Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4883 |
|---|---|
| ensemblid | ENSG00000113389.16 |
| hgncid | 7945 |
| symbol | NPR3 |
| name | natriuretic peptide receptor 3 |
| refseq_nuc | NM_001204375.2 |
| refseq_prot | NP_001191304.1 |
| ensembl_nuc | ENST00000265074.13 |
| ensembl_prot | ENSP00000265074.8 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 32711321 |
| end | 32791720 |
| strand | + |
| ver | v1.2 |
| region | chr5:32711321-32791720 |
| region5000 | chr5:32706321-32796720 |
| regionname0 | NPR3_chr5_32711321_32791720 |
| regionname5000 | NPR3_chr5_32706321_32796720 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 541 | 252 | 80 | 47 | 91 | 8 | 24 | 64 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0002 | 0/0 | 541 | 68 | 8 | 11 | 33 | 4 | 12 | 28 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1626 | 235 | 64 | 46 | 91 | 8 | 24 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| c0002 | 0/0 | 1626 | 68 | 8 | 11 | 33 | 4 | 12 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| c0003 | 0/0 | 1626 | 14 | 13 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| c0004 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| c0005 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| c0006 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 5838 | 91 | 14 | 17 | 41 | 4 | 15 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0002 | 0/0 | 5838 | 49 | 7 | 4 | 28 | 3 | 7 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0003 | 0/0 | 5836 | 47 | 1 | 3 | 39 | 0 | 4 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0004 | 0/0 | 5838 | 18 | 8 | 5 | 0 | 1 | 4 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0005 | 0/0 | 5852 | 9 | 9 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0006 | 0/0 | 5838 | 6 | 5 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0007 | 0/0 | 5838 | 6 | 4 | 2 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0008 | 0/0 | 5853 | 5 | 5 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0009 | 1/0 | 5832 | 5 | 0 | 1 | 3 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0010 | 0/1 | 5836 | 4 | 0 | 3 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0011 | 0/0 | 5838 | 4 | 0 | 1 | 1 | 1 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0012 | 0/0 | 5838 | 4 | 0 | 4 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0013 | 0/0 | 5844 | 3 | 0 | 3 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0014 | 0/0 | 5838 | 2 | 0 | 2 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0015 | 0/0 | 5838 | 2 | 0 | 1 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0016 | 0/0 | 5844 | 2 | 0 | 2 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0017 | 0/0 | 5838 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0018 | 0/0 | 5838 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0019 | 0/0 | 5838 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0020 | 0/0 | 5838 | 2 | 0 | 0 | 2 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0021 | 0/0 | 5838 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0022 | 0/0 | 5836 | 2 | 0 | 0 | 0 | 1 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0023 | 0/0 | 5852 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0024 | 0/0 | 5852 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0025 | 0/0 | 5839 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0026 | 0/0 | 5853 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0027 | 0/0 | 5832 | 2 | 1 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0028 | 0/0 | 5836 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0029 | 0/0 | 5838 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0030 | 0/0 | 5841 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0031 | 0/0 | 5842 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0032 | 0/0 | 5836 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0033 | 0/0 | 5838 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0034 | 0/0 | 5838 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0035 | 0/0 | 5838 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0036 | 0/0 | 5838 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0037 | 0/0 | 5838 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0038 | 0/0 | 5838 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0039 | 0/0 | 5838 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0040 | 0/0 | 5838 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0041 | 0/0 | 5838 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0042 | 0/0 | 5838 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0043 | 0/0 | 5838 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0044 | 0/0 | 5838 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0045 | 0/0 | 5838 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0046 | 0/0 | 5838 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0047 | 0/0 | 5838 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0048 | 0/0 | 5838 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0049 | 0/0 | 5838 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0050 | 0/0 | 5838 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0051 | 0/0 | 5838 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0052 | 0/0 | 5838 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0053 | 0/0 | 5836 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0054 | 0/0 | 5838 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0055 | 0/0 | 5838 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0056 | 0/0 | 5838 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0057 | 0/0 | 5838 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0058 | 0/0 | 5838 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0059 | 0/0 | 5840 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0060 | 0/0 | 5852 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0061 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0062 | 0/0 | 5852 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0063 | 0/0 | 5852 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0064 | 0/0 | 5839 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0065 | 0/0 | 5839 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0066 | 0/0 | 5837 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0067 | 0/0 | 5830 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| t0068 | 0/0 | 5830 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1626 | 235 | 64 | 46 | 91 | 8 | 24 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0003 | 0/0 | 1626 | 14 | 13 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0004 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0005 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0006 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0002c0002 | 0/0 | 1626 | 68 | 8 | 11 | 33 | 4 | 12 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7463 | 90 | 14 | 16 | 41 | 4 | 15 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0002 | 0/0 | 7463 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0003 | 0/0 | 7461 | 47 | 1 | 3 | 39 | 0 | 4 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0004 | 0/0 | 7463 | 17 | 7 | 5 | 0 | 1 | 4 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0005 | 0/0 | 7477 | 3 | 3 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0006 | 0/0 | 7463 | 6 | 5 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0007 | 0/0 | 7463 | 6 | 4 | 2 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0008 | 0/0 | 7478 | 4 | 4 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0009 | 1/0 | 7457 | 5 | 0 | 1 | 3 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0010 | 0/1 | 7461 | 4 | 0 | 3 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0013 | 0/0 | 7469 | 3 | 0 | 3 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0014 | 0/0 | 7463 | 2 | 0 | 2 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0015 | 0/0 | 7463 | 2 | 0 | 1 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0017 | 0/0 | 7463 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0019 | 0/0 | 7463 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0021 | 0/0 | 7463 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0022 | 0/0 | 7461 | 2 | 0 | 0 | 0 | 1 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0024 | 0/0 | 7477 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0025 | 0/0 | 7464 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0026 | 0/0 | 7478 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0028 | 0/0 | 7461 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0030 | 0/0 | 7466 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0031 | 0/0 | 7467 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0032 | 0/0 | 7461 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0034 | 0/0 | 7463 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0036 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0037 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0038 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0039 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0040 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0041 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0042 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0043 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0045 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0046 | 0/0 | 7463 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0047 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0048 | 0/0 | 7463 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0049 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0050 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0051 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0053 | 0/0 | 7461 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0055 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0057 | 0/0 | 7463 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0059 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0060 | 0/0 | 7477 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0064 | 0/0 | 7464 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0065 | 0/0 | 7464 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0066 | 0/0 | 7462 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0067 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0001t0068 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0003t0001 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0003t0004 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0003t0005 | 0/0 | 7477 | 6 | 6 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0003t0008 | 0/0 | 7478 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0003t0023 | 0/0 | 7477 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0003t0044 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0003t0058 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0003t0063 | 0/0 | 7477 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0004t0062 | 0/0 | 7477 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0005t0056 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0001c0006t0061 | 0/0 | 7478 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0002c0002t0002 | 0/0 | 7463 | 47 | 5 | 4 | 28 | 3 | 7 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0002c0002t0011 | 0/0 | 7463 | 4 | 0 | 1 | 1 | 1 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0002c0002t0012 | 0/0 | 7463 | 4 | 0 | 4 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0002c0002t0016 | 0/0 | 7469 | 2 | 0 | 2 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0002c0002t0018 | 0/0 | 7463 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0002c0002t0020 | 0/0 | 7463 | 2 | 0 | 0 | 2 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0002c0002t0027 | 0/0 | 7457 | 2 | 1 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0002c0002t0029 | 0/0 | 7463 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0002c0002t0033 | 0/0 | 7463 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0002c0002t0035 | 0/0 | 7463 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0002c0002t0052 | 0/0 | 7463 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| a0002c0002t0054 | 0/0 | 7463 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | copy fasta | chr5 | 32706321 | 32796720 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0007g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0009g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0009g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0009g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0009g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0009g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0010g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0010g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0010g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0010g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0013g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0013g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0013g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0014g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0014g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0015g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0015g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0017g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0017g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0019g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0019g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0021g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0021g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0022g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0022g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0024g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0024g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0025g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0025g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0026g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0026g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0028g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0030g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0031g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0032g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0034g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0036g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0037g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0038g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0039g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0040g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0041g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0042g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0043g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0045g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0046g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0047g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0048g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0049g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0050g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0051g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0053g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0055g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0057g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0059g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0060g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0064g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0065g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0066g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0067g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0001t0068g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0003t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0003t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0003t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0003t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0003t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0003t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0003t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0003t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0003t0023g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0003t0023g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0003t0044g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0003t0058g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0003t0063g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0004t0062g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0005t0056g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0001c0006t0061g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0011g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0011g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0011g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0011g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0012g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0012g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0012g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0012g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0016g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0016g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0018g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0018g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0020g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0020g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0027g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0027g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0029g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0033g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0035g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0052g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| a0002c0002t0054g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0228 | EUR | GBR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00280 | hp1 | a0001 | c0001 | t0015 | g0107 | EUR | FIN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00280 | hp2 | a0001 | c0001 | t0022 | g0223 | EUR | FIN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00323 | hp2 | a0001 | c0001 | t0046 | g0289 | EUR | FIN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0158 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00642 | hp2 | a0002 | c0002 | t0012 | g0082 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00735 | hp2 | a0001 | c0001 | t0045 | g0081 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0092 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00738 | hp2 | a0001 | c0001 | t0038 | g0018 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0146 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01070 | hp1 | a0001 | c0001 | t0010 | g0121 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0106 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01074 | hp1 | a0001 | c0001 | t0047 | g0110 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01099 | hp2 | a0002 | c0002 | t0012 | g0297 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01106 | hp1 | a0002 | c0002 | t0012 | g0083 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0150 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0032 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01168 | hp1 | a0001 | c0001 | t0010 | g0103 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01168 | hp2 | a0001 | c0001 | t0049 | g0013 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01169 | hp1 | a0001 | c0001 | t0010 | g0080 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01175 | hp2 | a0001 | c0001 | t0036 | g0009 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01192 | hp1 | a0001 | c0001 | t0055 | g0145 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0113 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01256 | hp1 | a0001 | c0001 | t0028 | g0100 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01257 | hp2 | a0001 | c0001 | t0014 | g0108 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01258 | hp2 | a0001 | c0001 | t0014 | g0109 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01261 | hp1 | a0001 | c0001 | t0040 | g0161 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0153 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0281 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01433 | hp1 | a0002 | c0002 | t0012 | g0014 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01516 | hp1 | a0002 | c0002 | t0011 | g0130 | EUR | IBS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0147 | EUR | IBS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01884 | hp1 | a0001 | c0001 | t0021 | g0084 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01934 | hp1 | a0001 | c0001 | t0013 | g0283 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0137 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01952 | hp1 | a0001 | c0001 | t0015 | g0123 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01952 | hp2 | a0001 | c0001 | t0013 | g0280 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01978 | hp1 | a0002 | c0002 | t0011 | g0262 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01978 | hp2 | a0001 | c0001 | t0009 | g0159 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01981 | hp2 | a0002 | c0002 | t0016 | g0276 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG01993 | hp2 | a0001 | c0001 | t0030 | g0288 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02040 | hp1 | a0002 | c0002 | t0020 | g0090 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02055 | hp1 | a0002 | c0002 | t0027 | g0128 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02055 | hp2 | a0001 | c0006 | t0061 | g0041 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02074 | hp1 | a0001 | c0001 | t0053 | g0315 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02080 | hp1 | a0001 | c0001 | t0032 | g0221 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0206 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0162 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | CDX | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CDX | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0305 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02258 | hp2 | a0001 | c0003 | t0005 | g0027 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0079 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02293 | hp1 | a0001 | c0001 | t0013 | g0279 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02293 | hp2 | a0002 | c0002 | t0016 | g0294 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0042 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0199 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0058 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02615 | hp2 | a0001 | c0001 | t0050 | g0047 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02622 | hp1 | a0001 | c0003 | t0023 | g0038 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02622 | hp2 | a0001 | c0001 | t0026 | g0049 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0066 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0114 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0008 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02698 | hp1 | a0002 | c0002 | t0054 | g0167 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02717 | hp1 | a0001 | c0001 | t0066 | g0053 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02717 | hp2 | a0001 | c0003 | t0008 | g0031 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02723 | hp1 | a0001 | c0001 | t0043 | g0067 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0298 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02735 | hp2 | a0001 | c0001 | t0022 | g0020 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0065 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0055 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0271 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02818 | hp2 | a0001 | c0001 | t0025 | g0048 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02886 | hp1 | a0001 | c0003 | t0058 | g0035 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02886 | hp2 | a0001 | c0001 | t0019 | g0003 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02895 | hp1 | a0002 | c0002 | t0018 | g0077 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02895 | hp2 | a0001 | c0001 | t0039 | g0267 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02896 | hp1 | a0001 | c0003 | t0023 | g0039 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02897 | hp1 | a0002 | c0002 | t0018 | g0076 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0304 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02922 | hp2 | a0001 | c0001 | t0026 | g0052 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0064 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02965 | hp2 | a0001 | c0003 | t0005 | g0034 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02970 | hp1 | a0001 | c0003 | t0005 | g0028 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02970 | hp2 | a0001 | c0001 | t0041 | g0148 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0127 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02976 | hp2 | a0001 | c0001 | t0021 | g0140 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03041 | hp1 | a0001 | c0003 | t0005 | g0029 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0303 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03130 | hp1 | a0001 | c0001 | t0060 | g0293 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0306 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03139 | hp1 | a0001 | c0001 | t0059 | g0155 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03139 | hp2 | a0001 | c0001 | t0025 | g0050 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0072 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03225 | hp1 | a0001 | c0001 | t0051 | g0270 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03225 | hp2 | a0001 | c0003 | t0005 | g0033 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0026 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03453 | hp1 | a0001 | c0001 | t0019 | g0002 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0074 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0241 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03516 | hp2 | a0001 | c0001 | t0042 | g0045 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03540 | hp2 | a0001 | c0003 | t0044 | g0036 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03579 | hp1 | a0001 | c0001 | t0017 | g0057 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03579 | hp2 | a0001 | c0003 | t0063 | g0040 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0073 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0179 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0125 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0111 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03831 | hp2 | a0002 | c0002 | t0029 | g0104 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03834 | hp1 | a0002 | c0002 | t0052 | g0165 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03927 | hp1 | a0002 | c0002 | t0035 | g0124 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0174 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0255 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0273 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0173 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG04228 | hp2 | a0002 | c0002 | t0011 | g0263 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18522 | hp1 | a0001 | c0001 | t0064 | g0054 | AFR | YRI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18522 | hp2 | a0001 | c0003 | t0005 | g0030 | AFR | YRI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18612 | hp1 | a0001 | c0001 | t0048 | g0307 | EAS | CHB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | CHB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0144 | AFR | YRI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18941 | hp2 | a0001 | c0001 | t0009 | g0310 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0312 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18963 | hp1 | a0002 | c0002 | t0033 | g0219 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18967 | hp1 | a0001 | c0001 | t0009 | g0160 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18967 | hp2 | a0001 | c0001 | t0068 | g0233 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18988 | hp2 | a0002 | c0002 | t0011 | g0264 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19011 | hp2 | a0001 | c0001 | t0009 | g0193 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19030 | hp1 | a0001 | c0005 | t0056 | g0268 | AFR | LWK | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0046 | AFR | LWK | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19043 | hp1 | a0001 | c0001 | t0024 | g0286 | AFR | LWK | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19043 | hp2 | a0001 | c0001 | t0065 | g0051 | AFR | LWK | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19058 | hp2 | a0002 | c0002 | t0027 | g0230 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19060 | hp2 | a0002 | c0002 | t0020 | g0227 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19070 | hp1 | a0001 | c0001 | t0031 | g0295 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19081 | hp1 | a0001 | c0001 | t0057 | g0282 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19087 | hp1 | a0001 | c0001 | t0034 | g0157 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19088 | hp2 | a0001 | c0001 | t0067 | g0266 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0314 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA19240 | hp2 | a0001 | c0003 | t0004 | g0037 | AFR | YRI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | ASW | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ASW | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0296 | EUR | TSI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0274 | EUR | TSI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0275 | EUR | TSI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0287 | EUR | TSI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02109 | hp1 | a0001 | c0001 | t0037 | g0059 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02109 | hp2 | a0001 | c0004 | t0062 | g0134 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0151 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0204 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03471 | hp1 | a0001 | c0001 | t0024 | g0265 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | LWK | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | LWK | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0010 | g0118 | REF | REF | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0009 | g0189 | REF | REF | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:32786283
|
A | G | 1 | a0002 | 68 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(65): Show |
missense_variant | MODERATE | c.1564A>G | p.Asn522Asp | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2020/7457 | 1564/1626 | 522/541 | chr5 | 32786283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:32712013
|
T | C | 1 | a0001c0003 | 14 | HG01109.hp2 HG02258.hp2 HG02622.hp1 others(11): Show |
synonymous_variant | LOW | c.237T>C | p.Ala79Ala | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 693/7457 | 237/1626 | 79/541 | chr5 | 32712013 | ||
| chr5:32774734
|
C | T | 1 | a0001c0006 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.1086C>T | p.His362His | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/8 | 1542/7457 | 1086/1626 | 362/541 | chr5 | 32774734 | ||
| chr5:32780759
|
C | T | 1 | a0001c0005 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1233C>T | p.Asp411Asp | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/8 | 1689/7457 | 1233/1626 | 411/541 | chr5 | 32780759 | ||
| chr5:32784833
|
C | T | 2 | a0001c0004a0001c0006 | 2 | HG02055.hp2 HG02109.hp2 |
synonymous_variant | LOW | c.1464C>T | p.Val488Val | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/8 | 1920/7457 | 1464/1626 | 488/541 | chr5 | 32784833 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:32711527
|
C | A | 6 | a0001c0001t0010a0001c0001t0014a0001c0001t0015others(3): Show | 14 | HG00280.hp1 HG01070.hp1 HG01168.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-250C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 250 | chr5 | 32711527 | |||||
| chr5:32711547
|
A | ACTTTTT | 60 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(57): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
5_prime_UTR_variant | MODIFIER | c.-211_-206dupCTTTTT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 205 | INFO_REALIGN_3_PRIME | chr5 | 32711547 | ||||
| chr5:32711547
|
A | ACTTTTTC others(5): Show |
3 | a0001c0001t0013a0001c0001t0031a0002c0002t0016 | 6 | HG01934.hp1 HG01952.hp2 HG01981.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-217_-206dupCTTTTT others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 205 | INFO_REALIGN_3_PRIME | chr5 | 32711547 | ||||
| chr5:32711566
|
C | CTTTTTCT | 5 | a0001c0001t0025a0001c0001t0026a0001c0001t0064others(2): Show | 7 | HG02622.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-206_-205insCTTTTT others(1): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 205 | INFO_REALIGN_3_PRIME | chr5 | 32711566 | ||||
| chr5:32711567
|
T | TTTTTCTT others(4): Show |
