| geneid | 57486 |
|---|---|
| ensemblid | ENSG00000123213.23 |
| hgncid | 16058 |
| symbol | NLN |
| name | neurolysin |
| refseq_nuc | NM_020726.5 |
| refseq_prot | NP_065777.1 |
| ensembl_nuc | ENST00000380985.10 |
| ensembl_prot | ENSP00000370372.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 65722205 |
| end | 65829283 |
| strand | + |
| ver | v1.2 |
| region | chr5:65722205-65829283 |
| region5000 | chr5:65717205-65834283 |
| regionname0 | NLN_chr5_65722205_65829283 |
| regionname5000 | NLN_chr5_65717205_65834283 |
| 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 | 704 | 292 | 56 | 63 | 126 | 14 | 31 | 106 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002 | 0/0 | 704 | 25 | 21 | 3 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0003 | 0/0 | 704 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0004 | 0/0 | 704 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0005 | 0/0 | 704 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0006 | 0/0 | 704 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0007 | 0/0 | 704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0008 | 0/0 | 704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2115 | 204 | 52 | 42 | 74 | 10 | 25 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0002 | 1/0 | 2115 | 81 | 1 | 21 | 48 | 4 | 6 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0003 | 0/0 | 2115 | 14 | 11 | 2 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0004 | 0/0 | 2115 | 10 | 9 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0005 | 0/0 | 2115 | 7 | 6 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0006 | 0/0 | 2115 | 6 | 6 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0007 | 0/0 | 2115 | 3 | 0 | 0 | 3 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0008 | 0/0 | 2115 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0009 | 0/0 | 2115 | 2 | 1 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0010 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0011 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0012 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0013 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0014 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0015 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| c0016 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 6538 | 107 | 11 | 28 | 44 | 8 | 15 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0002 | 0/0 | 6538 | 45 | 4 | 10 | 26 | 1 | 4 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0003 | 0/0 | 6538 | 22 | 0 | 5 | 15 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0004 | 0/0 | 6538 | 22 | 6 | 7 | 6 | 3 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0005 | 0/0 | 6538 | 19 | 2 | 0 | 15 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0006 | 0/0 | 6538 | 11 | 10 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0007 | 0/0 | 6537 | 9 | 4 | 3 | 0 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0008 | 0/0 | 6538 | 8 | 8 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0009 | 0/0 | 6538 | 8 | 0 | 6 | 0 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0010 | 0/0 | 6537 | 6 | 6 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0011 | 0/0 | 6538 | 4 | 1 | 0 | 0 | 2 | 1 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0012 | 0/0 | 6538 | 4 | 0 | 0 | 4 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0013 | 0/0 | 6538 | 4 | 0 | 0 | 4 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0014 | 0/0 | 6538 | 4 | 0 | 0 | 4 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0015 | 0/0 | 6538 | 3 | 3 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0016 | 0/0 | 6537 | 3 | 3 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0017 | 0/1 | 6535 | 3 | 0 | 1 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0018 | 0/0 | 6537 | 3 | 2 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0019 | 0/0 | 6538 | 3 | 0 | 0 | 3 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0020 | 0/0 | 6538 | 2 | 1 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0021 | 0/0 | 6538 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0022 | 0/0 | 6534 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0023 | 0/0 | 6538 | 2 | 1 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0024 | 0/0 | 6538 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0025 | 0/0 | 6538 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0026 | 0/0 | 6538 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0027 | 0/0 | 6538 | 2 | 0 | 0 | 0 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0028 | 0/0 | 6538 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0029 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0030 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0031 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0032 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0033 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0034 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0035 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0036 | 0/0 | 6537 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0037 | 0/0 | 6538 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0038 | 0/0 | 6538 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0039 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0040 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0041 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0042 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0043 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0044 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0045 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0046 | 0/0 | 6538 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0047 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0048 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0049 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0050 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0051 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0052 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0053 | 0/0 | 6538 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0054 | 0/0 | 6538 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0055 | 0/0 | 6548 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0056 | 0/0 | 6538 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0057 | 0/0 | 6538 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| t0058 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| 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 | 6 | 0 | 3 | 3 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0069 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| 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 | 0/1 | 2115 | 204 | 52 | 42 | 74 | 10 | 25 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0002 | 1/0 | 2115 | 81 | 1 | 21 | 48 | 4 | 6 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0007 | 0/0 | 2115 | 3 | 0 | 0 | 3 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0011 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0013 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0014 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0015 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0003 | 0/0 | 2115 | 14 | 11 | 2 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0004 | 0/0 | 2115 | 10 | 9 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0016 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0003c0005 | 0/0 | 2115 | 7 | 6 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0004c0006 | 0/0 | 2115 | 6 | 6 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0005c0009 | 0/0 | 2115 | 2 | 1 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0006c0008 | 0/0 | 2115 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0007c0012 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0008c0010 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8652 | 31 | 4 | 9 | 5 | 4 | 9 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0002 | 0/0 | 8652 | 45 | 4 | 10 | 26 | 1 | 4 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0003 | 0/0 | 8652 | 22 | 0 | 5 | 15 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0004 | 0/0 | 8652 | 20 | 5 | 6 | 6 | 3 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0005 | 0/0 | 8652 | 18 | 1 | 0 | 15 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0006 | 0/0 | 8652 | 9 | 8 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0007 | 0/0 | 8651 | 2 | 0 | 1 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0008 | 0/0 | 8652 | 7 | 7 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0009 | 0/0 | 8652 | 8 | 0 | 6 | 0 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0011 | 0/0 | 8652 | 4 | 1 | 0 | 0 | 2 | 1 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0014 | 0/0 | 8652 | 4 | 0 | 0 | 4 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0015 | 0/0 | 8652 | 3 | 3 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0017 | 0/1 | 8649 | 3 | 0 | 1 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0020 | 0/0 | 8652 | 2 | 1 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0022 | 0/0 | 8648 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0025 | 0/0 | 8652 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0026 | 0/0 | 8652 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0027 | 0/0 | 8652 | 2 | 0 | 0 | 0 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0028 | 0/0 | 8652 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0029 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0031 | 0/0 | 8648 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0032 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0033 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0034 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0037 | 0/0 | 8652 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0038 | 0/0 | 8652 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0040 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0043 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0047 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0048 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0050 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0051 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0052 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0053 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0055 | 0/0 | 8662 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0001t0056 | 0/0 | 8652 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0002t0001 | 1/0 | 8652 | 70 | 1 | 19 | 39 | 4 | 6 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0002t0004 | 0/0 | 8652 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0002t0012 | 0/0 | 8652 | 4 | 0 | 0 | 4 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0002t0013 | 0/0 | 8652 | 4 | 0 | 0 | 4 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0002t0046 | 0/0 | 8652 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0002t0054 | 0/0 | 8652 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0007t0019 | 0/0 | 8652 | 3 | 0 | 0 | 3 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0011t0005 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0013t0039 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0014t0057 | 0/0 | 8652 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0001c0015t0004 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0003t0007 | 0/0 | 8651 | 4 | 1 | 2 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0003t0010 | 0/0 | 8651 | 6 | 6 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0003t0018 | 0/0 | 8651 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0003t0042 | 0/0 | 8651 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0003t0049 | 0/0 | 8651 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0003t0058 | 0/0 | 8651 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0004t0007 | 0/0 | 8651 | 3 | 3 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0004t0016 | 0/0 | 8651 | 3 | 3 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0004t0018 | 0/0 | 8651 | 2 | 1 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0004t0041 | 0/0 | 8651 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0004t0044 | 0/0 | 8651 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0002c0016t0035 | 0/0 | 8651 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0003c0005t0021 | 0/0 | 8652 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0003c0005t0022 | 0/0 | 8648 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0003c0005t0023 | 0/0 | 8652 | 2 | 1 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0003c0005t0024 | 0/0 | 8652 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0004c0006t0001 | 0/0 | 8652 | 4 | 4 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0004c0006t0008 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0004c0006t0030 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0005c0009t0036 | 0/0 | 8651 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0005c0009t0045 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0006c0008t0006 | 0/0 | 8652 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0007c0012t0001 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| a0008c0010t0001 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | copy fasta | chr5 | 65717205 | 65834283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0008g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0008g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0008g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0008g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0009g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0009g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0009g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0009g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0009g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0009g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0009g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0009g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0011g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0011g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0011g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0014g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0014g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0014g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0014g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0015g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0015g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0015g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0017g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0017g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0017g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0020g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0022g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0025g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0025g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0026g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0027g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0027g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0028g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0028g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0029g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0031g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0032g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0033g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0034g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0037g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0038g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0040g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0043g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0047g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0048g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0050g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0051g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0052g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0053g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0055g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0001t0056g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0001 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0069 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0012g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0012g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0012g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0012g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0013g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0013g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0013g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0046g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0002t0054g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0007t0019g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0007t0019g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0007t0019g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0011t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0013t0039g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0014t0057g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0001c0015t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0003t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0003t0007g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0003t0007g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0003t0007g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0003t0010g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0003t0010g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0003t0010g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0003t0010g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0003t0010g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0003t0010g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0003t0018g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0003t0042g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0003t0049g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0003t0058g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0004t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0004t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0004t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0004t0016g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0004t0016g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0004t0016g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0004t0018g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0004t0018g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0004t0041g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0004t0044g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0002c0016t0035g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0003c0005t0021g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0003c0005t0022g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0003c0005t0023g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0003c0005t0023g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0003c0005t0024g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0003c0005t0024g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0004c0006t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0004c0006t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0004c0006t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0004c0006t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0004c0006t0030g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0005c0009t0036g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0005c0009t0045g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0006c0008t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0006c0008t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0007c0012t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| a0008c0010t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0031 | EUR | GBR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0191 | EUR | FIN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00438 | hp1 | a0001 | c0007 | t0019 | g0292 | EAS | CHS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | CHS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | CHS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00609 | hp2 | a0001 | c0002 | t0013 | g0204 | EAS | CHS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | CHS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0122 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0297 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0301 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00738 | hp1 | a0002 | c0003 | t0007 | g0181 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0045 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0303 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01070 | hp2 | a0001 | c0001 | t0009 | g0243 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01071 | hp2 | a0001 | c0001 | t0055 | g0304 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0176 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0298 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0272 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01106 | hp2 | a0001 | c0002 | t0004 | g0288 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01109 | hp1 | a0001 | c0001 | t0020 | g0018 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01167 | hp2 | a0002 | c0004 | t0018 | g0293 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0063 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01243 | hp1 | a0005 | c0009 | t0036 | g0256 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01243 | hp2 | a0003 | c0005 | t0023 | g0077 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0139 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01256 | hp1 | a0002 | c0003 | t0007 | g0229 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0280 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01358 | hp2 | a0001 | c0001 | t0009 | g0138 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0271 | EUR | IBS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0162 | EUR | IBS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01516 | hp2 | a0001 | c0001 | t0011 | g0228 | EUR | IBS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01517 | hp1 | a0001 | c0001 | t0011 | g0236 | EUR | IBS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0291 | EUR | IBS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01884 | hp1 | a0001 | c0001 | t0032 | g0255 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01884 | hp2 | a0002 | c0003 | t0042 | g0083 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01891 | hp1 | a0001 | c0001 | t0031 | g0054 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01891 | hp2 | a0001 | c0001 | t0026 | g0019 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0152 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01934 | hp1 | a0001 | c0001 | t0009 | g0026 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01952 | hp1 | a0001 | c0001 | t0017 | g0241 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01952 | hp2 | a0001 | c0001 | t0009 | g0144 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01975 | hp1 | a0001 | c0001 | t0009 | g0160 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0141 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01981 | hp1 | a0001 | c0002 | t0054 | g0273 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0199 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02004 | hp2 | a0001 | c0001 | t0038 | g0006 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02027 | hp2 | a0001 | c0002 | t0013 | g0172 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02040 | hp2 | a0001 | c0002 | t0013 | g0016 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02055 | hp1 | a0005 | c0009 | t0045 | g0043 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02055 | hp2 | a0002 | c0003 | t0010 | g0268 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02056 | hp1 | a0001 | c0001 | t0014 | g0174 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02129 | hp2 | a0001 | c0002 | t0013 | g0016 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02132 | hp1 | a0001 | c0014 | t0057 | g0306 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0201 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02145 | hp2 | a0002 | c0003 | t0007 | g0078 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0173 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02257 | hp1 | a0002 | c0016 | t0035 | g0257 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02258 | hp2 | a0002 | c0004 | t0044 | g0259 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02280 | hp1 | a0002 | c0003 | t0010 | g0287 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02280 | hp2 | a0001 | c0001 | t0015 | g0251 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0142 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02451 | hp1 | a0004 | c0006 | t0001 | g0088 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02451 | hp2 | a0001 | c0001 | t0051 | g0299 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02572 | hp2 | a0001 | c0001 | t0022 | g0084 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02622 | hp1 | a0003 | c0005 | t0024 | g0080 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0263 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02630 | hp1 | a0001 | c0001 | t0025 | g0046 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02647 | hp1 | a0002 | c0004 | t0016 | g0082 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02647 | hp2 | a0003 | c0005 | t0024 | g0055 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02717 | hp1 | a0001 | c0015 | t0004 | g0264 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02717 | hp2 | a0001 | c0001 | t0048 | g0265 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02723 | hp1 | a0002 | c0003 | t0010 | g0261 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02723 | hp2 | a0001 | c0001 | t0034 | g0219 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0047 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0150 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02809 | hp1 | a0001 | c0001 | t0029 | g0105 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02809 | hp2 | a0001 | c0001 | t0043 | g0094 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02818 | hp1 | a0001 | c0001 | t0015 | g0044 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02818 | hp2 | a0001 | c0001 | t0040 | g0195 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02886 | hp1 | a0002 | c0003 | t0049 | g0269 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0281 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02895 | hp2 | a0002 | c0003 | t0058 | g0285 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02896 | hp1 | a0002 | c0004 | t0041 | g0311 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02896 | hp2 | a0003 | c0005 | t0021 | g0017 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0244 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02897 | hp2 | a0003 | c0005 | t0021 | g0017 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0089 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02965 | hp1 | a0002 | c0004 | t0016 | g0056 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02965 | hp2 | a0002 | c0004 | t0007 | g0249 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02970 | hp1 | a0001 | c0001 | t0047 | g0248 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02970 | hp2 | a0001 | c0001 | t0026 | g0019 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0266 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02976 | hp2 | a0006 | c0008 | t0006 | g0090 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0305 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03041 | hp2 | a0001 | c0011 | t0005 | g0020 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03098 | hp1 | a0002 | c0004 | t0016 | g0058 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0050 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03130 | hp2 | a0002 | c0004 | t0007 | g0245 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03139 | hp2 | a0002 | c0004 | t0007 | g0246 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0095 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03195 | hp2 | a0002 | c0003 | t0010 | g0283 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03209 | hp2 | a0001 | c0001 | t0050 | g0310 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03225 | hp1 | a0004 | c0006 | t0008 | g0224 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03225 | hp2 | a0003 | c0005 | t0023 | g0081 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03486 | hp1 | a0004 | c0006 | t0030 | g0097 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03490 | hp2 | a0001 | c0001 | t0027 | g0278 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0060 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03492 | hp1 | a0001 | c0001 | t0027 | g0295 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03516 | hp1 | a0002 | c0003 | t0010 | g0270 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0091 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0262 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03540 | hp2 | a0007 | c0012 | t0001 | g0093 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03579 | hp1 | a0006 | c0008 | t0006 | g0103 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03579 | hp2 | a0002 | c0004 | t0018 | g0282 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0165 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03669 | hp2 | a0001 | c0001 | t0009 | g0023 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03688 | hp1 | a0001 | c0001 | t0056 | g0260 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03688 | hp2 | a0001 | c0001 | t0017 | g0242 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0158 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0208 | SAS | BEB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03834 | hp1 | a0001 | c0001 | t0009 | g0062 | SAS | BEB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG04115 | hp1 | a0002 | c0003 | t0007 | g0230 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0238 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0057 | SAS | BEB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0159 | SAS | BEB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | YRI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0279 | AFR | YRI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0225 | EAS | CHB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | CHB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18941 | hp1 | a0001 | c0002 | t0012 | g0102 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18957 | hp2 | a0001 | c0002 | t0012 | g0100 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18962 | hp1 | a0001 | c0007 | t0019 | g0290 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0218 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18968 | hp2 | a0001 | c0002 | t0012 | g0003 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18983 | hp1 | a0001 | c0001 | t0014 | g0194 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18991 | hp2 | a0001 | c0001 | t0028 | g0307 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18993 | hp1 | a0001 | c0001 | t0014 | g0146 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0231 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19000 | hp2 | a0001 | c0001 | t0037 | g0025 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19006 | hp2 | a0001 | c0007 | t0019 | g0309 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19009 | hp1 | a0001 | c0002 | t0046 | g0001 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19012 | hp2 | a0001 | c0001 | t0028 | g0308 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19030 | hp1 | a0004 | c0006 | t0001 | g0096 | AFR | LWK | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19030 | hp2 | a0002 | c0003 | t0018 | g0267 | AFR | LWK | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19043 | hp1 | a0002 | c0003 | t0010 | g0286 | AFR | LWK | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19043 | hp2 | a0004 | c0006 | t0001 | g0008 | AFR | LWK | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19054 | hp1 | a0001 | c0001 | t0014 | g0175 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0212 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19075 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19083 | hp1 | a0001 | c0002 | t0012 | g0101 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19083 | hp2 | a0001 | c0001 | t0005 | g0206 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19089 | hp1 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | YRI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA19240 | hp2 | a0004 | c0006 | t0001 | g0008 | AFR | YRI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA20129 | hp1 | a0001 | c0001 | t0025 | g0049 | AFR | ASW | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ASW | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0277 | EUR | TSI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0187 | EUR | TSI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0153 | EUR | TSI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA20905 | hp1 | a0001 | c0001 | t0011 | g0237 | SAS | GIH | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | GIH | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02109 | hp1 | a0001 | c0001 | t0052 | g0284 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02109 | hp2 | a0001 | c0001 | t0015 | g0250 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02559 | hp1 | a0001 | c0001 | t0033 | g0221 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0027 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03471 | hp1 | a0008 | c0010 | t0001 | g0092 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG03471 | hp2 | a0003 | c0005 | t0022 | g0079 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG06807 | hp1 | a0001 | c0001 | t0020 | g0018 | AFR | USA | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0289 | AFR | USA | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA20300 | hp1 | a0001 | c0001 | t0011 | g0222 | AFR | USA | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA20300 | hp2 | a0001 | c0001 | t0008 | g0220 | AFR | USA | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA21309 | hp1 | a0001 | c0013 | t0039 | g0021 | AFR | LWK | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| NA21309 | hp2 | a0001 | c0001 | t0053 | g0300 | AFR | LWK | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0017 | g0240 | REF | REF | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0069 | REF | REF | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:65758760
|
G | A | 3 | a0004a0006a0008 | 9 | HG02451.hp1 HG02976.hp2 HG03225.hp1 others(6): Show |
missense_variant | MODERATE | c.235G>A | p.Gly79Ser | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/13 | 404/8652 | 235/2115 | 79/704 | chr5 | 65758760 | ||
| chr5:65785895
