| geneid | 115677 |
|---|---|
| ensemblid | ENSG00000163072.16 |
| hgncid | 20203 |
| symbol | NOSTRIN |
| name | nitric oxide synthase trafficking |
| refseq_nuc | NM_001039724.4 |
| refseq_prot | NP_001034813.2 |
| ensembl_nuc | ENST00000317647.12 |
| ensembl_prot | ENSP00000318921.7 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 168802637 |
| end | 168865514 |
| strand | + |
| ver | v1.2 |
| region | chr2:168802637-168865514 |
| region5000 | chr2:168797637-168870514 |
| regionname0 | NOSTRIN_chr2_168802637_168865514 |
| regionname5000 | NOSTRIN_chr2_168797637_168870514 |
| 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 | 0/1 | 506 | 277 | 79 | 48 | 99 | 11 | 39 | 71 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0002 | 1/0 | 506 | 38 | 3 | 15 | 15 | 3 | 1 | 15 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0003 | 0/0 | 506 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0004 | 0/0 | 506 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0005 | 0/0 | 506 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1521 | 151 | 39 | 31 | 53 | 6 | 22 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| c0002 | 0/0 | 1521 | 49 | 2 | 4 | 35 | 0 | 8 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| c0003 | 1/0 | 1521 | 38 | 3 | 15 | 15 | 3 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| c0004 | 0/1 | 1521 | 32 | 6 | 10 | 5 | 3 | 7 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| c0005 | 0/0 | 1521 | 29 | 24 | 2 | 0 | 2 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| c0006 | 0/0 | 1521 | 8 | 7 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| c0007 | 0/0 | 1521 | 8 | 0 | 1 | 6 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| c0008 | 0/0 | 1521 | 3 | 3 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| c0009 | 0/0 | 1521 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| c0010 | 0/0 | 1521 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| c0011 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| c0012 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| c0013 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| c0014 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| 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 | 555 | 181 | 40 | 39 | 73 | 7 | 21 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| t0002 | 0/1 | 555 | 108 | 22 | 23 | 40 | 5 | 17 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| t0003 | 0/0 | 555 | 33 | 28 | 2 | 0 | 2 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| t0004 | 0/0 | 555 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| t0005 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| t0006 | 0/0 | 555 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| 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 | 4 | 0 | 4 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| 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 | 0/0 | 1521 | 151 | 39 | 31 | 53 | 6 | 22 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0002 | 0/0 | 1521 | 49 | 2 | 4 | 35 | 0 | 8 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0004 | 0/1 | 1521 | 32 | 6 | 10 | 5 | 3 | 7 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0005 | 0/0 | 1521 | 29 | 24 | 2 | 0 | 2 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0007 | 0/0 | 1521 | 8 | 0 | 1 | 6 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0008 | 0/0 | 1521 | 3 | 3 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0009 | 0/0 | 1521 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0010 | 0/0 | 1521 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0012 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0002c0003 | 1/0 | 1521 | 38 | 3 | 15 | 15 | 3 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0003c0006 | 0/0 | 1521 | 8 | 7 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0003c0013 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0004c0014 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0005c0011 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2075 | 122 | 24 | 22 | 52 | 4 | 20 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0001t0002 | 0/0 | 2075 | 26 | 13 | 9 | 0 | 2 | 2 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0001t0004 | 0/0 | 2075 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0001t0005 | 0/0 | 2075 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0002t0002 | 0/0 | 2075 | 49 | 2 | 4 | 35 | 0 | 8 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0004t0002 | 0/1 | 2075 | 32 | 6 | 10 | 5 | 3 | 7 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0005t0003 | 0/0 | 2075 | 29 | 24 | 2 | 0 | 2 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0007t0001 | 0/0 | 2075 | 7 | 0 | 1 | 6 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0007t0006 | 0/0 | 2075 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0008t0003 | 0/0 | 2075 | 3 | 3 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0009t0001 | 0/0 | 2075 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0010t0001 | 0/0 | 2075 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0001c0012t0001 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0002c0003t0001 | 1/0 | 2075 | 38 | 3 | 15 | 15 | 3 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0003c0006t0001 | 0/0 | 2075 | 7 | 6 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0003c0006t0002 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0003c0013t0003 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0004c0014t0001 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| a0005c0011t0001 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | copy fasta | chr2 | 168797637 | 168870514 