1 | a0001c0001t0030 | 1 | HG01993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-206_-205insCTTTTT others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 205 | INFO_REALIGN_3_PRIME | chr5 | 32711567 | ||||
| chr5:32711576
|
T | A | 2 | a0001c0001t0006a0001c0001t0017 | 8 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-201T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 201 | chr5 | 32711576 | |||||
| chr5:32711771
|
G | C | 5 | a0001c0001t0025a0001c0001t0026a0001c0001t0064others(2): Show | 7 | HG02622.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-6G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 6 | chr5 | 32711771 | |||||
| chr5:32786531
|
T | C | 1 | a0002c0002t0018 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*186T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 186 | chr5 | 32786531 | |||||
| chr5:32786545
|
A | G | 7 | a0001c0001t0005a0001c0001t0024a0001c0001t0026others(4): Show | 16 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*200A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 200 | chr5 | 32786545 | |||||
| chr5:32786573
|
T | C | 1 | a0001c0001t0019 | 2 | HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*228T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 228 | chr5 | 32786573 | |||||
| chr5:32786600
|
C | G | 12 | a0001c0001t0005a0001c0001t0008a0001c0001t0024others(9): Show | 25 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*255C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 255 | chr5 | 32786600 | |||||
| chr5:32786607
|
G | A | 1 | a0001c0001t0032 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*262G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 262 | chr5 | 32786607 | |||||
| chr5:32786680
|
T | C | 1 | a0002c0002t0020 | 2 | HG02040.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*335T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 335 | chr5 | 32786680 | |||||
| chr5:32786738
|
G | A | 1 | a0001c0001t0014 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*393G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 393 | chr5 | 32786738 | |||||
| chr5:32786894
|
A | G | 7 | a0001c0001t0005a0001c0001t0024a0001c0001t0026others(4): Show | 16 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*549A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 549 | chr5 | 32786894 | |||||
| chr5:32786942
|
C | T | 12 | a0001c0001t0005a0001c0001t0008a0001c0001t0024others(9): Show | 25 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*597C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 597 | chr5 | 32786942 | |||||
| chr5:32787025
|
T | TA | 8 | a0001c0001t0005a0001c0001t0024a0001c0001t0026others(5): Show | 18 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*691dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 692 | INFO_REALIGN_3_PRIME | chr5 | 32787025 | ||||
| chr5:32787025
|
T | TAA | 4 | a0001c0001t0008a0001c0001t0059a0001c0003t0008others(1): Show | 7 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*690_*691dupAA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 692 | INFO_REALIGN_3_PRIME | chr5 | 32787025 | ||||
| chr5:32787047
|
G | A | 1 | a0001c0003t0023 | 2 | HG02622.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*702G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 702 | chr5 | 32787047 | |||||
| chr5:32787095
|
A | G | 8 | a0001c0001t0005a0001c0001t0024a0001c0001t0026others(5): Show | 17 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*750A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 750 | chr5 | 32787095 | |||||
| chr5:32787182
|
G | C | 1 | a0002c0002t0033 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*837G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 837 | chr5 | 32787182 | |||||
| chr5:32787192
|
A | C | 8 | a0001c0001t0005a0001c0001t0024a0001c0001t0026others(5): Show | 17 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*847A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 847 | chr5 | 32787192 | |||||
| chr5:32787311
|
C | A | 5 | a0001c0001t0008a0001c0001t0059a0001c0001t0060others(2): Show | 9 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*966C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 966 | chr5 | 32787311 | |||||
| chr5:32787328
|
G | A | 1 | a0001c0001t0034 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*983G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 983 | chr5 | 32787328 | |||||
| chr5:32787387
|
C | T | 1 | a0001c0001t0068 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1042C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1042 | chr5 | 32787387 | |||||
| chr5:32787411
|
T | C | 4 | a0001c0001t0008a0001c0001t0059a0001c0001t0060others(1): Show | 7 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1066T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1066 | chr5 | 32787411 | |||||
| chr5:32787526
|
T | G | 1 | a0002c0002t0035 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1181T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1181 | chr5 | 32787526 | |||||
| chr5:32787564
|
T | A | 1 | a0001c0001t0036 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1219T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1219 | chr5 | 32787564 | |||||
| chr5:32787779
|
T | C | 1 | a0001c0001t0037 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1434T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1434 | chr5 | 32787779 | |||||
| chr5:32787871
|
A | G | 1 | a0001c0001t0057 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1526A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1526 | chr5 | 32787871 | |||||
| chr5:32787877
|
T | A | 1 | a0001c0001t0038 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1532T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1532 | chr5 | 32787877 | |||||
| chr5:32787939
|
T | G | 13 | a0001c0001t0005a0001c0001t0008a0001c0001t0024others(10): Show | 26 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1594T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1594 | chr5 | 32787939 | |||||
| chr5:32787995
|
A | G | 5 | a0001c0001t0008a0001c0001t0059a0001c0001t0060others(2): Show | 9 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1650A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1650 | chr5 | 32787995 | |||||
| chr5:32788078
|
C | T | 40 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(37): Show | 161 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*1733C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1733 | chr5 | 32788078 | |||||
| chr5:32788263
|
G | A | 25 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(22): Show | 133 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*1918G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1918 | chr5 | 32788263 | |||||
| chr5:32788300
|
C | A | 3 | a0001c0001t0007a0001c0001t0039a0001c0001t0064 | 8 | HG01106.hp2 HG01934.hp2 HG02451.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1955C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1955 | chr5 | 32788300 | |||||
| chr5:32788362
|
G | A | 1 | a0001c0001t0040 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2017G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2017 | chr5 | 32788362 | |||||
| chr5:32788368
|
C | T | 1 | a0001c0003t0063 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2023C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2023 | chr5 | 32788368 | |||||
| chr5:32788420
|
C | G | 8 | a0001c0001t0005a0001c0001t0024a0001c0001t0026others(5): Show | 17 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2075C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2075 | chr5 | 32788420 | |||||
| chr5:32788420
|
C | T | 1 | a0001c0001t0034 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2075C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2075 | chr5 | 32788420 | |||||
| chr5:32788441
|
G | T | 1 | a0001c0001t0051 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2096G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2096 | chr5 | 32788441 | |||||
| chr5:32788582
|
C | T | 1 | a0001c0001t0055 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2237C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2237 | chr5 | 32788582 | |||||
| chr5:32788590
|
G | A | 2 | a0001c0001t0022a0001c0001t0028 | 3 | HG00280.hp2 HG01256.hp1 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2245G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2245 | chr5 | 32788590 | |||||
| chr5:32788730
|
G | A | 5 | a0001c0001t0008a0001c0001t0059a0001c0001t0060others(2): Show | 9 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2385G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2385 | chr5 | 32788730 | |||||
| chr5:32788832
|
T | G | 1 | a0002c0002t0052 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2487T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2487 | chr5 | 32788832 | |||||
| chr5:32788975
|
G | A | 13 | a0001c0001t0005a0001c0001t0008a0001c0001t0024others(10): Show | 26 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2630G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2630 | chr5 | 32788975 | |||||
| chr5:32788999
|
T | C | 13 | a0001c0001t0005a0001c0001t0008a0001c0001t0024others(10): Show | 26 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2654T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2654 | chr5 | 32788999 | |||||
| chr5:32789089
|
CT | C | 11 | a0001c0001t0003a0001c0001t0010a0001c0001t0022others(8): Show | 61 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2747delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2747 | INFO_REALIGN_3_PRIME | chr5 | 32789089 | ||||
| chr5:32789286
|
G | A | 25 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(22): Show | 133 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*2941G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2941 | chr5 | 32789286 | |||||
| chr5:32789287
|
TA | T | 11 | a0001c0001t0003a0001c0001t0010a0001c0001t0022others(8): Show | 61 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2943delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2943 | chr5 | 32789287 | |||||
| chr5:32789366
|
G | T | 1 | a0001c0001t0050 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3021G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3021 | chr5 | 32789366 | |||||
| chr5:32789415
|
T | C | 1 | a0001c0001t0065 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3070T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3070 | chr5 | 32789415 | |||||
| chr5:32789507
|
T | C | 1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3162T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3162 | chr5 | 32789507 | |||||
| chr5:32789641
|
A | T | 1 | a0001c0001t0049 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3296A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3296 | chr5 | 32789641 | |||||
| chr5:32789702
|
A | T | 1 | a0001c0004t0062 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3357A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3357 | chr5 | 32789702 | |||||
| chr5:32789746
|
T | C | 57 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(54): Show | 202 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*3401T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3401 | chr5 | 32789746 | |||||
| chr5:32789813
|
G | A | 1 | a0002c0002t0054 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3468G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3468 | chr5 | 32789813 | |||||
| chr5:32789852
|
G | A | 7 | a0001c0001t0005a0001c0001t0024a0001c0001t0026others(4): Show | 16 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3507G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3507 | chr5 | 32789852 | |||||
| chr5:32790019
|
A | G | 3 | a0001c0001t0037a0001c0001t0065a0001c0003t0058 | 3 | HG02109.hp1 HG02886.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3674A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3674 | chr5 | 32790019 | |||||
| chr5:32790133
|
T | C | 1 | a0001c0001t0064 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3788T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3788 | chr5 | 32790133 | |||||
| chr5:32790168
|
G | A | 1 | a0001c0001t0019 | 2 | HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3823G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3823 | chr5 | 32790168 | |||||
| chr5:32790262
|
C | CAGCAAGA others(16): Show |
11 | a0001c0001t0005a0001c0001t0008a0001c0001t0024others(8): Show | 24 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3926_*3927insCATG others(19): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3927 | INFO_REALIGN_3_PRIME | chr5 | 32790262 | ||||
| chr5:32790325
|
C | G | 1 | a0001c0001t0045 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3980C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3980 | chr5 | 32790325 | |||||
| chr5:32790352
|
CTCCACCC others(3): Show |
C | 11 | a0001c0001t0005a0001c0001t0008a0001c0001t0024others(8): Show | 24 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4013_*4022delCCAC others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4013 | INFO_REALIGN_3_PRIME | chr5 | 32790352 | ||||
| chr5:32790384
|
A | G | 1 | a0001c0001t0019 | 2 | HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4039A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4039 | chr5 | 32790384 | |||||
| chr5:32790429
|
G | A | 5 | a0001c0001t0008a0001c0001t0059a0001c0001t0060others(2): Show | 9 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4084G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4084 | chr5 | 32790429 | |||||
| chr5:32790510
|
T | C | 27 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(24): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*4165T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4165 | chr5 | 32790510 | |||||
| chr5:32790535
|
G | A | 1 | a0001c0001t0039 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4190G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4190 | chr5 | 32790535 | |||||
| chr5:32790672
|
G | T | 1 | a0001c0003t0044 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4327G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4327 | chr5 | 32790672 | |||||
| chr5:32790673
|
G | C | 1 | a0001c0003t0044 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4328G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4328 | chr5 | 32790673 | |||||
| chr5:32790722
|
C | T | 1 | a0001c0001t0019 | 2 | HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4377C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4377 | chr5 | 32790722 | |||||
| chr5:32790729
|
A | G | 11 | a0001c0001t0005a0001c0001t0008a0001c0001t0024others(8): Show | 24 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4384A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4384 | chr5 | 32790729 | |||||
| chr5:32790739
|
A | T | 2 | a0001c0001t0024a0001c0003t0063 | 3 | HG03471.hp1 HG03579.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4394A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4394 | chr5 | 32790739 | |||||
| chr5:32790812
|
G | C | 13 | a0001c0001t0004a0001c0001t0007a0001c0001t0014others(10): Show | 37 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*4467G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4467 | chr5 | 32790812 | |||||
| chr5:32790814
|
T | C | 2 | a0001c0001t0037a0001c0003t0058 | 2 | HG02109.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4469T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4469 | chr5 | 32790814 | |||||
| chr5:32790865
|
G | A | 1 | a0001c0001t0053 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4520G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4520 | chr5 | 32790865 | |||||
| chr5:32790933
|
T | C | 12 | a0001c0001t0005a0001c0001t0008a0001c0001t0024others(9): Show | 25 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4588T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4588 | chr5 | 32790933 | |||||
| chr5:32791051
|
G | A | 1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4706G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4706 | chr5 | 32791051 | |||||
| chr5:32791058
|
G | A | 7 | a0001c0001t0005a0001c0001t0024a0001c0001t0026others(4): Show | 16 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4713G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4713 | chr5 | 32791058 | |||||
| chr5:32791147
|
T | G | 3 | a0001c0001t0017a0001c0001t0021a0001c0003t0044 | 5 | HG01884.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4802T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4802 | chr5 | 32791147 | |||||
| chr5:32791187
|
A | T | 1 | a0001c0001t0048 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4842A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4842 | chr5 | 32791187 | |||||
| chr5:32791205
|
G | C | 1 | a0001c0001t0046 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4860G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4860 | chr5 | 32791205 | |||||
| chr5:32791215
|
G | A | 12 | a0001c0001t0005a0001c0001t0008a0001c0001t0024others(9): Show | 25 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4870G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4870 | chr5 | 32791215 | |||||
| chr5:32791345
|
C | T | 1 | a0002c0002t0012 | 4 | HG00642.hp2 HG01099.hp2 HG01106.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5000C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 5000 | chr5 | 32791345 | |||||
| chr5:32791371
|
G | A | 1 | a0001c0001t0042 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5026G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 5026 | chr5 | 32791371 | |||||
| chr5:32791378
|
C | T | 1 | a0001c0001t0057 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5033C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 5033 | chr5 | 32791378 | |||||
| chr5:32791420
|
G | A | 1 | a0001c0001t0065 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5075G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 5075 | chr5 | 32791420 | |||||
| chr5:32791571
|
C | A | 1 | a0001c0001t0047 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5226C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 5226 | chr5 | 32791571 | |||||
| chr5:32791625
|
T | C | 1 | a0001c0006t0061 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5280T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 5280 | chr5 | 32791625 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:32712568
|
C | T | 13 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0311others(10): Show | 13 | HG00544.hp1 HG02074.hp1 NA18612.hp1 others(10): Show |
intron_variant | MODIFIER | c.769+23C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32712568 | ||||||
| chr5:32712689
|
C | T | 4 | a0001c0001t0004g0303a0001c0001t0004g0304a0001c0001t0004g0306others(1): Show | 4 | HG02257.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+144C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32712689 | ||||||
| chr5:32712693
|
T | A | 4 | a0001c0001t0002g0004a0001c0001t0019g0002a0001c0001t0019g0003others(1): Show | 4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+148T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32712693 | ||||||
| chr5:32712725
|
C | T | 35 | a0001c0001t0001g0269a0001c0001t0001g0272a0001c0001t0001g0275others(32): Show | 35 | HG00323.hp2 HG01099.hp2 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.769+180C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32712725 | ||||||
| chr5:32712795
|
A | C | 1 | a0001c0001t0039g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.769+250A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32712795 | ||||||
| chr5:32712843
|
T | A | 1 | a0001c0001t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.769+298T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32712843 | ||||||
| chr5:32713002
|
G | C | 106 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(103): Show | 106 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(103): Show |
intron_variant | MODIFIER | c.769+457G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713002 | ||||||
| chr5:32713026
|
G | A | 35 | a0001c0001t0001g0269a0001c0001t0001g0272a0001c0001t0001g0275others(32): Show | 35 | HG00323.hp2 HG01099.hp2 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.769+481G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713026 | ||||||
| chr5:32713151
|
C | T | 1 | a0001c0001t0043g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.769+606C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713151 | ||||||
| chr5:32713166
|
T | C | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0002c0002t0002g0070 | 3 | NA18954.hp2 NA18986.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.769+621T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713166 | ||||||
| chr5:32713221
|
T | C | 82 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(79): Show | 82 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.769+676T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713221 | ||||||
| chr5:32713259
|
T | G | 20 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(17): Show | 20 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.769+714T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713259 | ||||||
| chr5:32713392
|
C | A | 1 | a0001c0001t0001g0007 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.769+847C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713392 | ||||||
| chr5:32713562
|
C | A | 1 | a0001c0001t0043g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.769+1017C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713562 | ||||||
| chr5:32713563
|
G | T | 1 | a0001c0001t0067g0266 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.769+1018G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713563 | ||||||
| chr5:32713730
|
A | G | 82 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(79): Show | 82 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.769+1185A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713730 | ||||||
| chr5:32713781
|
G | A | 1 | a0002c0002t0002g0071 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.769+1236G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713781 | ||||||
| chr5:32713900
|
G | C | 1 | a0002c0002t0002g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.769+1355G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713900 | ||||||
| chr5:32713932
|
C | T | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.769+1387C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713932 | ||||||
| chr5:32714013
|
A | G | 2 | a0001c0001t0004g0025a0001c0001t0004g0026 | 2 | HG01496.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.769+1468A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714013 | ||||||
| chr5:32714017
|
A | C | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.769+1472A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714017 | ||||||
| chr5:32714079
|
C | G | 4 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0302others(1): Show | 4 | HG02083.hp1 NA18950.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+1534C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714079 | ||||||
| chr5:32714164
|
C | G | 82 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(79): Show | 82 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.769+1619C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714164 | ||||||
| chr5:32714165
|
G | T | 1 | a0001c0001t0004g0306 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.769+1620G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714165 | ||||||
| chr5:32714170
|
G | C | 1 | a0001c0001t0004g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.769+1625G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714170 | ||||||
| chr5:32714188
|
C | G | 1 | a0001c0001t0004g0298 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.769+1643C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714188 | ||||||
| chr5:32714258
|
G | T | 6 | a0001c0001t0001g0044a0001c0001t0004g0043a0001c0001t0008g0046others(3): Show | 6 | HG02055.hp2 HG02451.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+1713G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714258 | ||||||
| chr5:32714327
|
C | T | 12 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(9): Show | 12 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.769+1782C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714327 | ||||||
| chr5:32714360
|
C | G | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.769+1815C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714360 | ||||||
| chr5:32714370
|
G | C | 1 | a0001c0001t0007g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.769+1825G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714370 | ||||||
| chr5:32714491
|
C | A | 1 | a0001c0001t0001g0068 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.769+1946C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714491 | ||||||
| chr5:32714505
|
CT | C | 82 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(79): Show | 82 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.769+1975delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 32714505 | |||||
| chr5:32714505
|
CTT | C | 8 | a0001c0003t0001g0032a0001c0003t0005g0027a0001c0003t0005g0028others(5): Show | 8 | HG01109.hp2 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.769+1974_769+1975d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 32714505 | |||||
| chr5:32714514
|
T | C | 4 | a0001c0001t0002g0004a0001c0001t0019g0002a0001c0001t0019g0003others(1): Show | 4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+1969T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714514 | ||||||
| chr5:32714555
|
C | T | 41 | a0001c0001t0001g0044a0001c0001t0001g0269a0001c0001t0001g0272others(38): Show | 41 | HG00323.hp2 HG01099.hp2 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.769+2010C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714555 | ||||||
| chr5:32714781
|
A | G | 17 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(14): Show | 17 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.769+2236A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714781 | ||||||
| chr5:32715029
|
C | T | 42 | a0001c0001t0001g0044a0001c0001t0001g0269a0001c0001t0001g0272others(39): Show | 42 | HG00323.hp2 HG01099.hp2 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.769+2484C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32715029 | ||||||
| chr5:32715157
|
C | A | 2 | a0002c0002t0018g0076a0002c0002t0018g0077 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.769+2612C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32715157 | ||||||
| chr5:32715414
|
C | T | 1 | a0001c0001t0024g0265 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.769+2869C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32715414 | ||||||
| chr5:32715804
|
T | C | 4 | a0001c0001t0002g0004a0001c0001t0019g0002a0001c0001t0019g0003others(1): Show | 4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+3259T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32715804 | ||||||
| chr5:32716002
|
C | T | 2 | a0001c0001t0043g0067a0001c0001t0050g0047 | 2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.769+3457C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716002 | ||||||
| chr5:32716060
|
C | T | 3 | a0002c0002t0011g0262a0002c0002t0011g0263a0002c0002t0011g0264 | 3 | HG01978.hp1 HG04228.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.769+3515C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716060 | ||||||
| chr5:32716115
|
A | C | 4 | a0001c0001t0002g0004a0001c0001t0019g0002a0001c0001t0019g0003others(1): Show | 4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+3570A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716115 | ||||||
| chr5:32716202
|
A | G | 14 | a0001c0003t0001g0032a0001c0003t0004g0037a0001c0003t0005g0027others(11): Show | 14 | HG01109.hp2 HG02258.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+3657A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716202 | ||||||
| chr5:32716281
|
C | T | 1 | a0002c0002t0002g0261 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.769+3736C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716281 | ||||||
| chr5:32716368
|
C | CT | 90 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(87): Show | 90 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.769+3835dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 32716368 | |||||
| chr5:32716368
|
C | CTT | 16 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(13): Show | 16 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+3834_769+3835d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 32716368 | |||||
| chr5:32716429
|
C | T | 41 | a0001c0001t0001g0044a0001c0001t0001g0269a0001c0001t0001g0272others(38): Show | 41 | HG00323.hp2 HG01099.hp2 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.769+3884C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716429 | ||||||
| chr5:32716446
|
C | T | 16 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(13): Show | 16 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+3901C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716446 | ||||||
| chr5:32716483
|
T | C | 38 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(35): Show | 38 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.769+3938T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716483 | ||||||
| chr5:32716658
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0005g0079 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.769+4113T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716658 | ||||||
| chr5:32716894
|
G | A | 1 | a0001c0001t0067g0266 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.769+4349G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716894 | ||||||
| chr5:32716996
|
AC | A | 81 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0094others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.769+4458delC | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 32716996 | |||||
| chr5:32716998
|
C | A | 81 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0094others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.769+4453C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716998 | ||||||
| chr5:32717122
|
C | T | 81 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0094others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.769+4577C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717122 | ||||||
| chr5:32717151
|
G | A | 16 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(13): Show | 16 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+4606G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717151 | ||||||
| chr5:32717175
|
A | G | 4 | a0001c0001t0002g0004a0001c0001t0019g0002a0001c0001t0019g0003others(1): Show | 4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+4630A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717175 | ||||||
| chr5:32717212
|
A | G | 6 | a0001c0001t0001g0044a0001c0001t0004g0043a0001c0001t0008g0046others(3): Show | 6 | HG02055.hp2 HG02451.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+4667A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717212 | ||||||
| chr5:32717283
|
T | G | 4 | a0001c0001t0004g0303a0001c0001t0004g0304a0001c0001t0004g0306others(1): Show | 4 | HG02257.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+4738T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717283 | ||||||
| chr5:32717443
|
G | A | 1 | a0001c0001t0024g0265 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.769+4898G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717443 | ||||||
| chr5:32717853
|
AGT | A | 38 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(35): Show | 38 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.769+5309_769+5310d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717853 | ||||||
| chr5:32717938
|
C | T | 180 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(177): Show | 180 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.769+5393C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717938 | ||||||
| chr5:32718175
|
C | T | 62 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0207others(59): Show | 63 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.769+5630C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32718175 | ||||||
| chr5:32718275
|
A | G | 4 | a0001c0001t0006g0063a0001c0001t0006g0065a0001c0001t0006g0066others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+5730A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32718275 | ||||||
| chr5:32718391
|
C | T | 1 | a0001c0001t0031g0295 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.769+5846C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32718391 | ||||||
| chr5:32718501
|
C | T | 81 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0094others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.769+5956C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32718501 | ||||||
| chr5:32718752
|
A | C | 34 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.770-5946A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32718752 | ||||||
| chr5:32719324
|
C | T | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.770-5374C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719324 | ||||||
| chr5:32719484
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.770-5214T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719484 | ||||||
| chr5:32719509
|
G | A | 1 | a0001c0001t0003g0205 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.770-5189G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719509 | ||||||
| chr5:32719587
|
C | T | 180 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(177): Show | 180 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.770-5111C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719587 | ||||||
| chr5:32719651
|