|
G | A | 2 | a0007a0008 | 2 | HG03471.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.943G>A | p.Val315Ile | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/13 | 1112/8652 | 943/2115 | 315/704 | chr5 | 65785895 | ||
| chr5:65788274
|
A | G | 3 | a0003a0005a0006 | 11 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(8): Show |
missense_variant | MODERATE | c.1115A>G | p.Lys372Arg | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/13 | 1284/8652 | 1115/2115 | 372/704 | chr5 | 65788274 | ||
| chr5:65822910
|
C | T | 2 | a0002a0005 | 27 | HG00738.hp1 HG01167.hp2 HG01243.hp1 others(24): Show |
missense_variant | MODERATE | c.2110C>T | p.Pro704Ser | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2279/8652 | 2110/2115 | 704/704 | chr5 | 65822910 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:65758741
|
C | T | 1 | a0002c0016 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.216C>T | p.Tyr72Tyr | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/13 | 385/8652 | 216/2115 | 72/704 | chr5 | 65758741 | ||
| chr5:65758795
|
G | A | 1 | a0001c0011 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.270G>A | p.Gln90Gln | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/13 | 439/8652 | 270/2115 | 90/704 | chr5 | 65758795 | ||
| chr5:65785858
|
C | T | 1 | a0001c0007 | 3 | HG00438.hp1 NA18962.hp1 NA19006.hp2 |
synonymous_variant | LOW | c.906C>T | p.Phe302Phe | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/13 | 1075/8652 | 906/2115 | 302/704 | chr5 | 65785858 | ||
| chr5:65788143
|
C | T | 1 | a0001c0015 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.984C>T | p.Pro328Pro | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/13 | 1153/8652 | 984/2115 | 328/704 | chr5 | 65788143 | ||
| chr5:65792595
|
C | T | 1 | a0001c0014 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.1467C>T | p.His489His | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/13 | 1636/8652 | 1467/2115 | 489/704 | chr5 | 65792595 | ||
| chr5:65812292
|
G | A | 1 | a0001c0013 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1881G>A | p.Gly627Gly | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/13 | 2050/8652 | 1881/2115 | 627/704 | chr5 | 65812292 | ||
| chr5:65812388
|
A | G | 14 | a0001c0001a0001c0007a0001c0011others(11): Show | 241 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(238): Show |
synonymous_variant | LOW | c.1977A>G | p.Pro659Pro | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/13 | 2146/8652 | 1977/2115 | 659/704 | chr5 | 65812388 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:65722299
|
C | G | 21 | a0001c0001t0004a0001c0001t0026a0001c0001t0027others(18): Show | 51 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(48): Show |
5_prime_UTR_variant | MODIFIER | c.-75C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/13 | 75 | chr5 | 65722299 | |||||
| chr5:65722315
|
C | T | 1 | a0001c0001t0014 | 4 | HG02056.hp1 NA18983.hp1 NA18993.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-59C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/13 | 59 | chr5 | 65722315 | |||||
| chr5:65722351
|
G | T | 1 | a0002c0003t0058 | 1 | HG02895.hp2 | 5_prime_UTR_variant | MODIFIER | c.-23G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/13 | 23 | chr5 | 65722351 | |||||
| chr5:65823063
|
A | C | 1 | a0001c0001t0025 | 2 | HG02630.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*148A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 148 | chr5 | 65823063 | |||||
| chr5:65823292
|
G | A | 1 | a0001c0001t0020 | 2 | HG01109.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*377G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 377 | chr5 | 65823292 | |||||
| chr5:65823352
|
G | A | 7 | a0001c0001t0005a0001c0001t0011a0001c0001t0020others(4): Show | 28 | HG01109.hp1 HG01516.hp2 HG01517.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*437G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 437 | chr5 | 65823352 | |||||
| chr5:65823368
|
T | C | 1 | a0002c0003t0049 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*453T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 453 | chr5 | 65823368 | |||||
| chr5:65823788
|
A | G | 1 | a0001c0001t0047 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*873A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 873 | chr5 | 65823788 | |||||
| chr5:65824054
|
A | G | 1 | a0003c0005t0024 | 2 | HG02622.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1139A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1139 | chr5 | 65824054 | |||||
| chr5:65824144
|
T | A | 2 | a0001c0001t0015a0001c0001t0050 | 4 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1229T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1229 | chr5 | 65824144 | |||||
| chr5:65824199
|
G | A | 23 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(20): Show | 97 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1284G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1284 | chr5 | 65824199 | |||||
| chr5:65824226
|
C | T | 17 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(14): Show | 93 | HG00609.hp2 HG00621.hp2 HG00639.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1311C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1311 | chr5 | 65824226 | |||||
| chr5:65824316
|
T | C | 46 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(43): Show | 171 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*1401T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1401 | chr5 | 65824316 | |||||
| chr5:65824437
|
CA | C | 16 | a0001c0001t0007a0001c0001t0043a0002c0003t0007others(13): Show | 31 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1523delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1523 | chr5 | 65824437 | |||||
| chr5:65824544
|
T | C | 16 | a0001c0001t0007a0001c0001t0043a0002c0003t0007others(13): Show | 31 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1629T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1629 | chr5 | 65824544 | |||||
| chr5:65824582
|
G | T | 1 | a0003c0005t0023 | 2 | HG01243.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1667G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1667 | chr5 | 65824582 | |||||
| chr5:65824693
|
T | C | 1 | a0001c0001t0026 | 2 | HG01891.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1778T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1778 | chr5 | 65824693 | |||||
| chr5:65824770
|
G | A | 5 | a0001c0001t0003a0001c0001t0009a0001c0001t0037others(2): Show | 35 | HG00438.hp1 HG00609.hp1 HG01070.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1855G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1855 | chr5 | 65824770 | |||||
| chr5:65824828
|
G | A | 1 | a0005c0009t0036 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1913G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1913 | chr5 | 65824828 | |||||
| chr5:65824875
|
G | C | 15 | a0001c0001t0007a0001c0001t0043a0002c0003t0007others(12): Show | 30 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1960G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1960 | chr5 | 65824875 | |||||
| chr5:65824910
|
G | A | 15 | a0001c0001t0007a0001c0001t0043a0002c0003t0007others(12): Show | 30 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1995G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1995 | chr5 | 65824910 | |||||
| chr5:65825025
|
C | T | 1 | a0001c0001t0043 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2110C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2110 | chr5 | 65825025 | |||||
| chr5:65825117
|
CAAA | C | 1 | a0001c0001t0017 | 3 | HG01952.hp1 HG03688.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2203_*2205delAAA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2203 | chr5 | 65825117 | |||||
| chr5:65825162
|
TTCTC | T | 3 | a0001c0001t0022a0001c0001t0031a0003c0005t0022 | 3 | HG01891.hp1 HG02572.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2249_*2252delCTCT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2249 | INFO_REALIGN_3_PRIME | chr5 | 65825162 | ||||
| chr5:65825365
|
T | C | 15 | a0001c0001t0007a0001c0001t0043a0002c0003t0007others(12): Show | 30 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2450T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2450 | chr5 | 65825365 | |||||
| chr5:65825480
|
A | G | 1 | a0001c0001t0028 | 2 | NA18991.hp2 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2565A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2565 | chr5 | 65825480 | |||||
| chr5:65825499
|
G | C | 1 | a0001c0001t0052 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2584G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2584 | chr5 | 65825499 | |||||
| chr5:65825540
|
G | A | 32 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(29): Show | 105 | HG00438.hp1 HG00609.hp1 HG00738.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2625G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2625 | chr5 | 65825540 | |||||
| chr5:65825687
|
G | A | 2 | a0001c0001t0040a0001c0002t0054 | 2 | HG01981.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2772G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2772 | chr5 | 65825687 | |||||
| chr5:65825835
|
T | C | 6 | a0001c0001t0003a0001c0001t0009a0001c0001t0037others(3): Show | 36 | HG00438.hp1 HG00609.hp1 HG01070.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2920T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2920 | chr5 | 65825835 | |||||
| chr5:65826006
|
A | G | 9 | a0001c0001t0007a0002c0003t0007a0002c0003t0010others(6): Show | 21 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3091A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3091 | chr5 | 65826006 | |||||
| chr5:65826138
|
C | A | 1 | a0002c0003t0042 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3223C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3223 | chr5 | 65826138 | |||||
| chr5:65826199
|
T | C | 13 | a0001c0001t0007a0001c0001t0043a0002c0003t0007others(10): Show | 28 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3284T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3284 | chr5 | 65826199 | |||||
| chr5:65826219
|
A | G | 3 | a0001c0001t0033a0001c0001t0034a0001c0001t0051 | 3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3304A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3304 | chr5 | 65826219 | |||||
| chr5:65826255
|
C | T | 1 | a0001c0001t0038 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3340C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3340 | chr5 | 65826255 | |||||
| chr5:65826256
|
G | C | 1 | a0005c0009t0036 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3341G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3341 | chr5 | 65826256 | |||||
| chr5:65826262
|
A | T | 1 | a0001c0001t0043 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3347A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3347 | chr5 | 65826262 | |||||
| chr5:65826300
|
T | C | 1 | a0002c0004t0041 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3385T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3385 | chr5 | 65826300 | |||||
| chr5:65826380
|
G | C | 5 | a0001c0001t0003a0001c0001t0009a0001c0001t0037others(2): Show | 35 | HG00438.hp1 HG00609.hp1 HG01070.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3465G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3465 | chr5 | 65826380 | |||||
| chr5:65826474
|
C | T | 1 | a0001c0001t0056 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3559C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3559 | chr5 | 65826474 | |||||
| chr5:65826996
|
C | A | 1 | a0003c0005t0024 | 2 | HG02622.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4081C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4081 | chr5 | 65826996 | |||||
| chr5:65827005
|
G | C | 13 | a0001c0001t0007a0001c0001t0029a0001c0001t0043others(10): Show | 27 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4090G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4090 | chr5 | 65827005 | |||||
| chr5:65827007
|
G | C | 1 | a0001c0001t0029 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4092G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4092 | chr5 | 65827007 | |||||
| chr5:65827009
|
A | T | 1 | a0001c0001t0029 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4094A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4094 | chr5 | 65827009 | |||||
| chr5:65827010
|
A | C | 1 | a0001c0001t0029 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4095A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4095 | chr5 | 65827010 | |||||
| chr5:65827012
|
T | A | 1 | a0001c0001t0029 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4097T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4097 | chr5 | 65827012 | |||||
| chr5:65827015
|
C | A | 1 | a0001c0001t0029 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4100C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4100 | chr5 | 65827015 | |||||
| chr5:65827016
|
C | G | 1 | a0001c0001t0029 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4101C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4101 | chr5 | 65827016 | |||||
| chr5:65827017
|
A | G | 2 | a0002c0004t0041a0005c0009t0036 | 2 | HG01243.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4102A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4102 | chr5 | 65827017 | |||||
| chr5:65827018
|
C | T | 1 | a0001c0001t0029 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4103C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4103 | chr5 | 65827018 | |||||
| chr5:65827139
|
C | A | 40 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(37): Show | 158 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*4224C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4224 | chr5 | 65827139 | |||||
| chr5:65827274
|
G | A | 7 | a0001c0001t0005a0001c0001t0011a0001c0001t0020others(4): Show | 28 | HG01109.hp1 HG01516.hp2 HG01517.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4359G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4359 | chr5 | 65827274 | |||||
| chr5:65827598
|
T | A | 3 | a0002c0003t0010a0002c0003t0049a0002c0003t0058 | 8 | HG02055.hp2 HG02280.hp1 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4683T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4683 | chr5 | 65827598 | |||||
| chr5:65827740
|
G | A | 1 | a0004c0006t0030 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4825G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4825 | chr5 | 65827740 | |||||
| chr5:65827758
|
T | C | 1 | a0002c0004t0041 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4843T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4843 | chr5 | 65827758 | |||||
| chr5:65827761
|
A | C | 1 | a0001c0001t0027 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4846A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4846 | chr5 | 65827761 | |||||
| chr5:65827977
|
G | A | 1 | a0001c0001t0009 | 8 | HG01070.hp2 HG01169.hp2 HG01358.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5062G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5062 | chr5 | 65827977 | |||||
| chr5:65828002
|
G | A | 1 | a0001c0001t0037 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5087G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5087 | chr5 | 65828002 | |||||
| chr5:65828214
|
C | T | 1 | a0001c0002t0046 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5299C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5299 | chr5 | 65828214 | |||||
| chr5:65828229
|
A | C | 4 | a0001c0001t0025a0002c0004t0016a0002c0016t0035others(1): Show | 7 | HG02055.hp1 HG02257.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5314A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5314 | chr5 | 65828229 | |||||
| chr5:65828254
|
G | GAAAATAA others(3): Show |
1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5341_*5342insAATA others(6): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5342 | INFO_REALIGN_3_PRIME | chr5 | 65828254 | ||||
| chr5:65828257
|
G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5342G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5342 | chr5 | 65828257 | |||||
| chr5:65828258
|
T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5343T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5343 | chr5 | 65828258 | |||||
| chr5:65828260
|
T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5345T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5345 | chr5 | 65828260 | |||||
| chr5:65828261
|
G | T | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5346G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5346 | chr5 | 65828261 | |||||
| chr5:65828262
|
T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5347T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5347 | chr5 | 65828262 | |||||
| chr5:65828263
|
G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5348G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5348 | chr5 | 65828263 | |||||
| chr5:65828264
|
C | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5349C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5349 | chr5 | 65828264 | |||||
| chr5:65828265
|
C | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5350C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5350 | chr5 | 65828265 | |||||
| chr5:65828268
|
G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5353G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5353 | chr5 | 65828268 | |||||
| chr5:65828271
|
C | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5356C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5356 | chr5 | 65828271 | |||||
| chr5:65828276
|
G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5361G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5361 | chr5 | 65828276 | |||||
| chr5:65828279
|
T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5364T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5364 | chr5 | 65828279 | |||||
| chr5:65828292
|
C | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5377C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5377 | chr5 | 65828292 | |||||
| chr5:65828293
|
T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5378T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5378 | chr5 | 65828293 | |||||
| chr5:65828294
|
C | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5379C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5379 | chr5 | 65828294 | |||||
| chr5:65828295
|
C | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5380C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5380 | chr5 | 65828295 | |||||
| chr5:65828297
|
G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5382G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5382 | chr5 | 65828297 | |||||
| chr5:65828298
|
T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5383T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5383 | chr5 | 65828298 | |||||
| chr5:65828299
|
G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5384G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5384 | chr5 | 65828299 | |||||
| chr5:65828303
|
G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5388G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5388 | chr5 | 65828303 | |||||
| chr5:65828305
|
T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5390T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5390 | chr5 | 65828305 | |||||
| chr5:65828306
|
C | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5391C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5391 | chr5 | 65828306 | |||||
| chr5:65828310
|
T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5395T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5395 | chr5 | 65828310 | |||||
| chr5:65828314
|
G | T | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5399G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5399 | chr5 | 65828314 | |||||
| chr5:65828315
|
T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5400T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5400 | chr5 | 65828315 | |||||
| chr5:65828316
|
T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5401T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5401 | chr5 | 65828316 | |||||
| chr5:65828317
|
G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5402G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5402 | chr5 | 65828317 | |||||
| chr5:65828318
|
G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5403G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5403 | chr5 | 65828318 | |||||
| chr5:65828429
|
A | C | 1 | a0001c0001t0034 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5514A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5514 | chr5 | 65828429 | |||||
| chr5:65828587
|
C | T | 35 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(32): Show | 123 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*5672C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5672 | chr5 | 65828587 | |||||
| chr5:65828715
|
C | T | 1 | a0003c0005t0024 | 2 | HG02622.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5800C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5800 | chr5 | 65828715 | |||||
| chr5:65828750
|
T | G | 20 | a0001c0001t0003a0001c0001t0007a0001c0001t0009others(17): Show | 65 | HG00438.hp1 HG00609.hp1 HG00738.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*5835T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5835 | chr5 | 65828750 | |||||
| chr5:65828775
|
C | T | 1 | a0001c0002t0012 | 4 | NA18941.hp1 NA18957.hp2 NA18968.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5860C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5860 | chr5 | 65828775 | |||||
| chr5:65828952
|
A | AC | 2 | a0001c0001t0043a0003c0005t0024 | 3 | HG02622.hp1 HG02647.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6039dupC | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 6040 | INFO_REALIGN_3_PRIME | chr5 | 65828952 | ||||
| chr5:65829162
|
A | G | 1 | a0001c0001t0011 | 4 | HG01516.hp2 HG01517.hp1 NA20300.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6247A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 6247 | chr5 | 65829162 | |||||
| chr5:65829238
|
A | G | 1 | a0003c0005t0023 | 2 | HG01243.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6323A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 6323 | chr5 | 65829238 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:65722494
|
C | G | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+80C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65722494 | ||||||
| chr5:65722723
|
A | G | 1 | a0001c0001t0032g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.41+309A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65722723 | ||||||
| chr5:65722959
|
T | C | 4 | a0001c0001t0002g0258a0002c0004t0044g0259a0002c0016t0035g0257others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+545T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65722959 | ||||||
| chr5:65723104
|
C | A | 2 | a0001c0011t0005g0020a0001c0013t0039g0021 | 2 | HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.41+690C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723104 | ||||||
| chr5:65723315
|
T | C | 1 | a0001c0001t0056g0260 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.41+901T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723315 | ||||||
| chr5:65723552
|
T | C | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+1138T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723552 | ||||||
| chr5:65723577
|
G | A | 1 | a0001c0001t0032g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.41+1163G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723577 | ||||||
| chr5:65723629
|
A | G | 1 | a0002c0004t0041g0311 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.41+1215A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723629 | ||||||
| chr5:65723659
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.41+1245C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723659 | ||||||
| chr5:65723696
|
T | C | 1 | a0002c0003t0010g0261 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.41+1282T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723696 | ||||||
| chr5:65723699
|
C | T | 1 | a0001c0002t0001g0253 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.41+1285C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723699 | ||||||
| chr5:65723739
|
C | T | 4 | a0001c0001t0002g0258a0002c0004t0044g0259a0002c0016t0035g0257others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+1325C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723739 | ||||||
| chr5:65723763
|
C | G | 51 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(48): Show | 52 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.41+1349C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723763 | ||||||
| chr5:65723814
|
C | CA | 21 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(18): Show | 21 | HG00099.hp1 HG01123.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.41+1422dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | |||||
| chr5:65723814
|
C | CAAAAAAA others(2): Show |
8 | a0001c0001t0004g0302a0001c0001t0004g0303a0001c0001t0004g0305others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.41+1414_41+1422dup others(9): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | |||||
| chr5:65723814
|
C | CAAAAAAA others(3): Show |
20 | a0001c0001t0004g0289a0001c0001t0004g0291a0001c0001t0004g0294others(17): Show | 20 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.41+1413_41+1422dup others(10): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | |||||
| chr5:65723814
|
C | CAAAAAAA others(4): Show |
17 | a0001c0001t0004g0271a0001c0001t0004g0272a0001c0001t0004g0274others(14): Show | 18 | HG01106.hp1 HG01261.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.41+1412_41+1422dup others(11): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | |||||
| chr5:65723814
|
C | CAAAAAAA others(5): Show |
1 | a0002c0003t0018g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.41+1411_41+1422dup others(12): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | |||||
| chr5:65723814
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0004g0266a0002c0004t0041g0311 | 2 | HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.41+1410_41+1422dup others(13): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | |||||
| chr5:65723814
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0048g0265a0001c0015t0004g0264 | 2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.41+1409_41+1422dup others(14): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | |||||
| chr5:65723814
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0002g0258a0002c0004t0044g0259 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.41+1407_41+1422dup others(16): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | |||||
| chr5:65723814
|
C | CAAAAAAA others(10): Show |
1 | a0002c0016t0035g0257 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.41+1406_41+1422dup others(17): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | |||||
| chr5:65723814
|
C | CAAAAAAA others(11): Show |
1 | a0005c0009t0036g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+1405_41+1422dup others(18): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | |||||
| chr5:65723814
|
CA | C | 36 | a0001c0001t0001g0217a0001c0001t0001g0227a0001c0001t0002g0223others(33): Show | 36 | HG01070.hp2 HG01256.hp1 HG01516.hp2 others(33): Show |
intron_variant | MODIFIER | c.41+1422delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | |||||
| chr5:65723814
|
CAAAAAAA others(6): Show |
C | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+1410_41+1422del others(13): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | |||||
| chr5:65724018
|
G | A | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+1604G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724018 | ||||||
| chr5:65724112
|
T | A | 1 | a0001c0001t0002g0042 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.41+1698T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724112 | ||||||
| chr5:65724249
|
TAACTGCC others(10): Show |
T | 1 | a0001c0002t0001g0216 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.41+1836_41+1852del others(17): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724249 | ||||||
| chr5:65724261
|
A | G | 92 | a0001c0001t0001g0038a0001c0001t0001g0143a0001c0001t0001g0156others(89): Show | 100 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.41+1847A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724261 | ||||||
| chr5:65724348
|
T | C | 3 | a0001c0001t0052g0284a0002c0003t0010g0268a0002c0003t0010g0283 | 3 | HG02055.hp2 HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.41+1934T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724348 | ||||||
| chr5:65724427
|
T | C | 1 | a0005c0009t0045g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41+2013T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724427 | ||||||
| chr5:65724543
|
T | C | 1 | a0001c0001t0015g0044 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.41+2129T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724543 | ||||||
| chr5:65724557
|
A | G | 1 | a0001c0001t0009g0138 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.41+2143A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724557 | ||||||
| chr5:65724701
|
T | C | 9 | a0001c0001t0052g0284a0002c0003t0010g0261a0002c0003t0010g0268others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.41+2287T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724701 | ||||||
| chr5:65724789
|
GTTTCTTT others(4): Show |
G | 1 | a0001c0013t0039g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.41+2390_41+2400del others(11): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65724789 | |||||
| chr5:65724804
|
C | T | 4 | a0001c0001t0002g0258a0002c0004t0044g0259a0002c0016t0035g0257others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+2390C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724804 | ||||||
| chr5:65724804
|
CT | C | 50 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(47): Show | 51 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.41+2405delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65724804 | |||||
| chr5:65724805
|
T | C | 4 | a0001c0001t0002g0258a0002c0004t0044g0259a0002c0016t0035g0257others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+2391T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724805 | ||||||
| chr5:65724871
|
G | T | 9 | a0001c0001t0052g0284a0002c0003t0010g0261a0002c0003t0010g0268others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.41+2457G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724871 | ||||||
| chr5:65724978
|
T | A | 35 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(32): Show | 35 | HG00741.hp2 HG01256.hp1 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.41+2564T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724978 | ||||||
| chr5:65724996
|
G | A | 1 | a0002c0004t0041g0311 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.41+2582G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724996 | ||||||
| chr5:65725027
|
G | T | 1 | a0001c0002t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.41+2613G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725027 | ||||||
| chr5:65725085
|
G | A | 1 | a0001c0001t0005g0053 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.41+2671G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725085 | ||||||
| chr5:65725289
|
A | G | 1 | a0005c0009t0045g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41+2875A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725289 | ||||||
| chr5:65725339
|
T | C | 6 | a0001c0001t0001g0143a0001c0001t0003g0140a0001c0001t0003g0141others(3): Show | 6 | HG01081.hp2 HG01255.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+2925T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725339 | ||||||
| chr5:65725510
|
A | G | 1 | a0001c0002t0001g0214 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.41+3096A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725510 | ||||||
| chr5:65725842
|
G | A | 1 | a0002c0004t0041g0311 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.41+3428G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725842 | ||||||
| chr5:65725895
|
G | A | 35 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(32): Show | 35 | HG00741.hp2 HG01256.hp1 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.41+3481G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725895 | ||||||
| chr5:65725897
|
A | G | 158 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(155): Show | 166 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.41+3483A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725897 | ||||||
| chr5:65725929
|
G | A | 1 | a0001c0002t0004g0288 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.41+3515G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725929 | ||||||
| chr5:65725969
|
G | A | 5 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0002t0012g0100others(2): Show | 5 | HG02040.hp1 NA18941.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.41+3555G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725969 | ||||||
| chr5:65725972
|
C | T | 1 | a0001c0002t0001g0213 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.41+3558C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725972 | ||||||
| chr5:65726010
|
G | A | 1 | a0001c0001t0031g0054 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.41+3596G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726010 | ||||||
| chr5:65726106
|
C | T | 52 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(49): Show | 57 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.41+3692C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726106 | ||||||
| chr5:65726111
|
C | CA | 21 | a0001c0001t0001g0028a0001c0001t0001g0217a0001c0001t0002g0223others(18): Show | 21 | HG00741.hp2 HG02559.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.41+3716dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65726111 | |||||
| chr5:65726111
|
CA | C | 103 | a0001c0001t0001g0038a0001c0001t0001g0143a0001c0001t0001g0156others(100): Show | 113 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.41+3716delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65726111 | |||||
| chr5:65726111
|
CAA | C | 11 | a0001c0001t0002g0258a0001c0001t0004g0302a0001c0001t0005g0262others(8): Show | 13 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.41+3715_41+3716del others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65726111 | |||||
| chr5:65726111
|
CAAA | C | 49 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(46): Show | 50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.41+3714_41+3716del others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65726111 | |||||
| chr5:65726114
|
A | C | 4 | a0001c0001t0002g0258a0002c0004t0044g0259a0002c0016t0035g0257others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+3700A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726114 | ||||||
| chr5:65726131
|
T | A | 1 | a0003c0005t0024g0055 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.41+3717T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726131 | ||||||
| chr5:65726280
|
A | G | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+3866A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726280 | ||||||
| chr5:65726386