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0006g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0008t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0008t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0008t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0009t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0009t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0010t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0010t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0012t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0006t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0006t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0006t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0006t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0006t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0006t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0006t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0006t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0013t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0004c0014t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0005c0011t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0001 | g0025 | EUR | GBR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0282 | EUR | GBR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00140 | hp1 | a0001 | c0004 | t0002 | g0200 | EUR | GBR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | FIN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | FIN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00323 | hp1 | a0001 | c0004 | t0002 | g0038 | EUR | FIN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00323 | hp2 | a0002 | c0003 | t0001 | g0033 | EUR | FIN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0308 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00673 | hp2 | a0001 | c0004 | t0002 | g0294 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00733 | hp2 | a0001 | c0004 | t0002 | g0195 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00735 | hp2 | a0001 | c0004 | t0002 | g0199 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00738 | hp1 | a0001 | c0004 | t0002 | g0203 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00738 | hp2 | a0001 | c0004 | t0002 | g0241 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01069 | hp1 | a0002 | c0003 | t0001 | g0011 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01069 | hp2 | a0002 | c0003 | t0001 | g0028 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01070 | hp1 | a0001 | c0004 | t0002 | g0193 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01070 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0011 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01074 | hp2 | a0001 | c0004 | t0002 | g0044 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01099 | hp1 | a0002 | c0003 | t0001 | g0259 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01106 | hp2 | a0001 | c0004 | t0002 | g0194 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0163 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01167 | hp1 | a0002 | c0003 | t0001 | g0029 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01168 | hp1 | a0001 | c0004 | t0002 | g0160 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01175 | hp1 | a0001 | c0004 | t0002 | g0284 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01175 | hp2 | a0001 | c0004 | t0002 | g0230 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01255 | hp2 | a0001 | c0005 | t0003 | g0248 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0164 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0024 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0023 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01261 | hp1 | a0001 | c0005 | t0003 | g0138 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01261 | hp2 | a0003 | c0006 | t0001 | g0276 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0147 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0030 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0031 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01516 | hp1 | a0001 | c0005 | t0003 | g0263 | EUR | IBS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01516 | hp2 | a0002 | c0003 | t0001 | g0009 | EUR | IBS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01517 | hp2 | a0001 | c0005 | t0003 | g0262 | EUR | IBS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01884 | hp1 | a0001 | c0005 | t0003 | g0251 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01884 | hp2 | a0001 | c0005 | t0003 | g0002 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01928 | hp2 | a0002 | c0003 | t0001 | g0027 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01943 | hp2 | a0001 | c0007 | t0001 | g0211 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0204 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0302 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0032 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02015 | hp1 | a0001 | c0007 | t0001 | g0155 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02055 | hp2 | a0001 | c0005 | t0003 | g0081 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0159 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02074 | hp2 | a0001 | c0007 | t0001 | g0214 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02145 | hp2 | a0001 | c0005 | t0003 | g0039 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | CDX | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CDX | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02257 | hp2 | a0001 | c0005 | t0003 | g0002 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02258 | hp2 | a0001 | c0005 | t0003 | g0012 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02280 | hp1 | a0001 | c0004 | t0002 | g0197 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02280 | hp2 | a0001 | c0005 | t0003 | g0065 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02293 | hp2 | a0002 | c0003 | t0001 | g0009 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02451 | hp1 | a0001 | c0004 | t0002 | g0234 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02451 | hp2 | a0001 | c0008 | t0003 | g0219 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02572 | hp1 | a0003 | c0006 | t0001 | g0310 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02572 | hp2 | a0001 | c0005 | t0003 | g0040 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02615 | hp2 | a0001 | c0005 | t0003 | g0080 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02622 | hp1 | a0001 | c0005 | t0003 | g0250 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02622 | hp2 | a0001 | c0005 | t0003 | g0043 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02630 | hp2 | a0003 | c0013 | t0003 | g0275 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0252 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02698 | hp1 | a0001 | c0004 | t0002 | g0196 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02738 | hp1 | a0001 | c0004 | t0002 | g0198 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02809 | hp1 | a0001 | c0010 | t0001 | g0049 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02818 | hp1 | a0005 | c0011 | t0001 | g0014 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02886 | hp1 | a0001 | c0005 | t0003 | g0249 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02896 | hp1 | a0001 | c0005 | t0003 | g0247 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02896 | hp2 | a0003 | c0006 | t0001 | g0279 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02897 | hp1 | a0001 | c0005 | t0003 | g0246 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0216 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02970 | hp1 | a0001 | c0005 | t0003 | g0272 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02970 | hp2 | a0003 | c0006 | t0001 | g0311 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02976 | hp1 | a0003 | c0006 | t0001 | g0274 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02976 | hp2 | a0003 | c0006 | t0002 | g0266 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0177 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03041 | hp1 | a0001 | c0009 | t0001 | g0260 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03098 | hp2 | a0001 | c0010 | t0001 | g0048 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03130 | hp1 | a0001 | c0004 | t0002 | g0255 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03130 | hp2 | a0001 | c0008 | t0003 | g0221 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0018 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03195 | hp1 | a0001 | c0005 | t0003 | g0254 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03195 | hp2 | a0003 | c0006 | t0001 | g0277 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0222 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03486 | hp1 | a0001 | c0005 | t0003 | g0078 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03486 | hp2 | a0001 | c0005 | t0003 | g0035 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0010 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03516 | hp1 | a0001 | c0008 | t0003 | g0220 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03540 | hp1 | a0001 | c0005 | t0003 | g0015 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03579 | hp1 | a0001 | c0005 | t0003 | g0077 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0176 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03688 | hp2 | a0001 | c0007 | t0006 | g0167 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03704 | hp1 | a0001 | c0004 | t0002 | g0283 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03704 | hp2 | a0001 | c0004 | t0002 | g0243 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03710 | hp1 | a0001 | c0004 | t0002 | g0202 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0179 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0173 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03834 | hp2 | a0001 | c0004 | t0002 | g0224 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0166 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03942 | hp2 | a0002 | c0003 | t0001 | g0258 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04184 | hp2 | a0001 | c0005 | t0003 | g0034 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04199 | hp2 | a0001 | c0004 | t0002 | g0209 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18522 | hp1 | a0004 | c0014 | t0001 | g0235 | AFR | YRI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18522 | hp2 | a0001 | c0005 | t0003 | g0012 | AFR | YRI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18945 | hp1 | a0002 | c0003 | t0001 | g0300 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0299 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18950 | hp1 | a0001 | c0004 | t0002 | g0089 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18950 | hp2 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18954 | hp1 | a0002 | c0003 | t0001 | g0057 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0297 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18961 | hp2 | a0001 | c0004 | t0002 | g0056 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18969 | hp1 | a0002 | c0003 | t0001 | g0298 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18970 | hp2 | a0001 | c0007 | t0001 | g0165 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18973 | hp2 | a0001 | c0004 | t0002 | g0094 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18978 | hp1 | a0002 | c0003 | t0001 | g0231 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18978 | hp2 | a0001 | c0007 | t0001 | g0071 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18991 | hp1 | a0002 | c0003 | t0001 | g0306 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18992 | hp2 | a0002 | c0003 | t0001 | g0076 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18994 | hp2 | a0001 | c0004 | t0002 | g0058 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18997 | hp2 | a0002 | c0003 | t0001 | g0305 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19009 | hp2 | a0001 | c0007 | t0001 | g0151 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | LWK | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0264 | AFR | LWK | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19043 | hp2 | a0001 | c0012 | t0001 | g0042 | AFR | LWK | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19057 | hp1 | a0002 | c0003 | t0001 | g0285 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19070 | hp2 | a0002 | c0003 | t0001 | g0307 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19076 | hp1 | a0002 | c0003 | t0001 | g0017 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19078 | hp1 | a0002 | c0003 | t0001 | g0301 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19084 | hp2 | a0001 | c0007 | t0001 | g0213 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0223 | AFR | YRI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19240 | hp2 | a0001 | c0005 | t0003 | g0079 | AFR | YRI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0253 | AFR | ASW | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ASW | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20805 | hp1 | a0001 | c0004 | t0002 | g0239 | EUR | TSI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | GIH | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0180 | SAS | GIH | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02109 | hp2 | a0001 | c0005 | t0003 | g0037 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02559 | hp2 | a0001 | c0005 | t0003 | g0041 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | USA | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG06807 | hp2 | a0001 | c0009 | t0001 | g0267 | AFR | USA | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20300 | hp1 | a0003 | c0006 | t0001 | g0278 | AFR | USA | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | USA | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA21309 | hp1 | a0001 | c0004 | t0002 | g0158 | AFR | LWK | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA21309 | hp2 | a0001 | c0004 | t0002 | g0061 | AFR | LWK | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0002 | g0026 | REF | REF | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| homoSapiens_grch38 | hp1 | a0002 | c0003 | t0001 | g0271 | REF | REF | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:168834321
|
G | A | 2 | a0003a0004 | 10 | HG01261.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
missense_variant | MODERATE | c.500G>A | p.Arg167Gln | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/16 | 510/2075 | 500/1521 | 167/506 | chr2 | 168834321 | ||
| chr2:168860868
|
C | T | 2 | a0004a0005 | 2 | HG02818.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.1253C>T | p.Ala418Val | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/16 | 1263/2075 | 1253/1521 | 418/506 | chr2 | 168860868 | ||
| chr2:168864867
|
G | A | 4 | a0001a0003a0004others(1): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
missense_variant | MODERATE | c.1418G>A | p.Gly473Glu | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 16/16 | 1428/2075 | 1418/1521 | 473/506 | chr2 | 168864867 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:168824641
|
C | T | 4 | a0001c0002a0001c0007a0001c0008others(1): Show | 62 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(59): Show |
synonymous_variant | LOW | c.121C>T | p.Leu41Leu | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/16 | 131/2075 | 121/1521 | 41/506 | chr2 | 168824641 | ||
| chr2:168834238
|
A | G | 4 | a0001c0009a0003c0006a0003c0013others(1): Show | 12 | HG01261.hp2 HG02572.hp1 HG02630.hp2 others(9): Show |
synonymous_variant | LOW | c.417A>G | p.Lys139Lys | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/16 | 427/2075 | 417/1521 | 139/506 | chr2 | 168834238 | ||
| chr2:168851317
|
C | T | 2 | a0001c0010a0001c0012 | 3 | HG02809.hp1 HG03098.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.768C>T | p.Asp256Asp | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/16 | 778/2075 | 768/1521 | 256/506 | chr2 | 168851317 | ||
| chr2:168859604
|
T | C | 3 | a0001c0005a0001c0008a0003c0013 | 33 | HG01255.hp2 HG01261.hp1 HG01516.hp1 others(30): Show |
synonymous_variant | LOW | c.1146T>C | p.Pro382Pro | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/16 | 1156/2075 | 1146/1521 | 382/506 | chr2 | 168859604 | ||
| chr2:168864871
|
A | G | 2 | a0001c0002a0001c0004 | 81 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
synonymous_variant | LOW | c.1422A>G | p.Gly474Gly | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 16/16 | 1432/2075 | 1422/1521 | 474/506 | chr2 | 168864871 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:168864986
|
A | G | 1 | a0001c0007t0006 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 16/16 | 16 | chr2 | 168864986 | |||||
| chr2:168865054
|
T | C | 1 | a0001c0001t0005 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*84T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 16/16 | 84 | chr2 | 168865054 | |||||
| chr2:168865130
|
A | G | 3 | a0001c0005t0003a0001c0008t0003a0003c0013t0003 | 33 | HG01255.hp2 HG01261.hp1 HG01516.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*160A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 16/16 | 160 | chr2 | 168865130 | |||||
| chr2:168865390
|
G | C | 1 | a0001c0001t0004 | 2 | HG02145.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*420G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 16/16 | 420 | chr2 | 168865390 | |||||
| chr2:168865434
|
A | T | 4 | a0001c0001t0002a0001c0002t0002a0001c0004t0002others(1): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*464A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 16/16 | 464 | chr2 | 168865434 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:168802741
|
G | T | 2 | a0003c0006t0001g0310a0003c0006t0001g0311 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.27+68G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168802741 | ||||||
| chr2:168803071
|
A | G | 26 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(23): Show | 27 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.27+398A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803071 | ||||||