A | C | 1 | a0001c0001t0043g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.770-5047A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719651 | ||||||
| chr5:32719705
|
G | A | 81 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0094others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.770-4993G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719705 | ||||||
| chr5:32719723
|
ATGCTAGA others(120): Show |
A | 1 | a0001c0001t0025g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.770-4972_770-4846d others(2): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 32719723 | |||||
| chr5:32719785
|
G | GT | 9 | a0001c0001t0001g0044a0001c0001t0004g0043a0001c0001t0004g0303others(6): Show | 9 | HG02257.hp1 HG02451.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.770-4911dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 32719785 | |||||
| chr5:32719787
|
TG | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(113): Show | 116 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.770-4910delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719787 | ||||||
| chr5:32719788
|
G | T | 67 | a0001c0001t0001g0044a0001c0001t0001g0056a0001c0001t0001g0060others(64): Show | 67 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(64): Show |
intron_variant | MODIFIER | c.770-4910G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719788 | ||||||
| chr5:32719790
|
T | G | 3 | a0001c0001t0045g0081a0002c0002t0012g0082a0002c0002t0012g0083 | 3 | HG00642.hp2 HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.770-4908T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719790 | ||||||
| chr5:32719924
|
A | G | 4 | a0001c0001t0002g0004a0001c0001t0019g0002a0001c0001t0019g0003others(1): Show | 4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-4774A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719924 | ||||||
| chr5:32720000
|
C | T | 1 | a0002c0002t0011g0130 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.770-4698C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720000 | ||||||
| chr5:32720039
|
C | T | 4 | a0001c0001t0002g0004a0001c0001t0019g0002a0001c0001t0019g0003others(1): Show | 4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-4659C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720039 | ||||||
| chr5:32720053
|
G | T | 1 | a0001c0001t0001g0201 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.770-4645G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720053 | ||||||
| chr5:32720208
|
A | T | 1 | a0002c0002t0016g0294 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.770-4490A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720208 | ||||||
| chr5:32720393
|
A | G | 4 | a0001c0001t0002g0004a0001c0001t0019g0002a0001c0001t0019g0003others(1): Show | 4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-4305A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720393 | ||||||
| chr5:32720401
|
A | C | 3 | a0001c0001t0002g0129a0001c0001t0008g0127a0002c0002t0027g0128 | 3 | HG02055.hp1 HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.770-4297A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720401 | ||||||
| chr5:32720789
|
T | C | 4 | a0001c0001t0004g0303a0001c0001t0004g0304a0001c0001t0004g0306others(1): Show | 4 | HG02257.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-3909T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720789 | ||||||
| chr5:32720798
|
G | T | 1 | a0001c0001t0039g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.770-3900G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720798 | ||||||
| chr5:32720823
|
T | C | 1 | a0001c0001t0001g0272 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.770-3875T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720823 | ||||||
| chr5:32720877
|
G | T | 1 | a0001c0001t0001g0259 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.770-3821G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720877 | ||||||
| chr5:32721010
|
G | T | 12 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(9): Show | 12 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.770-3688G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721010 | ||||||
| chr5:32721283
|
A | T | 1 | a0001c0001t0001g0200 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.770-3415A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721283 | ||||||
| chr5:32721387
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0062 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.770-3311C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721387 | ||||||
| chr5:32721439
|
G | A | 26 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(23): Show | 26 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.770-3259G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721439 | ||||||
| chr5:32721454
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.770-3244C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721454 | ||||||
| chr5:32721488
|
C | G | 35 | a0001c0001t0001g0269a0001c0001t0001g0272a0001c0001t0001g0275others(32): Show | 35 | HG00323.hp2 HG01099.hp2 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.770-3210C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721488 | ||||||
| chr5:32721500
|
G | A | 2 | a0002c0002t0018g0076a0002c0002t0018g0077 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.770-3198G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721500 | ||||||
| chr5:32721690
|
A | C | 1 | a0001c0001t0067g0266 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.770-3008A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721690 | ||||||
| chr5:32721691
|
AG | A | 4 | a0001c0001t0002g0004a0001c0001t0019g0002a0001c0001t0019g0003others(1): Show | 4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-3006delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721691 | ||||||
| chr5:32722213
|
G | A | 34 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.770-2485G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722213 | ||||||
| chr5:32722214
|
G | A | 15 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0207others(12): Show | 15 | HG01069.hp2 HG02080.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.770-2484G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722214 | ||||||
| chr5:32722224
|
C | G | 17 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(14): Show | 17 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.770-2474C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722224 | ||||||
| chr5:32722228
|
G | C | 186 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(183): Show | 186 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.770-2470G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722228 | ||||||
| chr5:32722321
|
C | A | 4 | a0001c0001t0002g0004a0001c0001t0019g0002a0001c0001t0019g0003others(1): Show | 4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-2377C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722321 | ||||||
| chr5:32722327
|
T | A | 6 | a0001c0001t0001g0044a0001c0001t0004g0043a0001c0001t0008g0046others(3): Show | 6 | HG02055.hp2 HG02451.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.770-2371T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722327 | ||||||
| chr5:32722382
|
A | G | 4 | a0001c0001t0004g0303a0001c0001t0004g0304a0001c0001t0004g0306others(1): Show | 4 | HG02257.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-2316A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722382 | ||||||
| chr5:32722393
|
T | C | 186 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(183): Show | 186 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.770-2305T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722393 | ||||||
| chr5:32722529
|
T | C | 1 | a0001c0001t0048g0307 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.770-2169T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722529 | ||||||
| chr5:32722544
|
A | G | 1 | a0001c0001t0007g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.770-2154A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722544 | ||||||
| chr5:32722576
|
C | G | 6 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 6 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.770-2122C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722576 | ||||||
| chr5:32722615
|
C | G | 1 | a0001c0001t0001g0198 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.770-2083C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722615 | ||||||
| chr5:32722642
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0004g0025a0001c0001t0004g0026 | 3 | HG01496.hp1 HG03239.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.770-2056C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722642 | ||||||
| chr5:32722665
|
T | C | 7 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0008g0204others(4): Show | 7 | HG02145.hp2 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.770-2033T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722665 | ||||||
| chr5:32722795
|
A | T | 1 | a0001c0001t0039g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.770-1903A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722795 | ||||||
| chr5:32722930
|
C | T | 1 | a0001c0001t0039g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.770-1768C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722930 | ||||||
| chr5:32723029
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.770-1669G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723029 | ||||||
| chr5:32723057
|
A | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.770-1641A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723057 | ||||||
| chr5:32723171
|
G | T | 1 | a0001c0001t0003g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.770-1527G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723171 | ||||||
| chr5:32723285
|
T | C | 1 | a0001c0001t0043g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.770-1413T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723285 | ||||||
| chr5:32723372
|
G | A | 78 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0094others(75): Show | 78 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.770-1326G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723372 | ||||||
| chr5:32723463
|
G | A | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.770-1235G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723463 | ||||||
| chr5:32723524
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG01993.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.770-1174C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723524 | ||||||
| chr5:32723649
|
T | C | 1 | a0002c0002t0002g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.770-1049T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723649 | ||||||
| chr5:32723652
|
G | A | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.770-1046G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723652 | ||||||
| chr5:32723692
|
G | T | 1 | a0001c0001t0003g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.770-1006G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723692 | ||||||
| chr5:32723835
|
C | T | 1 | a0002c0002t0002g0257 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.770-863C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723835 | ||||||
| chr5:32723875
|
C | T | 6 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 6 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.770-823C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723875 | ||||||
| chr5:32723943
|
A | G | 1 | a0002c0002t0002g0070 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.770-755A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723943 | ||||||
| chr5:32723972
|
C | G | 135 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.770-726C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723972 | ||||||
| chr5:32724134
|
A | T | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0003g0075others(1): Show | 4 | HG01074.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-564A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32724134 | ||||||
| chr5:32724257
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.770-441C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32724257 | ||||||
| chr5:32724353
|
C | T | 2 | a0001c0001t0060g0293a0001c0005t0056g0268 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.770-345C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32724353 | ||||||
| chr5:32724368
|
T | C | 2 | a0002c0002t0002g0135a0002c0002t0002g0136 | 2 | NA18949.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.770-330T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32724368 | ||||||
| chr5:32724529
|
G | A | 2 | a0001c0001t0051g0270a0002c0002t0002g0271 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.770-169G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32724529 | ||||||
| chr5:32724836
|
C | A | 1 | a0001c0001t0007g0137 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.892+16C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32724836 | ||||||
| chr5:32724846
|
C | G | 1 | a0002c0002t0035g0124 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.892+26C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32724846 | ||||||
| chr5:32724924
|
C | G | 1 | a0001c0001t0002g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.892+104C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32724924 | ||||||
| chr5:32724965
|
C | T | 1 | a0001c0005t0056g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.892+145C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32724965 | ||||||
| chr5:32724966
|
T | C | 201 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(198): Show | 201 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.892+146T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32724966 | ||||||
| chr5:32724991
|
G | T | 2 | a0001c0001t0004g0154a0001c0001t0059g0155 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.892+171G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32724991 | ||||||
| chr5:32725053
|
A | G | 4 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 4 | NA18963.hp2 NA18975.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.892+233A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725053 | ||||||
| chr5:32725082
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.892+262C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725082 | ||||||
| chr5:32725112
|
G | A | 1 | a0001c0001t0003g0156 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.892+292G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725112 | ||||||
| chr5:32725132
|
G | A | 1 | a0001c0001t0003g0226 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.892+312G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725132 | ||||||
| chr5:32725153
|
T | C | 7 | a0001c0001t0002g0004a0001c0001t0007g0199a0001c0001t0019g0002others(4): Show | 7 | HG02451.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.892+333T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725153 | ||||||
| chr5:32725246
|
G | C | 95 | a0001c0001t0001g0044a0001c0001t0001g0056a0001c0001t0001g0062others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.892+426G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725246 | ||||||
| chr5:32725425
|
G | A | 70 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0094others(67): Show | 70 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.892+605G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725425 | ||||||
| chr5:32725439
|
T | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0078a0001c0001t0001g0269others(20): Show | 23 | HG01074.hp2 HG01175.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.892+619T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725439 | ||||||
| chr5:32725662
|
G | A | 20 | a0001c0001t0001g0044a0001c0001t0004g0011a0001c0001t0004g0012others(17): Show | 20 | HG00741.hp1 HG01070.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.892+842G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725662 | ||||||
| chr5:32725678
|
A | G | 6 | a0001c0001t0002g0004a0001c0001t0008g0204a0001c0001t0019g0002others(3): Show | 6 | HG02055.hp2 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.892+858A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725678 | ||||||
| chr5:32725749
|
T | C | 1 | a0001c0001t0004g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.892+929T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725749 | ||||||
| chr5:32725813
|
A | G | 1 | a0001c0001t0021g0084 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.892+993A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725813 | ||||||
| chr5:32725832
|
G | C | 2 | a0001c0001t0050g0047a0001c0003t0044g0036 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.892+1012G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725832 | ||||||
| chr5:32726083
|
C | T | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.892+1263C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726083 | ||||||
| chr5:32726137
|
A | G | 1 | a0001c0005t0056g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.892+1317A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726137 | ||||||
| chr5:32726232
|
G | A | 2 | a0001c0001t0068g0233a0002c0002t0002g0274 | 2 | NA18967.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.892+1412G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726232 | ||||||
| chr5:32726529
|
A | T | 1 | a0001c0003t0044g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.892+1709A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726529 | ||||||
| chr5:32726531
|
G | A | 143 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0089others(140): Show | 143 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.892+1711G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726531 | ||||||
| chr5:32726601
|
G | A | 1 | a0001c0001t0053g0315 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.892+1781G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726601 | ||||||
| chr5:32726628
|
A | G | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.892+1808A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726628 | ||||||
| chr5:32726910
|
A | G | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.892+2090A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726910 | ||||||
| chr5:32727395
|
A | G | 1 | a0001c0001t0005g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.892+2575A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32727395 | ||||||
| chr5:32727560
|
G | C | 3 | a0001c0001t0004g0025a0001c0001t0004g0026a0001c0001t0004g0106 | 3 | HG01070.hp2 HG01496.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.892+2740G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32727560 | ||||||
| chr5:32727578
|
G | T | 13 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0019others(10): Show | 13 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.892+2758G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32727578 | ||||||
| chr5:32727924
|
A | G | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.892+3104A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32727924 | ||||||
| chr5:32727990
|
G | A | 1 | a0001c0001t0009g0159 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.892+3170G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32727990 | ||||||
| chr5:32728070
|
G | A | 1 | a0001c0005t0056g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.892+3250G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728070 | ||||||
| chr5:32728217
|
C | G | 60 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(57): Show | 60 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.892+3397C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728217 | ||||||
| chr5:32728288
|
C | T | 11 | a0001c0001t0004g0139a0001c0001t0005g0079a0001c0001t0007g0151others(8): Show | 11 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.892+3468C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728288 | ||||||
| chr5:32728465
|
G | GA | 297 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(294): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.892+3660dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728465 | |||||
| chr5:32728465
|
G | GAA | 10 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0004g0025others(7): Show | 10 | HG01496.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.892+3659_892+3660d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728465 | |||||
| chr5:32728465
|
G | GAAA | 6 | a0001c0001t0006g0063a0001c0001t0006g0065a0001c0001t0017g0057others(3): Show | 6 | HG01891.hp2 HG02809.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.892+3658_892+3660d others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728465 | |||||
| chr5:32728502
|
A | G | 1 | a0002c0002t0002g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.892+3682A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728502 | ||||||
| chr5:32728618
|
G | A | 1 | a0001c0003t0058g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.892+3798G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728618 | ||||||
| chr5:32728700
|
A | G | 11 | a0001c0001t0004g0139a0001c0001t0005g0079a0001c0001t0007g0151others(8): Show | 11 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.892+3880A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728700 | ||||||
| chr5:32728779
|
T | C | 1 | a0001c0001t0002g0004 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.892+3959T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728779 | ||||||
| chr5:32728792
|
C | A | 2 | a0001c0001t0002g0004a0001c0004t0062g0134 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.892+3972C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728792 | ||||||
| chr5:32728815
|
TTG | T | 45 | a0001c0001t0001g0089a0001c0001t0001g0120a0001c0001t0001g0126others(42): Show | 46 | HG00423.hp2 HG00621.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.892+4017_892+4018d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728815 | |||||
| chr5:32728815
|
TTGTG | T | 26 | a0001c0001t0001g0044a0001c0001t0001g0149a0001c0001t0002g0004others(23): Show | 26 | HG00280.hp1 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.892+4015_892+4018d others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728815 | |||||
| chr5:32728815
|
TTGTGTG | T | 11 | a0001c0001t0001g0141a0001c0001t0001g0318a0001c0001t0001g0319others(8): Show | 11 | HG00738.hp1 HG01106.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.892+4013_892+4018d others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728815 | |||||
| chr5:32728815
|
TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0003g0231a0001c0003t0044g0036a0002c0002t0027g0230 | 3 | HG03540.hp2 NA18945.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.892+4011_892+4018d others(10): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728815 | |||||
| chr5:32728827
|
GTGTGTGT others(7): Show |
G | 1 | a0002c0002t0002g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.892+4009_892+4022d others(16): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728827 | |||||
| chr5:32728827
|
GTGTGTGT others(17): Show |
G | 1 | a0001c0005t0056g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.892+4009_892+4032d others(26): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728827 | |||||
| chr5:32728829
|
G | GTA | 6 | a0001c0001t0001g0085a0001c0001t0001g0229a0001c0001t0001g0308others(3): Show | 6 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.892+4010_892+4011i others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728829 | |||||
| chr5:32728829
|
G | GTATATAT others(3): Show |
1 | a0002c0002t0002g0132 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.892+4010_892+4011i others(12): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728829 | |||||
| chr5:32728829
|
GTGTGTGT others(9): Show |
G | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.892+4011_892+4026d others(18): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728829 | |||||
| chr5:32728829
|
GTGTGTGT others(25): Show |
G | 2 | a0001c0001t0024g0265a0002c0002t0002g0261 | 2 | HG03471.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.892+4011_892+4042d others(34): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728829 | |||||
| chr5:32728829
|
GTGTGTGT others(31): Show |
G | 1 | a0002c0002t0002g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.892+4011_892+4048d others(40): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728829 | |||||
| chr5:32728831
|
G | A | 17 | a0001c0001t0001g0085a0001c0001t0001g0202a0001c0001t0001g0229others(14): Show | 17 | HG00621.hp2 HG00642.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.892+4011G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728831 | ||||||
| chr5:32728831
|
G | GTA | 10 | a0001c0001t0004g0012a0001c0001t0004g0026a0001c0001t0004g0146others(7): Show | 10 | HG00741.hp1 HG01261.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.892+4012_892+4013i others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728831 | |||||
| chr5:32728831
|
G | GTATA | 7 | a0001c0001t0004g0011a0001c0001t0004g0303a0001c0001t0006g0063others(4): Show | 7 | HG01192.hp1 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.892+4012_892+4013i others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728831 | |||||
| chr5:32728831
|
GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0051g0270 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.892+4013_892+4022d others(12): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728831 | |||||
| chr5:32728831
|
GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0007g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.892+4013_892+4034d others(24): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728831 | |||||
| chr5:32728831
|
GTGTGTGT others(19): Show |
G | 3 | a0001c0001t0007g0137a0001c0001t0041g0148a0001c0001t0050g0047 | 3 | HG01934.hp2 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.892+4013_892+4038d others(28): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728831 | |||||
| chr5:32728831
|
GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0007g0058 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.892+4013_892+4040d others(30): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728831 | |||||
| chr5:32728831
|
GTGTGTGT others(23): Show |
G | 1 | a0001c0001t0004g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.892+4013_892+4042d others(32): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728831 | |||||
| chr5:32728833
|
G | A | 69 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(66): Show | 69 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.892+4013G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728833 | ||||||
| chr5:32728833
|
G | GTATATA | 4 | a0001c0001t0001g0168a0001c0001t0004g0025a0001c0001t0019g0002others(1): Show | 4 | HG01496.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.892+4014_892+4015i others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728833 | |||||
| chr5:32728833
|
GTGTGTAT others(17): Show |
G | 1 | a0001c0001t0005g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.892+4015_892+4038d others(26): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728833 | |||||
| chr5:32728833
|
GTGTGTAT others(21): Show |
G | 2 | a0001c0006t0061g0041a0002c0002t0002g0072 | 2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.892+4015_892+4042d others(30): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728833 | |||||
| chr5:32728835
|
G | A | 98 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(95): Show | 98 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.892+4015G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728835 | ||||||
| chr5:32728835
|
G | GTA | 22 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0021others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.892+4016_892+4017i others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | |||||
| chr5:32728835
|
G | GTATA | 30 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0097others(27): Show | 30 | HG01109.hp2 HG01934.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.892+4016_892+4017i others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | |||||
| chr5:32728835
|
G | GTATATA | 40 | a0001c0001t0001g0056a0001c0001t0001g0061a0001c0001t0001g0062others(37): Show | 40 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.892+4016_892+4017i others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | |||||
| chr5:32728835
|
G | GTATATAT others(1): Show |
4 | a0001c0001t0001g0010a0001c0001t0001g0190a0001c0001t0001g0316others(1): Show | 4 | HG00544.hp1 HG01069.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.892+4016_892+4017i others(10): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | |||||
| chr5:32728835
|
G | GTATATAT others(3): Show |
3 | a0001c0001t0001g0060a0001c0001t0001g0069a0002c0002t0002g0210 | 3 | HG01192.hp2 HG02523.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.892+4016_892+4017i others(12): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | |||||
| chr5:32728835
|
G | GTATATAT others(9): Show |
2 | a0001c0001t0001g0022a0002c0002t0002g0111 | 2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.892+4016_892+4017i others(18): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | |||||
| chr5:32728835
|
GTGTA | G | 4 | a0001c0001t0001g0185a0001c0001t0025g0048a0001c0001t0030g0288others(1): Show | 4 | HG01993.hp2 HG02818.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.892+4017_892+4020d others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | |||||
| chr5:32728835
|
GTGTATA | G | 3 | a0001c0001t0001g0194a0002c0002t0018g0076a0002c0002t0018g0077 | 3 | HG01993.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.892+4017_892+4022d others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | |||||
| chr5:32728835
|
GTGTATAT others(11): Show |
G | 1 | a0001c0001t0001g0275 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.892+4017_892+4034d others(20): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | |||||
| chr5:32728835
|
GTGTATAT others(13): Show |
G | 1 | a0002c0002t0002g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.892+4017_892+4036d others(22): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | |||||
| chr5:32728835
|
GTGTATAT others(15): Show |
G | 9 | a0001c0001t0004g0139a0001c0001t0007g0151a0001c0001t0008g0046others(6): Show | 9 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.892+4017_892+4038d others(24): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | |||||
| chr5:32728837
|
G | A | 228 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(225): Show | 228 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.892+4017G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728837 | ||||||
| chr5:32728837
|
G | GTA | 4 | a0001c0001t0001g0101a0001c0001t0001g0188a0001c0001t0003g0187others(1): Show | 4 | HG00099.hp1 HG02071.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.892+4055_892+4056d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | |||||
| chr5:32728837
|
G | GTATA | 6 | a0001c0001t0001g0017a0001c0001t0003g0122a0001c0001t0003g0186others(3): Show | 6 | HG00423.hp1 HG01256.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.892+4053_892+4056d others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | |||||
| chr5:32728837
|
G | GTATATA | 10 | a0001c0001t0001g0143a0001c0001t0003g0117a0001c0001t0003g0156others(7): Show | 10 | HG02027.hp1 HG02523.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.892+4051_892+4056d others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | |||||
| chr5:32728837
|
G | GTATATAT others(3): Show |
2 | a0001c0001t0003g0247a0001c0001t0003g0248 | 2 | NA18992.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.892+4047_892+4056d others(12): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | |||||
| chr5:32728837
|
G | GTATATAT others(7): Show |
1 | a0001c0001t0003g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.892+4043_892+4056d others(16): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | |||||
| chr5:32728837
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0003g0246 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.892+4039_892+4056d others(20): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | |||||
| chr5:32728837
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0001g0201 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.892+4037_892+4056d others(22): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | |||||
| chr5:32728837
|
GTA | G | 5 | a0001c0001t0003g0226a0001c0001t0003g0254a0001c0001t0010g0121others(2): Show | 5 | HG01070.hp1 HG02074.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.892+4055_892+4056d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | |||||
| chr5:32728841
|
A | G | 1 | a0001c0001t0003g0226 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.892+4021A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728841 | ||||||
| chr5:32728857
|
A | G | 1 | a0001c0003t0044g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.892+4037A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728857 | ||||||
| chr5:32728930
|
A | C | 1 | a0001c0003t0001g0032 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.892+4110A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728930 | ||||||
| chr5:32728976
|
A | T | 143 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0089others(140): Show | 143 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.892+4156A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728976 | ||||||
| chr5:32729014
|
G | GT | 8 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0201others(5): Show | 8 | HG01168.hp2 HG01175.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.892+4209dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32729014 | |||||