|
G | A | 55 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(52): Show | 58 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.41+3972G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726386 | ||||||
| chr5:65726587
|
G | A | 1 | a0001c0001t0022g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.41+4173G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726587 | ||||||
| chr5:65726684
|
T | A | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+4270T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726684 | ||||||
| chr5:65726700
|
A | G | 2 | a0001c0001t0006g0048a0001c0001t0025g0049 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.41+4286A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726700 | ||||||
| chr5:65726719
|
A | T | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+4305A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726719 | ||||||
| chr5:65726734
|
G | A | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+4320G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726734 | ||||||
| chr5:65726740
|
C | G | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+4326C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726740 | ||||||
| chr5:65726965
|
T | G | 2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.41+4551T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726965 | ||||||
| chr5:65727014
|
T | TG | 58 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(55): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.41+4600_41+4601ins others(1): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727014 | ||||||
| chr5:65727015
|
C | A | 58 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(55): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.41+4601C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727015 | ||||||
| chr5:65727261
|
G | A | 1 | a0001c0002t0001g0145 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.41+4847G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727261 | ||||||
| chr5:65727295
|
G | A | 51 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(48): Show | 52 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.41+4881G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727295 | ||||||
| chr5:65727370
|
A | G | 55 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(52): Show | 58 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.41+4956A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727370 | ||||||
| chr5:65727541
|
A | G | 56 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(53): Show | 61 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.41+5127A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727541 | ||||||
| chr5:65727559
|
T | C | 1 | a0002c0004t0016g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.41+5145T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727559 | ||||||
| chr5:65727575
|
G | A | 4 | a0001c0001t0006g0022a0001c0001t0006g0045a0001c0001t0006g0048others(1): Show | 4 | HG00741.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+5161G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727575 | ||||||
| chr5:65727821
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0001t0029g0105others(1): Show | 4 | HG02572.hp1 HG02809.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+5407C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727821 | ||||||
| chr5:65727912
|
C | G | 282 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(279): Show | 302 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.41+5498C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727912 | ||||||
| chr5:65727923
|
C | T | 1 | a0001c0011t0005g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.41+5509C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727923 | ||||||
| chr5:65728100
|
A | T | 1 | a0005c0009t0045g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41+5686A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728100 | ||||||
| chr5:65728138
|
A | G | 5 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0211others(2): Show | 5 | NA18949.hp1 NA18992.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+5724A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728138 | ||||||
| chr5:65728188
|
A | G | 2 | a0001c0002t0001g0209a0001c0002t0001g0216 | 2 | NA18988.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.41+5774A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728188 | ||||||
| chr5:65728454
|
T | C | 1 | a0001c0001t0002g0252 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.41+6040T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728454 | ||||||
| chr5:65728520
|
C | A | 1 | a0002c0003t0058g0285 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.41+6106C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728520 | ||||||
| chr5:65728859
|
T | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0001t0029g0105others(1): Show | 4 | HG02572.hp1 HG02809.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+6445T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728859 | ||||||
| chr5:65728936
|
C | T | 2 | a0002c0004t0016g0056a0002c0004t0016g0058 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.41+6522C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728936 | ||||||
| chr5:65728947
|
G | A | 8 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0001t0005g0262others(5): Show | 10 | HG01109.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.41+6533G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728947 | ||||||
| chr5:65728969
|
G | A | 19 | a0001c0001t0004g0271a0001c0001t0004g0272a0001c0001t0004g0274others(16): Show | 19 | HG00438.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.41+6555G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728969 | ||||||
| chr5:65729272
|
A | C | 93 | a0001c0001t0001g0038a0001c0001t0001g0143a0001c0001t0001g0156others(90): Show | 101 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.41+6858A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729272 | ||||||
| chr5:65729318
|
G | GTATCAAT others(16): Show |
7 | a0001c0001t0002g0247a0001c0001t0015g0250a0001c0001t0015g0251others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+6904_41+6905ins others(23): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729318 | ||||||
| chr5:65729321
|
T | A | 7 | a0001c0001t0002g0247a0001c0001t0015g0250a0001c0001t0015g0251others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+6907T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729321 | ||||||
| chr5:65729322
|
G | T | 7 | a0001c0001t0002g0247a0001c0001t0015g0250a0001c0001t0015g0251others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+6908G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729322 | ||||||
| chr5:65729323
|
A | C | 7 | a0001c0001t0002g0247a0001c0001t0015g0250a0001c0001t0015g0251others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+6909A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729323 | ||||||
| chr5:65729324
|
C | A | 7 | a0001c0001t0002g0247a0001c0001t0015g0250a0001c0001t0015g0251others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+6910C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729324 | ||||||
| chr5:65729369
|
C | CT | 9 | a0001c0001t0001g0205a0001c0001t0002g0074a0001c0001t0002g0075others(6): Show | 9 | HG00621.hp1 HG00642.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.41+6978dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65729369 | |||||
| chr5:65729369
|
CT | C | 88 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(85): Show | 95 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.41+6978delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65729369 | |||||
| chr5:65729369
|
CTT | C | 62 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0032others(59): Show | 66 | HG00099.hp1 HG00621.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.41+6977_41+6978del others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65729369 | |||||
| chr5:65729369
|
CTTT | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0106a0001c0001t0002g0009others(2): Show | 6 | HG00323.hp2 HG03017.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+6976_41+6978del others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65729369 | |||||
| chr5:65729394
|
G | A | 189 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(186): Show | 201 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.41+6980G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729394 | ||||||
| chr5:65729422
|
T | C | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+7008T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729422 | ||||||
| chr5:65729462
|
C | T | 1 | a0002c0004t0041g0311 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.41+7048C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729462 | ||||||
| chr5:65729621
|
G | A | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+7207G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729621 | ||||||
| chr5:65729654
|
G | A | 3 | a0001c0002t0001g0147a0001c0002t0001g0148a0001c0002t0001g0149 | 3 | NA18948.hp2 NA18954.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.41+7240G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729654 | ||||||
| chr5:65729658
|
A | G | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+7244A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729658 | ||||||
| chr5:65729666
|
G | A | 55 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(52): Show | 58 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.41+7252G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729666 | ||||||
| chr5:65729789
|
A | G | 1 | a0001c0001t0003g0060 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.41+7375A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729789 | ||||||
| chr5:65729822
|
A | G | 12 | a0001c0001t0002g0009a0001c0001t0002g0033a0001c0001t0002g0042others(9): Show | 13 | NA18942.hp1 NA18962.hp2 NA18964.hp1 others(10): Show |
intron_variant | MODIFIER | c.41+7408A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729822 | ||||||
| chr5:65729883
|
G | A | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+7469G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729883 | ||||||
| chr5:65730004
|
C | T | 1 | a0002c0003t0042g0083 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.41+7590C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730004 | ||||||
| chr5:65730237
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.41+7823G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730237 | ||||||
| chr5:65730352
|
A | G | 1 | a0001c0013t0039g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.41+7938A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730352 | ||||||
| chr5:65730392
|
G | A | 158 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(155): Show | 168 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.41+7978G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730392 | ||||||
| chr5:65730393
|
G | C | 1 | a0001c0001t0008g0002 | 3 | HG02258.hp1 HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.41+7979G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730393 | ||||||
| chr5:65730543
|
CT | C | 7 | a0001c0001t0001g0029a0001c0001t0002g0226a0001c0001t0003g0061others(4): Show | 8 | HG01243.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.41+8142delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65730543 | |||||
| chr5:65730562
|
A | G | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+8148A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730562 | ||||||
| chr5:65730613
|
A | G | 1 | a0006c0008t0006g0090 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.41+8199A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730613 | ||||||
| chr5:65730684
|
G | A | 2 | a0001c0001t0022g0084a0001c0001t0031g0054 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.41+8270G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730684 | ||||||
| chr5:65730829
|
G | A | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+8415G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730829 | ||||||
| chr5:65731127
|
G | A | 2 | a0007c0012t0001g0093a0008c0010t0001g0092 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.41+8713G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731127 | ||||||
| chr5:65731152
|
T | G | 49 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(46): Show | 50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.41+8738T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731152 | ||||||
| chr5:65731177
|
C | T | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+8763C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731177 | ||||||
| chr5:65731242
|
G | C | 1 | a0001c0001t0004g0294 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.41+8828G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731242 | ||||||
| chr5:65731334
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0029g0105 | 2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.41+8920A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731334 | ||||||
| chr5:65731451
|
T | C | 1 | a0001c0001t0048g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.41+9037T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731451 | ||||||
| chr5:65731604
|
C | G | 3 | a0001c0001t0052g0284a0002c0003t0010g0268a0002c0003t0010g0283 | 3 | HG02055.hp2 HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.41+9190C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731604 | ||||||
| chr5:65731636
|
A | C | 57 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(54): Show | 64 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.41+9222A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731636 | ||||||
| chr5:65731734
|
TAC | T | 2 | a0001c0002t0013g0016a0001c0002t0013g0204 | 3 | HG00609.hp2 HG02040.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.41+9322_41+9323del others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65731734 | |||||
| chr5:65731742
|
C | CT | 41 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0197others(38): Show | 43 | HG00323.hp2 HG00438.hp2 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.41+9354dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65731742 | |||||
| chr5:65731742
|
C | CTT | 44 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(41): Show | 51 | HG00099.hp1 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.41+9353_41+9354dup others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65731742 | |||||
| chr5:65731742
|
C | CTTT | 8 | a0001c0001t0001g0028a0001c0001t0001g0130a0001c0001t0002g0033others(5): Show | 8 | HG00621.hp2 HG02027.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.41+9352_41+9354dup others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65731742 | |||||
| chr5:65731742
|
CT | C | 6 | a0001c0001t0001g0156a0001c0001t0001g0227a0001c0001t0003g0061others(3): Show | 6 | HG00099.hp2 HG01516.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+9354delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65731742 | |||||
| chr5:65731742
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0005g0047 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.41+9340_41+9354del others(15): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65731742 | |||||
| chr5:65731747
|
T | C | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+9333T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731747 | ||||||
| chr5:65731751
|
TTTTTTTT others(11): Show |
T | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+9338_41+9355del others(18): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731751 | ||||||
| chr5:65731764
|
TTTTTC | T | 54 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(51): Show | 55 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.41+9351_41+9355del others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731764 | ||||||
| chr5:65731865
|
G | A | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+9451G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731865 | ||||||
| chr5:65731966
|
A | G | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+9552A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731966 | ||||||
| chr5:65732148
|
A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0001t0029g0105others(1): Show | 4 | HG02572.hp1 HG02809.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+9734A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65732148 | ||||||
| chr5:65732182
|
C | A | 1 | a0005c0009t0036g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+9768C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65732182 | ||||||
| chr5:65732256
|
TAGAAAGA others(2290): Show |
T | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+9859_41+12155de others(1): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65732256 | |||||
| chr5:65732351
|
T | A | 1 | a0003c0005t0024g0055 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.41+9937T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65732351 | ||||||
| chr5:65732385
|
G | T | 21 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0006g0089others(18): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.41+9971G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65732385 | ||||||
| chr5:65732386
|
A | T | 21 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0006g0089others(18): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.41+9972A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65732386 | ||||||
| chr5:65732645
|
C | T | 1 | a0003c0005t0023g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.41+10231C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65732645 | ||||||
| chr5:65733474
|
A | G | 225 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(222): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.41+11060A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65733474 | ||||||
| chr5:65733527
|
A | G | 1 | a0005c0009t0045g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41+11113A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65733527 | ||||||
| chr5:65733568
|
G | A | 2 | a0006c0008t0006g0090a0006c0008t0006g0103 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.41+11154G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65733568 | ||||||
| chr5:65733785
|
T | A | 1 | a0001c0001t0001g0030 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.41+11371T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65733785 | ||||||
| chr5:65733809
|
T | C | 1 | a0005c0009t0045g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41+11395T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65733809 | ||||||
| chr5:65733966
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(2): Show | 5 | HG00099.hp1 HG01123.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.41+11552C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65733966 | ||||||
| chr5:65733998
|
T | C | 111 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(108): Show | 119 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.41+11584T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65733998 | ||||||
| chr5:65734200
|
T | C | 1 | a0001c0001t0003g0060 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.41+11786T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734200 | ||||||
| chr5:65734342
|
C | T | 2 | a0001c0001t0002g0013a0001c0001t0002g0127 | 3 | NA18999.hp2 NA19009.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.41+11928C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734342 | ||||||
| chr5:65734541
|
G | GA | 102 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(99): Show | 110 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.41+12140dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65734541 | |||||
| chr5:65734622
|
T | A | 2 | a0001c0001t0006g0022a0001c0001t0006g0045 | 2 | HG00741.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.41+12208T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734622 | ||||||
| chr5:65734640
|
A | G | 1 | a0001c0001t0048g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.41+12226A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734640 | ||||||
| chr5:65734687
|
C | T | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+12273C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734687 | ||||||
| chr5:65734688
|
G | A | 91 | a0001c0001t0001g0038a0001c0001t0001g0143a0001c0001t0001g0156others(88): Show | 99 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.41+12274G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734688 | ||||||
| chr5:65734742
|
A | G | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+12328A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734742 | ||||||
| chr5:65734750
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.41+12336A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734750 | ||||||
| chr5:65734869
|
T | G | 1 | a0003c0005t0024g0055 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.41+12455T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734869 | ||||||
| chr5:65734894
|
C | T | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+12480C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734894 | ||||||
| chr5:65734905
|
A | G | 7 | a0001c0001t0006g0089a0001c0001t0006g0091a0001c0001t0006g0095others(4): Show | 8 | HG01243.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.41+12491A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734905 | ||||||
| chr5:65735000
|
C | T | 1 | a0001c0002t0001g0125 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.41+12586C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65735000 | ||||||
| chr5:65735117
|
G | T | 1 | a0002c0016t0035g0257 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.41+12703G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65735117 | ||||||
| chr5:65735122
|
T | C | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+12708T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65735122 | ||||||
| chr5:65735215
|
TA | T | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+12803delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65735215 | |||||
| chr5:65735665
|
A | G | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+13251A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65735665 | ||||||
| chr5:65735755
|
A | T | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+13341A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65735755 | ||||||
| chr5:65735811
|
A | G | 1 | a0001c0001t0005g0225 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.41+13397A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65735811 | ||||||
| chr5:65736104
|
T | C | 116 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(113): Show | 126 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.41+13690T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736104 | ||||||
| chr5:65736364
|
C | T | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+13950C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736364 | ||||||
| chr5:65736527
|
C | T | 1 | a0001c0001t0006g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.41+14113C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736527 | ||||||
| chr5:65736580
|
T | C | 1 | a0002c0016t0035g0257 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.41+14166T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736580 | ||||||
| chr5:65736640
|
AT | A | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+14229delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65736640 | |||||
| chr5:65736676
|
G | A | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+14262G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736676 | ||||||
| chr5:65736700
|
G | C | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+14286G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736700 | ||||||
| chr5:65736990
|
A | G | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+14576A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736990 | ||||||
| chr5:65736997
|
C | T | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+14583C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736997 | ||||||
| chr5:65737154
|
CTG | C | 13 | a0001c0001t0006g0022a0001c0001t0006g0045a0001c0001t0006g0048others(10): Show | 13 | HG00741.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.41+14744_41+14745d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65737154 | |||||
| chr5:65737221
|
G | A | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+14807G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737221 | ||||||
| chr5:65737263
|
A | G | 1 | a0001c0001t0040g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.41+14849A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737263 | ||||||
| chr5:65737306
|
G | A | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+14892G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737306 | ||||||
| chr5:65737311
|
C | T | 13 | a0001c0001t0006g0022a0001c0001t0006g0045a0001c0001t0006g0048others(10): Show | 13 | HG00741.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.41+14897C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737311 | ||||||
| chr5:65737541
|
A | G | 22 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(19): Show | 22 | HG01516.hp2 HG01517.hp1 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+15127A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737541 | ||||||
| chr5:65737627
|
T | C | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+15213T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737627 | ||||||
| chr5:65737637
|
G | A | 1 | a0001c0001t0040g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.41+15223G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737637 | ||||||
| chr5:65737739
|
G | A | 22 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(19): Show | 22 | HG01516.hp2 HG01517.hp1 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+15325G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737739 | ||||||
| chr5:65737755
|
A | G | 1 | a0001c0001t0004g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.41+15341A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737755 | ||||||
| chr5:65737821
|
C | T | 1 | a0001c0013t0039g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.41+15407C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737821 | ||||||
| chr5:65737881
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.41+15467G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737881 | ||||||
| chr5:65737898
|
G | A | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+15484G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737898 | ||||||
| chr5:65737909
|
C | T | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+15495C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737909 | ||||||
| chr5:65738025
|
A | G | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+15611A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738025 | ||||||
| chr5:65738043
|
G | A | 1 | a0001c0001t0009g0023 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.41+15629G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738043 | ||||||
| chr5:65738061
|
G | A | 51 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(48): Show | 52 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.41+15647G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738061 | ||||||
| chr5:65738068
|
G | A | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+15654G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738068 | ||||||
| chr5:65738135
|
GA | G | 135 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(132): Show | 146 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.41+15735delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738135 | |||||
| chr5:65738312
|
G | GGT | 57 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(54): Show | 64 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.41+15900_41+15901d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738312 | |||||
| chr5:65738487
|
A | C | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+16073A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738487 | ||||||
| chr5:65738552
|
G | A | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+16138G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738552 | ||||||
| chr5:65738610
|
T | C | 1 | a0001c0001t0006g0091 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.41+16196T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738610 | ||||||
| chr5:65738632
|
A | T | 6 | a0002c0003t0007g0078a0002c0003t0042g0083a0002c0004t0016g0082others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+16218A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738632 | ||||||
| chr5:65738744
|
A | G | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+16330A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738744 | ||||||
| chr5:65738904
|
G | A | 7 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0001t0002g0085others(4): Show | 7 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+16490G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738904 | ||||||
| chr5:65738926
|
G | GTATATAT others(26): Show |
10 | a0001c0001t0052g0284a0002c0003t0010g0261a0002c0003t0010g0268others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16513_41+16514i others(35): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738926 | |||||
| chr5:65738926
|
G | GTATATAT others(28): Show |
1 | a0005c0009t0036g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+16513_41+16514i others(37): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738926 | |||||
| chr5:65738926
|
GTGTATAT others(18): Show |
G | 2 | a0002c0004t0018g0282a0002c0004t0018g0293 | 2 | HG01167.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.41+16514_41+16538d others(27): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738926 | |||||
| chr5:65738928
|
G | A | 56 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(53): Show | 59 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.41+16514G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738928 | ||||||
| chr5:65738928
|
G | T | 1 | a0005c0009t0036g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+16514G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738928 | ||||||
| chr5:65738936
|
A | G | 46 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(43): Show | 49 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.41+16522A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738936 | ||||||
| chr5:65738937
|
T | TA | 42 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(39): Show | 43 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.41+16523_41+16524i others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738937 | ||||||
| chr5:65738937
|
T | TATATATA others(17): Show |
4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+16523_41+16524i others(26): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738937 | ||||||
| chr5:65738938
|
T | A | 1 | a0005c0009t0036g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+16524T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738938 | ||||||
| chr5:65738939
|
T | A | 42 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(39): Show | 43 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.41+16525T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738939 | ||||||
| chr5:65738940
|
T | TA | 10 | a0001c0001t0052g0284a0002c0003t0010g0261a0002c0003t0010g0268others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16526_41+16527i others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738940 | ||||||
| chr5:65738941
|
T | A | 46 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(43): Show | 49 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.41+16527T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738941 | ||||||
| chr5:65738942
|
T | A | 11 | a0001c0001t0052g0284a0001c0002t0001g0159a0002c0003t0010g0261others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+16528T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738942 | ||||||
| chr5:65738944
|
T | A | 42 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(39): Show | 43 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.41+16530T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738944 | ||||||
| chr5:65738949
|
G | A | 57 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(54): Show | 60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.41+16535G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738949 | ||||||
| chr5:65738951
|
T | A | 42 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(39): Show | 43 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.41+16537T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738951 | ||||||
| chr5:65738952
|
T | TTATA | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+16538_41+16539i others(6): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738952 | ||||||
| chr5:65738953
|
A | AT | 39 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(36): Show | 40 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.41+16540dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738953 | |||||
| chr5:65738955
|
A | AT | 3 | a0001c0001t0002g0258a0002c0004t0044g0259a0002c0016t0035g0257 | 3 | HG02257.hp1 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.41+16542dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738955 | |||||
| chr5:65738961
|
G | A | 11 | a0001c0001t0052g0284a0002c0003t0010g0261a0002c0003t0010g0268others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+16547G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738961 | ||||||
| chr5:65738961
|
G | T | 46 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(43): Show | 49 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.41+16547G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738961 | ||||||
| chr5:65738962
|
T | A | 11 | a0001c0001t0052g0284a0002c0003t0010g0261a0002c0003t0010g0268others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+16548T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738962 | ||||||
| chr5:65738970
|
A | ATATATAT others(5): Show |
10 | a0001c0001t0052g0284a0002c0003t0010g0261a0002c0003t0010g0268others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16556_41+16557i others(14): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738970 | ||||||
| chr5:65738970
|
A | T | 46 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(43): Show | 49 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.41+16556A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738970 | ||||||
| chr5:65738972
|
T | A | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+16558T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738972 | ||||||
| chr5:65738972
|
T | TTTTATA | 3 | a0001c0001t0002g0258a0002c0004t0044g0259a0002c0016t0035g0257 | 3 | HG02257.hp1 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.41+16558_41+16559i others(8): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738972 | ||||||
| chr5:65738972
|
TA | T | 39 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(36): Show | 40 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.41+16559delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738972 | ||||||
| chr5:65738975
|
A | T | 39 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(36): Show | 40 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.41+16561A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738975 | ||||||