| chr2:168803110
|
A | C | 4 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0004t0002g0283others(1): Show | 4 | HG00099.hp2 HG01074.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+437A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803110 | ||||||
| chr2:168803126
|
C | A | 28 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(25): Show | 29 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.27+453C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803126 | ||||||
| chr2:168803191
|
T | C | 2 | a0001c0001t0002g0016a0001c0005t0003g0002 | 3 | HG01884.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.27+518T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803191 | ||||||
| chr2:168803739
|
G | A | 2 | a0001c0001t0002g0016a0001c0005t0003g0002 | 3 | HG01884.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.27+1066G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803739 | ||||||
| chr2:168803747
|
T | A | 1 | a0002c0003t0001g0017 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.27+1074T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803747 | ||||||
| chr2:168803776
|
T | G | 3 | a0001c0005t0003g0015a0002c0003t0001g0018a0005c0011t0001g0014 | 3 | HG02818.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.27+1103T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803776 | ||||||
| chr2:168803847
|
T | C | 2 | a0001c0001t0002g0019a0001c0001t0002g0020 | 2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.27+1174T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803847 | ||||||
| chr2:168803912
|
T | A | 1 | a0001c0001t0002g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.27+1239T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803912 | ||||||
| chr2:168804022
|
A | T | 1 | a0001c0001t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.27+1349A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804022 | ||||||
| chr2:168804177
|
G | T | 5 | a0003c0006t0001g0276a0003c0006t0001g0277a0003c0006t0001g0278others(2): Show | 5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+1504G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804177 | ||||||
| chr2:168804260
|
C | T | 4 | a0001c0001t0001g0273a0003c0006t0001g0274a0003c0006t0001g0310others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+1587C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804260 | ||||||
| chr2:168804475
|
G | A | 14 | a0001c0001t0002g0022a0001c0004t0002g0026a0002c0003t0001g0003others(11): Show | 15 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.27+1802G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804475 | ||||||
| chr2:168804750
|
A | G | 29 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(26): Show | 30 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.27+2077A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804750 | ||||||
| chr2:168804922
|
T | C | 5 | a0003c0006t0001g0276a0003c0006t0001g0277a0003c0006t0001g0278others(2): Show | 5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+2249T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804922 | ||||||
| chr2:168804951
|
C | A | 310 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(307): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.27+2278C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804951 | ||||||
| chr2:168804966
|
G | T | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27+2293G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804966 | ||||||
| chr2:168805159
|
C | G | 9 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.27+2486C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168805159 | ||||||
| chr2:168805514
|
A | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.27+2841A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168805514 | ||||||
| chr2:168805687
|
A | G | 3 | a0001c0005t0003g0015a0002c0003t0001g0018a0005c0011t0001g0014 | 3 | HG02818.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.27+3014A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168805687 | ||||||
| chr2:168805789
|
A | G | 1 | a0001c0001t0001g0265 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.27+3116A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168805789 | ||||||
| chr2:168805815
|
C | T | 1 | a0001c0004t0002g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+3142C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168805815 | ||||||
| chr2:168806138
|
C | T | 2 | a0001c0005t0003g0262a0001c0005t0003g0263 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.27+3465C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806138 | ||||||
| chr2:168806183
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(4): Show | 8 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.27+3510G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806183 | ||||||
| chr2:168806226
|
G | A | 4 | a0001c0001t0001g0059a0001c0004t0002g0056a0001c0004t0002g0058others(1): Show | 4 | NA18954.hp1 NA18961.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+3553G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806226 | ||||||
| chr2:168806508
|
G | A | 2 | a0001c0001t0001g0060a0001c0004t0002g0061 | 2 | HG00733.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.27+3835G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806508 | ||||||
| chr2:168806530
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.27+3857C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806530 | ||||||
| chr2:168806572
|
GA | G | 24 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0002g0022others(21): Show | 26 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.27+3901delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 168806572 | |||||
| chr2:168806682
|
A | G | 1 | a0001c0009t0001g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27+4009A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806682 | ||||||
| chr2:168806787