| chr5:32729014
|
G | T | 9 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(6): Show | 9 | HG00280.hp1 HG01175.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.892+4194G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729014 | ||||||
| chr5:32729014
|
GTT | G | 9 | a0001c0001t0001g0229a0001c0001t0003g0086a0001c0001t0006g0066others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.892+4208_892+4209d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32729014 | |||||
| chr5:32729016
|
T | G | 1 | a0001c0001t0007g0058 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.892+4196T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729016 | ||||||
| chr5:32729025
|
T | G | 3 | a0001c0001t0001g0182a0001c0001t0001g0211a0001c0001t0013g0279 | 3 | HG01169.hp2 HG02293.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.892+4205T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729025 | ||||||
| chr5:32729028
|
TTG | T | 8 | a0001c0001t0006g0065a0001c0001t0017g0064a0001c0001t0019g0002others(5): Show | 8 | HG02055.hp2 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.892+4210_892+4211d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32729028 | |||||
| chr5:32729029
|
TG | T | 51 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(48): Show | 51 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.892+4210delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729029 | ||||||
| chr5:32729030
|
G | T | 19 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0002g0004others(16): Show | 19 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.892+4210G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729030 | ||||||
| chr5:32729032
|
T | G | 51 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(48): Show | 51 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.892+4212T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729032 | ||||||
| chr5:32729033
|
T | G | 9 | a0001c0001t0001g0229a0001c0001t0003g0086a0001c0001t0006g0066others(6): Show | 9 | HG00423.hp2 HG00621.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.892+4213T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729033 | ||||||
| chr5:32729033
|
TTG | T | 11 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0003g0075others(8): Show | 11 | HG00735.hp2 HG01074.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.892+4215_892+4216d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32729033 | |||||
| chr5:32729035
|
G | T | 14 | a0001c0001t0001g0229a0001c0001t0003g0086a0001c0001t0005g0142others(11): Show | 14 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.892+4215G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729035 | ||||||
| chr5:32729035
|
GT | G | 225 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(222): Show | 225 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.892+4227delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32729035 | |||||
| chr5:32729036
|
T | G | 23 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0229others(20): Show | 23 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.892+4216T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729036 | ||||||
| chr5:32729041
|
T | G | 1 | a0001c0001t0036g0009 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.892+4221T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729041 | ||||||
| chr5:32729091
|
G | A | 33 | a0001c0001t0001g0044a0001c0001t0001g0141a0001c0001t0001g0149others(30): Show | 33 | HG00741.hp1 HG01070.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.892+4271G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729091 | ||||||
| chr5:32729103
|
C | T | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.892+4283C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729103 | ||||||
| chr5:32729112
|
C | G | 8 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(5): Show | 8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.892+4292C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729112 | ||||||
| chr5:32729130
|
C | T | 63 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(60): Show | 63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.892+4310C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729130 | ||||||
| chr5:32729140
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.892+4320C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729140 | ||||||
| chr5:32729153
|
C | A | 1 | a0002c0002t0002g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.892+4333C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729153 | ||||||
| chr5:32729276
|
A | G | 143 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0089others(140): Show | 143 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.892+4456A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729276 | ||||||
| chr5:32729313
|
G | A | 1 | a0001c0001t0005g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.892+4493G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729313 | ||||||
| chr5:32729421
|
T | G | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.892+4601T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729421 | ||||||
| chr5:32729655
|
C | A | 1 | a0002c0002t0012g0297 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.892+4835C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729655 | ||||||
| chr5:32729908
|
T | G | 1 | a0002c0002t0002g0241 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.892+5088T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729908 | ||||||
| chr5:32729963
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.892+5143C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729963 | ||||||
| chr5:32730115
|
G | A | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.892+5295G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730115 | ||||||
| chr5:32730122
|
C | T | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0006g0006others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.892+5302C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730122 | ||||||
| chr5:32730198
|
TA | T | 14 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0168others(11): Show | 14 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.892+5388delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32730198 | |||||
| chr5:32730222
|
T | C | 1 | a0002c0002t0052g0165 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.892+5402T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730222 | ||||||
| chr5:32730314
|
AG | A | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0006g0006others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.892+5498delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32730314 | |||||
| chr5:32730358
|
G | T | 63 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(60): Show | 63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.892+5538G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730358 | ||||||
| chr5:32730360
|
A | G | 1 | a0001c0001t0007g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.892+5540A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730360 | ||||||
| chr5:32730540
|
T | C | 1 | a0001c0001t0008g0046 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.892+5720T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730540 | ||||||
| chr5:32730660
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.892+5840G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730660 | ||||||
| chr5:32730665
|
T | A | 1 | a0002c0002t0002g0255 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.892+5845T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730665 | ||||||
| chr5:32730859
|
T | C | 10 | a0001c0001t0002g0129a0001c0001t0004g0138a0001c0001t0015g0123others(7): Show | 10 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.892+6039T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730859 | ||||||
| chr5:32731204
|
C | T | 1 | a0002c0002t0002g0241 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.892+6384C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731204 | ||||||
| chr5:32731268
|
A | G | 1 | a0001c0001t0015g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.892+6448A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731268 | ||||||
| chr5:32731309
|
C | T | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.892+6489C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731309 | ||||||
| chr5:32731313
|
A | G | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.892+6493A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731313 | ||||||
| chr5:32731368
|
A | G | 2 | a0001c0001t0045g0081a0002c0002t0029g0104 | 2 | HG00735.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.892+6548A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731368 | ||||||
| chr5:32731442
|
A | G | 33 | a0001c0001t0001g0044a0001c0001t0001g0141a0001c0001t0001g0149others(30): Show | 33 | HG00741.hp1 HG01070.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.892+6622A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731442 | ||||||
| chr5:32731534
|
G | A | 6 | a0001c0001t0004g0138a0001c0001t0015g0123a0001c0001t0026g0049others(3): Show | 6 | HG00735.hp2 HG01891.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.892+6714G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731534 | ||||||
| chr5:32731726
|
T | C | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.892+6906T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731726 | ||||||
| chr5:32731820
|
T | G | 8 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(5): Show | 8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.892+7000T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731820 | ||||||
| chr5:32731960
|
G | A | 1 | a0001c0004t0062g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.893-6904G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731960 | ||||||
| chr5:32732008
|
A | G | 72 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(69): Show | 72 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.893-6856A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732008 | ||||||
| chr5:32732068
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.893-6796C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732068 | ||||||
| chr5:32732084
|
A | G | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.893-6780A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732084 | ||||||
| chr5:32732097
|
C | T | 1 | a0001c0001t0007g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.893-6767C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732097 | ||||||
| chr5:32732104
|
G | A | 11 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(8): Show | 11 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.893-6760G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732104 | ||||||
| chr5:32732131
|
C | T | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.893-6733C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732131 | ||||||
| chr5:32732134
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.893-6730G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732134 | ||||||
| chr5:32732135
|
G | A | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.893-6729G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732135 | ||||||
| chr5:32732247
|
C | CA | 75 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0094others(72): Show | 76 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.893-6586dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32732247 | |||||
| chr5:32732247
|
C | CAA | 23 | a0001c0001t0001g0044a0001c0001t0001g0069a0001c0001t0001g0318others(20): Show | 23 | HG00280.hp1 HG01175.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.893-6587_893-6586d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32732247 | |||||
| chr5:32732247
|
CA | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0197a0001c0001t0003g0087others(11): Show | 14 | HG00741.hp1 HG01516.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.893-6586delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32732247 | |||||
| chr5:32732247
|
CAA | C | 33 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0308others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.893-6587_893-6586d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32732247 | |||||
| chr5:32732247
|
CAAA | C | 43 | a0001c0001t0001g0120a0001c0001t0001g0126a0001c0001t0001g0229others(40): Show | 43 | HG00621.hp2 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.893-6588_893-6586d others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32732247 | |||||
| chr5:32732247
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.893-6596_893-6586d others(13): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32732247 | |||||
| chr5:32732369
|
G | A | 14 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0115others(11): Show | 14 | HG02040.hp2 HG02071.hp1 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.893-6495G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732369 | ||||||
| chr5:32732666
|
T | C | 5 | a0001c0001t0008g0204a0001c0001t0019g0002a0001c0001t0019g0003others(2): Show | 5 | HG02055.hp2 HG02486.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.893-6198T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732666 | ||||||
| chr5:32732754
|
A | G | 8 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(5): Show | 8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-6110A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732754 | ||||||
| chr5:32732853
|
C | T | 64 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(61): Show | 64 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.893-6011C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732853 | ||||||
| chr5:32733096
|
C | T | 1 | a0001c0001t0004g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.893-5768C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733096 | ||||||
| chr5:32733124
|
C | T | 1 | a0002c0002t0002g0216 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.893-5740C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733124 | ||||||
| chr5:32733140
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.893-5724C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733140 | ||||||
| chr5:32733159
|
T | C | 1 | a0002c0002t0002g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.893-5705T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733159 | ||||||
| chr5:32733312
|
C | T | 95 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(92): Show | 95 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.893-5552C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733312 | ||||||
| chr5:32733741
|
A | G | 10 | a0001c0001t0002g0129a0001c0001t0004g0138a0001c0001t0015g0123others(7): Show | 10 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.893-5123A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733741 | ||||||
| chr5:32733747
|
C | A | 1 | a0001c0001t0003g0247 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.893-5117C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733747 | ||||||
| chr5:32733806
|
A | G | 1 | a0001c0004t0062g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.893-5058A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733806 | ||||||
| chr5:32733807
|
T | G | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.893-5057T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733807 | ||||||
| chr5:32733834
|
C | T | 11 | a0001c0001t0004g0139a0001c0001t0005g0079a0001c0001t0007g0151others(8): Show | 11 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.893-5030C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733834 | ||||||
| chr5:32733862
|
C | T | 8 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(5): Show | 8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-5002C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733862 | ||||||
| chr5:32733907
|
T | C | 1 | a0002c0002t0002g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.893-4957T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733907 | ||||||
| chr5:32734034
|
A | G | 64 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(61): Show | 64 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.893-4830A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734034 | ||||||
| chr5:32734140
|
G | A | 2 | a0001c0003t0023g0038a0001c0003t0023g0039 | 2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.893-4724G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734140 | ||||||
| chr5:32734187
|
T | C | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.893-4677T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734187 | ||||||
| chr5:32734221
|
A | G | 60 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(57): Show | 60 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.893-4643A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734221 | ||||||
| chr5:32734302
|
T | G | 44 | a0001c0001t0001g0044a0001c0001t0001g0141a0001c0001t0001g0149others(41): Show | 44 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.893-4562T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734302 | ||||||
| chr5:32734364
|
C | T | 2 | a0001c0001t0003g0226a0001c0001t0003g0292 | 2 | NA18612.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.893-4500C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734364 | ||||||
| chr5:32734377
|
C | T | 1 | a0001c0001t0007g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.893-4487C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734377 | ||||||
| chr5:32734405
|
G | A | 64 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(61): Show | 64 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.893-4459G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734405 | ||||||
| chr5:32734427
|
T | C | 1 | a0001c0003t0058g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.893-4437T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734427 | ||||||
| chr5:32734463
|
G | A | 4 | a0001c0001t0015g0123a0001c0001t0045g0081a0001c0001t0047g0110others(1): Show | 4 | HG00735.hp2 HG01074.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.893-4401G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734463 | ||||||
| chr5:32734472
|
A | G | 3 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0009g0193 | 3 | NA18963.hp2 NA18977.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.893-4392A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734472 | ||||||
| chr5:32734584
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.893-4280C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734584 | ||||||
| chr5:32734711
|
G | A | 63 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(60): Show | 63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.893-4153G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734711 | ||||||
| chr5:32734762
|
A | G | 96 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(93): Show | 96 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.893-4102A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734762 | ||||||
| chr5:32734850
|
C | T | 1 | a0001c0001t0003g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.893-4014C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734850 | ||||||
| chr5:32735013
|
T | A | 70 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(67): Show | 70 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.893-3851T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735013 | ||||||
| chr5:32735039
|
T | A | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0006g0006others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.893-3825T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735039 | ||||||
| chr5:32735137
|
T | C | 1 | a0002c0002t0002g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.893-3727T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735137 | ||||||
| chr5:32735139
|
C | T | 1 | a0001c0001t0004g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.893-3725C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735139 | ||||||
| chr5:32735191
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0234a0001c0001t0003g0169 | 3 | HG02074.hp2 NA18949.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.893-3673G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735191 | ||||||
| chr5:32735213
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.893-3651A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735213 | ||||||
| chr5:32735289
|
G | C | 1 | a0002c0002t0002g0299 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.893-3575G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735289 | ||||||
| chr5:32735302
|
C | T | 31 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0002g0129others(28): Show | 31 | HG00280.hp1 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.893-3562C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735302 | ||||||
| chr5:32735303
|
T | A | 1 | a0001c0001t0005g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.893-3561T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735303 | ||||||
| chr5:32735412
|
CTA | C | 6 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 6 | HG01109.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.893-3450_893-3449d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32735412 | |||||
| chr5:32735426
|
T | A | 8 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(5): Show | 8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-3438T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735426 | ||||||
| chr5:32735479
|
C | CA | 23 | a0001c0001t0001g0019a0001c0001t0001g0094a0001c0001t0001g0098others(20): Show | 23 | HG00639.hp2 HG01099.hp1 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.893-3370dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32735479 | |||||
| chr5:32735479
|
C | CAAA | 58 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(55): Show | 58 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.893-3372_893-3370d others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32735479 | |||||
| chr5:32735479
|
CA | C | 36 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0001g0197others(33): Show | 36 | HG01074.hp2 HG01106.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.893-3370delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32735479 | |||||
| chr5:32735479
|
CAA | C | 9 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(6): Show | 9 | HG00280.hp1 HG01175.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.893-3371_893-3370d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32735479 | |||||
| chr5:32735543
|
G | A | 111 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(108): Show | 111 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.893-3321G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735543 | ||||||
| chr5:32735556
|
G | A | 1 | a0001c0004t0062g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.893-3308G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735556 | ||||||
| chr5:32735624
|
C | T | 1 | a0001c0001t0006g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.893-3240C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735624 | ||||||
| chr5:32735627
|
C | G | 6 | a0001c0001t0004g0139a0001c0001t0008g0046a0001c0001t0008g0127others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.893-3237C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735627 | ||||||
| chr5:32735679
|
T | C | 5 | a0001c0001t0006g0063a0001c0001t0006g0065a0001c0001t0017g0057others(2): Show | 5 | HG01891.hp2 HG02809.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.893-3185T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735679 | ||||||
| chr5:32735693
|
A | T | 7 | a0001c0001t0004g0138a0001c0001t0015g0123a0001c0001t0026g0049others(4): Show | 7 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.893-3171A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735693 | ||||||
| chr5:32735788
|
C | G | 8 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(5): Show | 8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-3076C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735788 | ||||||
| chr5:32735844
|
G | C | 23 | a0001c0001t0003g0075a0001c0001t0004g0139a0001c0001t0005g0079others(20): Show | 23 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.893-3020G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735844 | ||||||
| chr5:32735853
|
G | A | 6 | a0001c0001t0006g0063a0001c0001t0006g0065a0001c0001t0017g0057others(3): Show | 6 | HG01891.hp2 HG02809.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.893-3011G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735853 | ||||||
| chr5:32735969
|
G | A | 1 | a0002c0002t0002g0312 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.893-2895G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735969 | ||||||
| chr5:32736059
|
T | C | 63 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(60): Show | 63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.893-2805T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736059 | ||||||
| chr5:32736088
|
G | A | 1 | a0001c0003t0058g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.893-2776G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736088 | ||||||
| chr5:32736165
|
AG | A | 4 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0009g0310others(1): Show | 4 | NA18941.hp2 NA18984.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.893-2697delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32736165 | |||||
| chr5:32736213
|
A | T | 10 | a0001c0001t0002g0129a0001c0001t0004g0138a0001c0001t0015g0123others(7): Show | 10 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.893-2651A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736213 | ||||||
| chr5:32736230
|
C | CA | 8 | a0001c0001t0001g0183a0001c0001t0010g0118a0001c0001t0010g0121others(5): Show | 8 | HG01070.hp1 HG02109.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.893-2616dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32736230 | |||||
| chr5:32736230
|
CA | C | 43 | a0001c0001t0001g0044a0001c0001t0001g0141a0001c0001t0001g0149others(40): Show | 43 | HG00741.hp1 HG01070.hp2 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.893-2616delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32736230 | |||||
| chr5:32736239
|
A | G | 4 | a0001c0001t0003g0096a0001c0001t0003g0300a0001c0001t0003g0301others(1): Show | 4 | HG02083.hp1 NA18950.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.893-2625A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736239 | ||||||
| chr5:32736248
|
A | AAAG | 15 | a0001c0001t0002g0129a0001c0001t0004g0138a0001c0001t0008g0204others(12): Show | 15 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.893-2616_893-2615i others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736248 | ||||||
| chr5:32736249
|
G | A | 32 | a0001c0001t0001g0211a0001c0001t0001g0318a0001c0001t0001g0319others(29): Show | 32 | HG00280.hp1 HG00735.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.893-2615G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736249 | ||||||
| chr5:32736250
|
A | AAAG | 5 | a0001c0001t0015g0107a0001c0001t0036g0009a0001c0003t0044g0036others(2): Show | 5 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.893-2612_893-2611i others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32736250 | |||||
| chr5:32736363
|
G | A | 86 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(83): Show | 86 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.893-2501G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736363 | ||||||
| chr5:32736368
|
G | A | 8 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(5): Show | 8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-2496G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736368 | ||||||
| chr5:32736394
|
A | T | 3 | a0001c0001t0004g0138a0001c0001t0026g0049a0001c0001t0026g0052 | 3 | HG01891.hp1 HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.893-2470A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736394 | ||||||
| chr5:32736614
|
G | A | 1 | a0001c0001t0055g0145 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.893-2250G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736614 | ||||||
| chr5:32736629
|
G | A | 23 | a0001c0001t0002g0129a0001c0001t0003g0075a0001c0001t0004g0138others(20): Show | 23 | HG00735.hp2 HG01074.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.893-2235G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736629 | ||||||
| chr5:32736729
|
C | T | 13 | a0001c0001t0003g0075a0001c0001t0005g0079a0001c0001t0006g0063others(10): Show | 13 | HG01074.hp2 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.893-2135C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736729 | ||||||
| chr5:32736821
|
C | T | 1 | a0001c0001t0005g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.893-2043C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736821 | ||||||
| chr5:32736895
|
C | T | 23 | a0001c0001t0002g0129a0001c0001t0003g0075a0001c0001t0004g0138others(20): Show | 23 | HG00735.hp2 HG01074.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.893-1969C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736895 | ||||||
| chr5:32737037
|
T | C | 11 | a0001c0001t0004g0139a0001c0001t0007g0151a0001c0001t0008g0046others(8): Show | 11 | HG01261.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.893-1827T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737037 | ||||||
| chr5:32737128
|
A | T | 11 | a0001c0001t0004g0139a0001c0001t0007g0151a0001c0001t0008g0046others(8): Show | 11 | HG01261.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.893-1736A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737128 | ||||||
| chr5:32737204
|
G | A | 23 | a0001c0001t0002g0129a0001c0001t0003g0075a0001c0001t0004g0138others(20): Show | 23 | HG00735.hp2 HG01074.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.893-1660G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737204 | ||||||
| chr5:32737213
|
T | C | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.893-1651T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737213 | ||||||
| chr5:32737237
|
T | C | 2 | a0001c0001t0010g0118a0001c0001t0010g0121 | 2 | HG01070.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.893-1627T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737237 | ||||||
| chr5:32737243
|
C | T | 1 | a0001c0001t0008g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.893-1621C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737243 | ||||||
| chr5:32737259
|
T | C | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.893-1605T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737259 | ||||||
| chr5:32737371
|
G | A | 1 | a0002c0002t0002g0093 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.893-1493G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737371 | ||||||
| chr5:32737477
|
C | T | 12 | a0001c0001t0003g0205a0001c0001t0004g0139a0001c0001t0007g0151others(9): Show | 12 | HG01261.hp1 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.893-1387C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737477 | ||||||
| chr5:32737478
|
G | A | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.893-1386G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737478 | ||||||
| chr5:32737508
|
C | A | 1 | a0001c0001t0001g0175 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.893-1356C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737508 | ||||||
| chr5:32737509
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.893-1355T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737509 | ||||||
| chr5:32737510
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.893-1354G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737510 | ||||||
| chr5:32737515
|
G | T | 2 | a0002c0002t0002g0042a0002c0002t0002g0055 | 2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.893-1349G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737515 | ||||||
| chr5:32737516
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.893-1348T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737516 | ||||||
| chr5:32737653
|
G | A | 1 | a0002c0002t0002g0312 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.893-1211G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737653 | ||||||
| chr5:32737826
|
T | C | 7 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(4): Show | 7 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.893-1038T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737826 | ||||||
| chr5:32737861
|
C | T | 7 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(4): Show | 7 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.893-1003C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737861 | ||||||
| chr5:32737942
|
A | G | 2 | a0001c0001t0045g0081a0002c0002t0029g0104 | 2 | HG00735.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.893-922A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737942 | ||||||
| chr5:32738122
|
T | G | 1 | a0001c0001t0004g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.893-742T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738122 | ||||||
| chr5:32738341
|
T | C | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0006g0006others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.893-523T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738341 | ||||||
| chr5:32738401
|
C | T | 4 | a0001c0001t0003g0224a0001c0001t0003g0317a0001c0001t0067g0266others(1): Show | 4 | HG02155.hp1 NA18967.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.893-463C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738401 | ||||||
| chr5:32738433
|