| chr5:65738976
|
TA | T | 11 | a0001c0001t0006g0027a0001c0001t0032g0255a0004c0006t0001g0008others(8): Show | 12 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.41+16563delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738976 | ||||||
| chr5:65738979
|
AT | A | 11 | a0001c0001t0006g0027a0001c0001t0032g0255a0004c0006t0001g0008others(8): Show | 12 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.41+16567delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738979 | |||||
| chr5:65738980
|
T | A | 44 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(41): Show | 47 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.41+16566T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738980 | ||||||
| chr5:65738980
|
T | TAAATA | 10 | a0001c0001t0052g0284a0002c0003t0010g0261a0002c0003t0010g0268others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16566_41+16567i others(7): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738980 | ||||||
| chr5:65738981
|
T | A | 1 | a0005c0009t0036g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+16567T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738981 | ||||||
| chr5:65738983
|
T | TA | 10 | a0001c0001t0052g0284a0002c0003t0010g0261a0002c0003t0010g0268others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16570dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738983 | |||||
| chr5:65738986
|
A | G | 7 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0001t0002g0085others(4): Show | 7 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+16572A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738986 | ||||||
| chr5:65738986
|
A | T | 11 | a0001c0001t0006g0027a0001c0001t0032g0255a0004c0006t0001g0008others(8): Show | 12 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.41+16572A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738986 | ||||||
| chr5:65738988
|
T | A | 29 | a0001c0001t0002g0258a0001c0001t0005g0262a0001c0001t0006g0027others(26): Show | 32 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.41+16574T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738988 | ||||||
| chr5:65738988
|
T | TTA | 224 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(221): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.41+16582_41+16583d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738988 | |||||
| chr5:65738991
|
T | A | 7 | a0001c0001t0002g0258a0001c0001t0005g0262a0001c0001t0006g0263others(4): Show | 9 | HG01109.hp1 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.41+16577T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738991 | ||||||
| chr5:65738993
|
T | A | 1 | a0005c0009t0036g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+16579T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738993 | ||||||
| chr5:65738997
|
T | A | 10 | a0001c0001t0052g0284a0002c0003t0010g0261a0002c0003t0010g0268others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16583T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738997 | ||||||
| chr5:65738997
|
T | TAAA | 39 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(36): Show | 40 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.41+16583_41+16584i others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738997 | ||||||
| chr5:65738998
|
T | A | 12 | a0001c0001t0002g0258a0001c0001t0005g0262a0001c0001t0006g0263others(9): Show | 16 | HG01109.hp1 HG01243.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.41+16584T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738998 | ||||||
| chr5:65738999
|
T | A | 56 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(53): Show | 59 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.41+16585T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738999 | ||||||
| chr5:65739000
|
T | A | 1 | a0005c0009t0036g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+16586T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739000 | ||||||
| chr5:65739003
|
A | AT | 8 | a0001c0001t0002g0258a0001c0001t0005g0262a0001c0001t0006g0263others(5): Show | 10 | HG01109.hp1 HG01243.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16589_41+16590i others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739003 | ||||||
| chr5:65739008
|
AT | A | 7 | a0001c0001t0002g0258a0001c0001t0005g0262a0001c0001t0006g0263others(4): Show | 9 | HG01109.hp1 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.41+16595delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739008 | ||||||
| chr5:65739009
|
T | TATAAAAT others(50): Show |
2 | a0001c0001t0004g0303a0001c0001t0055g0304 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.41+16597_41+16598i others(59): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65739009 | |||||
| chr5:65739009
|
T | TATAAAAT others(52): Show |
35 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(32): Show | 36 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.41+16597_41+16598i others(61): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65739009 | |||||
| chr5:65739009
|
T | TATATAAA | 10 | a0001c0001t0048g0265a0002c0003t0010g0261a0002c0003t0010g0268others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.41+16597_41+16598i others(9): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65739009 | |||||
| chr5:65739011
|
T | A | 8 | a0001c0001t0002g0258a0001c0001t0005g0262a0001c0001t0006g0263others(5): Show | 10 | HG01109.hp1 HG01243.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16597T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739011 | ||||||
| chr5:65739012
|
T | A | 57 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(54): Show | 60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.41+16598T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739012 | ||||||
| chr5:65739023
|
A | T | 2 | a0002c0004t0018g0282a0002c0004t0018g0293 | 2 | HG01167.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.41+16609A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739023 | ||||||
| chr5:65739032
|
TATATATA others(6): Show |
T | 2 | a0002c0004t0018g0282a0002c0004t0018g0293 | 2 | HG01167.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.41+16630_41+16642d others(15): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65739032 | |||||
| chr5:65739042
|
A | T | 58 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(55): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.41+16628A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739042 | ||||||
| chr5:65739045
|
A | T | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+16631A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739045 | ||||||
| chr5:65739109
|
G | A | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+16695G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739109 | ||||||
| chr5:65739185
|
G | A | 51 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(48): Show | 52 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.41+16771G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739185 | ||||||
| chr5:65739321
|
G | A | 1 | a0003c0005t0021g0017 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.41+16907G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739321 | ||||||
| chr5:65739432
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.41+17018G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739432 | ||||||
| chr5:65739484
|
T | C | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+17070T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739484 | ||||||
| chr5:65739601
|
T | G | 1 | a0001c0001t0032g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.41+17187T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739601 | ||||||
| chr5:65739880
|
C | T | 8 | a0001c0001t0006g0089a0001c0001t0006g0091a0001c0001t0006g0095others(5): Show | 9 | HG01243.hp2 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.41+17466C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739880 | ||||||
| chr5:65740068
|
C | G | 7 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0001t0002g0085others(4): Show | 7 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+17654C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740068 | ||||||
| chr5:65740082
|
T | C | 1 | a0006c0008t0006g0103 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41+17668T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740082 | ||||||
| chr5:65740092
|
C | G | 4 | a0001c0001t0006g0022a0001c0001t0006g0045a0001c0001t0006g0048others(1): Show | 4 | HG00741.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+17678C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740092 | ||||||
| chr5:65740472
|
A | G | 4 | a0001c0001t0002g0012a0001c0001t0002g0123a0001c0001t0002g0124others(1): Show | 5 | HG01496.hp1 HG01928.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+18058A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740472 | ||||||
| chr5:65740601
|
G | C | 1 | a0001c0001t0032g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.42-17966G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740601 | ||||||
| chr5:65740757
|
A | G | 1 | a0001c0001t0005g0238 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.42-17810A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740757 | ||||||
| chr5:65740813
|
T | TTA | 78 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(75): Show | 86 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.42-17742_42-17741d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65740813 | |||||
| chr5:65740813
|
T | TTATA | 7 | a0001c0001t0002g0247a0001c0001t0015g0044a0001c0001t0015g0250others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-17744_42-17741d others(6): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65740813 | |||||
| chr5:65740870
|
CT | C | 6 | a0001c0001t0003g0060a0001c0001t0037g0025a0004c0006t0001g0088others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-17679delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65740870 | |||||
| chr5:65740870
|
CTT | C | 57 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(54): Show | 60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.42-17680_42-17679d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65740870 | |||||
| chr5:65740934
|
C | T | 1 | a0001c0001t0002g0252 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.42-17633C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740934 | ||||||
| chr5:65740976
|
C | A | 1 | a0003c0005t0023g0077 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.42-17591C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740976 | ||||||
| chr5:65741135
|
G | A | 1 | a0001c0002t0001g0014 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.42-17432G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65741135 | ||||||
| chr5:65741192
|
G | C | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-17375G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65741192 | ||||||
| chr5:65741389
|
C | T | 1 | a0001c0001t0014g0194 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.42-17178C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65741389 | ||||||
| chr5:65741436
|
T | C | 1 | a0001c0001t0006g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.42-17131T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65741436 | ||||||
| chr5:65741459
|
A | G | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-17108A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65741459 | ||||||
| chr5:65741624
|
C | T | 85 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(82): Show | 93 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.42-16943C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65741624 | ||||||
| chr5:65741852
|
A | G | 2 | a0002c0004t0018g0282a0002c0004t0018g0293 | 2 | HG01167.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.42-16715A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65741852 | ||||||
| chr5:65742013
|
T | G | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-16554T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742013 | ||||||
| chr5:65742179
|
T | C | 92 | a0001c0001t0001g0038a0001c0001t0001g0143a0001c0001t0001g0156others(89): Show | 100 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.42-16388T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742179 | ||||||
| chr5:65742223
|
G | A | 1 | a0001c0001t0005g0262 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.42-16344G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742223 | ||||||
| chr5:65742244
|
AAG | A | 3 | a0001c0001t0015g0044a0001c0001t0015g0250a0001c0001t0015g0251 | 3 | HG02109.hp2 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.42-16320_42-16319d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65742244 | |||||
| chr5:65742269
|
TAA | T | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-16297_42-16296d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742269 | ||||||
| chr5:65742284
|
G | A | 3 | a0001c0001t0002g0258a0002c0004t0044g0259a0002c0016t0035g0257 | 3 | HG02257.hp1 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.42-16283G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742284 | ||||||
| chr5:65742314
|
G | A | 92 | a0001c0001t0001g0038a0001c0001t0001g0143a0001c0001t0001g0156others(89): Show | 100 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.42-16253G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742314 | ||||||
| chr5:65742380
|
A | G | 4 | a0001c0001t0002g0258a0002c0004t0044g0259a0002c0016t0035g0257others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-16187A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742380 | ||||||
| chr5:65742404
|
C | T | 306 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(303): Show | 327 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.42-16163C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742404 | ||||||
| chr5:65742504
|
G | A | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-16063G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742504 | ||||||
| chr5:65742548
|
C | A | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-16019C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742548 | ||||||
| chr5:65742627
|
T | A | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-15940T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742627 | ||||||
| chr5:65742654
|
G | A | 1 | a0001c0002t0001g0153 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.42-15913G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742654 | ||||||
| chr5:65742698
|
A | T | 1 | a0005c0009t0045g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42-15869A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742698 | ||||||
| chr5:65742737
|
G | A | 63 | a0001c0001t0002g0012a0001c0001t0002g0123a0001c0001t0002g0124others(60): Show | 67 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.42-15830G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742737 | ||||||
| chr5:65742850
|
C | G | 2 | a0001c0001t0006g0050a0001c0001t0025g0046 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.42-15717C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742850 | ||||||
| chr5:65742902
|
C | T | 1 | a0001c0002t0001g0208 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.42-15665C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742902 | ||||||
| chr5:65742928
|
G | A | 4 | a0001c0001t0002g0258a0002c0004t0044g0259a0002c0016t0035g0257others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-15639G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742928 | ||||||
| chr5:65743000
|
A | G | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-15567A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743000 | ||||||
| chr5:65743156
|
T | TGCTGGTA others(2): Show |
5 | a0001c0001t0017g0240a0001c0001t0017g0241a0001c0001t0017g0242others(2): Show | 5 | HG01256.hp1 HG01952.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-15407_42-15399d others(11): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65743156 | |||||
| chr5:65743223
|
TCAA | T | 5 | a0001c0001t0017g0240a0001c0001t0017g0241a0001c0001t0017g0242others(2): Show | 5 | HG01256.hp1 HG01952.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-15340_42-15338d others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65743223 | |||||
| chr5:65743572
|
G | A | 49 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(46): Show | 50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.42-14995G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743572 | ||||||
| chr5:65743605
|
G | T | 2 | a0001c0001t0028g0307a0001c0001t0028g0308 | 2 | NA18991.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.42-14962G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743605 | ||||||
| chr5:65743779
|
A | C | 9 | a0001c0001t0052g0284a0002c0003t0010g0261a0002c0003t0010g0268others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.42-14788A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743779 | ||||||
| chr5:65743783
|
C | A | 1 | a0001c0001t0032g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.42-14784C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743783 | ||||||
| chr5:65743840
|
G | T | 55 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(52): Show | 58 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.42-14727G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743840 | ||||||
| chr5:65743891
|
G | A | 1 | a0001c0002t0001g0110 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.42-14676G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743891 | ||||||
| chr5:65743948
|
C | T | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-14619C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743948 | ||||||
| chr5:65744053
|
G | T | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-14514G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744053 | ||||||
| chr5:65744138
|
C | CT | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-14428dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65744138 | |||||
| chr5:65744162
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0001g0205 | 2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.42-14405G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744162 | ||||||
| chr5:65744171
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.42-14396A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744171 | ||||||
| chr5:65744415
|
G | T | 2 | a0001c0001t0048g0265a0002c0004t0041g0311 | 2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.42-14152G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744415 | ||||||
| chr5:65744440
|
A | G | 59 | a0001c0001t0002g0258a0001c0001t0004g0266a0001c0001t0004g0271others(56): Show | 62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-14127A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744440 | ||||||
| chr5:65744472
|
C | CT | 8 | a0001c0001t0001g0203a0001c0001t0002g0192a0001c0001t0003g0060others(5): Show | 8 | HG01243.hp1 HG03041.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.42-14079dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65744472 | |||||
| chr5:65744472
|
C | CTTT | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-14081_42-14079d others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65744472 | |||||
| chr5:65744472
|
CT | C | 62 | a0001c0001t0002g0252a0001c0001t0004g0266a0001c0001t0004g0271others(59): Show | 64 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.42-14079delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65744472 | |||||
| chr5:65744473
|
T | C | 4 | a0001c0001t0006g0022a0001c0001t0006g0045a0001c0001t0006g0048others(1): Show | 4 | HG00741.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-14094T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744473 | ||||||
| chr5:65744474
|
T | C | 2 | a0001c0001t0027g0278a0001c0001t0027g0295 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.42-14093T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744474 | ||||||
| chr5:65744489
|
G | T | 4 | a0001c0001t0002g0258a0002c0004t0044g0259a0002c0016t0035g0257others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-14078G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744489 | ||||||
| chr5:65744618
|
G | A | 51 | a0001c0001t0004g0266a0001c0001t0004g0271a0001c0001t0004g0272others(48): Show | 52 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.42-13949G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744618 | ||||||
| chr5:65744647
|
C | T | 1 | a0001c0001t0017g0242 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.42-13920C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744647 | ||||||
| chr5:65744834
|
C | T | 2 | a0001c0001t0002g0258a0002c0004t0044g0259 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.42-13733C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744834 | ||||||
| chr5:65744883
|
G | GAGAAA | 64 | a0001c0001t0001g0217a0001c0001t0001g0227a0001c0001t0002g0226others(61): Show | 65 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.42-13674_42-13670d others(7): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65744883 | |||||
| chr5:65745047
|
G | A | 1 | a0001c0001t0004g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.42-13520G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745047 | ||||||
| chr5:65745110
|
C | A | 108 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(105): Show | 116 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.42-13457C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745110 | ||||||
| chr5:65745143
|
C | T | 1 | a0001c0001t0006g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.42-13424C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745143 | ||||||
| chr5:65745247
|
A | T | 1 | a0001c0001t0001g0217 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.42-13320A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745247 | ||||||
| chr5:65745690
|
G | A | 2 | a0001c0001t0001g0028a0001c0015t0004g0264 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.42-12877G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745690 | ||||||
| chr5:65745824
|
T | C | 1 | a0001c0007t0019g0290 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.42-12743T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745824 | ||||||
| chr5:65745858
|
C | T | 3 | a0001c0001t0004g0274a0001c0001t0004g0275a0001c0001t0004g0276 | 3 | NA18948.hp1 NA18980.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.42-12709C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745858 | ||||||
| chr5:65745869
|
G | A | 22 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(19): Show | 22 | HG01516.hp2 HG01517.hp1 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.42-12698G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745869 | ||||||
| chr5:65745922
|
A | G | 155 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(152): Show | 166 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.42-12645A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745922 | ||||||
| chr5:65745963
|
G | A | 3 | a0001c0001t0004g0294a0001c0001t0004g0296a0001c0001t0056g0260 | 3 | HG03688.hp1 NA18973.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.42-12604G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745963 | ||||||
| chr5:65746141
|
G | A | 1 | a0005c0009t0036g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.42-12426G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746141 | ||||||
| chr5:65746211
|
G | A | 1 | a0003c0005t0021g0017 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.42-12356G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746211 | ||||||
| chr5:65746248
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.42-12319A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746248 | ||||||
| chr5:65746304
|
T | C | 2 | a0001c0001t0002g0232a0001c0001t0005g0231 | 2 | NA18994.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.42-12263T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746304 | ||||||
| chr5:65746420
|
G | C | 1 | a0001c0001t0006g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.42-12147G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746420 | ||||||
| chr5:65746497
|
A | G | 2 | a0001c0001t0006g0027a0001c0001t0032g0255 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.42-12070A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746497 | ||||||
| chr5:65746637
|
T | C | 1 | a0002c0004t0007g0245 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42-11930T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746637 | ||||||
| chr5:65746990
|
C | T | 5 | a0001c0001t0002g0121a0001c0002t0001g0011a0001c0002t0001g0110others(2): Show | 6 | HG00733.hp1 HG00735.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-11577C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746990 | ||||||
| chr5:65746991
|
G | A | 3 | a0001c0001t0004g0271a0001c0001t0004g0272a0001c0001t0004g0291 | 3 | HG01106.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.42-11576G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746991 | ||||||
| chr5:65747042
|
A | G | 4 | a0004c0006t0001g0008a0004c0006t0001g0088a0004c0006t0001g0096others(1): Show | 5 | HG02451.hp1 HG03486.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-11525A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65747042 | ||||||
| chr5:65747192
|
T | C | 2 | a0001c0001t0048g0265a0002c0004t0041g0311 | 2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.42-11375T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65747192 | ||||||
| chr5:65747200
|
AT | A | 4 | a0004c0006t0001g0008a0004c0006t0001g0088a0004c0006t0001g0096others(1): Show | 5 | HG02451.hp1 HG03486.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-11364delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65747200 | |||||
| chr5:65747266
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0120 | 2 | NA20805.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.42-11301C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65747266 | ||||||
| chr5:65747534
|
T | G | 1 | a0001c0001t0001g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.42-11033T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65747534 | ||||||
| chr5:65748036
|
A | G | 7 | a0001c0001t0002g0247a0001c0001t0015g0044a0001c0001t0015g0250others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-10531A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748036 | ||||||
| chr5:65748073
|
C | T | 1 | a0005c0009t0045g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42-10494C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748073 | ||||||
| chr5:65748100
|
C | T | 1 | a0005c0009t0045g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42-10467C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748100 | ||||||
| chr5:65748235
|
C | T | 7 | a0001c0001t0001g0143a0001c0001t0003g0140a0001c0001t0003g0141others(4): Show | 7 | HG01081.hp2 HG01255.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-10332C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748235 | ||||||
| chr5:65748381
|
T | C | 1 | a0002c0004t0018g0293 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.42-10186T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748381 | ||||||
| chr5:65748495
|
C | T | 1 | a0001c0002t0001g0122 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.42-10072C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748495 | ||||||
| chr5:65748637
|
C | G | 1 | a0001c0001t0026g0019 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.42-9930C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748637 | ||||||
| chr5:65748695
|
A | G | 1 | a0001c0001t0004g0301 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.42-9872A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748695 | ||||||
| chr5:65748782
|
A | G | 2 | a0001c0001t0006g0089a0001c0001t0006g0095 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.42-9785A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748782 | ||||||
| chr5:65748902
|
A | T | 1 | a0001c0002t0001g0191 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.42-9665A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748902 | ||||||
| chr5:65749144
|
G | A | 143 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(140): Show | 154 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.42-9423G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65749144 | ||||||
| chr5:65749245
|
A | C | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-9322A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65749245 | ||||||
| chr5:65749284
|
A | G | 1 | a0001c0001t0011g0237 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.42-9283A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65749284 | ||||||
| chr5:65749375
|
G | C | 1 | a0005c0009t0045g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42-9192G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65749375 | ||||||
| chr5:65750152
|
G | C | 109 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(106): Show | 117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.42-8415G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750152 | ||||||
| chr5:65750175
|
G | A | 1 | a0001c0001t0002g0010 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.42-8392G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750175 | ||||||
| chr5:65750223
|
G | C | 2 | a0004c0006t0001g0008a0004c0006t0001g0096 | 3 | NA19030.hp1 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.42-8344G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750223 | ||||||
| chr5:65750259
|
T | A | 4 | a0001c0001t0002g0258a0002c0004t0044g0259a0002c0016t0035g0257others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-8308T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750259 | ||||||
| chr5:65750408
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0009g0160 | 2 | HG01975.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.42-8159G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750408 | ||||||
| chr5:65750445
|
A | G | 114 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(111): Show | 122 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.42-8122A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750445 | ||||||
| chr5:65750860
|
A | C | 2 | a0001c0001t0004g0281a0001c0001t0053g0300 | 2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.42-7707A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750860 | ||||||
| chr5:65750986
|
G | A | 169 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(166): Show | 180 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.42-7581G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750986 | ||||||
| chr5:65751025
|
A | C | 7 | a0001c0001t0002g0247a0001c0001t0015g0044a0001c0001t0015g0250others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-7542A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751025 | ||||||
| chr5:65751061
|
G | A | 6 | a0001c0001t0001g0143a0001c0001t0003g0140a0001c0001t0003g0141others(3): Show | 6 | HG01081.hp2 HG01255.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-7506G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751061 | ||||||
| chr5:65751124
|
CA | C | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-7440delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65751124 | |||||
| chr5:65751218
|
A | G | 2 | a0001c0001t0027g0278a0001c0001t0027g0295 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.42-7349A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751218 | ||||||
| chr5:65751299
|
A | G | 1 | a0001c0001t0006g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.42-7268A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751299 | ||||||
| chr5:65751418
|
A | G | 1 | a0001c0001t0005g0234 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.42-7149A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751418 | ||||||
| chr5:65751630
|
G | A | 49 | a0001c0001t0001g0028a0001c0001t0004g0266a0001c0001t0004g0271others(46): Show | 50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.42-6937G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751630 | ||||||
| chr5:65751722
|
C | T | 114 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(111): Show | 122 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.42-6845C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751722 | ||||||
| chr5:65751841
|
T | TATG | 3 | a0001c0001t0002g0258a0002c0004t0044g0259a0002c0016t0035g0257 | 3 | HG02257.hp1 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.42-6714_42-6712dup others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65751841 | |||||
| chr5:65751856
|
A | G | 9 | a0001c0001t0006g0089a0001c0001t0006g0091a0001c0001t0006g0095others(6): Show | 10 | HG01243.hp2 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.42-6711A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751856 | ||||||
| chr5:65751912
|
C | T | 109 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(106): Show | 117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.42-6655C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751912 | ||||||
| chr5:65751913
|
G | A | 1 | a0001c0002t0001g0161 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.42-6654G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751913 | ||||||
| chr5:65752010
|
T | C | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-6557T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752010 | ||||||
| chr5:65752115
|
A | G | 1 | a0001c0002t0004g0288 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.42-6452A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752115 | ||||||
| chr5:65752137
|
T | C | 118 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(115): Show | 128 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.42-6430T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752137 | ||||||
| chr5:65752237
|
CA | C | 109 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(106): Show | 117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.42-6317delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65752237 | |||||
| chr5:65752510
|
G | A | 1 | a0001c0001t0009g0062 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.42-6057G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752510 | ||||||
| chr5:65752554
|
T | G | 1 | a0001c0002t0001g0162 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.42-6013T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752554 | ||||||
| chr5:65752660
|
T | C | 49 | a0001c0001t0001g0028a0001c0001t0004g0266a0001c0001t0004g0271others(46): Show | 50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.42-5907T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752660 | ||||||
| chr5:65752706
|
C | T | 1 | a0001c0002t0001g0108 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.42-5861C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752706 | ||||||
| chr5:65752800
|
G | A | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-5767G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752800 | ||||||
| chr5:65752901
|
T | G | 4 | a0001c0002t0001g0003a0001c0002t0001g0191a0001c0002t0001g0207others(1): Show | 5 | HG00323.hp1 HG00621.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-5666T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752901 | ||||||
| chr5:65753052
|
C | T | 75 | a0001c0001t0001g0028a0001c0001t0001g0051a0001c0001t0001g0217others(72): Show | 76 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.42-5515C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753052 | ||||||