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.27+4114T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806787 | ||||||
| chr2:168806899
|
C | G | 1 | a0001c0001t0001g0059 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.27+4226C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806899 | ||||||
| chr2:168806909
|
C | T | 2 | a0001c0005t0003g0015a0005c0011t0001g0014 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.27+4236C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806909 | ||||||
| chr2:168807283
|
G | C | 8 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0067others(5): Show | 8 | HG01496.hp2 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-4284G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807283 | ||||||
| chr2:168807517
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.28-4050G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807517 | ||||||
| chr2:168807613
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.28-3954T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807613 | ||||||
| chr2:168807717
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(188): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.28-3850G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807717 | ||||||
| chr2:168807733
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.28-3834C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807733 | ||||||
| chr2:168807742
|
G | A | 3 | a0001c0005t0003g0015a0002c0003t0001g0018a0005c0011t0001g0014 | 3 | HG02818.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.28-3825G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807742 | ||||||
| chr2:168807757
|
C | T | 1 | a0001c0002t0002g0232 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.28-3810C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807757 | ||||||
| chr2:168807948
|
A | C | 16 | a0001c0001t0002g0022a0001c0004t0002g0026a0002c0003t0001g0003others(13): Show | 17 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.28-3619A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807948 | ||||||
| chr2:168808019
|
A | C | 8 | a0001c0001t0001g0055a0001c0001t0001g0268a0001c0001t0001g0269others(5): Show | 8 | HG01891.hp1 HG02572.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-3548A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808019 | ||||||
| chr2:168808020
|
A | G | 26 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(23): Show | 27 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-3547A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808020 | ||||||
| chr2:168808449
|
C | G | 1 | a0002c0003t0001g0231 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.28-3118C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808449 | ||||||
| chr2:168808611
|
A | G | 37 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0238others(34): Show | 38 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.28-2956A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808611 | ||||||
| chr2:168808668
|
A | G | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.28-2899A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808668 | ||||||
| chr2:168808772
|
A | G | 1 | a0001c0001t0002g0257 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.28-2795A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808772 | ||||||
| chr2:168808797
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.28-2770T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808797 | ||||||
| chr2:168808810
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.28-2757A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808810 | ||||||
| chr2:168808853
|
A | G | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.28-2714A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808853 | ||||||
| chr2:168809527
|
A | G | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.28-2040A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168809527 | ||||||
| chr2:168809591
|
C | A | 2 | a0001c0005t0003g0015a0005c0011t0001g0014 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.28-1976C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168809591 | ||||||
| chr2:168809620
|
A | C | 1 | a0003c0006t0001g0311 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.28-1947A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168809620 | ||||||
| chr2:168810039
|
T | C | 5 | a0001c0001t0001g0055a0001c0001t0001g0273a0003c0006t0001g0274others(2): Show | 5 | HG01891.hp1 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-1528T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168810039 | ||||||
| chr2:168810235
|
A | G | 31 | a0001c0001t0001g0280a0001c0001t0001g0286a0001c0001t0001g0287others(28): Show | 32 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.28-1332A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168810235 | ||||||
| chr2:168810590
|
T | G | 1 | a0002c0003t0001g0285 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.28-977T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168810590 | ||||||
| chr2:168810918
|
A | C | 2 | a0001c0005t0003g0015a0005c0011t0001g0014 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.28-649A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168810918 | ||||||
| chr2:168810944
|
C | T | 3 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229 | 3 | HG02738.hp2 HG03490.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.28-623C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168810944 | ||||||
| chr2:168810945
|
G | A | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG00423.hp1 HG02027.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.28-622G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168810945 | ||||||
| chr2:168810985
|
T | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.28-582T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168810985 | ||||||
| chr2:168811182
|
T | G | 3 | a0001c0002t0002g0154a0001c0002t0002g0156a0001c0007t0001g0155 | 3 | HG00438.hp2 HG02015.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.28-385T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168811182 | ||||||