C | T | 2 | a0001c0003t0023g0038a0001c0003t0023g0039 | 2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.893-431C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738433 | ||||||
| chr5:32738547
|
A | C | 8 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(5): Show | 8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-317A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738547 | ||||||
| chr5:32738548
|
G | A | 144 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0089others(141): Show | 144 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.893-316G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738548 | ||||||
| chr5:32738652
|
G | A | 11 | a0001c0001t0002g0129a0001c0001t0004g0138a0001c0001t0015g0123others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.893-212G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738652 | ||||||
| chr5:32738702
|
G | A | 1 | a0002c0002t0002g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.893-162G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738702 | ||||||
| chr5:32738758
|
C | T | 1 | a0001c0001t0003g0179 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.893-106C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738758 | ||||||
| chr5:32738780
|
G | A | 8 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(5): Show | 8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-84G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738780 | ||||||
| chr5:32738785
|
C | T | 63 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(60): Show | 63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.893-79C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738785 | ||||||
| chr5:32739165
|
C | CTG | 5 | a0001c0001t0001g0097a0001c0001t0001g0316a0001c0001t0003g0246others(2): Show | 5 | HG00544.hp1 HG00544.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+153_1059+154d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32739165 | |||||
| chr5:32739165
|
CTG | C | 17 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1059+153_1059+154d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32739165 | |||||
| chr5:32739181
|
G | T | 1 | a0001c0001t0002g0004 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1059+151G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739181 | ||||||
| chr5:32739183
|
G | GT | 14 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0025others(11): Show | 14 | HG00741.hp1 HG01070.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1059+165dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32739183 | |||||
| chr5:32739183
|
G | T | 106 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0089others(103): Show | 106 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.1059+153G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739183 | ||||||
| chr5:32739185
|
T | G | 31 | a0001c0001t0001g0184a0001c0001t0001g0188a0001c0001t0001g0237others(28): Show | 32 | HG00621.hp1 HG01168.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.1059+155T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739185 | ||||||
| chr5:32739191
|
T | TA | 16 | a0001c0001t0002g0129a0001c0001t0003g0075a0001c0001t0004g0138others(13): Show | 16 | HG00735.hp2 HG01074.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1059+161_1059+162i others(3): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739191 | ||||||
| chr5:32739191
|
T | TTTA | 6 | a0001c0001t0006g0063a0001c0001t0006g0065a0001c0001t0017g0057others(3): Show | 6 | HG01891.hp2 HG02809.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+163_1059+164i others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32739191 | |||||
| chr5:32739555
|
A | G | 71 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(68): Show | 71 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1059+525A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739555 | ||||||
| chr5:32739556
|
C | A | 1 | a0001c0001t0003g0243 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1059+526C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739556 | ||||||
| chr5:32739625
|
G | T | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1059+595G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739625 | ||||||
| chr5:32739642
|
G | A | 1 | a0001c0001t0003g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1059+612G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739642 | ||||||
| chr5:32739679
|
C | T | 1 | a0002c0002t0002g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1059+649C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739679 | ||||||
| chr5:32739854
|
T | A | 1 | a0001c0001t0007g0137 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1059+824T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739854 | ||||||
| chr5:32739869
|
G | A | 3 | a0001c0001t0002g0004a0001c0001t0065g0051a0001c0004t0062g0134 | 3 | HG02109.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1059+839G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739869 | ||||||
| chr5:32739953
|
T | C | 63 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(60): Show | 63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1059+923T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739953 | ||||||
| chr5:32740078
|
G | A | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1059+1048G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740078 | ||||||
| chr5:32740120
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1059+1090A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740120 | ||||||
| chr5:32740240
|
G | T | 75 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(72): Show | 75 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1059+1210G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740240 | ||||||
| chr5:32740255
|
T | C | 75 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(72): Show | 75 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1059+1225T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740255 | ||||||
| chr5:32740302
|
T | C | 75 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(72): Show | 75 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1059+1272T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740302 | ||||||
| chr5:32740326
|
A | G | 143 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0089others(140): Show | 143 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.1059+1296A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740326 | ||||||
| chr5:32740437
|
T | A | 139 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0089others(136): Show | 139 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.1059+1407T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740437 | ||||||
| chr5:32740471
|
A | G | 1 | a0001c0003t0058g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1059+1441A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740471 | ||||||
| chr5:32740493
|
T | C | 9 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(6): Show | 9 | HG00280.hp1 HG01175.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059+1463T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740493 | ||||||
| chr5:32740608
|
G | GA | 49 | a0001c0001t0001g0044a0001c0001t0001g0141a0001c0001t0001g0149others(46): Show | 49 | HG00741.hp1 HG01070.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1059+1588dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32740608 | |||||
| chr5:32740630
|
G | A | 143 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0089others(140): Show | 143 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.1059+1600G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740630 | ||||||
| chr5:32740660
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1059+1630C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740660 | ||||||
| chr5:32740674
|
T | C | 8 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(5): Show | 8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+1644T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740674 | ||||||
| chr5:32740737
|
G | A | 63 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(60): Show | 63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1059+1707G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740737 | ||||||
| chr5:32740767
|
G | A | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1059+1737G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740767 | ||||||
| chr5:32740878
|
G | A | 65 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(62): Show | 65 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1059+1848G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740878 | ||||||
| chr5:32740930
|
A | C | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1059+1900A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740930 | ||||||
| chr5:32740953
|
C | T | 1 | a0001c0001t0008g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1059+1923C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740953 | ||||||
| chr5:32740977
|
T | C | 85 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(82): Show | 85 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1059+1947T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740977 | ||||||
| chr5:32741018
|
TA | T | 11 | a0001c0001t0002g0129a0001c0001t0004g0138a0001c0001t0015g0123others(8): Show | 11 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1059+1989delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741018 | ||||||
| chr5:32741027
|
C | T | 9 | a0001c0001t0004g0138a0001c0001t0015g0123a0001c0001t0026g0049others(6): Show | 9 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059+1997C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741027 | ||||||
| chr5:32741050
|
T | TAGGTTCA others(309): Show |
1 | a0002c0002t0054g0167 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1059+2037_1059+203 others(320): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741050
|
T | TAGGTTCA others(317): Show |
1 | a0002c0002t0011g0262 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1059+2037_1059+203 others(328): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741050
|
T | TAGGTTCA others(322): Show |
1 | a0001c0001t0003g0086 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1059+2037_1059+203 others(333): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741050
|
T | TAGGTTCA others(326): Show |
7 | a0001c0001t0001g0126a0002c0002t0002g0070a0002c0002t0002g0092others(4): Show | 7 | HG00639.hp1 HG00738.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(337): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741050
|
T | TAGGTTCA others(327): Show |
14 | a0001c0001t0001g0089a0001c0001t0001g0309a0001c0001t0032g0221others(11): Show | 14 | HG01516.hp1 HG02080.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(338): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741050
|
T | TAGGTTCA others(328): Show |
5 | a0001c0001t0001g0229a0001c0001t0003g0166a0001c0001t0009g0160others(2): Show | 5 | HG00621.hp2 HG01981.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(339): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741050
|
T | TAGGTTCA others(329): Show |
2 | a0001c0001t0009g0310a0002c0002t0002g0278 | 2 | NA18941.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(340): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741050
|
T | TAGGTTCA others(330): Show |
4 | a0001c0001t0003g0087a0002c0002t0012g0082a0002c0002t0012g0297others(1): Show | 4 | HG00642.hp2 HG01099.hp2 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(341): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741050
|
T | TAGGTTCA others(331): Show |
7 | a0001c0001t0001g0120a0001c0001t0003g0163a0002c0002t0002g0257others(4): Show | 7 | HG00609.hp2 HG01106.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(342): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741050
|
T | TAGGTTCA others(332): Show |
6 | a0001c0001t0001g0085a0001c0001t0003g0231a0001c0001t0021g0084others(3): Show | 6 | HG00609.hp1 HG00741.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(343): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741050
|
T | TAGGTTCA others(333): Show |
4 | a0002c0002t0002g0005a0002c0002t0002g0220a0002c0002t0020g0090others(1): Show | 4 | HG01257.hp1 HG02040.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(344): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741050
|
T | TAGGTTCA others(334): Show |
2 | a0002c0002t0002g0042a0002c0002t0033g0219 | 2 | HG02451.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(345): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741050
|
T | TAGGTTCA others(335): Show |
3 | a0001c0001t0001g0308a0001c0001t0006g0066a0002c0002t0002g0055 | 3 | HG02630.hp1 HG02809.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(346): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741050
|
T | TAGGTTCA others(336): Show |
1 | a0002c0002t0011g0264 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1059+2037_1059+203 others(347): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741050
|
T | TAGGTTCA others(337): Show |
2 | a0002c0002t0002g0091a0002c0002t0011g0263 | 2 | HG04228.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(348): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | |||||
| chr5:32741097
|
G | GTTGT | 8 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(5): Show | 8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+2068_1059+207 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741097 | |||||
| chr5:32741116
|
C | T | 111 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(108): Show | 111 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1059+2086C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741116 | ||||||
| chr5:32741156
|
C | T | 12 | a0001c0001t0002g0129a0001c0001t0004g0138a0001c0001t0015g0123others(9): Show | 12 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1059+2126C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741156 | ||||||
| chr5:32741279
|
A | G | 1 | a0002c0002t0002g0070 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1059+2249A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741279 | ||||||
| chr5:32741409
|
A | T | 1 | a0001c0001t0060g0293 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1059+2379A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741409 | ||||||
| chr5:32741482
|
T | C | 9 | a0001c0001t0004g0138a0001c0001t0015g0123a0001c0001t0026g0049others(6): Show | 9 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059+2452T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741482 | ||||||
| chr5:32741499
|
T | G | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1059+2469T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741499 | ||||||
| chr5:32741507
|
A | G | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1059+2477A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741507 | ||||||
| chr5:32741749
|
G | T | 1 | a0001c0003t0008g0031 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1059+2719G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741749 | ||||||
| chr5:32741771
|
C | CT | 64 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(61): Show | 64 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1059+2752dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741771 | |||||
| chr5:32741771
|
C | CTT | 13 | a0001c0001t0002g0129a0001c0001t0004g0138a0001c0001t0015g0123others(10): Show | 13 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1059+2751_1059+275 others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741771 | |||||
| chr5:32741792
|
C | G | 83 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(80): Show | 83 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1059+2762C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741792 | ||||||
| chr5:32742046
|
C | T | 1 | a0001c0003t0008g0031 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1059+3016C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742046 | ||||||
| chr5:32742047
|
G | A | 5 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0006g0113others(2): Show | 5 | HG01243.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+3017G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742047 | ||||||
| chr5:32742186
|
C | T | 1 | a0001c0003t0058g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1059+3156C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742186 | ||||||
| chr5:32742240
|
T | C | 77 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(74): Show | 77 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.1059+3210T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742240 | ||||||
| chr5:32742264
|
C | G | 8 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(5): Show | 8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+3234C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742264 | ||||||
| chr5:32742353
|
G | C | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1059+3323G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742353 | ||||||
| chr5:32742359
|
C | T | 84 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(81): Show | 84 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1059+3329C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742359 | ||||||
| chr5:32742439
|
T | A | 1 | a0001c0001t0017g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1059+3409T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742439 | ||||||
| chr5:32742857
|
G | A | 1 | a0001c0001t0003g0173 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1059+3827G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742857 | ||||||
| chr5:32742982
|
A | G | 1 | a0001c0001t0025g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1059+3952A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742982 | ||||||
| chr5:32743134
|
A | C | 3 | a0001c0001t0002g0004a0001c0001t0065g0051a0001c0004t0062g0134 | 3 | HG02109.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1059+4104A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743134 | ||||||
| chr5:32743392
|
A | ATG | 8 | a0001c0001t0003g0122a0001c0001t0005g0142a0001c0001t0007g0058others(5): Show | 8 | HG01257.hp1 HG01978.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+4378_1059+437 others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743392 | |||||
| chr5:32743392
|
A | ATGTG | 7 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(4): Show | 7 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1059+4376_1059+437 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743392 | |||||
| chr5:32743648
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1059+4618C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743648 | ||||||
| chr5:32743696
|
G | A | 1 | a0001c0001t0008g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1059+4666G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743696 | ||||||
| chr5:32743717
|
G | A | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1059+4687G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743717 | ||||||
| chr5:32743832
|
G | A | 1 | a0002c0002t0002g0111 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1059+4802G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743832 | ||||||
| chr5:32743919
|
A | G | 6 | a0001c0001t0004g0139a0001c0001t0008g0046a0001c0001t0008g0127others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+4889A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743919 | ||||||
| chr5:32743987
|
A | AT | 31 | a0001c0001t0001g0021a0001c0001t0001g0060a0001c0001t0001g0094others(28): Show | 31 | HG01192.hp2 HG01243.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.1059+4981dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743987 | |||||
| chr5:32743987
|
A | ATCT | 11 | a0001c0001t0001g0044a0001c0001t0004g0139a0001c0001t0008g0046others(8): Show | 11 | HG01257.hp2 HG01261.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1059+4958_1059+495 others(7): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743987 | |||||
| chr5:32743987
|
A | ATCTT | 32 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0001g0318others(29): Show | 32 | HG00280.hp1 HG00741.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1059+4958_1059+495 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743987 | |||||
| chr5:32743987
|
A | ATCTTT | 14 | a0001c0001t0004g0011a0001c0001t0004g0073a0001c0001t0004g0303others(11): Show | 14 | HG01106.hp2 HG01192.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.1059+4958_1059+495 others(9): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743987 | |||||
| chr5:32743987
|
AT | A | 13 | a0001c0001t0001g0101a0001c0001t0001g0175a0001c0001t0001g0185others(10): Show | 13 | HG00099.hp1 HG00099.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1059+4981delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743987 | |||||
| chr5:32743987
|
ATTTTTT | A | 74 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(71): Show | 74 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.1059+4976_1059+498 others(10): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743987 | |||||
| chr5:32743989
|
T | C | 2 | a0001c0003t0023g0038a0001c0003t0023g0039 | 2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1059+4959T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743989 | ||||||
| chr5:32743990
|
T | C | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1059+4960T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743990 | ||||||
| chr5:32743994
|
T | C | 1 | a0001c0001t0004g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1059+4964T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743994 | ||||||
| chr5:32743995
|
T | C | 74 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(71): Show | 74 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.1059+4965T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743995 | ||||||
| chr5:32744123
|
G | A | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1059+5093G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744123 | ||||||
| chr5:32744125
|
T | C | 1 | a0002c0002t0002g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1059+5095T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744125 | ||||||
| chr5:32744135
|
G | A | 2 | a0001c0001t0003g0251a0001c0001t0003g0253 | 2 | HG00423.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1059+5105G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744135 | ||||||
| chr5:32744273
|
G | A | 8 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0003g0232others(5): Show | 8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+5243G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744273 | ||||||
| chr5:32744597
|
G | A | 6 | a0002c0002t0002g0008a0002c0002t0002g0111a0002c0002t0002g0273others(3): Show | 6 | HG01346.hp1 HG02683.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+5567G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744597 | ||||||
| chr5:32744635
|
C | T | 2 | a0001c0001t0002g0004a0001c0004t0062g0134 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1059+5605C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744635 | ||||||
| chr5:32744687
|
C | T | 2 | a0001c0001t0014g0108a0001c0001t0014g0109 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1059+5657C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744687 | ||||||
| chr5:32744731
|
T | C | 83 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(80): Show | 83 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1059+5701T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744731 | ||||||
| chr5:32744790
|
C | T | 112 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(109): Show | 112 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1059+5760C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744790 | ||||||
| chr5:32744803
|
C | T | 61 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(58): Show | 61 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1059+5773C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744803 | ||||||
| chr5:32744804
|
A | G | 4 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG01192.hp2 HG01884.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+5774A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744804 | ||||||
| chr5:32744810
|
T | G | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0006g0006others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+5780T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744810 | ||||||
| chr5:32744901
|
T | A | 6 | a0001c0001t0015g0123a0001c0001t0045g0081a0001c0001t0047g0110others(3): Show | 6 | HG00735.hp2 HG01074.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+5871T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744901 | ||||||
| chr5:32744923
|
C | T | 86 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(83): Show | 86 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.1059+5893C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744923 | ||||||
| chr5:32745105
|
A | G | 1 | a0002c0002t0002g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1059+6075A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745105 | ||||||
| chr5:32745153
|
C | T | 7 | a0002c0002t0002g0070a0002c0002t0002g0135a0002c0002t0002g0277others(4): Show | 7 | HG01981.hp2 HG02293.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059+6123C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745153 | ||||||
| chr5:32745177
|
A | C | 125 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(122): Show | 125 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1059+6147A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745177 | ||||||
| chr5:32745242
|
C | T | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1059+6212C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745242 | ||||||
| chr5:32745251
|
C | A | 14 | a0001c0001t0002g0004a0001c0001t0003g0075a0001c0001t0004g0139others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1059+6221C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745251 | ||||||
| chr5:32745328
|
A | C | 1 | a0001c0001t0003g0250 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1059+6298A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745328 | ||||||
| chr5:32745490
|
T | G | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1059+6460T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745490 | ||||||
| chr5:32745527
|
A | G | 8 | a0001c0001t0006g0063a0001c0001t0006g0065a0001c0001t0008g0204others(5): Show | 8 | HG01891.hp2 HG02486.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+6497A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745527 | ||||||
| chr5:32745562
|
A | G | 1 | a0001c0001t0004g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1059+6532A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745562 | ||||||
| chr5:32745592
|
A | G | 2 | a0001c0006t0061g0041a0002c0002t0002g0072 | 2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1059+6562A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745592 | ||||||
| chr5:32745646
|
C | A | 146 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(143): Show | 146 | HG00323.hp1 HG00423.hp2 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.1059+6616C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745646 | ||||||
| chr5:32745720
|
G | C | 1 | a0002c0002t0011g0264 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1059+6690G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745720 | ||||||
| chr5:32745949
|
T | C | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1059+6919T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745949 | ||||||
| chr5:32746071
|
G | A | 1 | a0002c0002t0027g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1059+7041G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32746071 | ||||||
| chr5:32746173
|
T | C | 2 | a0001c0004t0062g0134a0001c0005t0056g0268 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1059+7143T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32746173 | ||||||
| chr5:32746320
|
T | C | 1 | a0001c0003t0008g0031 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1059+7290T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32746320 | ||||||
| chr5:32746399
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1059+7369C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32746399 | ||||||
| chr5:32746441
|
A | G | 123 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0089others(120): Show | 123 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.1059+7411A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32746441 | ||||||
| chr5:32746459
|
G | A | 1 | a0001c0001t0015g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1059+7429G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32746459 | ||||||
| chr5:32746475
|
A | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0066g0053 | 3 | HG01243.hp2 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1059+7445A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32746475 | ||||||
| chr5:32747073
|
T | C | 14 | a0001c0001t0005g0079a0001c0001t0005g0152a0001c0001t0024g0265others(11): Show | 14 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1059+8043T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32747073 | ||||||
| chr5:32747082
|
A | G | 63 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(60): Show | 63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1059+8052A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32747082 | ||||||
| chr5:32747198
|
C | A | 1 | a0001c0001t0004g0012 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1059+8168C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32747198 | ||||||
| chr5:32747605
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1059+8575C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32747605 | ||||||
| chr5:32747728
|
C | T | 15 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0025others(12): Show | 15 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1059+8698C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32747728 | ||||||
| chr5:32747748
|
G | A | 17 | a0001c0001t0005g0079a0001c0001t0005g0142a0001c0001t0005g0152others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1059+8718G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32747748 | ||||||
| chr5:32747757
|
AT | A | 113 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(110): Show | 113 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.1059+8743delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32747757 | |||||
| chr5:32748049
|
C | T | 1 | a0001c0001t0022g0223 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1059+9019C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748049 | ||||||
| chr5:32748156
|
C | A | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1059+9126C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748156 | ||||||
| chr5:32748206
|
C | T | 4 | a0001c0001t0015g0123a0001c0006t0061g0041a0002c0002t0002g0072others(1): Show | 4 | HG01952.hp1 HG02055.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+9176C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748206 | ||||||
| chr5:32748247
|
A | G | 1 | a0001c0001t0057g0282 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1059+9217A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748247 | ||||||
| chr5:32748433
|
A | AGCAT | 118 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0089others(115): Show | 118 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1059+9404_1059+940 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32748433 | |||||
| chr5:32748531
|
G | A | 118 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0089others(115): Show | 118 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1059+9501G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748531 | ||||||
| chr5:32748552
|
G | A | 118 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0089others(115): Show | 118 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1059+9522G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748552 | ||||||
| chr5:32748582
|
G | A | 1 | a0001c0001t0008g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1059+9552G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748582 | ||||||
| chr5:32748635
|
A | G | 5 | a0001c0001t0004g0139a0001c0001t0008g0046a0001c0001t0008g0127others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+9605A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748635 | ||||||
| chr5:32748956
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1059+9926A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748956 | ||||||
| chr5:32748966
|
T | C | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1059+9936T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748966 | ||||||
| chr5:32749042
|
G | A | 1 | a0001c0001t0034g0157 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1059+10012G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749042 | ||||||
| chr5:32749049
|
C | T | 2 | a0001c0001t0004g0146a0001c0001t0004g0147 | 2 | HG00741.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1059+10019C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749049 | ||||||
| chr5:32749196
|
AT | A | 153 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0085others(150): Show | 153 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(150): Show |
intron_variant | MODIFIER | c.1059+10173delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32749196 | |||||
| chr5:32749228
|
A | C | 1 | a0001c0001t0003g0246 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1059+10198A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749228 | ||||||
| chr5:32749234
|
C | T | 36 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0004g0011others(33): Show | 36 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1059+10204C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749234 | ||||||