| chr5:65753107
|
A | G | 3 | a0001c0001t0051g0299a0002c0004t0018g0282a0002c0004t0018g0293 | 3 | HG01167.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.42-5460A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753107 | ||||||
| chr5:65753187
|
T | A | 1 | a0001c0002t0001g0163 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.42-5380T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753187 | ||||||
| chr5:65753200
|
G | T | 8 | a0002c0003t0007g0078a0002c0003t0042g0083a0002c0004t0016g0056others(5): Show | 8 | HG01884.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.42-5367G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753200 | ||||||
| chr5:65753207
|
A | G | 1 | a0002c0016t0035g0257 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.42-5360A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753207 | ||||||
| chr5:65753317
|
A | T | 109 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(106): Show | 117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.42-5250A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753317 | ||||||
| chr5:65753497
|
A | G | 26 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(23): Show | 26 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.42-5070A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753497 | ||||||
| chr5:65753539
|
C | A | 285 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(282): Show | 305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.42-5028C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753539 | ||||||
| chr5:65753564
|
C | T | 49 | a0001c0001t0001g0028a0001c0001t0004g0266a0001c0001t0004g0271others(46): Show | 50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.42-5003C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753564 | ||||||
| chr5:65753650
|
C | CA | 23 | a0001c0001t0001g0111a0001c0001t0001g0164a0001c0001t0002g0033others(20): Show | 25 | HG01074.hp2 HG01109.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.42-4902dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65753650 | |||||
| chr5:65753765
|
T | C | 1 | a0001c0002t0001g0199 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.42-4802T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753765 | ||||||
| chr5:65753837
|
C | G | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-4730C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753837 | ||||||
| chr5:65754204
|
C | T | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-4363C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754204 | ||||||
| chr5:65754225
|
T | C | 15 | a0001c0001t0005g0166a0001c0001t0005g0206a0001c0002t0001g0015others(12): Show | 16 | NA18941.hp2 NA18955.hp1 NA18961.hp1 others(13): Show |
intron_variant | MODIFIER | c.42-4342T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754225 | ||||||
| chr5:65754255
|
AG | A | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-4311delG | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754255 | ||||||
| chr5:65754307
|
C | G | 1 | a0001c0002t0001g0190 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.42-4260C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754307 | ||||||
| chr5:65754371
|
C | T | 8 | a0001c0001t0006g0089a0001c0001t0006g0091a0001c0001t0006g0095others(5): Show | 9 | HG01243.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.42-4196C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754371 | ||||||
| chr5:65754419
|
G | A | 127 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(124): Show | 137 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.42-4148G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754419 | ||||||
| chr5:65754564
|
A | G | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0196 | 3 | NA18953.hp1 NA19005.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.42-4003A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754564 | ||||||
| chr5:65754608
|
T | G | 1 | a0001c0001t0040g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.42-3959T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754608 | ||||||
| chr5:65754620
|
C | T | 1 | a0001c0001t0002g0252 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.42-3947C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754620 | ||||||
| chr5:65754639
|
C | T | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-3928C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754639 | ||||||
| chr5:65754680
|
C | A | 3 | a0001c0001t0004g0274a0001c0001t0004g0275a0001c0001t0004g0276 | 3 | NA18948.hp1 NA18980.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.42-3887C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754680 | ||||||
| chr5:65754718
|
A | G | 5 | a0001c0001t0017g0240a0001c0001t0017g0241a0001c0001t0017g0242others(2): Show | 5 | HG01256.hp1 HG01952.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-3849A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754718 | ||||||
| chr5:65754743
|
C | T | 56 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(53): Show | 63 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.42-3824C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754743 | ||||||
| chr5:65754808
|
A | C | 3 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0212 | 3 | NA18949.hp1 NA18992.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.42-3759A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754808 | ||||||
| chr5:65755065
|
C | T | 109 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(106): Show | 117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.42-3502C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65755065 | ||||||
| chr5:65755378
|
T | C | 1 | a0002c0003t0007g0230 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.42-3189T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65755378 | ||||||
| chr5:65755677
|
ATTAG | A | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-2885_42-2882del others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65755677 | |||||
| chr5:65755764
|
A | G | 1 | a0002c0004t0007g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.42-2803A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65755764 | ||||||
| chr5:65755829
|
G | A | 118 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(115): Show | 128 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.42-2738G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65755829 | ||||||
| chr5:65755928
|
T | G | 118 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(115): Show | 128 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.42-2639T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65755928 | ||||||
| chr5:65755977
|
G | A | 19 | a0001c0001t0001g0164a0001c0001t0001g0171a0001c0001t0005g0053others(16): Show | 24 | HG00609.hp2 HG01258.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.42-2590G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65755977 | ||||||
| chr5:65756030
|
A | G | 113 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(110): Show | 123 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.42-2537A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65756030 | ||||||
| chr5:65756188
|
A | G | 109 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(106): Show | 117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.42-2379A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65756188 | ||||||
| chr5:65756229
|
C | G | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-2338C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65756229 | ||||||
| chr5:65756390
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.42-2177A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65756390 | ||||||
| chr5:65756604
|
A | G | 2 | a0001c0001t0022g0084a0001c0001t0031g0054 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.42-1963A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65756604 | ||||||
| chr5:65757032
|
A | G | 3 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170 | 3 | NA18941.hp2 NA18955.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.42-1535A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757032 | ||||||
| chr5:65757390
|
G | A | 26 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0247others(23): Show | 27 | HG01243.hp2 HG01256.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.42-1177G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757390 | ||||||
| chr5:65757541
|
A | G | 1 | a0003c0005t0024g0055 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.42-1026A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757541 | ||||||
| chr5:65757573
|
G | T | 1 | a0001c0011t0005g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.42-994G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757573 | ||||||
| chr5:65757596
|
T | TTA | 49 | a0001c0001t0001g0028a0001c0001t0004g0266a0001c0001t0004g0271others(46): Show | 50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.42-963_42-962dupAT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65757596 | |||||
| chr5:65757662
|
G | C | 1 | a0001c0001t0032g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.42-905G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757662 | ||||||
| chr5:65757696
|
A | G | 2 | a0001c0001t0048g0265a0002c0004t0041g0311 | 2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.42-871A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757696 | ||||||
| chr5:65757918
|
G | C | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-649G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757918 | ||||||
| chr5:65757926
|
A | G | 49 | a0001c0001t0001g0028a0001c0001t0004g0266a0001c0001t0004g0271others(46): Show | 50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.42-641A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757926 | ||||||
| chr5:65758102
|
G | A | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-465G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65758102 | ||||||
| chr5:65758209
|
G | A | 2 | a0007c0012t0001g0093a0008c0010t0001g0092 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.42-358G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65758209 | ||||||
| chr5:65758247
|
G | A | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-320G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65758247 | ||||||
| chr5:65758298
|
A | T | 1 | a0001c0002t0001g0036 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.42-269A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65758298 | ||||||
| chr5:65758321
|
A | G | 56 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(53): Show | 63 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.42-246A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65758321 | ||||||
| chr5:65758424
|
A | G | 3 | a0001c0001t0004g0302a0001c0001t0028g0307a0001c0001t0028g0308 | 3 | NA18988.hp1 NA18991.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.42-143A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65758424 | ||||||
| chr5:65758556
|
A | G | 7 | a0001c0001t0002g0247a0001c0001t0015g0044a0001c0001t0015g0250others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-11A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65758556 | ||||||
| chr5:65758984
|
A | G | 139 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(136): Show | 150 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.301+158A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65758984 | ||||||
| chr5:65758997
|
A | G | 1 | a0001c0002t0001g0137 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.301+171A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65758997 | ||||||
| chr5:65759309
|
G | A | 1 | a0001c0001t0032g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.301+483G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65759309 | ||||||
| chr5:65759396
|
GTGTC | G | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+574_301+577del others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 65759396 | |||||
| chr5:65759400
|
CTG | C | 161 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(158): Show | 170 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.301+590_301+591del others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 65759400 | |||||
| chr5:65759491
|
T | C | 2 | a0001c0001t0027g0278a0001c0001t0027g0295 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.301+665T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65759491 | ||||||
| chr5:65759543
|
G | A | 1 | a0001c0001t0047g0248 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.301+717G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65759543 | ||||||
| chr5:65760270
|
C | A | 2 | a0001c0007t0019g0292a0001c0007t0019g0309 | 2 | HG00438.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.301+1444C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760270 | ||||||
| chr5:65760368
|
T | C | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1542T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760368 | ||||||
| chr5:65760371
|
A | T | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1545A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760371 | ||||||
| chr5:65760372
|
A | C | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1546A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760372 | ||||||
| chr5:65760373
|
G | C | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1547G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760373 | ||||||
| chr5:65760384
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1558A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760384 | ||||||
| chr5:65760385
|
G | T | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1559G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760385 | ||||||
| chr5:65760386
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1560A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760386 | ||||||
| chr5:65760390
|
A | T | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1564A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760390 | ||||||
| chr5:65760395
|
C | T | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1569C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760395 | ||||||
| chr5:65760397
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1571A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760397 | ||||||
| chr5:65760403
|
T | G | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1577T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760403 | ||||||
| chr5:65760404
|
A | T | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1578A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760404 | ||||||
| chr5:65760406
|
A | C | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1580A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760406 | ||||||
| chr5:65760407
|
G | T | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1581G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760407 | ||||||
| chr5:65760409
|
T | A | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1583T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760409 | ||||||
| chr5:65760410
|
T | C | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1584T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760410 | ||||||
| chr5:65760419
|
G | A | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1593G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760419 | ||||||
| chr5:65760420
|
G | T | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1594G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760420 | ||||||
| chr5:65760423
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1597A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760423 | ||||||
| chr5:65760428
|
A | C | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1602A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760428 | ||||||
| chr5:65760430
|
G | C | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1604G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760430 | ||||||
| chr5:65760432
|
G | T | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1606G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760432 | ||||||
| chr5:65760434
|
G | C | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1608G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760434 | ||||||
| chr5:65760440
|
C | T | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1614C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760440 | ||||||
| chr5:65760441
|
A | C | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1615A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760441 | ||||||
| chr5:65760443
|
C | A | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1617C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760443 | ||||||
| chr5:65760446
|
G | T | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1620G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760446 | ||||||
| chr5:65760447
|
G | A | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1621G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760447 | ||||||
| chr5:65760454
|
T | G | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1628T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760454 | ||||||
| chr5:65760455
|
T | A | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1629T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760455 | ||||||
| chr5:65760814
|
A | G | 6 | a0001c0001t0002g0258a0001c0001t0004g0281a0001c0001t0005g0047others(3): Show | 6 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+1988A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760814 | ||||||
| chr5:65761291
|
A | T | 1 | a0001c0001t0002g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.302-1669A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65761291 | ||||||
| chr5:65761448
|
G | A | 165 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(162): Show | 176 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.302-1512G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65761448 | ||||||
| chr5:65761536
|
C | T | 2 | a0001c0001t0005g0262a0001c0001t0020g0018 | 3 | HG01109.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.302-1424C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65761536 | ||||||
| chr5:65761816
|
A | G | 92 | a0001c0001t0001g0038a0001c0001t0001g0143a0001c0001t0001g0156others(89): Show | 100 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.302-1144A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65761816 | ||||||
| chr5:65761841
|
G | A | 56 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(53): Show | 63 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.302-1119G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65761841 | ||||||
| chr5:65762000
|
C | T | 1 | a0001c0001t0005g0201 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.302-960C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65762000 | ||||||
| chr5:65762108
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.302-852T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65762108 | ||||||
| chr5:65762532
|
A | G | 1 | a0001c0001t0037g0025 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.302-428A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65762532 | ||||||
| chr5:65762623
|
AG | A | 8 | a0001c0001t0006g0089a0001c0001t0006g0091a0001c0001t0006g0095others(5): Show | 9 | HG01243.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-336delG | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65762623 | ||||||
| chr5:65762702
|
C | CA | 108 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(105): Show | 116 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.302-244dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 65762702 | |||||
| chr5:65763153
|
A | G | 1 | a0001c0001t0002g0136 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.450+45A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763153 | ||||||
| chr5:65763272
|
G | A | 1 | a0001c0001t0032g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.450+164G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763272 | ||||||
| chr5:65763282
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.450+174T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763282 | ||||||
| chr5:65763385
|
A | G | 1 | a0001c0002t0004g0288 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.450+277A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763385 | ||||||
| chr5:65763706
|
T | G | 2 | a0002c0004t0016g0056a0002c0004t0016g0058 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.450+598T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763706 | ||||||
| chr5:65763744
|
TA | T | 165 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(162): Show | 176 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.450+637delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763744 | ||||||
| chr5:65763746
|
C | T | 165 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(162): Show | 176 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.450+638C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763746 | ||||||
| chr5:65763767
|
G | A | 3 | a0001c0001t0004g0294a0001c0001t0004g0296a0001c0001t0056g0260 | 3 | HG03688.hp1 NA18973.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.450+659G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763767 | ||||||
| chr5:65763827
|
T | C | 1 | a0001c0001t0032g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.450+719T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763827 | ||||||
| chr5:65764026
|
T | G | 2 | a0007c0012t0001g0093a0008c0010t0001g0092 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.450+918T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65764026 | ||||||
| chr5:65764118
|
A | G | 1 | a0001c0002t0012g0101 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.450+1010A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65764118 | ||||||
| chr5:65764259
|
C | CA | 12 | a0001c0001t0006g0027a0001c0001t0032g0255a0003c0005t0023g0081others(9): Show | 13 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.450+1153dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65764259 | |||||
| chr5:65764285
|
C | G | 165 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(162): Show | 176 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.450+1177C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65764285 | ||||||
| chr5:65764644
|
C | T | 6 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0130others(3): Show | 6 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+1536C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65764644 | ||||||
| chr5:65764685
|
G | A | 1 | a0001c0001t0003g0065 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.450+1577G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65764685 | ||||||
| chr5:65764913
|
T | A | 2 | a0001c0001t0048g0265a0002c0004t0041g0311 | 2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.450+1805T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65764913 | ||||||
| chr5:65765074
|
G | C | 6 | a0001c0001t0001g0038a0001c0001t0001g0203a0001c0001t0014g0174others(3): Show | 6 | HG02056.hp1 NA18983.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+1966G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765074 | ||||||
| chr5:65765274
|
T | A | 1 | a0001c0001t0002g0013 | 2 | NA18999.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.450+2166T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765274 | ||||||
| chr5:65765349
|
C | T | 4 | a0001c0001t0002g0012a0001c0001t0002g0123a0001c0001t0002g0124others(1): Show | 5 | HG01496.hp1 HG01928.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+2241C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765349 | ||||||
| chr5:65765454
|
G | A | 165 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(162): Show | 176 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.450+2346G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765454 | ||||||
| chr5:65765458
|
C | T | 1 | a0001c0001t0048g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.450+2350C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765458 | ||||||
| chr5:65765506
|
A | G | 1 | a0003c0005t0023g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.450+2398A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765506 | ||||||
| chr5:65765578
|
A | G | 165 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(162): Show | 176 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.450+2470A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765578 | ||||||
| chr5:65765631
|
C | T | 165 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(162): Show | 176 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.450+2523C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765631 | ||||||
| chr5:65765678
|
C | G | 6 | a0001c0001t0009g0023a0001c0001t0009g0026a0001c0001t0009g0062others(3): Show | 6 | HG01070.hp2 HG01169.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+2570C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765678 | ||||||
| chr5:65765706
|
C | T | 1 | a0001c0002t0001g0190 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.450+2598C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765706 | ||||||
| chr5:65765966
|
C | T | 2 | a0007c0012t0001g0093a0008c0010t0001g0092 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.450+2858C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765966 | ||||||
| chr5:65766004
|
A | G | 165 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(162): Show | 176 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.450+2896A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65766004 | ||||||
| chr5:65766041
|
G | A | 26 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(23): Show | 26 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+2933G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65766041 | ||||||
| chr5:65766088
|
G | A | 165 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(162): Show | 176 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.450+2980G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65766088 | ||||||
| chr5:65766513
|
G | A | 56 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(53): Show | 63 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.450+3405G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65766513 | ||||||
| chr5:65766801
|
T | C | 1 | a0001c0001t0004g0294 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.450+3693T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65766801 | ||||||
| chr5:65767015
|
G | T | 48 | a0001c0001t0001g0028a0001c0001t0004g0266a0001c0001t0004g0271others(45): Show | 49 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.450+3907G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65767015 | ||||||
| chr5:65767349
|
G | T | 1 | a0005c0009t0045g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.450+4241G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65767349 | ||||||
| chr5:65767362
|
G | A | 4 | a0001c0001t0001g0164a0001c0002t0013g0016a0001c0002t0013g0172others(1): Show | 5 | HG00609.hp2 HG02027.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+4254G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65767362 | ||||||
| chr5:65767508
|
G | C | 9 | a0001c0001t0006g0089a0001c0001t0006g0091a0001c0001t0006g0095others(6): Show | 10 | HG01243.hp2 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.450+4400G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65767508 | ||||||
| chr5:65767641
|
T | G | 2 | a0002c0004t0016g0056a0002c0004t0016g0058 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.450+4533T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65767641 | ||||||
| chr5:65767898
|
G | C | 1 | a0001c0001t0002g0157 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.450+4790G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65767898 | ||||||
| chr5:65768035
|
A | G | 165 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(162): Show | 176 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.450+4927A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768035 | ||||||
| chr5:65768196
|
C | A | 112 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(109): Show | 122 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.450+5088C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768196 | ||||||
| chr5:65768277
|
G | A | 26 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(23): Show | 26 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+5169G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768277 | ||||||
| chr5:65768412
|
C | G | 26 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(23): Show | 26 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+5304C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768412 | ||||||
| chr5:65768462
|
C | A | 2 | a0002c0004t0016g0082a0003c0005t0022g0079 | 2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.450+5354C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768462 | ||||||
| chr5:65768757
|
C | T | 1 | a0001c0001t0007g0057 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.450+5649C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768757 | ||||||
| chr5:65768784
|
C | T | 2 | a0001c0001t0033g0221a0001c0001t0034g0219 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.450+5676C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768784 | ||||||
| chr5:65768914
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.450+5806C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768914 | ||||||
| chr5:65769118
|
T | G | 2 | a0002c0004t0018g0282a0002c0004t0018g0293 | 2 | HG01167.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.450+6010T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769118 | ||||||
| chr5:65769201
|
A | G | 165 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(162): Show | 176 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.450+6093A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769201 | ||||||
| chr5:65769332
|
C | G | 6 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0118others(3): Show | 6 | HG00323.hp2 HG02257.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+6224C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769332 | ||||||
| chr5:65769404
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.450+6296G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769404 | ||||||
| chr5:65769547
|
T | A | 1 | a0001c0001t0004g0281 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.450+6439T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769547 | ||||||
| chr5:65769582
|
T | C | 165 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(162): Show | 176 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.450+6474T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769582 | ||||||
| chr5:65769624
|
G | A | 165 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(162): Show | 176 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.450+6516G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769624 | ||||||
| chr5:65769666
|
A | T | 113 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(110): Show | 123 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.450+6558A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769666 | ||||||
| chr5:65769724
|
A | G | 190 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(187): Show | 202 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.450+6616A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769724 | ||||||
| chr5:65769725
|
T | G | 9 | a0001c0001t0006g0089a0001c0001t0006g0091a0001c0001t0006g0095others(6): Show | 10 | HG01243.hp2 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.450+6617T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769725 | ||||||
| chr5:65769907
|
C | T | 1 | a0001c0001t0003g0072 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.450+6799C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769907 | ||||||
| chr5:65770163
|
C | T | 2 | a0001c0001t0048g0265a0002c0004t0041g0311 | 2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.450+7055C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770163 | ||||||
| chr5:65770278
|
A | T | 1 | a0001c0001t0003g0065 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.451-7149A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770278 | ||||||
| chr5:65770498
|
A | G | 109 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(106): Show | 117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-6929A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770498 | ||||||
| chr5:65770519
|
G | T | 1 | a0001c0002t0001g0191 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.451-6908G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770519 | ||||||
| chr5:65770656
|
C | T | 3 | a0001c0001t0002g0187a0001c0002t0001g0153a0001c0002t0001g0199 | 3 | HG01981.hp2 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.451-6771C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770656 | ||||||
| chr5:65770659
|
C | T | 1 | a0001c0001t0053g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451-6768C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770659 | ||||||
| chr5:65770680
|
A | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0130 | 3 | HG00323.hp2 HG02257.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.451-6747A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770680 | ||||||
| chr5:65770764
|
T | A | 7 | a0001c0001t0002g0247a0001c0001t0015g0044a0001c0001t0015g0250others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.451-6663T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770764 | ||||||
| chr5:65770915
|
G | A | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-6512G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770915 | ||||||
| chr5:65771046
|
C | G | 2 | a0001c0001t0001g0104a0001c0001t0029g0105 | 2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.451-6381C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65771046 | ||||||
| chr5:65771214
|
A | G | 92 | a0001c0001t0001g0038a0001c0001t0001g0143a0001c0001t0001g0156others(89): Show | 100 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.451-6213A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65771214 | ||||||
| chr5:65771376
|
G | A | 1 | a0001c0001t0017g0240 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.451-6051G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65771376 | ||||||
| chr5:65771683
|
C | T | 9 | a0001c0001t0006g0089a0001c0001t0006g0091a0001c0001t0006g0095others(6): Show | 10 | HG01243.hp2 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.451-5744C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65771683 | ||||||
| chr5:65771923
|
A | T | 109 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(106): Show | 117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-5504A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65771923 | ||||||
| chr5:65771963
|
C | CA | 39 | a0001c0001t0001g0217a0001c0001t0001g0227a0001c0001t0002g0223others(36): Show | 39 | HG00741.hp2 HG01070.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.451-5450dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65771963 | |||||
| chr5:65771963
|
C | CAA | 20 | a0001c0001t0001g0051a0001c0001t0002g0239a0001c0001t0005g0262others(17): Show | 23 | HG01109.hp1 HG01243.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.451-5451_451-5450d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65771963 | |||||
