t0022g0128 | 3 | HG01346.hp1 HG02602.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.366+1272C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50622980 | ||||||
| chr16:50623213
|
T | C | 32 | a0001c0001t0005g0146a0001c0001t0005g0164a0001c0001t0005g0166others(29): Show | 33 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.366+1505T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50623213 | ||||||
| chr16:50623415
|
G | A | 1 | a0001c0001t0018g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.366+1707G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50623415 | ||||||
| chr16:50623482
|
G | C | 7 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(4): Show | 7 | HG01109.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.366+1774G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50623482 | ||||||
| chr16:50623567
|
A | C | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.366+1859A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50623567 | ||||||
| chr16:50623725
|
C | CTG | 16 | a0001c0001t0001g0098a0001c0001t0002g0163a0001c0001t0003g0185others(13): Show | 17 | HG01993.hp2 HG02074.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.367-1722_367-1721d others(4): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 50623725 | |||||
| chr16:50623725
|
C | CTGTG | 8 | a0001c0001t0003g0092a0001c0001t0003g0097a0001c0001t0014g0013others(5): Show | 8 | HG00558.hp1 HG02559.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.367-1724_367-1721d others(6): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 50623725 | |||||
| chr16:50623725
|
C | CTGTGTG | 2 | a0001c0001t0003g0198a0001c0001t0047g0204 | 2 | HG03098.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.367-1726_367-1721d others(8): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 50623725 | |||||
| chr16:50623725
|
C | CTGTGTGT others(3): Show |
3 | a0001c0001t0005g0164a0001c0001t0005g0167a0001c0001t0053g0160 | 3 | HG01943.hp2 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.367-1730_367-1721d others(12): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 50623725 | |||||
| chr16:50623725
|
C | CTGTGTGT others(5): Show |
8 | a0001c0001t0005g0146a0001c0001t0005g0166a0001c0001t0005g0174others(5): Show | 8 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.367-1732_367-1721d others(14): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 50623725 | |||||
| chr16:50623725
|
C | CTGTGTGT others(7): Show |
1 | a0001c0001t0005g0171 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.367-1734_367-1721d others(16): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 50623725 | |||||
| chr16:50623725
|
CTG | C | 26 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(23): Show | 26 | HG00741.hp2 HG01884.hp2 HG01943.hp1 others(23): Show |
intron_variant | MODIFIER | c.367-1722_367-1721d others(4): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 50623725 | |||||
| chr16:50623725
|
CTGTG | C | 11 | a0001c0001t0002g0033a0001c0001t0002g0040a0001c0001t0012g0207others(8): Show | 11 | HG02451.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.367-1724_367-1721d others(6): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | 50623725 | |||||
| chr16:50623751
|
G | A | 1 | a0001c0001t0019g0201 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.367-1734G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50623751 | ||||||
| chr16:50623996
|
G | A | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.367-1489G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50623996 | ||||||
| chr16:50624248
|
C | G | 1 | a0001c0001t0004g0196 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.367-1237C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50624248 | ||||||
| chr16:50624338
|
G | A | 5 | a0001c0001t0007g0100a0001c0001t0007g0113a0001c0001t0007g0125others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.367-1147G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50624338 | ||||||
| chr16:50624634
|
G | T | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.367-851G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50624634 | ||||||
| chr16:50624651
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.367-834C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50624651 | ||||||
| chr16:50624737
|
G | A | 2 | a0001c0001t0020g0001a0001c0001t0051g0172 | 3 | HG02109.hp1 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.367-748G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50624737 | ||||||
| chr16:50625107
|
C | T | 1 | a0001c0002t0054g0026 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.367-378C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50625107 | ||||||
| chr16:50625124
|
G | T | 7 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(4): Show | 7 | HG01109.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-361G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50625124 | ||||||
| chr16:50625394
|
C | T | 1 | a0001c0001t0066g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.367-91C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 5/9 | chr16 | 50625394 | ||||||
| chr16:50625621
|
G | A | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.462+41G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50625621 | ||||||
| chr16:50625676
|
C | T | 1 | a0001c0001t0004g0054 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.462+96C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50625676 | ||||||
| chr16:50625848
|
G | GA | 94 | a0001c0001t0002g0003a0001c0001t0002g0027a0001c0001t0002g0029others(91): Show | 95 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.462+268_462+269ins others(1): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50625848 | ||||||
| chr16:50625900
|
G | A | 1 | a0001c0001t0066g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.462+320G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50625900 | ||||||
| chr16:50625952