| chr5:32749317
|
T | A | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1059+10287T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749317 | ||||||
| chr5:32749318
|
A | T | 128 | a0001c0001t0001g0022a0001c0001t0001g0085a0001c0001t0001g0089others(125): Show | 128 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.1059+10288A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749318 | ||||||
| chr5:32749355
|
C | T | 1 | a0001c0001t0003g0252 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1059+10325C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749355 | ||||||
| chr5:32749432
|
T | C | 1 | a0001c0001t0004g0146 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1059+10402T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749432 | ||||||
| chr5:32749486
|
G | A | 117 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0120others(114): Show | 117 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.1059+10456G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749486 | ||||||
| chr5:32749523
|
A | G | 1 | a0001c0001t0003g0186 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1059+10493A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749523 | ||||||
| chr5:32749643
|
T | C | 1 | a0002c0002t0002g0277 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1059+10613T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749643 | ||||||
| chr5:32749745
|
C | T | 2 | a0001c0004t0062g0134a0001c0005t0056g0268 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1059+10715C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749745 | ||||||
| chr5:32749774
|
C | A | 1 | a0002c0002t0002g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1059+10744C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749774 | ||||||
| chr5:32749845
|
C | T | 1 | a0002c0002t0002g0135 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1059+10815C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749845 | ||||||
| chr5:32749883
|
C | T | 1 | a0001c0001t0025g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1059+10853C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749883 | ||||||
| chr5:32749896
|
A | G | 11 | a0001c0001t0003g0117a0001c0001t0003g0119a0001c0001t0003g0156others(8): Show | 11 | HG00544.hp2 HG02027.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.1059+10866A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749896 | ||||||
| chr5:32749969
|
A | G | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1059+10939A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749969 | ||||||
| chr5:32750276
|
C | T | 1 | a0001c0003t0005g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1059+11246C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750276 | ||||||
| chr5:32750292
|
C | T | 36 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0004g0011others(33): Show | 36 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1059+11262C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750292 | ||||||
| chr5:32750309
|
G | T | 115 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0089others(112): Show | 115 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1059+11279G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750309 | ||||||
| chr5:32750641
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1059+11611G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750641 | ||||||
| chr5:32750675
|
A | C | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1059+11645A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750675 | ||||||
| chr5:32750783
|
T | C | 1 | a0001c0001t0064g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1059+11753T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750783 | ||||||
| chr5:32750784
|
C | T | 1 | a0002c0002t0002g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1059+11754C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750784 | ||||||
| chr5:32750801
|
C | T | 2 | a0001c0001t0019g0002a0001c0001t0019g0003 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1059+11771C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750801 | ||||||
| chr5:32750877
|
T | C | 141 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0085others(138): Show | 141 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.1059+11847T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750877 | ||||||
| chr5:32751044
|
G | A | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1059+12014G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751044 | ||||||
| chr5:32751155
|
TA | T | 63 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(60): Show | 63 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1059+12131delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32751155 | |||||
| chr5:32751155
|
TAA | T | 5 | a0001c0001t0001g0172a0001c0001t0003g0179a0001c0001t0013g0279others(2): Show | 5 | HG01496.hp2 HG01934.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+12130_1059+12 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32751155 | |||||
| chr5:32751436
|
G | A | 5 | a0001c0001t0015g0123a0001c0001t0047g0110a0001c0006t0061g0041others(2): Show | 5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+12406G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751436 | ||||||
| chr5:32751560
|
G | A | 5 | a0001c0001t0015g0123a0001c0001t0047g0110a0001c0006t0061g0041others(2): Show | 5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+12530G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751560 | ||||||
| chr5:32751683
|
G | A | 2 | a0001c0001t0019g0002a0001c0001t0019g0003 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1059+12653G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751683 | ||||||
| chr5:32751880
|
G | A | 5 | a0001c0001t0004g0139a0001c0001t0008g0046a0001c0001t0008g0127others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+12850G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751880 | ||||||
| chr5:32751921
|
G | A | 43 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0004g0011others(40): Show | 43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1059+12891G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751921 | ||||||
| chr5:32751989
|
G | A | 1 | a0001c0001t0007g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1059+12959G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751989 | ||||||
| chr5:32751992
|
G | A | 72 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(69): Show | 72 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1059+12962G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751992 | ||||||
| chr5:32752022
|
T | G | 67 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(64): Show | 67 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1059+12992T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752022 | ||||||
| chr5:32752029
|
C | T | 2 | a0001c0001t0004g0043a0001c0001t0042g0045 | 2 | HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1059+12999C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752029 | ||||||
| chr5:32752030
|
C | T | 1 | a0001c0001t0024g0265 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1059+13000C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752030 | ||||||
| chr5:32752045
|
T | C | 72 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(69): Show | 72 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1059+13015T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752045 | ||||||
| chr5:32752051
|
A | C | 1 | a0001c0001t0004g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1059+13021A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752051 | ||||||
| chr5:32752068
|
G | T | 5 | a0001c0001t0015g0123a0001c0001t0047g0110a0001c0006t0061g0041others(2): Show | 5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+13038G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752068 | ||||||
| chr5:32752160
|
T | C | 4 | a0001c0001t0004g0303a0001c0001t0004g0304a0001c0001t0004g0306others(1): Show | 4 | HG02922.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+13130T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752160 | ||||||
| chr5:32752201
|
C | T | 4 | a0001c0001t0003g0096a0001c0001t0003g0300a0001c0001t0003g0301others(1): Show | 4 | HG02083.hp1 NA18950.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+13171C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752201 | ||||||
| chr5:32752207
|
CCAAAAA | C | 52 | a0001c0001t0001g0044a0001c0001t0001g0141a0001c0001t0001g0149others(49): Show | 52 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.1059+13216_1059+13 others(12): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32752207 | |||||
| chr5:32752207
|
CCAAAAAC others(5): Show |
C | 73 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(70): Show | 73 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1059+13210_1059+13 others(18): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32752207 | |||||
| chr5:32752207
|
CCAAAAAC others(11): Show |
C | 16 | a0001c0001t0005g0079a0001c0001t0005g0152a0001c0001t0007g0151others(13): Show | 16 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1059+13204_1059+13 others(24): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32752207 | |||||
| chr5:32752258
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1059+13228C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752258 | ||||||
| chr5:32752333
|
C | T | 5 | a0001c0001t0003g0117a0001c0001t0003g0156a0001c0001t0003g0187others(2): Show | 5 | HG02027.hp1 HG02523.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+13303C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752333 | ||||||
| chr5:32752469
|
C | T | 1 | a0002c0002t0002g0218 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1059+13439C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752469 | ||||||
| chr5:32752493
|
G | T | 41 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0004g0011others(38): Show | 41 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.1059+13463G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752493 | ||||||
| chr5:32752533
|
G | T | 4 | a0001c0001t0004g0303a0001c0001t0004g0304a0001c0001t0004g0306others(1): Show | 4 | HG02922.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+13503G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752533 | ||||||
| chr5:32752545
|
C | T | 1 | a0001c0001t0006g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1059+13515C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752545 | ||||||
| chr5:32752582
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0316 | 2 | HG00544.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1059+13552A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752582 | ||||||
| chr5:32753080
|
G | A | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1059+14050G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753080 | ||||||
| chr5:32753120
|
A | G | 1 | a0001c0001t0003g0179 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1059+14090A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753120 | ||||||
| chr5:32753190
|
A | G | 1 | a0001c0001t0021g0084 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1059+14160A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753190 | ||||||
| chr5:32753323
|
C | CT | 6 | a0001c0001t0006g0063a0001c0001t0006g0065a0001c0001t0017g0057others(3): Show | 6 | HG01891.hp2 HG02809.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+14306dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753323 | |||||
| chr5:32753323
|
C | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 7 | HG00323.hp1 HG00639.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059+14293C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753323 | ||||||
| chr5:32753323
|
CTT | C | 69 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(66): Show | 69 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1059+14305_1059+14 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753323 | |||||
| chr5:32753331
|
T | C | 5 | a0001c0001t0015g0123a0001c0001t0047g0110a0001c0006t0061g0041others(2): Show | 5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+14301T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753331 | ||||||
| chr5:32753387
|
A | G | 1 | a0001c0001t0003g0301 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1059+14357A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753387 | ||||||
| chr5:32753439
|
G | A | 2 | a0001c0001t0026g0049a0001c0001t0026g0052 | 2 | HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1059+14409G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753439 | ||||||
| chr5:32753501
|
C | G | 2 | a0001c0001t0004g0138a0001c0001t0055g0145 | 2 | HG01192.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1059+14471C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753501 | ||||||
| chr5:32753501
|
C | T | 5 | a0001c0001t0015g0123a0001c0001t0047g0110a0001c0006t0061g0041others(2): Show | 5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+14471C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753501 | ||||||
| chr5:32753566
|
T | C | 64 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(61): Show | 64 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1059+14536T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753566 | ||||||
| chr5:32753585
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1059+14555C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753585 | ||||||
| chr5:32753624
|
C | CT | 28 | a0001c0001t0001g0060a0001c0001t0001g0168a0001c0001t0001g0175others(25): Show | 28 | HG01069.hp1 HG01069.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1059+14620dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753624 | |||||
| chr5:32753624
|
CT | C | 22 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0062others(19): Show | 22 | HG01074.hp2 HG01192.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1059+14620delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753624 | |||||
| chr5:32753624
|
CTT | C | 59 | a0001c0001t0001g0069a0001c0001t0001g0085a0001c0001t0001g0229others(56): Show | 59 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1059+14619_1059+14 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753624 | |||||
| chr5:32753624
|
CTTT | C | 8 | a0001c0001t0001g0126a0001c0001t0005g0142a0001c0001t0015g0107others(5): Show | 8 | HG00280.hp1 HG01261.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+14618_1059+14 others(9): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753624 | |||||
| chr5:32753624
|
CTTTT | C | 17 | a0001c0001t0001g0023a0001c0001t0005g0079a0001c0001t0005g0152others(14): Show | 17 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1059+14617_1059+14 others(10): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753624 | |||||
| chr5:32753624
|
CTTTTT | C | 34 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0001g0202others(31): Show | 34 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1059+14616_1059+14 others(11): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753624 | |||||
| chr5:32753624
|
CTTTTTT | C | 12 | a0001c0001t0006g0063a0001c0001t0006g0065a0001c0001t0008g0204others(9): Show | 12 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1059+14615_1059+14 others(12): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753624 | |||||
| chr5:32753674
|
A | G | 1 | a0001c0001t0008g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1059+14644A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753674 | ||||||
| chr5:32753744
|
A | G | 5 | a0001c0001t0015g0123a0001c0001t0047g0110a0001c0006t0061g0041others(2): Show | 5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+14714A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753744 | ||||||
| chr5:32754004
|
C | T | 2 | a0001c0004t0062g0134a0001c0005t0056g0268 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1059+14974C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754004 | ||||||
| chr5:32754053
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1059+15023C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754053 | ||||||
| chr5:32754129
|
A | G | 2 | a0001c0001t0001g0269a0001c0001t0009g0193 | 2 | NA19011.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1059+15099A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754129 | ||||||
| chr5:32754326
|
T | C | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0006g0006 | 3 | HG02145.hp2 HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1059+15296T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754326 | ||||||
| chr5:32754347
|
G | GT | 55 | a0001c0001t0001g0023a0001c0001t0001g0099a0001c0001t0001g0141others(52): Show | 55 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.1059+15327dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32754347 | |||||
| chr5:32754384
|
T | C | 1 | a0001c0003t0044g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1059+15354T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754384 | ||||||
| chr5:32754696
|
G | T | 5 | a0001c0001t0015g0123a0001c0001t0047g0110a0001c0006t0061g0041others(2): Show | 5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+15666G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754696 | ||||||
| chr5:32754979
|
G | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+15949G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754979 | ||||||
| chr5:32754996
|
G | A | 5 | a0001c0001t0015g0123a0001c0001t0047g0110a0001c0006t0061g0041others(2): Show | 5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+15966G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754996 | ||||||
| chr5:32755093
|
C | T | 1 | a0002c0002t0002g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1059+16063C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755093 | ||||||
| chr5:32755155
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1059+16125C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755155 | ||||||
| chr5:32755248
|
T | C | 1 | a0001c0001t0007g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1059+16218T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755248 | ||||||
| chr5:32755275
|
G | C | 1 | a0001c0001t0001g0171 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1059+16245G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755275 | ||||||
| chr5:32755416
|
T | C | 43 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0004g0011others(40): Show | 43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1059+16386T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755416 | ||||||
| chr5:32755418
|
G | T | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0006g0006 | 3 | HG02145.hp2 HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1059+16388G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755418 | ||||||
| chr5:32755483
|
T | C | 70 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(67): Show | 70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1059+16453T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755483 | ||||||
| chr5:32755858
|
G | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+16828G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755858 | ||||||
| chr5:32756101
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG02683.hp2 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1059+17071C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756101 | ||||||
| chr5:32756162
|
T | C | 1 | a0001c0001t0007g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1059+17132T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756162 | ||||||
| chr5:32756237
|
A | T | 2 | a0002c0002t0002g0042a0002c0002t0002g0055 | 2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1059+17207A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756237 | ||||||
| chr5:32756238
|
G | A | 2 | a0002c0002t0002g0042a0002c0002t0002g0055 | 2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1059+17208G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756238 | ||||||
| chr5:32756288
|
C | T | 1 | a0002c0002t0027g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1059+17258C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756288 | ||||||
| chr5:32756289
|
A | G | 1 | a0002c0002t0027g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1059+17259A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756289 | ||||||
| chr5:32756321
|
T | A | 36 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0004g0011others(33): Show | 36 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1059+17291T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756321 | ||||||
| chr5:32756373
|
A | T | 1 | a0001c0001t0007g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1059+17343A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756373 | ||||||
| chr5:32756433
|
T | C | 70 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(67): Show | 70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1059+17403T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756433 | ||||||
| chr5:32756486
|
G | A | 5 | a0001c0001t0004g0139a0001c0001t0008g0046a0001c0001t0008g0127others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+17456G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756486 | ||||||
| chr5:32756494
|
C | T | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1059+17464C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756494 | ||||||
| chr5:32756544
|
T | A | 2 | a0001c0003t0023g0038a0001c0003t0023g0039 | 2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1059+17514T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756544 | ||||||
| chr5:32756669
|
C | G | 6 | a0001c0001t0003g0096a0001c0001t0003g0300a0001c0001t0003g0301others(3): Show | 6 | HG02083.hp1 HG02723.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+17639C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756669 | ||||||
| chr5:32756683
|
C | T | 1 | a0001c0001t0021g0084 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1059+17653C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756683 | ||||||
| chr5:32756854
|
A | C | 1 | a0002c0002t0002g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1059+17824A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756854 | ||||||
| chr5:32756857
|
G | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0126 | 2 | HG00741.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1059+17827G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756857 | ||||||
| chr5:32756875
|
T | G | 1 | a0001c0001t0001g0184 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1060-17833T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756875 | ||||||
| chr5:32756911
|
T | A | 1 | a0001c0001t0003g0096 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1060-17797T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756911 | ||||||
| chr5:32756938
|
G | C | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0006g0006 | 3 | HG02145.hp2 HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1060-17770G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756938 | ||||||
| chr5:32757035
|
C | T | 1 | a0001c0001t0007g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1060-17673C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757035 | ||||||
| chr5:32757036
|
A | G | 1 | a0001c0001t0007g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1060-17672A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757036 | ||||||
| chr5:32757062
|
G | A | 2 | a0001c0001t0010g0080a0001c0001t0010g0103 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1060-17646G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757062 | ||||||
| chr5:32757102
|
C | T | 1 | a0001c0001t0007g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1060-17606C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757102 | ||||||
| chr5:32757143
|
A | C | 8 | a0001c0001t0001g0237a0001c0001t0003g0001a0001c0001t0003g0166others(5): Show | 9 | HG00621.hp1 HG02015.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-17565A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757143 | ||||||
| chr5:32757166
|
A | T | 70 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(67): Show | 70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-17542A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757166 | ||||||
| chr5:32757175
|
A | G | 29 | a0001c0001t0001g0237a0001c0001t0003g0001a0001c0001t0003g0095others(26): Show | 30 | HG00621.hp1 HG01109.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1060-17533A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757175 | ||||||
| chr5:32757185
|
G | T | 2 | a0002c0002t0020g0090a0002c0002t0020g0227 | 2 | HG02040.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1060-17523G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757185 | ||||||
| chr5:32757202
|
C | A | 4 | a0001c0001t0015g0123a0001c0001t0047g0110a0001c0006t0061g0041others(1): Show | 4 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-17506C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757202 | ||||||
| chr5:32757211
|
C | T | 2 | a0001c0001t0006g0113a0001c0001t0006g0114 | 2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1060-17497C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757211 | ||||||
| chr5:32757226
|
C | G | 1 | a0001c0001t0015g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1060-17482C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757226 | ||||||
| chr5:32757299
|
T | C | 1 | a0001c0001t0003g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1060-17409T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757299 | ||||||
| chr5:32757335
|
G | T | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-17373G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757335 | ||||||
| chr5:32757349
|
T | G | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-17359T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757349 | ||||||
| chr5:32757538
|
A | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0021others(1): Show | 4 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-17170A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757538 | ||||||
| chr5:32757546
|
A | C | 1 | a0001c0001t0001g0116 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1060-17162A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757546 | ||||||
| chr5:32757585
|
C | G | 1 | a0002c0002t0002g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1060-17123C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757585 | ||||||
| chr5:32757679
|
A | G | 1 | a0002c0002t0002g0314 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1060-17029A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757679 | ||||||
| chr5:32757756
|
T | C | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | NA19060.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1060-16952T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757756 | ||||||
| chr5:32757759
|
T | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-16949T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757759 | ||||||
| chr5:32757797
|
G | A | 1 | a0002c0002t0002g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1060-16911G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757797 | ||||||
| chr5:32757817
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1060-16891T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757817 | ||||||
| chr5:32757832
|
G | A | 2 | a0001c0003t0023g0038a0001c0003t0023g0039 | 2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1060-16876G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757832 | ||||||
| chr5:32758043
|
G | T | 2 | a0001c0001t0003g0095a0001c0001t0003g0205 | 2 | NA18940.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1060-16665G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758043 | ||||||
| chr5:32758051
|
T | C | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-16657T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758051 | ||||||
| chr5:32758060
|
CT | C | 3 | a0001c0001t0001g0023a0001c0001t0015g0107a0002c0002t0002g0271 | 3 | HG00280.hp1 HG02818.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1060-16647delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758060 | ||||||
| chr5:32758062
|
CT | C | 134 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0126others(131): Show | 134 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(131): Show |
intron_variant | MODIFIER | c.1060-16638delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32758062 | |||||
| chr5:32758063
|
T | C | 3 | a0001c0001t0001g0023a0001c0001t0015g0107a0002c0002t0002g0271 | 3 | HG00280.hp1 HG02818.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1060-16645T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758063 | ||||||
| chr5:32758114
|
C | G | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-16594C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758114 | ||||||
| chr5:32758256
|
A | C | 1 | a0001c0001t0001g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1060-16452A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758256 | ||||||
| chr5:32758348
|
G | A | 43 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0004g0011others(40): Show | 43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1060-16360G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758348 | ||||||
| chr5:32758404
|
T | C | 60 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(57): Show | 60 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1060-16304T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758404 | ||||||
| chr5:32758472
|
G | A | 2 | a0002c0002t0011g0263a0002c0002t0054g0167 | 2 | HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1060-16236G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758472 | ||||||
| chr5:32758551
|
T | C | 70 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(67): Show | 70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-16157T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758551 | ||||||
| chr5:32758582
|
G | GT | 69 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(66): Show | 69 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1060-16120dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32758582 | |||||
| chr5:32758758
|
T | G | 1 | a0001c0001t0051g0270 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1060-15950T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758758 | ||||||
| chr5:32758815
|
A | G | 1 | a0001c0001t0008g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1060-15893A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758815 | ||||||
| chr5:32758923
|
T | A | 17 | a0001c0001t0005g0079a0001c0001t0005g0142a0001c0001t0005g0152others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1060-15785T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758923 | ||||||
| chr5:32758939
|
T | G | 5 | a0001c0001t0015g0123a0001c0001t0047g0110a0001c0006t0061g0041others(2): Show | 5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-15769T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758939 | ||||||
| chr5:32758980
|
A | C | 5 | a0001c0001t0004g0139a0001c0001t0008g0046a0001c0001t0008g0127others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-15728A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758980 | ||||||
| chr5:32759035
|
A | G | 1 | a0001c0005t0056g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1060-15673A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759035 | ||||||
| chr5:32759233
|
G | A | 1 | a0002c0002t0002g0135 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1060-15475G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759233 | ||||||
| chr5:32759285
|
T | C | 70 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(67): Show | 70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-15423T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759285 | ||||||
| chr5:32759422
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1060-15286G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759422 | ||||||
| chr5:32759436
|
T | G | 70 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(67): Show | 70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-15272T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759436 | ||||||
| chr5:32759446
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1060-15262T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759446 | ||||||
| chr5:32759451
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1060-15257T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759451 | ||||||
| chr5:32759457
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1060-15251C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759457 | ||||||
| chr5:32759458
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1060-15250C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759458 | ||||||
| chr5:32759475
|
C | T | 15 | a0001c0001t0001g0115a0001c0001t0005g0079a0001c0001t0005g0152others(12): Show | 15 | HG02040.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1060-15233C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759475 | ||||||
| chr5:32759487
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-15221C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759487 | ||||||
| chr5:32759488
|
G | A | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1060-15220G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759488 | ||||||
| chr5:32759488
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1060-15220G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759488 | ||||||
| chr5:32759507
|
T | G | 43 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0004g0011others(40): Show | 43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1060-15201T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759507 | ||||||