| chr5:65771963
|
C | CAAA | 16 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0118others(13): Show | 18 | HG00323.hp2 HG01081.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-5452_451-5450d others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65771963 | |||||
| chr5:65771963
|
C | CAAAA | 88 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(85): Show | 93 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.451-5453_451-5450d others(6): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65771963 | |||||
| chr5:65771963
|
C | CAAAAA | 9 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0004g0275others(6): Show | 10 | HG00733.hp1 HG00735.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.451-5454_451-5450d others(7): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65771963 | |||||
| chr5:65772094
|
T | G | 2 | a0001c0001t0002g0013a0001c0001t0002g0127 | 3 | NA18999.hp2 NA19009.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.451-5333T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65772094 | ||||||
| chr5:65772220
|
A | C | 171 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(168): Show | 182 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.451-5207A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65772220 | ||||||
| chr5:65772451
|
G | A | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-4976G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65772451 | ||||||
| chr5:65772451
|
G | C | 2 | a0001c0001t0048g0265a0002c0004t0041g0311 | 2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.451-4976G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65772451 | ||||||
| chr5:65772879
|
C | T | 109 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(106): Show | 117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-4548C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65772879 | ||||||
| chr5:65772891
|
C | T | 1 | a0001c0002t0001g0186 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.451-4536C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65772891 | ||||||
| chr5:65772898
|
A | G | 1 | a0001c0001t0005g0233 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.451-4529A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65772898 | ||||||
| chr5:65772953
|
GT | G | 162 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(159): Show | 173 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.451-4460delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65772953 | |||||
| chr5:65773127
|
A | AT | 169 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(166): Show | 180 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.451-4280dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65773127 | |||||
| chr5:65773255
|
C | A | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-4172C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65773255 | ||||||
| chr5:65773592
|
GAAGAAA | G | 8 | a0002c0003t0007g0078a0002c0003t0042g0083a0002c0004t0016g0056others(5): Show | 8 | HG01884.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-3830_451-3825d others(8): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65773592 | |||||
| chr5:65773616
|
C | T | 1 | a0001c0001t0002g0232 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.451-3811C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65773616 | ||||||
| chr5:65773797
|
G | A | 1 | a0001c0001t0032g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.451-3630G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65773797 | ||||||
| chr5:65774043
|
A | C | 167 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(164): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.451-3384A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774043 | ||||||
| chr5:65774055
|
G | GT | 55 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(52): Show | 62 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.451-3356dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65774055 | |||||
| chr5:65774055
|
G | GTT | 78 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0001t0001g0119others(75): Show | 82 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.451-3357_451-3356d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65774055 | |||||
| chr5:65774055
|
G | GTTT | 37 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(34): Show | 37 | HG00741.hp2 HG01256.hp1 HG01516.hp2 others(34): Show |
intron_variant | MODIFIER | c.451-3358_451-3356d others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65774055 | |||||
| chr5:65774147
|
G | GT | 4 | a0001c0001t0002g0012a0001c0001t0002g0123a0001c0001t0002g0124others(1): Show | 5 | HG01496.hp1 HG01928.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-3279dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65774147 | |||||
| chr5:65774468
|
T | C | 1 | a0002c0003t0049g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.451-2959T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774468 | ||||||
| chr5:65774573
|
C | G | 111 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(108): Show | 119 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.451-2854C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774573 | ||||||
| chr5:65774580
|
A | G | 167 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(164): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.451-2847A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774580 | ||||||
| chr5:65774647
|
T | C | 1 | a0001c0001t0014g0194 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.451-2780T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774647 | ||||||
| chr5:65774715
|
T | TTA | 7 | a0001c0001t0001g0104a0001c0001t0002g0157a0001c0001t0029g0105others(4): Show | 7 | HG01261.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.451-2698_451-2697d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65774715 | |||||
| chr5:65774729
|
AT | A | 14 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0005g0052others(11): Show | 14 | HG01256.hp1 HG01891.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.451-2683delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65774729 | |||||
| chr5:65774729
|
ATT | A | 11 | a0001c0001t0005g0262a0001c0001t0006g0089a0001c0001t0006g0091others(8): Show | 13 | HG01109.hp1 HG01243.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.451-2684_451-2683d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65774729 | |||||
| chr5:65774730
|
T | TA | 66 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(63): Show | 72 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.451-2697_451-2696i others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774730 | ||||||
| chr5:65774730
|
T | TATA | 41 | a0001c0001t0001g0028a0001c0001t0001g0156a0001c0001t0001g0193others(38): Show | 44 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.451-2697_451-2696i others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774730 | ||||||
| chr5:65774730
|
T | TATATA | 11 | a0001c0001t0052g0284a0002c0003t0010g0261a0002c0003t0010g0268others(8): Show | 11 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.451-2697_451-2696i others(7): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774730 | ||||||
| chr5:65774731
|
T | A | 167 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0104others(164): Show | 177 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(174): Show |
intron_variant | MODIFIER | c.451-2696T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774731 | ||||||
| chr5:65774732
|
T | A | 125 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(122): Show | 134 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.451-2695T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774732 | ||||||
| chr5:65774733
|
T | A | 131 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0143others(128): Show | 138 | HG00438.hp2 HG00609.hp2 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.451-2694T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774733 | ||||||
| chr5:65774734
|
T | A | 71 | a0001c0001t0001g0028a0001c0001t0001g0156a0001c0001t0001g0193others(68): Show | 75 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.451-2693T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774734 | ||||||
| chr5:65774735
|
T | A | 6 | a0001c0001t0002g0247a0001c0001t0002g0258a0001c0002t0001g0215others(3): Show | 6 | HG00738.hp2 HG02258.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-2692T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774735 | ||||||
| chr5:65774736
|
T | A | 6 | a0001c0001t0004g0271a0001c0001t0004g0272a0001c0001t0004g0291others(3): Show | 6 | HG01106.hp1 HG01167.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-2691T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774736 | ||||||
| chr5:65774761
|
G | A | 115 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(112): Show | 125 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.451-2666G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774761 | ||||||
| chr5:65774782
|
T | C | 90 | a0001c0001t0001g0038a0001c0001t0001g0143a0001c0001t0001g0164others(87): Show | 98 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.451-2645T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774782 | ||||||
| chr5:65774945
|
G | A | 2 | a0001c0001t0027g0278a0001c0001t0027g0295 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.451-2482G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774945 | ||||||
| chr5:65774968
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.451-2459G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774968 | ||||||
| chr5:65774976
|
C | T | 1 | a0001c0001t0002g0116 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.451-2451C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774976 | ||||||
| chr5:65774977
|
G | A | 1 | a0001c0001t0002g0226 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.451-2450G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774977 | ||||||
| chr5:65775017
|
C | G | 2 | a0001c0001t0004g0277a0001c0001t0004g0297 | 2 | HG00733.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.451-2410C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775017 | ||||||
| chr5:65775167
|
A | G | 2 | a0001c0001t0002g0074a0001c0001t0002g0075 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.451-2260A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775167 | ||||||
| chr5:65775291
|
G | A | 1 | a0001c0001t0005g0211 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.451-2136G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775291 | ||||||
| chr5:65775306
|
T | G | 1 | a0003c0005t0023g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.451-2121T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775306 | ||||||
| chr5:65775355
|
G | A | 167 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(164): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.451-2072G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775355 | ||||||
| chr5:65775446
|
C | T | 3 | a0001c0002t0001g0011a0001c0002t0001g0110a0001c0002t0001g0122 | 4 | HG00733.hp1 HG00735.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-1981C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775446 | ||||||
| chr5:65775447
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.451-1980G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775447 | ||||||
| chr5:65775467
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0029g0105 | 2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.451-1960A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775467 | ||||||
| chr5:65775556
|
T | C | 6 | a0001c0001t0009g0023a0001c0001t0009g0026a0001c0001t0009g0062others(3): Show | 6 | HG01070.hp2 HG01169.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-1871T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775556 | ||||||
| chr5:65775870
|
A | G | 167 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(164): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.451-1557A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775870 | ||||||
| chr5:65776005
|
C | A | 1 | a0001c0002t0001g0190 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.451-1422C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65776005 | ||||||
| chr5:65776127
|
C | G | 1 | a0001c0001t0017g0240 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.451-1300C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65776127 | ||||||
| chr5:65776479
|
C | T | 90 | a0001c0001t0001g0038a0001c0001t0001g0143a0001c0001t0001g0164others(87): Show | 98 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.451-948C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65776479 | ||||||
| chr5:65776798
|
C | T | 1 | a0001c0001t0043g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.451-629C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65776798 | ||||||
| chr5:65777036
|
C | T | 167 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(164): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.451-391C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65777036 | ||||||
| chr5:65777079
|
G | A | 167 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(164): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.451-348G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65777079 | ||||||
| chr5:65777330
|
C | T | 8 | a0001c0001t0002g0247a0001c0001t0015g0044a0001c0001t0015g0250others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.451-97C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65777330 | ||||||
| chr5:65777397
|
C | A | 284 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(281): Show | 304 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.451-30C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65777397 | ||||||
| chr5:65777562
|
G | GA | 9 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0017g0240others(6): Show | 9 | HG01256.hp1 HG01891.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.558+38dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 65777562 | |||||
| chr5:65777722
|
G | A | 1 | a0001c0002t0001g0162 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.558+188G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65777722 | ||||||
| chr5:65777890
|
G | T | 167 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(164): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.558+356G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65777890 | ||||||
| chr5:65777915
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.558+381A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65777915 | ||||||
| chr5:65777923
|
G | A | 51 | a0001c0001t0001g0028a0001c0001t0001g0156a0001c0001t0001g0193others(48): Show | 52 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.558+389G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65777923 | ||||||
| chr5:65778310
|
A | G | 2 | a0002c0003t0010g0261a0002c0003t0010g0270 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.558+776A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778310 | ||||||
| chr5:65778331
|
G | T | 1 | a0002c0004t0007g0245 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.558+797G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778331 | ||||||
| chr5:65778334
|
C | G | 3 | a0004c0006t0008g0224a0006c0008t0006g0090a0006c0008t0006g0103 | 3 | HG02976.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.558+800C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778334 | ||||||
| chr5:65778656
|
G | A | 2 | a0004c0006t0001g0008a0004c0006t0001g0096 | 3 | NA19030.hp1 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.558+1122G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778656 | ||||||
| chr5:65778703
|
G | A | 167 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(164): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.558+1169G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778703 | ||||||
| chr5:65778865
|
T | G | 1 | a0001c0001t0002g0099 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.559-1314T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778865 | ||||||
| chr5:65778890
|
G | A | 1 | a0001c0001t0032g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.559-1289G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778890 | ||||||
| chr5:65778891
|
T | C | 167 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(164): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.559-1288T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778891 | ||||||
| chr5:65778934
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.559-1245G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778934 | ||||||
| chr5:65779009
|
G | T | 1 | a0001c0001t0004g0301 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.559-1170G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779009 | ||||||
| chr5:65779113
|
G | A | 1 | a0001c0001t0005g0231 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.559-1066G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779113 | ||||||
| chr5:65779117
|
G | A | 52 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(49): Show | 53 | HG00741.hp2 HG01243.hp2 HG01256.hp1 others(50): Show |
intron_variant | MODIFIER | c.559-1062G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779117 | ||||||
| chr5:65779210
|
C | T | 284 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(281): Show | 304 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.559-969C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779210 | ||||||
| chr5:65779427
|
C | T | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.559-752C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779427 | ||||||
| chr5:65779487
|
C | A | 1 | a0001c0001t0004g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.559-692C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779487 | ||||||
| chr5:65779496
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.559-683C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779496 | ||||||
| chr5:65779704
|
A | G | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.559-475A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779704 | ||||||
| chr5:65779835
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.559-344G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779835 | ||||||
| chr5:65779869
|
T | G | 1 | a0001c0001t0006g0050 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.559-310T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779869 | ||||||
| chr5:65779887
|
T | TA | 26 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(23): Show | 26 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.559-291dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 65779887 | |||||
| chr5:65780022
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0193 | 2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.559-157C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65780022 | ||||||
| chr5:65780031
|
A | G | 167 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(164): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.559-148A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65780031 | ||||||
| chr5:65780038
|
C | A | 2 | a0001c0001t0048g0265a0002c0004t0041g0311 | 2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.559-141C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65780038 | ||||||
| chr5:65780115
|
C | A | 13 | a0001c0001t0006g0027a0001c0001t0032g0255a0001c0011t0005g0020others(10): Show | 14 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.559-64C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65780115 | ||||||
| chr5:65780133
|
A | C | 3 | a0004c0006t0008g0224a0006c0008t0006g0090a0006c0008t0006g0103 | 3 | HG02976.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.559-46A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65780133 | ||||||
| chr5:65780311
|
C | A | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+30C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 5/12 | chr5 | 65780311 | ||||||
| chr5:65780329
|
A | C | 1 | a0005c0009t0045g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.661+48A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 5/12 | chr5 | 65780329 | ||||||
| chr5:65780444
|
A | G | 2 | a0007c0012t0001g0093a0008c0010t0001g0092 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.661+163A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 5/12 | chr5 | 65780444 | ||||||
| chr5:65780643
|
C | G | 1 | a0002c0004t0016g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.661+362C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 5/12 | chr5 | 65780643 | ||||||
| chr5:65780735
|
G | A | 1 | a0001c0001t0004g0277 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.661+454G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 5/12 | chr5 | 65780735 | ||||||
| chr5:65780791
|
A | T | 1 | a0001c0001t0005g0235 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.662-470A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 5/12 | chr5 | 65780791 | ||||||
| chr5:65780831
|
G | A | 9 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0017g0240others(6): Show | 9 | HG01256.hp1 HG01891.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.662-430G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 5/12 | chr5 | 65780831 | ||||||
| chr5:65781705
|
G | A | 1 | a0002c0004t0007g0249 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.822+284G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65781705 | ||||||
| chr5:65781909
|
G | C | 20 | a0001c0001t0001g0104a0001c0001t0002g0085a0001c0001t0002g0086others(17): Show | 21 | HG01243.hp2 HG01256.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.822+488G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65781909 | ||||||
| chr5:65782018
|
C | T | 1 | a0002c0004t0007g0249 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.822+597C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782018 | ||||||
| chr5:65782045
|
G | T | 1 | a0001c0001t0002g0123 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.822+624G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782045 | ||||||
| chr5:65782083
|
T | G | 52 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(49): Show | 53 | HG00741.hp2 HG01074.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.822+662T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782083 | ||||||
| chr5:65782198
|
T | A | 135 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(132): Show | 144 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.822+777T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782198 | ||||||
| chr5:65782358
|
T | C | 7 | a0001c0001t0002g0247a0001c0001t0015g0044a0001c0001t0015g0250others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+937T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782358 | ||||||
| chr5:65782417
|
A | G | 1 | a0002c0004t0007g0245 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.822+996A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782417 | ||||||
| chr5:65782504
|
T | G | 1 | a0001c0001t0002g0099 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.822+1083T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782504 | ||||||
| chr5:65782808
|
A | G | 1 | a0002c0004t0007g0249 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.822+1387A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782808 | ||||||
| chr5:65783008
|
C | G | 2 | a0001c0001t0003g0065a0001c0001t0003g0068 | 2 | NA18974.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.822+1587C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783008 | ||||||
| chr5:65783219
|
T | C | 2 | a0001c0001t0004g0280a0001c0001t0004g0298 | 2 | HG01081.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.822+1798T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783219 | ||||||
| chr5:65783292
|
C | T | 26 | a0001c0001t0002g0258a0001c0001t0004g0281a0001c0001t0006g0027others(23): Show | 27 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.822+1871C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783292 | ||||||
| chr5:65783506
|
G | T | 1 | a0001c0001t0026g0019 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.822+2085G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783506 | ||||||
| chr5:65783533
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0029g0105 | 2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.822+2112G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783533 | ||||||
| chr5:65783538
|
G | A | 2 | a0001c0001t0005g0053a0001c0001t0005g0211 | 2 | NA19063.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.822+2117G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783538 | ||||||
| chr5:65783584
|
G | A | 52 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(49): Show | 53 | HG00741.hp2 HG01243.hp1 HG01516.hp2 others(50): Show |
intron_variant | MODIFIER | c.822+2163G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783584 | ||||||
| chr5:65783651
|
G | A | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-2124G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783651 | ||||||
| chr5:65783703
|
T | TA | 144 | a0001c0001t0001g0038a0001c0001t0001g0164a0001c0001t0001g0171others(141): Show | 155 | HG00323.hp1 HG00438.hp2 HG00609.hp1 others(152): Show |
intron_variant | MODIFIER | c.823-2056dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 65783703 | |||||
| chr5:65783784
|
G | T | 1 | a0005c0009t0045g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.823-1991G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783784 | ||||||
| chr5:65784017
|
T | G | 203 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0143others(200): Show | 217 | HG00323.hp1 HG00438.hp2 HG00609.hp1 others(214): Show |
intron_variant | MODIFIER | c.823-1758T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784017 | ||||||
| chr5:65784264
|
C | T | 257 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0051others(254): Show | 272 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(269): Show |
intron_variant | MODIFIER | c.823-1511C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784264 | ||||||
| chr5:65784273
|
TAATAA | T | 146 | a0001c0001t0001g0038a0001c0001t0001g0143a0001c0001t0001g0164others(143): Show | 157 | HG00323.hp1 HG00438.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.823-1496_823-1492d others(7): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 65784273 | |||||
| chr5:65784322
|
A | C | 9 | a0001c0001t0006g0089a0001c0001t0006g0091a0001c0001t0006g0095others(6): Show | 10 | HG01243.hp2 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.823-1453A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784322 | ||||||
| chr5:65784369
|
A | G | 1 | a0002c0003t0010g0287 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.823-1406A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784369 | ||||||
| chr5:65784594
|
A | G | 1 | a0001c0002t0012g0101 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.823-1181A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784594 | ||||||
| chr5:65784657
|
G | T | 3 | a0004c0006t0008g0224a0006c0008t0006g0090a0006c0008t0006g0103 | 3 | HG02976.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.823-1118G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784657 | ||||||
| chr5:65784707
|
G | T | 21 | a0001c0001t0006g0027a0001c0001t0032g0255a0001c0011t0005g0020others(18): Show | 22 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.823-1068G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784707 | ||||||
| chr5:65784753
|
G | A | 91 | a0001c0001t0001g0038a0001c0001t0001g0143a0001c0001t0001g0164others(88): Show | 99 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.823-1022G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784753 | ||||||
| chr5:65784982
|
T | C | 1 | a0001c0001t0037g0025 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.823-793T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784982 | ||||||
| chr5:65785038
|
T | C | 9 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0017g0240others(6): Show | 9 | HG01256.hp1 HG01891.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.823-737T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65785038 | ||||||
| chr5:65785169
|
A | G | 121 | a0001c0001t0001g0038a0001c0001t0001g0143a0001c0001t0001g0164others(118): Show | 131 | HG00323.hp1 HG00438.hp2 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.823-606A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65785169 | ||||||
| chr5:65785219
|
A | G | 1 | a0001c0002t0001g0158 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.823-556A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65785219 | ||||||
| chr5:65785242
|
C | T | 5 | a0001c0001t0002g0258a0001c0001t0004g0281a0002c0004t0044g0259others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-533C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65785242 | ||||||
| chr5:65785339
|
A | T | 26 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(23): Show | 26 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.823-436A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65785339 | ||||||
| chr5:65785389
|
G | A | 1 | a0001c0001t0005g0262 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.823-386G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65785389 | ||||||
| chr5:65785605
|
CA | C | 32 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(29): Show | 32 | HG00741.hp2 HG01243.hp1 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.823-154delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 65785605 | |||||
| chr5:65785605
|
CAA | C | 25 | a0001c0001t0005g0262a0001c0001t0006g0027a0001c0001t0006g0263others(22): Show | 28 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.823-155_823-154del others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 65785605 | |||||
| chr5:65785623
|
C | T | 1 | a0001c0002t0012g0102 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.823-152C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65785623 | ||||||
| chr5:65786046
|
G | A | 1 | a0001c0001t0004g0302 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.958+136G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65786046 | ||||||
| chr5:65786050
|
T | A | 55 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0001t0001g0156others(52): Show | 56 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.958+140T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65786050 | ||||||
| chr5:65786278
|
C | T | 52 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(49): Show | 53 | HG00741.hp2 HG01243.hp1 HG01516.hp2 others(50): Show |
intron_variant | MODIFIER | c.958+368C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65786278 | ||||||
| chr5:65786617
|
G | T | 1 | a0001c0001t0002g0128 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.958+707G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65786617 | ||||||
| chr5:65786753
|
T | C | 3 | a0001c0007t0019g0290a0001c0007t0019g0292a0001c0007t0019g0309 | 3 | HG00438.hp1 NA18962.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.958+843T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65786753 | ||||||
| chr5:65786974
|
G | A | 1 | a0001c0001t0007g0176 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.958+1064G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65786974 | ||||||
| chr5:65787023
|
T | G | 21 | a0001c0001t0006g0027a0001c0001t0032g0255a0001c0011t0005g0020others(18): Show | 22 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.959-1095T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787023 | ||||||
| chr5:65787030
|
G | A | 2 | a0001c0001t0004g0303a0001c0001t0055g0304 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.959-1088G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787030 | ||||||
| chr5:65787115
|
T | C | 26 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0227others(23): Show | 26 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.959-1003T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787115 | ||||||
| chr5:65787156
|
G | A | 4 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018others(1): Show | 6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.959-962G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787156 | ||||||
| chr5:65787173
|
A | T | 49 | a0001c0001t0001g0028a0001c0001t0001g0156a0001c0001t0001g0193others(46): Show | 50 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.959-945A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787173 | ||||||
| chr5:65787252
|
G | A | 3 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018 | 4 | HG01109.hp1 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.959-866G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787252 | ||||||
| chr5:65787254
|
A | ATG | 63 | a0001c0001t0001g0051a0001c0001t0001g0104a0001c0001t0001g0217others(60): Show | 67 | HG00741.hp2 HG01243.hp2 HG01516.hp2 others(64): Show |
intron_variant | MODIFIER | c.959-844_959-843dup others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 65787254 | |||||
| chr5:65787254
|
A | G | 3 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018 | 4 | HG01109.hp1 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.959-864A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787254 | ||||||
| chr5:65787254
|
ATG | A | 2 | a0001c0002t0001g0163a0003c0005t0021g0017 | 3 | HG02896.hp2 HG02897.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.959-844_959-843del others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 65787254 | |||||
| chr5:65787256
|
G | A | 3 | a0001c0001t0005g0262a0001c0001t0006g0263a0001c0001t0020g0018 | 4 | HG01109.hp1 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.959-862G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787256 | ||||||
| chr5:65787288
|
GCA | G | 3 | a0001c0001t0015g0044a0001c0001t0015g0250a0001c0001t0015g0251 | 3 | HG02109.hp2 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.959-823_959-822del others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 65787288 | |||||
| chr5:65787308
|
G | A | 20 | a0001c0001t0006g0027a0001c0011t0005g0020a0002c0003t0007g0078others(17): Show | 21 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.959-810G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787308 | ||||||
| chr5:65787321
|
T | C | 110 | a0001c0001t0001g0028a0001c0001t0001g0051a0001c0001t0001g0104others(107): Show | 115 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.959-797T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787321 | ||||||
| chr5:65787332
|
A | G | 1 | a0001c0002t0001g0035 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.959-786A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787332 | ||||||
| chr5:65787382
|
C | T | 7 | a0001c0001t0001g0106a0001c0001t0009g0023a0001c0001t0009g0026others(4): Show | 7 | HG00323.hp2 HG01070.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.959-736C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787382 | ||||||
| chr5:65787435
|
A | G | 1 | a0001c0013t0039g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.959-683A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787435 | ||||||
| chr5:65787515
|
A | G | 1 | a0001c0001t0003g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.959-603A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787515 | ||||||
| chr5:65787869
|