|
C | T | 2 | a0001c0001t0020g0001a0001c0001t0051g0172 | 3 | HG02109.hp1 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.462+372C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50625952 | ||||||
| chr16:50626033
|
C | T | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.462+453C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50626033 | ||||||
| chr16:50626234
|
A | G | 111 | a0001c0001t0002g0003a0001c0001t0002g0027a0001c0001t0002g0029others(108): Show | 112 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.462+654A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50626234 | ||||||
| chr16:50626393
|
G | T | 1 | a0001c0001t0066g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.462+813G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50626393 | ||||||
| chr16:50626417
|
A | G | 1 | a0001c0001t0007g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.462+837A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50626417 | ||||||
| chr16:50626575
|
G | A | 1 | a0001c0001t0003g0074 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.462+995G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50626575 | ||||||
| chr16:50626588
|
A | G | 1 | a0001c0001t0066g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.462+1008A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50626588 | ||||||
| chr16:50626735
|
CCCTGTCC others(11): Show |
C | 2 | a0001c0001t0017g0032a0001c0001t0017g0206 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.462+1166_462+1183d others(20): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr16 | 50626735 | |||||
| chr16:50626765
|
C | T | 4 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0056g0118others(1): Show | 4 | HG02818.hp1 HG03130.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+1185C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50626765 | ||||||
| chr16:50626767
|
G | A | 4 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0056g0118others(1): Show | 4 | HG02818.hp1 HG03130.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+1187G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50626767 | ||||||
| chr16:50626827
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.462+1247C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50626827 | ||||||
| chr16:50626853
|
G | A | 90 | a0001c0001t0002g0003a0001c0001t0002g0027a0001c0001t0002g0029others(87): Show | 91 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.462+1273G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50626853 | ||||||
| chr16:50626928
|
C | T | 1 | a0001c0001t0066g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.462+1348C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50626928 | ||||||
| chr16:50627051
|
G | A | 90 | a0001c0001t0002g0003a0001c0001t0002g0027a0001c0001t0002g0029others(87): Show | 91 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.462+1471G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50627051 | ||||||
| chr16:50627053
|
G | T | 1 | a0001c0001t0002g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.462+1473G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50627053 | ||||||
| chr16:50627138
|
T | G | 1 | a0001c0001t0046g0082 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.462+1558T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50627138 | ||||||
| chr16:50627362
|
A | C | 17 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0050others(14): Show | 17 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.462+1782A>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50627362 | ||||||
| chr16:50627397
|
G | A | 1 | a0001c0001t0004g0111 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.462+1817G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50627397 | ||||||
| chr16:50627431
|
A | G | 3 | a0001c0001t0012g0207a0001c0001t0012g0208a0001c0001t0012g0209 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.462+1851A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50627431 | ||||||
| chr16:50628222
|
C | T | 1 | a0001c0001t0010g0068 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.463-1964C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50628222 | ||||||
| chr16:50628293
|
C | T | 4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0098others(1): Show | 4 | HG01496.hp2 HG03831.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-1893C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50628293 | ||||||
| chr16:50628398
|
C | G | 1 | a0001c0001t0066g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.463-1788C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50628398 | ||||||
| chr16:50628539
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.463-1647C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50628539 | ||||||
| chr16:50628881
|
C | T | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-1305C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50628881 | ||||||
| chr16:50628933
|
G | A | 79 | a0001c0001t0002g0003a0001c0001t0002g0027a0001c0001t0002g0029others(76): Show | 80 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.463-1253G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50628933 | ||||||
| chr16:50628946
|
G | C | 2 | a0001c0001t0009g0018a0001c0001t0009g0019 | 2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.463-1240G>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50628946 | ||||||
| chr16:50628956
|
C | CT | 101 | a0001c0001t0001g0134a0001c0001t0002g0003a0001c0001t0002g0027others(98): Show | 102 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.463-1214dupT | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr16 | 50628956 | |||||
| chr16:50628956
|
C | CTT | 7 | a0001c0001t0004g0142a0001c0002t0008g0024a0001c0002t0008g0025others(4): Show | 7 | HG02451.hp2 HG02615.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.463-1215_463-1214d others(4): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr16 | 50628956 | |||||