| chr5:32759515
|
G | T | 1 | a0001c0001t0053g0315 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1060-15193G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759515 | ||||||
| chr5:32759538
|
T | C | 1 | a0002c0002t0052g0165 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1060-15170T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759538 | ||||||
| chr5:32759652
|
G | T | 1 | a0001c0001t0001g0275 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1060-15056G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759652 | ||||||
| chr5:32759671
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-15037C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759671 | ||||||
| chr5:32759681
|
TG | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-15025delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32759681 | |||||
| chr5:32759713
|
C | T | 3 | a0001c0001t0008g0127a0001c0001t0008g0305a0001c0001t0059g0155 | 3 | HG02257.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1060-14995C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759713 | ||||||
| chr5:32759716
|
T | G | 6 | a0001c0001t0001g0023a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-14992T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759716 | ||||||
| chr5:32759740
|
G | C | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-14968G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759740 | ||||||
| chr5:32759830
|
G | T | 1 | a0001c0004t0062g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1060-14878G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759830 | ||||||
| chr5:32760089
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1060-14619G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760089 | ||||||
| chr5:32760125
|
GT | G | 53 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(50): Show | 53 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1060-14572delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32760125 | |||||
| chr5:32760159
|
G | A | 1 | a0001c0001t0007g0058 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1060-14549G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760159 | ||||||
| chr5:32760269
|
T | C | 70 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(67): Show | 70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-14439T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760269 | ||||||
| chr5:32760277
|
T | C | 53 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(50): Show | 53 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1060-14431T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760277 | ||||||
| chr5:32760547
|
T | C | 2 | a0001c0001t0003g0251a0001c0001t0003g0253 | 2 | HG00423.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1060-14161T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760547 | ||||||
| chr5:32760574
|
T | C | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1060-14134T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760574 | ||||||
| chr5:32760649
|
G | A | 6 | a0001c0001t0015g0123a0001c0001t0040g0161a0001c0001t0047g0110others(3): Show | 6 | HG01074.hp1 HG01261.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-14059G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760649 | ||||||
| chr5:32760655
|
T | G | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1060-14053T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760655 | ||||||
| chr5:32760667
|
G | T | 58 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(55): Show | 58 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1060-14041G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760667 | ||||||
| chr5:32760667
|
GT | G | 9 | a0001c0001t0015g0123a0001c0001t0019g0002a0001c0001t0047g0110others(6): Show | 9 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-14028delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32760667 | |||||
| chr5:32760681
|
A | T | 5 | a0001c0001t0001g0044a0001c0001t0002g0004a0001c0001t0002g0129others(2): Show | 5 | HG02109.hp1 HG03098.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-14027A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760681 | ||||||
| chr5:32760742
|
T | C | 2 | a0001c0001t0004g0025a0001c0001t0004g0026 | 2 | HG01496.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1060-13966T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760742 | ||||||
| chr5:32760988
|
G | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-13720G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760988 | ||||||
| chr5:32761211
|
TA | T | 13 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0202others(10): Show | 13 | HG00280.hp1 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1060-13486delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32761211 | |||||
| chr5:32761231
|
T | C | 1 | a0001c0001t0003g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1060-13477T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761231 | ||||||
| chr5:32761258
|
C | T | 5 | a0001c0001t0015g0123a0001c0001t0047g0110a0001c0006t0061g0041others(2): Show | 5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-13450C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761258 | ||||||
| chr5:32761323
|
C | T | 59 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(56): Show | 59 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1060-13385C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761323 | ||||||
| chr5:32761349
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1060-13359A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761349 | ||||||
| chr5:32761404
|
A | T | 2 | a0001c0001t0001g0185a0001c0001t0003g0186 | 2 | HG03704.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1060-13304A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761404 | ||||||
| chr5:32761472
|
T | C | 6 | a0002c0002t0002g0008a0002c0002t0002g0111a0002c0002t0002g0273others(3): Show | 6 | HG01346.hp1 HG02683.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-13236T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761472 | ||||||
| chr5:32761512
|
T | C | 5 | a0001c0001t0015g0123a0001c0001t0047g0110a0001c0006t0061g0041others(2): Show | 5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-13196T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761512 | ||||||
| chr5:32761591
|
C | T | 14 | a0001c0001t0005g0079a0001c0001t0005g0152a0001c0001t0024g0265others(11): Show | 14 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1060-13117C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761591 | ||||||
| chr5:32761646
|
T | G | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1060-13062T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761646 | ||||||
| chr5:32761658
|
AT | A | 5 | a0001c0001t0015g0123a0001c0001t0047g0110a0001c0006t0061g0041others(2): Show | 5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-13041delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32761658 | |||||
| chr5:32761737
|
T | TTTTTA | 70 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(67): Show | 70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-12961_1060-12 others(11): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32761737 | |||||
| chr5:32761794
|
A | T | 1 | a0001c0005t0056g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1060-12914A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761794 | ||||||
| chr5:32761962
|
G | T | 4 | a0001c0001t0004g0303a0001c0001t0004g0304a0001c0001t0004g0306others(1): Show | 4 | HG02922.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-12746G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761962 | ||||||
| chr5:32762012
|
A | T | 4 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG01192.hp2 HG01884.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-12696A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762012 | ||||||
| chr5:32762148
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1060-12560A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762148 | ||||||
| chr5:32762196
|
A | G | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1060-12512A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762196 | ||||||
| chr5:32762332
|
T | C | 2 | a0001c0003t0005g0028a0001c0003t0005g0029 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1060-12376T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762332 | ||||||
| chr5:32762333
|
G | A | 43 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0004g0011others(40): Show | 43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1060-12375G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762333 | ||||||
| chr5:32762427
|
C | T | 2 | a0001c0001t0004g0138a0001c0001t0055g0145 | 2 | HG01192.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1060-12281C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762427 | ||||||
| chr5:32762456
|
T | TTGTTTCC others(326): Show |
2 | a0002c0002t0002g0214a0002c0002t0002g0215 | 2 | NA18974.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1060-12236_1060-12 others(339): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32762456 | |||||
| chr5:32762456
|
T | TTGTTTCC others(327): Show |
34 | a0001c0001t0003g0095a0001c0001t0003g0112a0001c0001t0003g0117others(31): Show | 34 | HG00280.hp2 HG01069.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1060-12236_1060-12 others(340): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32762456 | |||||
| chr5:32762456
|
T | TTGTTTCC others(327): Show |
1 | a0001c0001t0003g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1060-12236_1060-12 others(340): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32762456 | |||||
| chr5:32762456
|
T | TTGTTTCC others(328): Show |
23 | a0001c0001t0001g0237a0001c0001t0003g0096a0001c0001t0003g0105others(20): Show | 23 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.1060-12236_1060-12 others(341): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32762456 | |||||
| chr5:32762456
|
T | TTGTTTCC others(328): Show |
1 | a0001c0001t0003g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1060-12236_1060-12 others(341): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32762456 | |||||
| chr5:32762456
|
T | TTGTTTCC others(329): Show |
4 | a0001c0001t0003g0001a0001c0001t0003g0258a0001c0001t0010g0080others(1): Show | 5 | HG00621.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-12236_1060-12 others(342): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32762456 | |||||
| chr5:32762583
|
A | G | 1 | a0002c0002t0002g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1060-12125A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762583 | ||||||
| chr5:32762913
|
A | G | 1 | a0001c0003t0008g0031 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1060-11795A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762913 | ||||||
| chr5:32763012
|
G | A | 65 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(62): Show | 65 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1060-11696G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763012 | ||||||
| chr5:32763022
|
A | C | 1 | a0001c0003t0058g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1060-11686A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763022 | ||||||
| chr5:32763154
|
T | C | 1 | a0002c0002t0054g0167 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1060-11554T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763154 | ||||||
| chr5:32763181
|
A | C | 70 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(67): Show | 70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-11527A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763181 | ||||||
| chr5:32763363
|
A | C | 70 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(67): Show | 70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-11345A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763363 | ||||||
| chr5:32763461
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1060-11247C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763461 | ||||||
| chr5:32763466
|
C | T | 1 | a0001c0001t0008g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1060-11242C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763466 | ||||||
| chr5:32763476
|
A | AT | 30 | a0001c0001t0001g0044a0001c0001t0001g0175a0001c0001t0001g0260others(27): Show | 30 | HG00639.hp1 HG01069.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1060-11213dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32763476 | |||||
| chr5:32763476
|
A | ATT | 61 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1060-11214_1060-11 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32763476 | |||||
| chr5:32763476
|
AT | A | 9 | a0001c0001t0001g0062a0001c0001t0001g0094a0001c0001t0001g0171others(6): Show | 9 | HG00099.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-11213delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32763476 | |||||
| chr5:32763657
|
A | G | 1 | a0001c0001t0064g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1060-11051A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763657 | ||||||
| chr5:32763740
|
G | A | 140 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0085others(137): Show | 140 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.1060-10968G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763740 | ||||||
| chr5:32764025
|
T | C | 43 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0004g0011others(40): Show | 43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1060-10683T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764025 | ||||||
| chr5:32764091
|
G | A | 6 | a0001c0001t0015g0123a0001c0001t0040g0161a0001c0001t0047g0110others(3): Show | 6 | HG01074.hp1 HG01261.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-10617G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764091 | ||||||
| chr5:32764120
|
C | T | 1 | a0001c0001t0008g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1060-10588C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764120 | ||||||
| chr5:32764219
|
C | G | 4 | a0001c0001t0001g0044a0001c0001t0002g0004a0001c0001t0002g0129others(1): Show | 4 | HG02109.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-10489C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764219 | ||||||
| chr5:32764466
|
A | G | 59 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(56): Show | 59 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1060-10242A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764466 | ||||||
| chr5:32764516
|
G | A | 43 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0004g0011others(40): Show | 43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1060-10192G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764516 | ||||||
| chr5:32764655
|
G | T | 1 | a0001c0001t0051g0270 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1060-10053G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764655 | ||||||
| chr5:32764657
|
G | A | 1 | a0002c0002t0002g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1060-10051G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764657 | ||||||
| chr5:32764785
|
T | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | NA19060.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1060-9923T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764785 | ||||||
| chr5:32764788
|
C | CA | 20 | a0001c0001t0001g0089a0001c0001t0001g0116a0001c0001t0001g0178others(17): Show | 20 | HG01952.hp1 HG01952.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1060-9892dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | |||||
| chr5:32764788
|
C | CAAAAAAA others(1): Show |
9 | a0001c0001t0001g0203a0001c0001t0004g0025a0001c0001t0004g0026others(6): Show | 9 | HG00735.hp2 HG01070.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-9899_1060-989 others(12): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | |||||
| chr5:32764788
|
C | CAAAAAAA others(2): Show |
7 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0073others(4): Show | 7 | HG00741.hp1 HG01168.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1060-9900_1060-989 others(13): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | |||||
| chr5:32764788
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0141 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1060-9901_1060-989 others(14): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | |||||
| chr5:32764788
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0004g0154a0001c0001t0007g0199a0001c0001t0066g0053 | 3 | HG02257.hp2 HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1060-9902_1060-989 others(15): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | |||||
| chr5:32764788
|
C | CAAAAAAA others(5): Show |
5 | a0001c0001t0001g0149a0001c0001t0021g0084a0001c0001t0039g0267others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-9903_1060-989 others(16): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | |||||
| chr5:32764788
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0007g0058a0001c0001t0007g0074a0001c0001t0007g0150 | 3 | HG01106.hp2 HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1060-9904_1060-989 others(17): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | |||||
| chr5:32764788
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0007g0137a0001c0001t0008g0204a0001c0001t0040g0161 | 3 | HG01261.hp1 HG01934.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1060-9905_1060-989 others(18): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | |||||
| chr5:32764788
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0004g0043a0001c0001t0019g0002a0001c0001t0042g0045 | 3 | HG03453.hp1 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1060-9906_1060-989 others(19): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | |||||
| chr5:32764788
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0019g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1060-9908_1060-989 others(21): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | |||||
| chr5:32764788
|
CA | C | 35 | a0001c0001t0001g0044a0001c0001t0001g0115a0001c0001t0001g0188others(32): Show | 36 | HG00609.hp2 HG00621.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1060-9892delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | |||||
| chr5:32764788
|
CAA | C | 60 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(57): Show | 60 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1060-9893_1060-989 others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | |||||
| chr5:32764788
|
CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0023a0001c0001t0015g0107a0002c0002t0002g0271 | 3 | HG00280.hp1 HG02818.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1060-9906_1060-989 others(19): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | |||||
| chr5:32765010
|
C | T | 1 | a0001c0004t0062g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1060-9698C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765010 | ||||||
| chr5:32765036
|
T | C | 1 | a0001c0001t0007g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1060-9672T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765036 | ||||||
| chr5:32765105
|
G | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-9603G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765105 | ||||||
| chr5:32765351
|
C | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-9357C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765351 | ||||||
| chr5:32765383
|
C | A | 115 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(112): Show | 115 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1060-9325C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765383 | ||||||
| chr5:32765398
|
C | G | 1 | a0001c0005t0056g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1060-9310C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765398 | ||||||
| chr5:32765468
|
C | T | 10 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0006g0063others(7): Show | 10 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1060-9240C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765468 | ||||||
| chr5:32765477
|
T | A | 1 | a0001c0001t0006g0063 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1060-9231T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765477 | ||||||
| chr5:32765560
|
C | A | 17 | a0001c0001t0005g0079a0001c0001t0005g0142a0001c0001t0005g0152others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1060-9148C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765560 | ||||||
| chr5:32765685
|
G | A | 2 | a0001c0006t0061g0041a0002c0002t0002g0072 | 2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1060-9023G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765685 | ||||||
| chr5:32765830
|
A | G | 1 | a0001c0005t0056g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1060-8878A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765830 | ||||||
| chr5:32765983
|
A | G | 224 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(221): Show | 225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1060-8725A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765983 | ||||||
| chr5:32765991
|
C | G | 135 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(132): Show | 135 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1060-8717C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765991 | ||||||
| chr5:32765991
|
C | T | 1 | a0002c0002t0002g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1060-8717C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765991 | ||||||
| chr5:32766039
|
T | A | 61 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(58): Show | 61 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1060-8669T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766039 | ||||||
| chr5:32766102
|
G | A | 1 | a0002c0002t0002g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1060-8606G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766102 | ||||||
| chr5:32766106
|
G | T | 43 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0004g0011others(40): Show | 43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1060-8602G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766106 | ||||||
| chr5:32766149
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1060-8559G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766149 | ||||||
| chr5:32766159
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1060-8549G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766159 | ||||||
| chr5:32766174
|
G | A | 61 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(58): Show | 61 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1060-8534G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766174 | ||||||
| chr5:32766311
|
T | C | 139 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0085others(136): Show | 139 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.1060-8397T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766311 | ||||||
| chr5:32766327
|
A | G | 1 | a0002c0002t0002g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1060-8381A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766327 | ||||||
| chr5:32766360
|
A | G | 112 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(109): Show | 112 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1060-8348A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766360 | ||||||
| chr5:32766400
|
C | G | 2 | a0001c0001t0007g0137a0001c0001t0041g0148 | 2 | HG01934.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1060-8308C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766400 | ||||||
| chr5:32766487
|
C | G | 1 | a0001c0001t0007g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1060-8221C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766487 | ||||||
| chr5:32766577
|
A | G | 61 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(58): Show | 61 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1060-8131A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766577 | ||||||
| chr5:32766623
|
T | C | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0006g0006 | 3 | HG02145.hp2 HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1060-8085T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766623 | ||||||
| chr5:32766716
|
T | C | 112 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(109): Show | 112 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1060-7992T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766716 | ||||||
| chr5:32766920
|
C | A | 1 | a0001c0001t0024g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1060-7788C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766920 | ||||||
| chr5:32767341
|
T | C | 1 | a0001c0001t0007g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1060-7367T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767341 | ||||||
| chr5:32767351
|
C | G | 1 | a0001c0001t0004g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1060-7357C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767351 | ||||||
| chr5:32767580
|
A | T | 1 | a0001c0001t0003g0087 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1060-7128A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767580 | ||||||
| chr5:32767621
|
A | G | 112 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(109): Show | 112 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1060-7087A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767621 | ||||||
| chr5:32767663
|
C | T | 1 | a0001c0001t0043g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1060-7045C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767663 | ||||||
| chr5:32767676
|
T | C | 112 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(109): Show | 112 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1060-7032T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767676 | ||||||
| chr5:32767775
|
C | A | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-6933C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767775 | ||||||
| chr5:32767822
|
T | G | 110 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(107): Show | 110 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1060-6886T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767822 | ||||||
| chr5:32768009
|
T | G | 1 | a0001c0001t0047g0110 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1060-6699T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768009 | ||||||
| chr5:32768064
|
C | T | 1 | a0001c0001t0004g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1060-6644C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768064 | ||||||
| chr5:32768151
|
G | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-6557G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768151 | ||||||
| chr5:32768347
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1060-6361G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768347 | ||||||
| chr5:32768367
|
G | A | 2 | a0001c0004t0062g0134a0001c0005t0056g0268 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1060-6341G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768367 | ||||||
| chr5:32768416
|
T | C | 2 | a0001c0001t0019g0002a0001c0001t0019g0003 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1060-6292T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768416 | ||||||
| chr5:32768428
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0200 | 2 | NA18956.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1060-6280G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768428 | ||||||
| chr5:32768520
|
C | A | 2 | a0001c0001t0004g0138a0001c0001t0055g0145 | 2 | HG01192.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1060-6188C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768520 | ||||||
| chr5:32768528
|
A | G | 112 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(109): Show | 112 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1060-6180A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768528 | ||||||
| chr5:32768594
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0126 | 2 | HG00741.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1060-6114T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768594 | ||||||
| chr5:32768614
|
G | C | 1 | a0002c0002t0033g0219 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1060-6094G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768614 | ||||||
| chr5:32768789
|
C | T | 2 | a0001c0006t0061g0041a0002c0002t0002g0072 | 2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1060-5919C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768789 | ||||||
| chr5:32768829
|
C | A | 2 | a0001c0006t0061g0041a0002c0002t0002g0072 | 2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1060-5879C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768829 | ||||||
| chr5:32768864
|
G | A | 1 | a0001c0003t0001g0032 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1060-5844G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768864 | ||||||
| chr5:32768963
|
C | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0066g0053 | 3 | HG01243.hp2 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1060-5745C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768963 | ||||||
| chr5:32769072
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1060-5636A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769072 | ||||||
| chr5:32769075
|
C | T | 61 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(58): Show | 61 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1060-5633C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769075 | ||||||
| chr5:32769081
|
A | G | 1 | a0001c0005t0056g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1060-5627A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769081 | ||||||
| chr5:32769197
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1060-5511A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769197 | ||||||
| chr5:32769251
|
A | T | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1060-5457A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769251 | ||||||
| chr5:32769354
|
A | G | 14 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0025others(11): Show | 14 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.1060-5354A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769354 | ||||||
| chr5:32769421
|
C | G | 1 | a0001c0001t0001g0238 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1060-5287C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769421 | ||||||
| chr5:32769602
|
A | G | 7 | a0001c0001t0004g0139a0001c0001t0008g0046a0001c0001t0008g0127others(4): Show | 7 | HG02257.hp1 HG02976.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-5106A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769602 | ||||||
| chr5:32769663
|
C | T | 1 | a0001c0001t0019g0002 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1060-5045C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769663 | ||||||
| chr5:32769857
|
T | C | 3 | a0001c0001t0036g0009a0001c0004t0062g0134a0001c0005t0056g0268 | 3 | HG01175.hp2 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1060-4851T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769857 | ||||||
| chr5:32769987
|
A | G | 5 | a0001c0001t0006g0063a0001c0001t0006g0065a0001c0001t0017g0057others(2): Show | 5 | HG01891.hp2 HG02809.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-4721A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769987 | ||||||
| chr5:32769993
|
G | T | 115 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(112): Show | 115 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1060-4715G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769993 | ||||||
| chr5:32770116
|
T | G | 1 | a0001c0001t0003g0226 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1060-4592T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770116 | ||||||
| chr5:32770220
|
T | G | 2 | a0001c0004t0062g0134a0001c0005t0056g0268 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1060-4488T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770220 | ||||||
| chr5:32770266
|
C | CA | 7 | a0001c0001t0004g0139a0001c0001t0008g0046a0001c0001t0008g0127others(4): Show | 7 | HG02257.hp1 HG02976.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-4436dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32770266 | |||||
| chr5:32770362
|
C | A | 2 | a0001c0001t0026g0049a0001c0001t0026g0052 | 2 | HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1060-4346C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770362 | ||||||
| chr5:32770429
|
C | CA | 17 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(14): Show | 17 | HG00323.hp1 HG00639.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1060-4268dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32770429 | |||||
| chr5:32770431
|
A | G | 1 | a0002c0002t0002g0136 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1060-4277A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770431 | ||||||
| chr5:32770483
|
C | T | 2 | a0001c0006t0061g0041a0002c0002t0002g0072 | 2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1060-4225C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770483 | ||||||
| chr5:32770644
|
G | A | 52 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(49): Show | 52 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1060-4064G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770644 | ||||||
| chr5:32770707
|
A | G | 1 | a0001c0001t0017g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1060-4001A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770707 | ||||||
| chr5:32770913
|
A | G | 6 | a0001c0001t0001g0044a0001c0001t0002g0004a0001c0001t0002g0129others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-3795A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770913 | ||||||