G | C | 9 | a0001c0001t0006g0089a0001c0001t0006g0091a0001c0001t0006g0095others(6): Show | 12 | HG01884.hp1 HG02258.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.959-249G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787869 | ||||||
| chr5:65787907
|
A | G | 1 | a0001c0001t0004g0272 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.959-211A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787907 | ||||||
| chr5:65787969
|
G | T | 74 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(71): Show | 81 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.959-149G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787969 | ||||||
| chr5:65787981
|
C | T | 1 | a0001c0001t0029g0105 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.959-137C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787981 | ||||||
| chr5:65788038
|
A | G | 51 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(48): Show | 58 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.959-80A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65788038 | ||||||
| chr5:65788738
|
G | A | 2 | a0001c0001t0003g0061a0001c0001t0003g0202 | 2 | NA19057.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1325+254G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65788738 | ||||||
| chr5:65788769
|
C | G | 1 | a0001c0002t0001g0189 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1325+285C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65788769 | ||||||
| chr5:65788859
|
G | A | 5 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0183others(2): Show | 5 | HG00642.hp2 HG01123.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325+375G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65788859 | ||||||
| chr5:65788971
|
C | CA | 93 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(90): Show | 95 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1325+500dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr5 | 65788971 | |||||
| chr5:65788971
|
CA | C | 10 | a0001c0001t0008g0002a0001c0001t0008g0007a0001c0001t0008g0220others(7): Show | 13 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1325+500delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr5 | 65788971 | |||||
| chr5:65789067
|
A | G | 2 | a0001c0001t0032g0255a0005c0009t0036g0256 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1325+583A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789067 | ||||||
| chr5:65789116
|
G | A | 10 | a0001c0001t0008g0002a0001c0001t0008g0007a0001c0001t0008g0220others(7): Show | 13 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1325+632G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789116 | ||||||
| chr5:65789323
|
A | G | 1 | a0004c0006t0008g0224 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1325+839A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789323 | ||||||
| chr5:65789371
|
T | C | 3 | a0002c0004t0007g0245a0002c0004t0007g0246a0002c0004t0007g0249 | 3 | HG02965.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1325+887T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789371 | ||||||
| chr5:65789493
|
C | A | 1 | a0001c0002t0001g0117 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1325+1009C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789493 | ||||||
| chr5:65789503
|
A | G | 99 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(96): Show | 103 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1325+1019A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789503 | ||||||
| chr5:65789755
|
A | T | 6 | a0001c0001t0001g0038a0001c0001t0001g0203a0001c0001t0004g0296others(3): Show | 6 | NA18983.hp1 NA18993.hp1 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325+1271A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789755 | ||||||
| chr5:65789756
|
T | C | 1 | a0001c0001t0022g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1325+1272T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789756 | ||||||
| chr5:65789797
|
C | T | 35 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0047others(32): Show | 38 | HG01516.hp2 HG01517.hp1 HG02132.hp2 others(35): Show |
intron_variant | MODIFIER | c.1325+1313C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789797 | ||||||
| chr5:65789845
|
A | G | 35 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0047others(32): Show | 38 | HG01516.hp2 HG01517.hp1 HG02132.hp2 others(35): Show |
intron_variant | MODIFIER | c.1325+1361A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789845 | ||||||
| chr5:65790081
|
A | T | 1 | a0002c0004t0016g0082 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1325+1597A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790081 | ||||||
| chr5:65790130
|
C | A | 2 | a0003c0005t0023g0077a0003c0005t0023g0081 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1325+1646C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790130 | ||||||
| chr5:65790204
|
T | G | 25 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0047others(22): Show | 25 | HG01516.hp2 HG01517.hp1 HG02132.hp2 others(22): Show |
intron_variant | MODIFIER | c.1325+1720T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790204 | ||||||
| chr5:65790469
|
A | G | 169 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(166): Show | 176 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.1325+1985A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790469 | ||||||
| chr5:65790541
|
A | C | 6 | a0001c0001t0002g0107a0001c0001t0002g0112a0001c0001t0002g0113others(3): Show | 6 | HG00621.hp2 NA18747.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-1913A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790541 | ||||||
| chr5:65790571
|
A | G | 4 | a0001c0001t0011g0222a0001c0001t0011g0228a0001c0001t0011g0236others(1): Show | 4 | HG01516.hp2 HG01517.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-1883A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790571 | ||||||
| chr5:65790624
|
C | T | 1 | a0002c0004t0041g0311 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1326-1830C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790624 | ||||||
| chr5:65790641
|
G | A | 11 | a0001c0001t0032g0255a0001c0001t0040g0195a0001c0001t0052g0284others(8): Show | 11 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1326-1813G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790641 | ||||||
| chr5:65790800
|
T | G | 45 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0012others(42): Show | 51 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1326-1654T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790800 | ||||||
| chr5:65790806
|
G | A | 1 | a0001c0001t0004g0298 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1326-1648G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790806 | ||||||
| chr5:65790877
|
G | A | 1 | a0001c0002t0013g0204 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1326-1577G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790877 | ||||||
| chr5:65790949
|
G | A | 2 | a0003c0005t0024g0055a0003c0005t0024g0080 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1326-1505G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790949 | ||||||
| chr5:65791023
|
A | C | 34 | a0001c0001t0001g0143a0001c0001t0001g0171a0001c0001t0001g0198others(31): Show | 36 | HG00609.hp1 HG01070.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1326-1431A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791023 | ||||||
| chr5:65791106
|
A | G | 1 | a0001c0002t0001g0190 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1326-1348A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791106 | ||||||
| chr5:65791258
|
G | C | 169 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(166): Show | 176 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.1326-1196G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791258 | ||||||
| chr5:65791284
|
A | C | 1 | a0002c0004t0041g0311 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1326-1170A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791284 | ||||||
| chr5:65791378
|
G | C | 169 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(166): Show | 176 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.1326-1076G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791378 | ||||||
| chr5:65791409
|
T | G | 1 | a0002c0004t0041g0311 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1326-1045T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791409 | ||||||
| chr5:65791493
|
C | T | 1 | a0001c0001t0005g0225 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1326-961C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791493 | ||||||
| chr5:65791494
|
A | G | 169 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(166): Show | 176 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.1326-960A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791494 | ||||||
| chr5:65791530
|
C | A | 69 | a0001c0001t0001g0051a0001c0001t0001g0106a0001c0001t0001g0109others(66): Show | 72 | HG00323.hp2 HG00438.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.1326-924C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791530 | ||||||
| chr5:65791543
|
G | A | 7 | a0001c0001t0040g0195a0001c0001t0052g0284a0001c0001t0053g0300others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1326-911G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791543 | ||||||
| chr5:65791553
|
G | A | 7 | a0001c0001t0040g0195a0001c0001t0052g0284a0001c0001t0053g0300others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1326-901G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791553 | ||||||
| chr5:65791593
|
T | C | 169 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(166): Show | 176 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.1326-861T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791593 | ||||||
| chr5:65791602
|
A | G | 2 | a0003c0005t0024g0055a0003c0005t0024g0080 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1326-852A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791602 | ||||||
| chr5:65791704
|
C | T | 88 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(85): Show | 92 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.1326-750C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791704 | ||||||
| chr5:65791729
|
A | T | 1 | a0001c0001t0005g0201 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1326-725A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791729 | ||||||
| chr5:65791730
|
A | T | 11 | a0001c0001t0032g0255a0001c0001t0040g0195a0001c0001t0052g0284others(8): Show | 11 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1326-724A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791730 | ||||||
| chr5:65792348
|
G | A | 100 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(97): Show | 105 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.1326-106G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65792348 | ||||||
| chr5:65792434
|
C | T | 2 | a0003c0005t0024g0055a0003c0005t0024g0080 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1326-20C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65792434 | ||||||
| chr5:65792660
|
GT | G | 7 | a0001c0001t0001g0120a0001c0001t0032g0255a0003c0005t0023g0077others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1527+15delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65792660 | |||||
| chr5:65792751
|
GA | G | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(3): Show | 6 | HG01123.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1527+98delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65792751 | |||||
| chr5:65792905
|
T | C | 1 | a0001c0001t0002g0129 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1527+250T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65792905 | ||||||
| chr5:65792941
|
T | G | 1 | a0005c0009t0045g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1527+286T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65792941 | ||||||
| chr5:65793340
|
G | A | 127 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(124): Show | 130 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1527+685G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65793340 | ||||||
| chr5:65793505
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1527+850G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65793505 | ||||||
| chr5:65793630
|
TA | T | 122 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(119): Show | 125 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1527+989delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65793630 | |||||
| chr5:65793698
|
T | C | 2 | a0003c0005t0023g0077a0003c0005t0023g0081 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1527+1043T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65793698 | ||||||
| chr5:65793952
|
T | G | 65 | a0001c0001t0001g0051a0001c0001t0001g0106a0001c0001t0001g0109others(62): Show | 66 | HG00323.hp2 HG00438.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.1527+1297T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65793952 | ||||||
| chr5:65793995
|
G | A | 2 | a0001c0001t0002g0258a0002c0004t0044g0259 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1527+1340G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65793995 | ||||||
| chr5:65794098
|
G | T | 1 | a0001c0001t0001g0185 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1527+1443G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794098 | ||||||
| chr5:65794154
|
G | T | 3 | a0001c0001t0002g0258a0002c0004t0041g0311a0002c0004t0044g0259 | 3 | HG02258.hp2 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1527+1499G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794154 | ||||||
| chr5:65794183
|
C | T | 3 | a0001c0001t0002g0258a0002c0004t0041g0311a0002c0004t0044g0259 | 3 | HG02258.hp2 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1527+1528C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794183 | ||||||
| chr5:65794263
|
A | G | 1 | a0002c0003t0010g0270 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1527+1608A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794263 | ||||||
| chr5:65794400
|
C | G | 42 | a0001c0001t0001g0143a0001c0001t0001g0171a0001c0001t0001g0198others(39): Show | 44 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1527+1745C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794400 | ||||||
| chr5:65794427
|
A | G | 1 | a0001c0001t0056g0260 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1527+1772A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794427 | ||||||
| chr5:65794561
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1527+1906C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794561 | ||||||
| chr5:65794656
|
C | T | 1 | a0007c0012t0001g0093 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1527+2001C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794656 | ||||||
| chr5:65794717
|
C | T | 4 | a0001c0001t0001g0171a0001c0001t0001g0198a0001c0001t0009g0144others(1): Show | 4 | HG01496.hp2 HG01952.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1527+2062C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794717 | ||||||
| chr5:65794718
|
G | A | 126 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(123): Show | 129 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1527+2063G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794718 | ||||||
| chr5:65794727
|
A | G | 1 | a0002c0004t0041g0311 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1527+2072A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794727 | ||||||
| chr5:65794804
|
C | T | 1 | a0001c0002t0001g0208 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1527+2149C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794804 | ||||||
| chr5:65794983
|
TTTTAATC others(32): Show |
T | 3 | a0001c0001t0005g0041a0001c0001t0005g0053a0001c0001t0005g0211 | 3 | NA18992.hp1 NA19063.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1527+2329_1527+236 others(43): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794983 | ||||||
| chr5:65795082
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1527+2427G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795082 | ||||||
| chr5:65795118
|
C | T | 1 | a0001c0001t0004g0301 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1527+2463C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795118 | ||||||
| chr5:65795217
|
C | T | 228 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(225): Show | 241 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(238): Show |
intron_variant | MODIFIER | c.1527+2562C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795217 | ||||||
| chr5:65795241
|
G | A | 52 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0012others(49): Show | 60 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1527+2586G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795241 | ||||||
| chr5:65795247
|
G | A | 1 | a0001c0001t0014g0175 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1527+2592G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795247 | ||||||
| chr5:65795351
|
G | T | 3 | a0002c0003t0007g0181a0002c0003t0007g0229a0002c0003t0007g0230 | 3 | HG00738.hp1 HG01256.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1527+2696G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795351 | ||||||
| chr5:65795638
|
G | A | 4 | a0003c0005t0023g0077a0003c0005t0023g0081a0003c0005t0024g0055others(1): Show | 4 | HG01243.hp2 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1527+2983G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795638 | ||||||
| chr5:65795746
|
G | A | 1 | a0001c0002t0001g0158 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1527+3091G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795746 | ||||||
| chr5:65795825
|
T | A | 1 | a0002c0004t0007g0249 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1527+3170T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795825 | ||||||
| chr5:65796060
|
C | T | 4 | a0003c0005t0023g0077a0003c0005t0023g0081a0003c0005t0024g0055others(1): Show | 4 | HG01243.hp2 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1527+3405C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65796060 | ||||||
| chr5:65796118
|
C | T | 2 | a0001c0001t0002g0258a0002c0004t0044g0259 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1527+3463C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65796118 | ||||||
| chr5:65796153
|
C | A | 2 | a0003c0005t0023g0077a0003c0005t0023g0081 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1527+3498C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65796153 | ||||||
| chr5:65796270
|
T | G | 1 | a0001c0001t0003g0070 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1527+3615T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65796270 | ||||||
| chr5:65796320
|
T | G | 2 | a0003c0005t0024g0055a0003c0005t0024g0080 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1527+3665T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65796320 | ||||||
| chr5:65796896
|
T | A | 27 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0047others(24): Show | 28 | HG01109.hp1 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.1527+4241T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65796896 | ||||||
| chr5:65797052
|
C | T | 3 | a0002c0004t0007g0245a0002c0004t0007g0246a0002c0004t0007g0249 | 3 | HG02965.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1527+4397C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797052 | ||||||
| chr5:65797143
|
T | C | 1 | a0001c0001t0002g0232 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1527+4488T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797143 | ||||||
| chr5:65797313
|
C | A | 1 | a0001c0002t0001g0145 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1527+4658C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797313 | ||||||
| chr5:65797812
|
C | T | 1 | a0001c0001t0002g0010 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1527+5157C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797812 | ||||||
| chr5:65797826
|
C | G | 42 | a0001c0001t0001g0143a0001c0001t0001g0171a0001c0001t0001g0198others(39): Show | 44 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1527+5171C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797826 | ||||||
| chr5:65797883
|
T | C | 2 | a0001c0001t0015g0250a0001c0001t0015g0251 | 2 | HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1527+5228T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797883 | ||||||
| chr5:65797896
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1527+5241C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797896 | ||||||
| chr5:65797937
|
A | G | 1 | a0001c0001t0004g0301 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1527+5282A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797937 | ||||||
| chr5:65798000
|
G | A | 2 | a0001c0001t0002g0258a0002c0004t0044g0259 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1527+5345G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798000 | ||||||
| chr5:65798018
|
T | C | 54 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(51): Show | 56 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1527+5363T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798018 | ||||||
| chr5:65798052
|
GAAGCGAA others(4): Show |
G | 1 | a0001c0001t0052g0284 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1527+5412_1527+542 others(15): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65798052 | |||||
| chr5:65798181
|
C | T | 42 | a0001c0001t0001g0143a0001c0001t0001g0171a0001c0001t0001g0198others(39): Show | 44 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1527+5526C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798181 | ||||||
| chr5:65798417
|
C | T | 1 | a0001c0001t0032g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1527+5762C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798417 | ||||||
| chr5:65798478
|
A | G | 1 | a0002c0003t0042g0083 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1527+5823A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798478 | ||||||
| chr5:65798577
|
C | T | 1 | a0001c0001t0002g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1527+5922C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798577 | ||||||
| chr5:65798642
|
A | G | 21 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0047others(18): Show | 21 | HG01516.hp2 HG01517.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.1527+5987A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798642 | ||||||
| chr5:65798907
|
G | T | 52 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0012others(49): Show | 60 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1527+6252G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798907 | ||||||
| chr5:65798982
|
G | A | 1 | a0003c0005t0022g0079 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1527+6327G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798982 | ||||||
| chr5:65799035
|
C | T | 5 | a0002c0004t0016g0056a0002c0004t0016g0058a0002c0004t0016g0082others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1527+6380C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799035 | ||||||
| chr5:65799050
|
T | G | 89 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(86): Show | 91 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1527+6395T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799050 | ||||||
| chr5:65799080
|
C | G | 1 | a0002c0004t0041g0311 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1527+6425C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799080 | ||||||
| chr5:65799276
|
A | G | 1 | a0001c0002t0004g0288 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1527+6621A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799276 | ||||||
| chr5:65799295
|
A | G | 55 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0012others(52): Show | 63 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1527+6640A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799295 | ||||||
| chr5:65799424
|
C | G | 4 | a0001c0001t0002g0009a0001c0001t0002g0033a0001c0001t0002g0131others(1): Show | 5 | NA18962.hp2 NA18964.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1527+6769C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799424 | ||||||
| chr5:65799427
|
G | C | 4 | a0002c0004t0016g0056a0002c0004t0016g0058a0002c0004t0016g0082others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1527+6772G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799427 | ||||||
| chr5:65799573
|
C | A | 1 | a0001c0001t0043g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1527+6918C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799573 | ||||||
| chr5:65799637
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1527+6982G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799637 | ||||||
| chr5:65799654
|
A | T | 1 | a0002c0004t0041g0311 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1527+6999A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799654 | ||||||
| chr5:65799714
|
A | G | 3 | a0001c0001t0033g0221a0001c0001t0034g0219a0001c0001t0051g0299 | 3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1527+7059A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799714 | ||||||
| chr5:65799724
|
A | G | 2 | a0001c0002t0001g0125a0001c0002t0001g0170 | 2 | NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1527+7069A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799724 | ||||||
| chr5:65799917
|
T | TA | 57 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0012others(54): Show | 65 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.1527+7272dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65799917 | |||||
| chr5:65800156
|
T | C | 10 | a0001c0001t0006g0022a0001c0001t0006g0045a0001c0001t0006g0048others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1527+7501T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65800156 | ||||||
| chr5:65800234
|
T | G | 1 | a0001c0001t0029g0105 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1527+7579T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65800234 | ||||||
| chr5:65800339
|
C | T | 2 | a0003c0005t0024g0055a0003c0005t0024g0080 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1527+7684C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65800339 | ||||||
| chr5:65800472
|
G | A | 3 | a0001c0001t0033g0221a0001c0001t0034g0219a0001c0001t0051g0299 | 3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1527+7817G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65800472 | ||||||
| chr5:65800489
|
C | T | 1 | a0001c0001t0014g0194 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1527+7834C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65800489 | ||||||
| chr5:65800663
|
C | CTTAT | 147 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(144): Show | 158 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(155): Show |
intron_variant | MODIFIER | c.1527+8043_1527+804 others(8): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65800663 | |||||
| chr5:65800663
|
C | CTTATTTA others(1): Show |
27 | a0001c0001t0001g0227a0001c0001t0002g0085a0001c0001t0002g0086others(24): Show | 28 | HG00738.hp1 HG00741.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1527+8039_1527+804 others(12): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65800663 | |||||
| chr5:65800663
|
C | CTTATTTA others(5): Show |
8 | a0001c0001t0033g0221a0001c0001t0034g0219a0001c0001t0051g0299others(5): Show | 8 | HG02257.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1527+8035_1527+804 others(16): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65800663 | |||||
| chr5:65800663
|
C | CTTATTTA others(9): Show |
2 | a0001c0001t0002g0258a0003c0005t0024g0055 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1527+8031_1527+804 others(20): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65800663 | |||||
| chr5:65800663
|
C | CTTTTTAT others(4): Show |
1 | a0001c0001t0005g0233 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1527+8010_1527+801 others(15): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65800663 | |||||
| chr5:65800663
|
C | CTTTTTAT others(8): Show |
54 | a0001c0001t0001g0051a0001c0001t0001g0106a0001c0001t0001g0109others(51): Show | 55 | HG00323.hp2 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1527+8010_1527+801 others(19): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65800663 | |||||
| chr5:65800663
|
C | CTTTTTAT others(12): Show |
7 | a0001c0001t0001g0119a0001c0001t0001g0130a0001c0001t0004g0280others(4): Show | 7 | HG01261.hp1 HG02132.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1527+8010_1527+801 others(23): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65800663 | |||||
| chr5:65800840
|
A | G | 220 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(217): Show | 233 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.1527+8185A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65800840 | ||||||
| chr5:65801237
|
T | G | 1 | a0001c0001t0006g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1528-8278T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801237 | ||||||
| chr5:65801404
|
G | T | 2 | a0001c0001t0006g0089a0001c0001t0006g0095 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1528-8111G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801404 | ||||||
| chr5:65801427
|
T | C | 1 | a0001c0002t0001g0189 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1528-8088T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801427 | ||||||
| chr5:65801474
|
G | T | 30 | a0001c0001t0002g0258a0001c0001t0005g0040a0001c0001t0005g0041others(27): Show | 31 | HG01109.hp1 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.1528-8041G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801474 | ||||||
| chr5:65801509
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1528-8006A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801509 | ||||||
| chr5:65801631
|
C | G | 2 | a0001c0002t0001g0180a0001c0002t0004g0288 | 2 | HG01106.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1528-7884C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801631 | ||||||
| chr5:65801806
|
A | AT | 220 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(217): Show | 233 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.1528-7708dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65801806 | |||||
| chr5:65801818
|
T | TG | 220 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(217): Show | 233 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.1528-7697_1528-769 others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801818 | ||||||
| chr5:65801923
|
G | A | 1 | a0001c0002t0001g0147 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1528-7592G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801923 | ||||||
| chr5:65801977
|
A | T | 1 | a0002c0004t0041g0311 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1528-7538A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801977 | ||||||
| chr5:65802043
|
C | T | 1 | a0001c0001t0009g0026 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1528-7472C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802043 | ||||||
| chr5:65802185
|
C | G | 1 | a0001c0001t0004g0294 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1528-7330C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802185 | ||||||
| chr5:65802300
|
G | A | 1 | a0002c0003t0018g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1528-7215G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802300 | ||||||
| chr5:65802301
|
G | T | 62 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0012others(59): Show | 70 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.1528-7214G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802301 | ||||||
| chr5:65802363
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1528-7152C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802363 | ||||||
| chr5:65802404
|
G | T | 30 | a0001c0001t0002g0258a0001c0001t0005g0040a0001c0001t0005g0041others(27): Show | 31 | HG01109.hp1 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.1528-7111G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802404 | ||||||
| chr5:65802427
|
C | T | 1 | a0001c0001t0002g0232 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1528-7088C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802427 | ||||||
| chr5:65802435
|
C | T | 1 | a0001c0013t0039g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1528-7080C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802435 | ||||||
| chr5:65802436
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1528-7079G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802436 | ||||||
| chr5:65802668
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1528-6847G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802668 | ||||||
| chr5:65802718
|
C | T | 158 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(155): Show | 163 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.1528-6797C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802718 | ||||||
| chr5:65802885
|
G | A | 54 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0012others(51): Show | 62 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.1528-6630G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802885 | ||||||
| chr5:65803098
|
G | A | 2 | a0003c0005t0023g0077a0003c0005t0023g0081 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1528-6417G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803098 | ||||||
| chr5:65803211
|
T | C | 3 | a0001c0001t0033g0221a0001c0001t0034g0219a0001c0001t0051g0299 | 3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1528-6304T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803211 | ||||||
| chr5:65803251
|
C | T | 62 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0012others(59): Show | 70 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.1528-6264C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803251 | ||||||
| chr5:65803255
|
C | T | 1 | a0002c0004t0018g0293 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1528-6260C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803255 | ||||||
| chr5:65803336
|
C | T | 62 | a0001c0001t0001g0051a0001c0001t0001g0106a0001c0001t0001g0109others(59): Show | 63 | HG00323.hp2 HG00438.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1528-6179C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803336 | ||||||
| chr5:65803401
|
G | T | 1 | a0001c0001t0002g0187 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1528-6114G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803401 | ||||||
| chr5:65803408
|
A | C | 2 | a0003c0005t0021g0017a0003c0005t0022g0079 | 3 | HG02896.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1528-6107A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803408 | ||||||
| chr5:65803417
|
C | T | 55 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0012others(52): Show | 63 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1528-6098C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803417 | ||||||
| chr5:65803510
|
G | C | 42 | a0001c0001t0001g0143a0001c0001t0001g0171a0001c0001t0001g0198others(39): Show | 44 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1528-6005G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803510 | ||||||
| chr5:65803602
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1528-5913C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803602 | ||||||