| chr2:168811284
|
A | T | 5 | a0003c0006t0001g0276a0003c0006t0001g0277a0003c0006t0001g0278others(2): Show | 5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-283A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168811284 | ||||||
| chr2:168811418
|
T | C | 1 | a0001c0007t0001g0071 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.28-149T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168811418 | ||||||
| chr2:168812010
|
G | A | 5 | a0003c0006t0001g0276a0003c0006t0001g0277a0003c0006t0001g0278others(2): Show | 5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+358G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812010 | ||||||
| chr2:168812118
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0002g0045a0001c0001t0002g0046others(2): Show | 6 | HG01074.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+466G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812118 | ||||||
| chr2:168812160
|
T | C | 6 | a0001c0001t0001g0055a0001c0001t0001g0273a0001c0001t0001g0280others(3): Show | 6 | HG01891.hp1 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+508T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812160 | ||||||
| chr2:168812451
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.113+799G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812451 | ||||||
| chr2:168812521
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.113+869T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812521 | ||||||
| chr2:168812532
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.113+880C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812532 | ||||||
| chr2:168812799
|
G | T | 1 | a0001c0002t0002g0226 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.113+1147G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812799 | ||||||
| chr2:168812952
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 119 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.113+1300G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812952 | ||||||
| chr2:168813014
|
AC | A | 80 | a0001c0001t0001g0162a0001c0001t0001g0192a0001c0001t0001g0201others(77): Show | 83 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.113+1363delC | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168813014 | ||||||
| chr2:168813067
|
A | G | 1 | a0001c0002t0002g0225 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.113+1415A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168813067 | ||||||
| chr2:168813198
|
C | T | 16 | a0001c0001t0002g0022a0001c0004t0002g0026a0002c0003t0001g0003others(13): Show | 17 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.113+1546C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168813198 | ||||||
| chr2:168813269
|
G | A | 26 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0238others(23): Show | 27 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.113+1617G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168813269 | ||||||
| chr2:168813451
|
T | C | 84 | a0001c0001t0001g0162a0001c0001t0001g0192a0001c0001t0001g0201others(81): Show | 87 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.113+1799T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168813451 | ||||||
| chr2:168813552
|
G | A | 1 | a0001c0002t0002g0159 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.113+1900G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168813552 | ||||||
| chr2:168813725
|
G | C | 1 | a0001c0005t0003g0034 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.113+2073G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168813725 | ||||||
| chr2:168813776
|
TACAAAGA others(9): Show |
T | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.113+2126_113+2141d others(18): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168813776 | |||||
| chr2:168814022
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.113+2370T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168814022 | ||||||
| chr2:168814051
|
A | C | 8 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(5): Show | 8 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.113+2399A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168814051 | ||||||
| chr2:168814219
|
C | T | 14 | a0001c0001t0002g0022a0001c0004t0002g0026a0002c0003t0001g0003others(11): Show | 15 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.113+2567C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168814219 | ||||||
| chr2:168814302
|
A | T | 2 | a0001c0005t0003g0015a0005c0011t0001g0014 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.113+2650A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168814302 | ||||||
| chr2:168814651
|
C | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0273a0003c0006t0001g0274others(2): Show | 5 | HG01891.hp1 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+2999C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168814651 | ||||||
| chr2:168814654
|
T | C | 1 | a0001c0005t0003g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.113+3002T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168814654 | ||||||
| chr2:168814693
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.113+3041A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168814693 | ||||||
| chr2:168814697
|
AAGG | A | 4 | a0001c0001t0001g0060a0001c0004t0002g0061a0001c0004t0002g0255others(1): Show | 4 | HG00733.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+3050_113+3052d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168814697 | |||||
| chr2:168815225
|
A | G | 29 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(26): Show | 30 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.113+3573A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168815225 | ||||||
| chr2:168815304
|
G | C | 2 | a0001c0005t0003g0015a0005c0011t0001g0014 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.113+3652G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168815304 | ||||||