| chr16:50628975
|
T | C | 1 | a0001c0001t0040g0123 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.463-1211T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50628975 | ||||||
| chr16:50629014
|
G | A | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-1172G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50629014 | ||||||
| chr16:50629034
|
C | T | 1 | a0001c0001t0012g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.463-1152C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50629034 | ||||||
| chr16:50629250
|
A | G | 1 | a0001c0001t0066g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.463-936A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50629250 | ||||||
| chr16:50629566
|
G | A | 1 | a0001c0001t0049g0170 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.463-620G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50629566 | ||||||
| chr16:50629792
|
A | G | 1 | a0001c0001t0066g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.463-394A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50629792 | ||||||
| chr16:50629912
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.463-274G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50629912 | ||||||
| chr16:50629963
|
C | G | 1 | a0001c0001t0027g0043 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.463-223C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50629963 | ||||||
| chr16:50630050
|
C | T | 1 | a0001c0001t0026g0120 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.463-136C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50630050 | ||||||
| chr16:50630062
|
C | T | 1 | a0001c0001t0003g0186 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.463-124C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50630062 | ||||||
| chr16:50630123
|
G | A | 1 | a0001c0001t0036g0157 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.463-63G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 6/9 | chr16 | 50630123 | ||||||
| chr16:50630610
|
G | T | 4 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0056g0118others(1): Show | 4 | HG02818.hp1 HG03130.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.611-216G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 7/9 | chr16 | 50630610 | ||||||
| chr16:50630817
|
C | T | 1 | a0001c0001t0011g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.611-9C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 7/9 | chr16 | 50630817 | ||||||
| chr16:50631178
|
T | G | 86 | a0001c0001t0002g0003a0001c0001t0002g0027a0001c0001t0002g0029others(83): Show | 87 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.695+268T>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 8/9 | chr16 | 50631178 | ||||||
| chr16:50631333
|
A | G | 1 | a0001c0001t0052g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.695+423A>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 8/9 | chr16 | 50631333 | ||||||
| chr16:50631337
|
G | T | 1 | a0001c0001t0066g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.695+427G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 8/9 | chr16 | 50631337 | ||||||
| chr16:50631371
|
A | T | 1 | a0001c0001t0066g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.695+461A>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 8/9 | chr16 | 50631371 | ||||||
| chr16:50631523
|
C | T | 1 | a0001c0001t0048g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.695+613C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 8/9 | chr16 | 50631523 | ||||||
| chr16:50631544
|
G | A | 6 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0008g0083others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+634G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 8/9 | chr16 | 50631544 | ||||||
| chr16:50631553
|
G | A | 11 | a0001c0001t0005g0146a0001c0001t0005g0164a0001c0001t0005g0166others(8): Show | 11 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.695+643G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 8/9 | chr16 | 50631553 | ||||||
| chr16:50631999
|
C | G | 1 | a0001c0001t0042g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.696-282C>G | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 8/9 | chr16 | 50631999 | ||||||
| chr16:50632099
|
C | T | 1 | a0001c0001t0016g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.696-182C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 8/9 | chr16 | 50632099 | ||||||
| chr16:50632462
|
G | T | 1 | a0002c0006t0001g0052 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.823+54G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 9/9 | chr16 | 50632462 | ||||||
| chr16:50632481
|
G | A | 1 | a0001c0001t0038g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.823+73G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 9/9 | chr16 | 50632481 | ||||||
| chr16:50632655
|
T | C | 103 | a0001c0001t0002g0003a0001c0001t0002g0027a0001c0001t0002g0029others(100): Show | 104 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.823+247T>C | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 9/9 | chr16 | 50632655 | ||||||
| chr16:50632740
|
G | T | 1 | a0001c0001t0004g0196 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.823+332G>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 9/9 | chr16 | 50632740 | ||||||
| chr16:50632908
|
C | T | 6 | a0001c0002t0008g0024a0001c0002t0008g0025a0001c0002t0008g0083others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-284C>T | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 9/9 | chr16 | 50632908 | ||||||
| chr16:50632970
|
G | A | 5 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-222G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 9/9 | chr16 | 50632970 | ||||||
| chr16:50633141
|
G | A | 3 | a0001c0001t0048g0069a0001c0001t0068g0161a0001c0001t0069g0162 | 3 | HG01109.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.824-51G>A | NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 9/9 | chr16 | 50633141 |