| chr5:32771089
|
C | T | 5 | a0001c0001t0004g0139a0001c0001t0008g0046a0001c0001t0008g0127others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-3619C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771089 | ||||||
| chr5:32771273
|
A | G | 140 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0085others(137): Show | 140 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.1060-3435A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771273 | ||||||
| chr5:32771286
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1060-3422C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771286 | ||||||
| chr5:32771336
|
G | C | 4 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | NA18962.hp1 NA18974.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-3372G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771336 | ||||||
| chr5:32771443
|
G | A | 2 | a0001c0001t0006g0113a0001c0001t0006g0114 | 2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1060-3265G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771443 | ||||||
| chr5:32771445
|
C | T | 1 | a0002c0002t0002g0215 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1060-3263C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771445 | ||||||
| chr5:32771476
|
A | G | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-3232A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771476 | ||||||
| chr5:32771706
|
C | T | 61 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(58): Show | 61 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1060-3002C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771706 | ||||||
| chr5:32771719
|
A | G | 117 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(114): Show | 117 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.1060-2989A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771719 | ||||||
| chr5:32771730
|
G | C | 2 | a0001c0001t0026g0049a0001c0001t0026g0052 | 2 | HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1060-2978G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771730 | ||||||
| chr5:32771832
|
A | G | 138 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0085others(135): Show | 138 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.1060-2876A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771832 | ||||||
| chr5:32771937
|
A | G | 115 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(112): Show | 115 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.1060-2771A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771937 | ||||||
| chr5:32771967
|
A | T | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1060-2741A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771967 | ||||||
| chr5:32771974
|
A | G | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-2734A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771974 | ||||||
| chr5:32772221
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0021 | 2 | HG00735.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1060-2487C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772221 | ||||||
| chr5:32772230
|
T | C | 26 | a0001c0001t0001g0044a0001c0001t0002g0004a0001c0001t0002g0129others(23): Show | 26 | HG01074.hp2 HG01192.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1060-2478T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772230 | ||||||
| chr5:32772237
|
C | T | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-2471C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772237 | ||||||
| chr5:32772520
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0066g0053 | 3 | HG01243.hp2 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1060-2188G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772520 | ||||||
| chr5:32772585
|
T | C | 114 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0141others(111): Show | 114 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(111): Show |
intron_variant | MODIFIER | c.1060-2123T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772585 | ||||||
| chr5:32772656
|
A | G | 1 | a0002c0002t0035g0124 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1060-2052A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772656 | ||||||
| chr5:32772658
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1060-2050T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772658 | ||||||
| chr5:32772781
|
A | AT | 26 | a0001c0001t0001g0044a0001c0001t0002g0004a0001c0001t0002g0129others(23): Show | 26 | HG01074.hp2 HG01192.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1060-1921dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32772781 | |||||
| chr5:32772796
|
C | T | 26 | a0001c0001t0001g0044a0001c0001t0002g0004a0001c0001t0002g0129others(23): Show | 26 | HG01074.hp2 HG01192.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1060-1912C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772796 | ||||||
| chr5:32772807
|
C | T | 1 | a0001c0001t0004g0298 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1060-1901C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772807 | ||||||
| chr5:32772808
|
G | A | 3 | a0001c0001t0005g0142a0001c0001t0043g0067a0001c0001t0065g0051 | 3 | HG02723.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1060-1900G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772808 | ||||||
| chr5:32772886
|
G | C | 62 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(59): Show | 62 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1060-1822G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772886 | ||||||
| chr5:32772910
|
T | A | 22 | a0001c0001t0001g0044a0001c0001t0002g0004a0001c0001t0002g0129others(19): Show | 22 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1060-1798T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772910 | ||||||
| chr5:32772927
|
G | A | 25 | a0001c0001t0001g0044a0001c0001t0002g0004a0001c0001t0002g0129others(22): Show | 25 | HG01074.hp2 HG01192.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1060-1781G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772927 | ||||||
| chr5:32772948
|
C | T | 1 | a0001c0001t0007g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1060-1760C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772948 | ||||||
| chr5:32772964
|
G | A | 26 | a0001c0001t0001g0044a0001c0001t0002g0004a0001c0001t0002g0129others(23): Show | 26 | HG01074.hp2 HG01192.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1060-1744G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772964 | ||||||
| chr5:32773035
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1060-1673A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773035 | ||||||
| chr5:32773049
|
TG | T | 60 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(57): Show | 60 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1060-1658delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773049 | ||||||
| chr5:32773169
|
A | G | 5 | a0001c0001t0001g0023a0001c0001t0015g0107a0001c0001t0019g0002others(2): Show | 5 | HG00280.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-1539A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773169 | ||||||
| chr5:32773208
|
C | T | 110 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0126others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1060-1500C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773208 | ||||||
| chr5:32773250
|
C | T | 64 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(61): Show | 64 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.1060-1458C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773250 | ||||||
| chr5:32773363
|
G | A | 2 | a0001c0001t0005g0142a0001c0001t0043g0067 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1060-1345G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773363 | ||||||
| chr5:32773542
|
A | C | 9 | a0001c0001t0004g0138a0001c0001t0041g0148a0001c0001t0043g0067others(6): Show | 9 | HG01192.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-1166A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773542 | ||||||
| chr5:32773545
|
C | T | 65 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0229others(62): Show | 65 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1060-1163C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773545 | ||||||
| chr5:32773580
|
T | G | 1 | a0001c0001t0049g0013 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1060-1128T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773580 | ||||||
| chr5:32773667
|
C | G | 2 | a0001c0001t0019g0003a0001c0001t0037g0059 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1060-1041C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773667 | ||||||
| chr5:32773683
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1060-1025A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773683 | ||||||
| chr5:32774153
|
G | A | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1060-555G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32774153 | ||||||
| chr5:32774225
|
A | G | 1 | a0001c0001t0003g0112 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1060-483A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32774225 | ||||||
| chr5:32774228
|
A | G | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1060-480A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32774228 | ||||||
| chr5:32774240
|
A | G | 2 | a0001c0001t0043g0067a0001c0001t0065g0051 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1060-468A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32774240 | ||||||
| chr5:32774327
|
T | C | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1060-381T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32774327 | ||||||
| chr5:32774889
|
G | A | 2 | a0001c0003t0023g0038a0001c0003t0023g0039 | 2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1195+46G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32774889 | ||||||
| chr5:32774908
|
A | T | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1195+65A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32774908 | ||||||
| chr5:32774941
|
G | T | 200 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0126others(197): Show | 201 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.1195+98G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32774941 | ||||||
| chr5:32775144
|
T | C | 73 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0004g0139others(70): Show | 73 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1195+301T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32775144 | ||||||
| chr5:32775155
|
G | A | 17 | a0001c0001t0005g0079a0001c0001t0005g0142a0001c0001t0005g0152others(14): Show | 17 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1195+312G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32775155 | ||||||
| chr5:32775294
|
AT | A | 54 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0025others(51): Show | 54 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.1195+467delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 32775294 | |||||
| chr5:32775294
|
ATT | A | 70 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0002g0004others(67): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1195+466_1195+467d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 32775294 | |||||
| chr5:32775294
|
ATTT | A | 72 | a0001c0001t0004g0139a0001c0001t0008g0046a0001c0001t0008g0127others(69): Show | 72 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1195+465_1195+467d others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 32775294 | |||||
| chr5:32775358
|
G | A | 1 | a0001c0001t0017g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1195+515G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32775358 | ||||||
| chr5:32775577
|
T | A | 1 | a0002c0002t0016g0276 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1195+734T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32775577 | ||||||
| chr5:32775738
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1195+895C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32775738 | ||||||
| chr5:32775907
|
A | C | 2 | a0001c0001t0001g0168a0001c0001t0001g0207 | 2 | NA18942.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1195+1064A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32775907 | ||||||
| chr5:32775909
|
T | A | 142 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0002g0004others(139): Show | 143 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1195+1066T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32775909 | ||||||
| chr5:32776291
|
T | C | 78 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0004g0139others(75): Show | 78 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.1195+1448T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776291 | ||||||
| chr5:32776335
|
A | T | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1195+1492A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776335 | ||||||
| chr5:32776356
|
A | G | 1 | a0001c0001t0015g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1195+1513A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776356 | ||||||
| chr5:32776426
|
C | T | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1195+1583C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776426 | ||||||
| chr5:32776567
|
C | T | 74 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0004g0139others(71): Show | 74 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1195+1724C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776567 | ||||||
| chr5:32776617
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1195+1774C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776617 | ||||||
| chr5:32776938
|
A | C | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1195+2095A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776938 | ||||||
| chr5:32776949
|
C | A | 1 | a0001c0001t0001g0176 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1195+2106C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776949 | ||||||
| chr5:32776994
|
G | A | 1 | a0001c0003t0008g0031 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1195+2151G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776994 | ||||||
| chr5:32777035
|
C | T | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0006g0006 | 3 | HG02145.hp2 HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1195+2192C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777035 | ||||||
| chr5:32777239
|
G | C | 64 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0003g0001others(61): Show | 65 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1195+2396G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777239 | ||||||
| chr5:32777289
|
A | G | 1 | a0001c0001t0049g0013 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1195+2446A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777289 | ||||||
| chr5:32777548
|
G | A | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1195+2705G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777548 | ||||||
| chr5:32777549
|
T | C | 2 | a0001c0001t0002g0004a0001c0001t0002g0129 | 2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1195+2706T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777549 | ||||||
| chr5:32777564
|
C | T | 14 | a0001c0001t0005g0079a0001c0001t0005g0142a0001c0001t0005g0152others(11): Show | 14 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1195+2721C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777564 | ||||||
| chr5:32777580
|
G | A | 5 | a0001c0001t0004g0138a0001c0001t0004g0303a0001c0001t0004g0304others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1195+2737G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777580 | ||||||
| chr5:32777713
|
G | A | 1 | a0001c0005t0056g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1195+2870G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777713 | ||||||
| chr5:32777830
|
A | G | 1 | a0001c0001t0003g0240 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1196-2892A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777830 | ||||||
| chr5:32777853
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1196-2869A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777853 | ||||||
| chr5:32778062
|
G | A | 3 | a0001c0001t0019g0002a0001c0001t0019g0003a0001c0001t0055g0145 | 3 | HG01192.hp1 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1196-2660G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32778062 | ||||||
| chr5:32778127
|
A | C | 79 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0004g0139others(76): Show | 79 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1196-2595A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32778127 | ||||||
| chr5:32778295
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1196-2427C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32778295 | ||||||
| chr5:32778588
|
T | C | 3 | a0001c0001t0019g0002a0001c0001t0019g0003a0001c0001t0055g0145 | 3 | HG01192.hp1 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1196-2134T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32778588 | ||||||
| chr5:32778813
|
C | G | 3 | a0001c0001t0008g0127a0001c0001t0008g0305a0001c0001t0059g0155 | 3 | HG02257.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1196-1909C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32778813 | ||||||
| chr5:32778932
|
G | T | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1196-1790G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32778932 | ||||||
| chr5:32779205
|
T | C | 2 | a0001c0001t0043g0067a0001c0001t0065g0051 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1196-1517T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779205 | ||||||
| chr5:32779228
|
GAGAGAAC others(6): Show |
G | 9 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0025others(6): Show | 9 | HG00735.hp2 HG01070.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1196-1479_1196-146 others(17): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 32779228 | |||||
| chr5:32779341
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1196-1381G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779341 | ||||||
| chr5:32779396
|
G | A | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1196-1326G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779396 | ||||||
| chr5:32779490
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1196-1232C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779490 | ||||||
| chr5:32779491
|
G | A | 14 | a0001c0001t0005g0079a0001c0001t0005g0142a0001c0001t0005g0152others(11): Show | 14 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1196-1231G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779491 | ||||||
| chr5:32779504
|
G | A | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1196-1218G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779504 | ||||||
| chr5:32779541
|
C | T | 1 | a0001c0001t0003g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1196-1181C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779541 | ||||||
| chr5:32779643
|
G | T | 1 | a0001c0004t0062g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1196-1079G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779643 | ||||||
| chr5:32779715
|
A | G | 2 | a0002c0002t0002g0042a0002c0002t0002g0055 | 2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1196-1007A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779715 | ||||||
| chr5:32779819
|
C | T | 1 | a0001c0001t0047g0110 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1196-903C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779819 | ||||||
| chr5:32779847
|
C | T | 1 | a0001c0001t0039g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1196-875C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779847 | ||||||
| chr5:32779908
|
G | T | 2 | a0001c0001t0004g0043a0001c0001t0042g0045 | 2 | HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1196-814G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779908 | ||||||
| chr5:32779926
|
T | C | 1 | a0001c0001t0003g0086 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1196-796T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779926 | ||||||
| chr5:32780021
|
G | A | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1196-701G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32780021 | ||||||
| chr5:32780167
|
T | C | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1196-555T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32780167 | ||||||
| chr5:32780185
|
A | G | 79 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0008g0046others(76): Show | 79 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1196-537A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32780185 | ||||||
| chr5:32780210
|
G | C | 37 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0025others(34): Show | 37 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1196-512G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32780210 | ||||||
| chr5:32780341
|
G | A | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1196-381G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32780341 | ||||||
| chr5:32780452
|
AATCTTTT others(9): Show |
A | 1 | a0001c0001t0037g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1196-266_1196-251d others(18): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 32780452 | |||||
| chr5:32780575
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1196-147A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32780575 | ||||||
| chr5:32780695
|
T | C | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | NA19060.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1196-27T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32780695 | ||||||
| chr5:32780828
|
AG | A | 3 | a0001c0001t0001g0149a0001c0001t0006g0066a0001c0001t0006g0114 | 3 | HG01243.hp2 HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1290+13delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32780828 | ||||||
| chr5:32780857
|
C | T | 1 | a0001c0001t0038g0018 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1290+41C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32780857 | ||||||
| chr5:32781090
|
T | G | 76 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0008g0046others(73): Show | 76 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1290+274T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781090 | ||||||
| chr5:32781298
|
C | T | 75 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0008g0046others(72): Show | 75 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1290+482C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781298 | ||||||
| chr5:32781415
|
T | C | 66 | a0001c0001t0001g0085a0001c0001t0001g0126a0002c0002t0002g0005others(63): Show | 66 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1290+599T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781415 | ||||||
| chr5:32781422
|
T | C | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1290+606T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781422 | ||||||
| chr5:32781475
|
G | GT | 202 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0002g0004others(199): Show | 203 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1290+659_1290+660i others(3): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781475 | ||||||
| chr5:32781495
|
A | G | 37 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0025others(34): Show | 37 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1290+679A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781495 | ||||||
| chr5:32781747
|
C | A | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1290+931C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781747 | ||||||
| chr5:32781808
|
G | A | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1290+992G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781808 | ||||||
| chr5:32782046
|
C | A | 202 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0002g0004others(199): Show | 203 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1291-847C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782046 | ||||||
| chr5:32782188
|
A | G | 2 | a0002c0002t0020g0090a0002c0002t0020g0227 | 2 | HG02040.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1291-705A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782188 | ||||||
| chr5:32782270
|
T | C | 1 | a0001c0005t0056g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1291-623T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782270 | ||||||
| chr5:32782325
|
C | T | 1 | a0001c0001t0003g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1291-568C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782325 | ||||||
| chr5:32782339
|
ACCCTGGC others(14): Show |
A | 37 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0025others(34): Show | 37 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1291-548_1291-528d others(23): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 32782339 | |||||
| chr5:32782487
|
C | A | 1 | a0001c0005t0056g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1291-406C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782487 | ||||||
| chr5:32782573
|
C | T | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1291-320C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782573 | ||||||
| chr5:32782576
|
C | T | 2 | a0001c0001t0043g0067a0001c0001t0065g0051 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1291-317C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782576 | ||||||
| chr5:32782687
|
T | A | 3 | a0001c0001t0003g0001a0001c0001t0003g0243a0001c0001t0003g0258 | 4 | HG00621.hp1 HG02015.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291-206T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782687 | ||||||
| chr5:32782698
|
G | A | 1 | a0001c0001t0003g0243 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1291-195G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782698 | ||||||
| chr5:32782720
|
C | T | 1 | a0002c0002t0002g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1291-173C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782720 | ||||||
| chr5:32782783
|
C | T | 2 | a0001c0001t0050g0047a0001c0003t0058g0035 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1291-110C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782783 | ||||||
| chr5:32782834
|
C | T | 1 | a0001c0001t0036g0009 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1291-59C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782834 | ||||||
| chr5:32783490
|
A | G | 2 | a0001c0001t0043g0067a0001c0001t0065g0051 | 2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1426+462A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32783490 | ||||||
| chr5:32783560
|
T | A | 1 | a0001c0001t0037g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1426+532T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32783560 | ||||||
| chr5:32783602
|
C | T | 28 | a0001c0001t0003g0001a0001c0001t0003g0086a0001c0001t0003g0095others(25): Show | 29 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1426+574C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32783602 | ||||||
| chr5:32783603
|
C | T | 75 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0008g0046others(72): Show | 75 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1426+575C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32783603 | ||||||
| chr5:32783631
|
C | G | 1 | a0001c0006t0061g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1426+603C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32783631 | ||||||
| chr5:32783690
|
A | T | 1 | a0001c0001t0003g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1426+662A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32783690 | ||||||
| chr5:32783990
|
T | G | 1 | a0001c0001t0008g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1427-806T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32783990 | ||||||
| chr5:32784020
|
T | C | 2 | a0001c0004t0062g0134a0001c0006t0061g0041 | 2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1427-776T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784020 | ||||||
| chr5:32784023
|
A | G | 1 | a0001c0001t0060g0293 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1427-773A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784023 | ||||||
| chr5:32784087
|
A | G | 2 | a0001c0004t0062g0134a0001c0006t0061g0041 | 2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1427-709A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784087 | ||||||
| chr5:32784097
|
C | A | 1 | a0001c0001t0040g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1427-699C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784097 | ||||||
| chr5:32784177
|
G | C | 5 | a0001c0001t0008g0046a0001c0001t0008g0127a0001c0001t0008g0204others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427-619G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784177 | ||||||
| chr5:32784251
|
T | C | 77 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0008g0046others(74): Show | 77 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1427-545T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784251 | ||||||
| chr5:32784262
|
C | T | 1 | a0001c0001t0017g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1427-534C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784262 | ||||||
| chr5:32784670
|
A | G | 74 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0008g0046others(71): Show | 74 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1427-126A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784670 | ||||||
| chr5:32784891
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18962.hp1 | splice_region_variant&intron_variant | LOW | c.1514+8C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32784891 | ||||||
| chr5:32784991
|
G | A | 1 | a0001c0001t0004g0012 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1514+108G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32784991 | ||||||
| chr5:32785101
|
A | G | 2 | a0001c0001t0009g0160a0001c0001t0048g0307 | 2 | NA18612.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1514+218A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785101 | ||||||
| chr5:32785138
|
A | AT | 61 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1514+283dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 32785138 | |||||
| chr5:32785138
|
A | ATT | 7 | a0001c0001t0001g0203a0001c0001t0006g0006a0001c0001t0006g0063others(4): Show | 7 | HG01891.hp2 HG01978.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1514+282_1514+283d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 32785138 | |||||
| chr5:32785138
|
AT | A | 6 | a0001c0001t0004g0147a0001c0001t0007g0199a0001c0001t0037g0059others(3): Show | 6 | HG01516.hp2 HG02109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1514+283delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 32785138 | |||||
| chr5:32785138
|
ATT | A | 8 | a0001c0001t0008g0046a0001c0001t0008g0127a0001c0001t0008g0204others(5): Show | 8 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1514+282_1514+283d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 32785138 | |||||
| chr5:32785138
|
ATTTT | A | 12 | a0001c0001t0001g0085a0001c0001t0019g0003a0001c0006t0061g0041others(9): Show | 12 | HG00741.hp2 HG01433.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1514+280_1514+283d others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 32785138 | |||||
| chr5:32785138
|
ATTTTT | A | 66 | a0001c0001t0001g0126a0001c0001t0003g0105a0001c0001t0003g0166others(63): Show | 66 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1514+279_1514+283d others(7): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 32785138 | |||||
| chr5:32785138
|
ATTTTTT | A | 54 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0003g0001others(51): Show | 55 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1514+278_1514+283d others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 32785138 | |||||
| chr5:32785177
|
C | G | 1 | a0001c0001t0002g0004 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1514+294C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785177 | ||||||
| chr5:32785181
|
G | C | 10 | a0001c0001t0008g0046a0001c0001t0008g0127a0001c0001t0008g0204others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1514+298G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785181 | ||||||
| chr5:32785314
|
T | G | 10 | a0001c0001t0008g0046a0001c0001t0008g0127a0001c0001t0008g0204others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1514+431T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785314 | ||||||
| chr5:32785720
|
G | A | 5 | a0001c0003t0005g0027a0001c0003t0005g0028a0001c0003t0005g0029others(2): Show | 5 | HG02258.hp2 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1515-514G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785720 | ||||||
| chr5:32785749
|
G | A | 4 | a0001c0001t0017g0057a0001c0001t0017g0064a0001c0001t0021g0084others(1): Show | 4 | HG01884.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515-485G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785749 | ||||||
| chr5:32785807
|
G | A | 1 | a0001c0004t0062g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1515-427G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785807 | ||||||
| chr5:32785973
|
C | G | 1 | a0001c0005t0056g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1515-261C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785973 | ||||||
| chr5:32786009
|
G | A | 9 | a0001c0001t0008g0046a0001c0001t0008g0127a0001c0001t0008g0204others(6): Show | 9 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1515-225G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32786009 |