| chr5:65803799
|
C | T | 93 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(90): Show | 97 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.1528-5716C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803799 | ||||||
| chr5:65803807
|
G | C | 1 | a0001c0001t0001g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1528-5708G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803807 | ||||||
| chr5:65803850
|
T | C | 3 | a0004c0006t0001g0008a0004c0006t0001g0088a0004c0006t0001g0096 | 4 | HG02451.hp1 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1528-5665T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803850 | ||||||
| chr5:65803889
|
C | T | 2 | a0003c0005t0023g0077a0003c0005t0023g0081 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1528-5626C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803889 | ||||||
| chr5:65804331
|
G | C | 3 | a0001c0001t0033g0221a0001c0001t0034g0219a0001c0001t0051g0299 | 3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1528-5184G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804331 | ||||||
| chr5:65804390
|
T | C | 1 | a0001c0001t0003g0073 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1528-5125T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804390 | ||||||
| chr5:65804397
|
T | A | 1 | a0001c0001t0001g0164 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1528-5118T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804397 | ||||||
| chr5:65804571
|
T | C | 220 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(217): Show | 233 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.1528-4944T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804571 | ||||||
| chr5:65804690
|
A | C | 1 | a0001c0014t0057g0306 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1528-4825A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804690 | ||||||
| chr5:65804741
|
A | G | 225 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(222): Show | 238 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.1528-4774A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804741 | ||||||
| chr5:65804833
|
T | C | 220 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(217): Show | 233 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.1528-4682T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804833 | ||||||
| chr5:65804942
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1528-4573A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804942 | ||||||
| chr5:65804954
|
G | A | 3 | a0001c0001t0006g0027a0001c0001t0032g0255a0005c0009t0036g0256 | 3 | HG01243.hp1 HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1528-4561G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804954 | ||||||
| chr5:65805135
|
A | G | 62 | a0001c0001t0001g0051a0001c0001t0001g0106a0001c0001t0001g0109others(59): Show | 63 | HG00323.hp2 HG00438.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1528-4380A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65805135 | ||||||
| chr5:65805632
|
T | G | 220 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(217): Show | 233 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.1528-3883T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65805632 | ||||||
| chr5:65805749
|
C | T | 2 | a0003c0005t0023g0077a0003c0005t0023g0081 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1528-3766C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65805749 | ||||||
| chr5:65805809
|
G | A | 2 | a0003c0005t0023g0077a0003c0005t0023g0081 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1528-3706G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65805809 | ||||||
| chr5:65805843
|
A | G | 4 | a0001c0001t0015g0044a0001c0001t0015g0250a0001c0001t0015g0251others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1528-3672A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65805843 | ||||||
| chr5:65805886
|
T | G | 1 | a0002c0003t0042g0083 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1528-3629T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65805886 | ||||||
| chr5:65806233
|
T | C | 3 | a0001c0001t0033g0221a0001c0001t0034g0219a0001c0001t0051g0299 | 3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1528-3282T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806233 | ||||||
| chr5:65806294
|
A | G | 4 | a0002c0004t0016g0056a0002c0004t0016g0058a0002c0004t0016g0082others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1528-3221A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806294 | ||||||
| chr5:65806413
|
T | C | 1 | a0001c0001t0002g0232 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1528-3102T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806413 | ||||||
| chr5:65806426
|
G | C | 2 | a0001c0001t0006g0089a0001c0001t0006g0095 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1528-3089G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806426 | ||||||
| chr5:65806450
|
T | C | 3 | a0001c0001t0033g0221a0001c0001t0034g0219a0001c0001t0051g0299 | 3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1528-3065T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806450 | ||||||
| chr5:65806639
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1528-2876A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806639 | ||||||
| chr5:65806674
|
C | T | 2 | a0003c0005t0023g0077a0003c0005t0023g0081 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1528-2841C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806674 | ||||||
| chr5:65806735
|
T | G | 2 | a0003c0005t0023g0077a0003c0005t0023g0081 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1528-2780T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806735 | ||||||
| chr5:65807012
|
A | G | 2 | a0001c0001t0002g0258a0002c0004t0044g0259 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1528-2503A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65807012 | ||||||
| chr5:65807071
|
G | A | 1 | a0001c0002t0001g0110 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1528-2444G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65807071 | ||||||
| chr5:65807173
|
T | C | 3 | a0001c0001t0033g0221a0001c0001t0034g0219a0001c0001t0051g0299 | 3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1528-2342T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65807173 | ||||||
| chr5:65807176
|
CA | C | 219 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(216): Show | 232 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.1528-2326delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65807176 | |||||
| chr5:65807338
|
C | T | 93 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(90): Show | 97 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.1528-2177C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65807338 | ||||||
| chr5:65807438
|
A | AT | 6 | a0001c0001t0002g0133a0001c0002t0001g0200a0002c0004t0018g0282others(3): Show | 6 | HG01167.hp2 HG03471.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1528-2065dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65807438 | |||||
| chr5:65807561
|
C | T | 2 | a0003c0005t0024g0055a0003c0005t0024g0080 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1528-1954C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65807561 | ||||||
| chr5:65807589
|
C | T | 1 | a0002c0016t0035g0257 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1528-1926C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65807589 | ||||||
| chr5:65807597
|
T | G | 6 | a0001c0001t0008g0002a0001c0001t0008g0007a0001c0001t0008g0220others(3): Show | 9 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1528-1918T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65807597 | ||||||
| chr5:65808088
|
G | A | 4 | a0001c0002t0001g0014a0001c0002t0001g0162a0001c0002t0001g0184others(1): Show | 5 | HG01255.hp2 HG01358.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1528-1427G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808088 | ||||||
| chr5:65808098
|
G | A | 30 | a0001c0001t0002g0258a0001c0001t0005g0040a0001c0001t0005g0041others(27): Show | 31 | HG01109.hp1 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.1528-1417G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808098 | ||||||
| chr5:65808319
|
G | A | 2 | a0001c0002t0001g0137a0001c0002t0001g0215 | 2 | HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1528-1196G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808319 | ||||||
| chr5:65808516
|
A | G | 1 | a0002c0004t0007g0249 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1528-999A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808516 | ||||||
| chr5:65808845
|
A | T | 4 | a0001c0001t0015g0044a0001c0001t0015g0250a0001c0001t0015g0251others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1528-670A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808845 | ||||||
| chr5:65808909
|
C | T | 3 | a0001c0001t0033g0221a0001c0001t0034g0219a0001c0001t0051g0299 | 3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1528-606C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808909 | ||||||
| chr5:65808942
|
A | G | 1 | a0001c0001t0002g0113 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1528-573A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808942 | ||||||
| chr5:65808972
|
C | G | 1 | a0001c0002t0001g0169 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1528-543C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808972 | ||||||
| chr5:65809130
|
C | T | 3 | a0001c0001t0033g0221a0001c0001t0034g0219a0001c0001t0051g0299 | 3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1528-385C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65809130 | ||||||
| chr5:65809369
|
C | T | 2 | a0003c0005t0023g0077a0003c0005t0023g0081 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1528-146C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65809369 | ||||||
| chr5:65809381
|
G | A | 3 | a0001c0002t0001g0014a0001c0002t0001g0162a0001c0002t0001g0184 | 4 | HG01255.hp2 HG01358.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1528-134G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65809381 | ||||||
| chr5:65809795
|
G | A | 220 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(217): Show | 233 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.1714+94G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 10/12 | chr5 | 65809795 | ||||||
| chr5:65810354
|
G | C | 5 | a0001c0001t0002g0107a0001c0001t0002g0112a0001c0001t0002g0113others(2): Show | 5 | NA18747.hp2 NA18942.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1843+189G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65810354 | ||||||
| chr5:65810400
|
T | C | 2 | a0001c0001t0002g0258a0002c0004t0044g0259 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1843+235T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65810400 | ||||||
| chr5:65810433
|
G | A | 2 | a0001c0001t0004g0266a0001c0001t0004g0279 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1843+268G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65810433 | ||||||
| chr5:65810607
|
C | T | 10 | a0001c0001t0006g0022a0001c0001t0006g0045a0001c0001t0006g0048others(7): Show | 10 | HG00741.hp2 HG01167.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1843+442C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65810607 | ||||||
| chr5:65810965
|
T | C | 3 | a0001c0001t0033g0221a0001c0001t0034g0219a0001c0001t0051g0299 | 3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1843+800T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65810965 | ||||||
| chr5:65810973
|
T | C | 1 | a0001c0001t0003g0072 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1843+808T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65810973 | ||||||
| chr5:65811111
|
T | G | 1 | a0001c0001t0002g0239 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1843+946T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811111 | ||||||
| chr5:65811112
|
T | A | 1 | a0001c0001t0002g0239 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1843+947T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811112 | ||||||
| chr5:65811152
|
A | T | 4 | a0002c0004t0016g0056a0002c0004t0016g0058a0002c0004t0016g0082others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1843+987A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811152 | ||||||
| chr5:65811170
|
G | A | 5 | a0002c0004t0016g0056a0002c0004t0016g0058a0002c0004t0016g0082others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1843+1005G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811170 | ||||||
| chr5:65811425
|
C | G | 46 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0012others(43): Show | 51 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1844-830C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811425 | ||||||
| chr5:65811447
|
G | A | 1 | a0001c0002t0001g0213 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1844-808G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811447 | ||||||
| chr5:65811515
|
T | C | 96 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(93): Show | 100 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1844-740T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811515 | ||||||
| chr5:65811546
|
G | A | 6 | a0001c0001t0008g0002a0001c0001t0008g0007a0001c0001t0008g0220others(3): Show | 9 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1844-709G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811546 | ||||||
| chr5:65811570
|
C | G | 2 | a0001c0001t0002g0258a0002c0004t0044g0259 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1844-685C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811570 | ||||||
| chr5:65811628
|
C | A | 3 | a0001c0001t0033g0221a0001c0001t0034g0219a0001c0001t0051g0299 | 3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1844-627C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811628 | ||||||
| chr5:65811668
|
T | C | 220 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(217): Show | 233 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.1844-587T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811668 | ||||||
| chr5:65811762
|
C | T | 93 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(90): Show | 97 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.1844-493C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811762 | ||||||
| chr5:65811851
|
A | T | 2 | a0002c0004t0016g0082a0002c0016t0035g0257 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1844-404A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811851 | ||||||
| chr5:65811989
|
C | T | 1 | a0001c0002t0001g0024 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1844-266C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811989 | ||||||
| chr5:65812215
|
G | A | 1 | a0001c0001t0002g0115 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1844-40G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65812215 | ||||||
| chr5:65812222
|
A | G | 1 | a0001c0001t0004g0294 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1844-33A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65812222 | ||||||
| chr5:65812242
|
T | C | 1 | a0002c0003t0042g0083 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1844-13T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65812242 | ||||||
| chr5:65812428
|
G | A | 3 | a0001c0007t0019g0290a0001c0007t0019g0292a0001c0007t0019g0309 | 3 | HG00438.hp1 NA18962.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1980+37G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65812428 | ||||||
| chr5:65812485
|
G | T | 4 | a0002c0004t0016g0056a0002c0004t0016g0058a0002c0004t0016g0082others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1980+94G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65812485 | ||||||
| chr5:65812582
|
T | C | 225 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(222): Show | 238 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.1980+191T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65812582 | ||||||
| chr5:65812739
|
G | T | 3 | a0001c0001t0002g0258a0002c0004t0041g0311a0002c0004t0044g0259 | 3 | HG02258.hp2 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1980+348G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65812739 | ||||||
| chr5:65812947
|
C | A | 1 | a0001c0002t0001g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1980+556C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65812947 | ||||||
| chr5:65813049
|
C | T | 220 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(217): Show | 233 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.1980+658C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813049 | ||||||
| chr5:65813179
|
A | C | 42 | a0001c0001t0001g0143a0001c0001t0001g0171a0001c0001t0001g0198others(39): Show | 44 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1980+788A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813179 | ||||||
| chr5:65813365
|
C | G | 5 | a0002c0004t0016g0056a0002c0004t0016g0058a0002c0004t0016g0082others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1980+974C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813365 | ||||||
| chr5:65813423
|
C | T | 1 | a0001c0001t0002g0187 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1980+1032C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813423 | ||||||
| chr5:65813782
|
G | A | 3 | a0001c0001t0002g0258a0002c0004t0041g0311a0002c0004t0044g0259 | 3 | HG02258.hp2 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1980+1391G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813782 | ||||||
| chr5:65813829
|
G | C | 1 | a0001c0002t0001g0087 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1980+1438G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813829 | ||||||
| chr5:65813927
|
C | CA | 8 | a0001c0001t0001g0111a0001c0001t0001g0114a0001c0001t0022g0084others(5): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1980+1549dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 65813927 | |||||
| chr5:65813941
|
T | A | 2 | a0003c0005t0024g0055a0003c0005t0024g0080 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1980+1550T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813941 | ||||||
| chr5:65813992
|
C | A | 8 | a0002c0003t0010g0261a0002c0003t0010g0268a0002c0003t0010g0270others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1980+1601C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813992 | ||||||
| chr5:65814013
|
G | A | 36 | a0001c0001t0001g0143a0001c0001t0001g0171a0001c0001t0001g0198others(33): Show | 38 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1980+1622G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814013 | ||||||
| chr5:65814014
|
G | A | 3 | a0001c0001t0005g0041a0001c0001t0005g0053a0001c0001t0005g0211 | 3 | NA18992.hp1 NA19063.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1980+1623G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814014 | ||||||
| chr5:65814116
|
T | C | 1 | a0001c0001t0043g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1980+1725T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814116 | ||||||
| chr5:65814416
|
G | A | 4 | a0001c0001t0001g0177a0001c0001t0033g0221a0001c0001t0034g0219others(1): Show | 4 | HG02451.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1980+2025G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814416 | ||||||
| chr5:65814544
|
A | C | 1 | a0001c0001t0005g0201 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1980+2153A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814544 | ||||||
| chr5:65814725
|
A | G | 214 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(211): Show | 227 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.1980+2334A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814725 | ||||||
| chr5:65814930
|
T | G | 6 | a0001c0001t0002g0258a0001c0001t0006g0027a0001c0001t0032g0255others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1980+2539T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814930 | ||||||
| chr5:65814961
|
A | G | 128 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(125): Show | 132 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1980+2570A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814961 | ||||||
| chr5:65815030
|
C | T | 1 | a0001c0001t0004g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1980+2639C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65815030 | ||||||
| chr5:65815072
|
A | T | 1 | a0001c0002t0001g0214 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1980+2681A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65815072 | ||||||
| chr5:65815411
|
A | T | 2 | a0001c0001t0002g0258a0002c0004t0044g0259 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1980+3020A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65815411 | ||||||
| chr5:65816011
|
C | G | 1 | a0001c0002t0001g0253 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1980+3620C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816011 | ||||||
| chr5:65816018
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1980+3627T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816018 | ||||||
| chr5:65816051
|
C | T | 35 | a0001c0001t0001g0143a0001c0001t0001g0171a0001c0001t0001g0198others(32): Show | 37 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1980+3660C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816051 | ||||||
| chr5:65816064
|
A | G | 1 | a0001c0001t0032g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1980+3673A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816064 | ||||||
| chr5:65816126
|
G | C | 163 | a0001c0001t0001g0051a0001c0001t0001g0106a0001c0001t0001g0109others(160): Show | 174 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(171): Show |
intron_variant | MODIFIER | c.1980+3735G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816126 | ||||||
| chr5:65816287
|
C | G | 53 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(50): Show | 55 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1980+3896C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816287 | ||||||
| chr5:65816345
|
C | T | 2 | a0001c0001t0004g0303a0001c0001t0055g0304 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1980+3954C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816345 | ||||||
| chr5:65816356
|
A | G | 90 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(87): Show | 92 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1980+3965A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816356 | ||||||
| chr5:65816523
|
G | A | 1 | a0002c0004t0041g0311 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1980+4132G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816523 | ||||||
| chr5:65816610
|
C | T | 1 | a0004c0006t0030g0097 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1980+4219C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816610 | ||||||
| chr5:65816694
|
G | A | 2 | a0001c0001t0033g0221a0001c0001t0051g0299 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1980+4303G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816694 | ||||||
| chr5:65816830
|
C | G | 1 | a0001c0011t0005g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1980+4439C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816830 | ||||||
| chr5:65816901
|
T | G | 214 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(211): Show | 227 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.1980+4510T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816901 | ||||||
| chr5:65817007
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1980+4616G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65817007 | ||||||
| chr5:65817025
|
A | G | 1 | a0001c0001t0002g0127 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1980+4634A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65817025 | ||||||
| chr5:65817326
|
C | T | 2 | a0003c0005t0023g0077a0003c0005t0023g0081 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1980+4935C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65817326 | ||||||
| chr5:65817637
|
C | G | 4 | a0001c0001t0015g0044a0001c0001t0015g0250a0001c0001t0015g0251others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-5144C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65817637 | ||||||
| chr5:65817715
|
A | G | 5 | a0001c0001t0005g0052a0001c0001t0005g0206a0001c0001t0005g0218others(2): Show | 5 | NA18954.hp2 NA18964.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1981-5066A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65817715 | ||||||
| chr5:65817868
|
C | G | 2 | a0001c0002t0001g0135a0001c0002t0001g0179 | 2 | NA19062.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1981-4913C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65817868 | ||||||
| chr5:65818256
|
C | A | 2 | a0001c0001t0002g0258a0002c0004t0044g0259 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1981-4525C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65818256 | ||||||
| chr5:65818331
|
T | C | 6 | a0001c0001t0004g0301a0002c0003t0007g0078a0002c0003t0007g0181others(3): Show | 6 | HG00735.hp1 HG00738.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1981-4450T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65818331 | ||||||
| chr5:65818372
|
C | T | 1 | a0001c0001t0056g0260 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1981-4409C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65818372 | ||||||
| chr5:65818389
|
C | A | 1 | a0001c0001t0001g0178 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1981-4392C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65818389 | ||||||
| chr5:65818766
|
G | C | 44 | a0001c0001t0001g0143a0001c0001t0001g0171a0001c0001t0001g0198others(41): Show | 46 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.1981-4015G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65818766 | ||||||
| chr5:65818769
|
G | A | 1 | a0001c0001t0004g0296 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1981-4012G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65818769 | ||||||
| chr5:65819019
|
G | A | 2 | a0003c0005t0024g0055a0003c0005t0024g0080 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1981-3762G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819019 | ||||||
| chr5:65819175
|
G | A | 177 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(174): Show | 188 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.1981-3606G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819175 | ||||||
| chr5:65819190
|
T | A | 1 | a0005c0009t0045g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1981-3591T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819190 | ||||||
| chr5:65819190
|
T | C | 3 | a0001c0001t0002g0258a0002c0004t0041g0311a0002c0004t0044g0259 | 3 | HG02258.hp2 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1981-3591T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819190 | ||||||
| chr5:65819437
|
A | G | 1 | a0001c0001t0043g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1981-3344A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819437 | ||||||
| chr5:65819460
|
C | T | 241 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(238): Show | 254 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.1981-3321C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819460 | ||||||
| chr5:65819525
|
G | A | 2 | a0002c0004t0016g0082a0002c0016t0035g0257 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1981-3256G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819525 | ||||||
| chr5:65819721
|
A | G | 173 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(170): Show | 184 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.1981-3060A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819721 | ||||||
| chr5:65820011
|
T | C | 1 | a0001c0002t0001g0135 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1981-2770T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820011 | ||||||
| chr5:65820061
|
C | A | 1 | a0003c0005t0024g0055 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1981-2720C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820061 | ||||||
| chr5:65820261
|
A | G | 224 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(221): Show | 237 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1981-2520A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820261 | ||||||
| chr5:65820290
|
C | T | 177 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(174): Show | 188 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.1981-2491C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820290 | ||||||
| chr5:65820716
|
G | GT | 7 | a0001c0001t0005g0262a0001c0001t0020g0018a0001c0002t0001g0087others(4): Show | 8 | HG01109.hp1 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1981-2056dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 65820716 | |||||
| chr5:65820718
|
T | C | 6 | a0001c0001t0009g0023a0001c0001t0009g0026a0001c0001t0009g0062others(3): Show | 6 | HG01070.hp2 HG01169.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1981-2063T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820718 | ||||||
| chr5:65820722
|
T | G | 1 | a0001c0007t0019g0290 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1981-2059T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820722 | ||||||
| chr5:65820722
|
T | TTTTG | 87 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(84): Show | 89 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1981-2043_1981-204 others(8): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 65820722 | |||||
| chr5:65820745
|
C | T | 3 | a0004c0006t0001g0008a0004c0006t0001g0088a0004c0006t0001g0096 | 4 | HG02451.hp1 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1981-2036C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820745 | ||||||
| chr5:65820746
|
G | A | 1 | a0002c0016t0035g0257 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1981-2035G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820746 | ||||||
| chr5:65820799
|
T | C | 1 | a0001c0001t0002g0115 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1982T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820799 | ||||||
| chr5:65820800
|
G | T | 1 | a0001c0001t0002g0115 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1981G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820800 | ||||||
| chr5:65820804
|
G | A | 1 | a0001c0001t0002g0115 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1977G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820804 | ||||||
| chr5:65820899
|
C | A | 1 | a0001c0001t0002g0115 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1882C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820899 | ||||||
| chr5:65820900
|
A | G | 215 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(212): Show | 228 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(225): Show |
intron_variant | MODIFIER | c.1981-1881A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820900 | ||||||
| chr5:65820962
|
AC | A | 312 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(309): Show | 334 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.1981-1815delC | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 65820962 | |||||
| chr5:65820965
|
C | T | 1 | a0001c0001t0002g0115 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1816C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820965 | ||||||
| chr5:65821042
|
CA | C | 6 | a0001c0001t0040g0195a0002c0004t0016g0056a0002c0004t0016g0058others(3): Show | 6 | HG02257.hp1 HG02258.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1981-1723delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 65821042 | |||||
| chr5:65821069
|
A | C | 42 | a0001c0001t0001g0143a0001c0001t0001g0171a0001c0001t0001g0198others(39): Show | 44 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1981-1712A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821069 | ||||||
| chr5:65821098
|
G | A | 1 | a0001c0001t0002g0115 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1683G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821098 | ||||||
| chr5:65821103
|
A | T | 1 | a0001c0001t0002g0115 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1678A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821103 | ||||||
| chr5:65821104
|
G | A | 1 | a0001c0001t0002g0115 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1677G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821104 | ||||||
| chr5:65821122
|
G | T | 1 | a0001c0001t0002g0115 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1659G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821122 | ||||||
| chr5:65821125
|
A | G | 1 | a0001c0001t0002g0115 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1656A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821125 | ||||||
| chr5:65821259
|
T | C | 4 | a0001c0001t0001g0143a0001c0001t0003g0140a0001c0001t0003g0141others(1): Show | 4 | HG01081.hp2 HG01978.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1981-1522T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821259 | ||||||
| chr5:65821293
|
T | C | 1 | a0001c0001t0003g0071 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1981-1488T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821293 | ||||||
| chr5:65821561
|
CTT | C | 4 | a0002c0004t0016g0056a0002c0004t0016g0058a0002c0004t0016g0082others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-1218_1981-121 others(6): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 65821561 | |||||
| chr5:65821580
|
G | T | 3 | a0001c0001t0005g0166a0001c0001t0005g0231a0001c0001t0005g0233 | 3 | NA18973.hp1 NA18994.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1981-1201G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821580 | ||||||
| chr5:65821599
|
A | C | 2 | a0002c0004t0016g0056a0002c0004t0016g0058 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1981-1182A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821599 | ||||||
| chr5:65821606
|
C | T | 1 | a0004c0006t0030g0097 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1981-1175C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821606 | ||||||
| chr5:65821807
|
C | A | 4 | a0002c0004t0016g0056a0002c0004t0016g0058a0002c0004t0016g0082others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-974C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821807 | ||||||
| chr5:65821943
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1981-838T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821943 | ||||||
| chr5:65822185
|
C | T | 1 | a0002c0003t0018g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1981-596C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65822185 | ||||||
| chr5:65822281
|
C | T | 1 | a0001c0001t0005g0238 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1981-500C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65822281 | ||||||
| chr5:65822357
|
ACCATTTG others(7): Show |
A | 3 | a0001c0001t0033g0221a0001c0001t0034g0219a0001c0001t0051g0299 | 3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1981-419_1981-406d others(16): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 65822357 | |||||
| chr5:65822584
|
G | A | 1 | a0001c0001t0002g0115 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-197G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65822584 | ||||||
| chr5:65822678
|
A | G | 1 | a0001c0002t0001g0167 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1981-103A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65822678 |