| chr2:168815327
|
T | G | 1 | a0001c0004t0002g0160 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.113+3675T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168815327 | ||||||
| chr2:168815437
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.113+3785T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168815437 | ||||||
| chr2:168815443
|
C | G | 1 | a0001c0004t0002g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.113+3791C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168815443 | ||||||
| chr2:168815829
|
T | C | 4 | a0001c0001t0001g0060a0001c0004t0002g0061a0001c0004t0002g0255others(1): Show | 4 | HG00733.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+4177T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168815829 | ||||||
| chr2:168816037
|
G | T | 1 | a0001c0001t0001g0004 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.113+4385G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816037 | ||||||
| chr2:168816115
|
G | A | 5 | a0003c0006t0001g0276a0003c0006t0001g0277a0003c0006t0001g0278others(2): Show | 5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+4463G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816115 | ||||||
| chr2:168816123
|
A | G | 310 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(307): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.113+4471A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816123 | ||||||
| chr2:168816291
|
A | G | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG06807.hp1 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.113+4639A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816291 | ||||||
| chr2:168816369
|
C | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0060others(41): Show | 48 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.113+4717C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816369 | ||||||
| chr2:168816413
|
C | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG06807.hp1 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.113+4761C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816413 | ||||||
| chr2:168816515
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.113+4863G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816515 | ||||||
| chr2:168816899
|
G | A | 42 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(39): Show | 44 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.113+5247G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816899 | ||||||
| chr2:168817045
|
A | G | 2 | a0001c0005t0003g0262a0001c0005t0003g0263 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.113+5393A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817045 | ||||||
| chr2:168817066
|
G | A | 42 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(39): Show | 44 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.113+5414G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817066 | ||||||
| chr2:168817104
|
C | A | 42 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(39): Show | 44 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.113+5452C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817104 | ||||||
| chr2:168817108
|
A | G | 14 | a0001c0001t0002g0022a0001c0004t0002g0026a0002c0003t0001g0003others(11): Show | 15 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.113+5456A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817108 | ||||||
| chr2:168817289
|
CAG | C | 6 | a0001c0002t0002g0222a0001c0002t0002g0223a0001c0004t0002g0234others(3): Show | 6 | HG02451.hp1 HG02451.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+5640_113+5641d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168817289 | |||||
| chr2:168817301
|
G | A | 3 | a0001c0001t0001g0047a0001c0010t0001g0048a0001c0010t0001g0049 | 3 | HG02809.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.113+5649G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817301 | ||||||
| chr2:168817357
|
T | A | 120 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.113+5705T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817357 | ||||||
| chr2:168817379
|
G | A | 14 | a0001c0001t0002g0022a0001c0004t0002g0026a0002c0003t0001g0003others(11): Show | 15 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.113+5727G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817379 | ||||||
| chr2:168817383
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(166): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.113+5731A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817383 | ||||||
| chr2:168817469
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(166): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.113+5817A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817469 | ||||||
| chr2:168817498
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(166): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.113+5846A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817498 | ||||||
| chr2:168817557
|
AC | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(166): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.113+5906delC | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817557 | ||||||
| chr2:168817589
|
C | T | 5 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0004t0002g0230others(2): Show | 5 | HG00099.hp2 HG01074.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+5937C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817589 | ||||||
| chr2:168817632
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.113+5980T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817632 | ||||||
| chr2:168817645
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.113+5993T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817645 | ||||||
| chr2:168817665
|
C | T | 1 | a0001c0001t0001g0309 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.113+6013C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817665 | ||||||
| chr2:168817669
|
C | T | 14 | a0001c0001t0002g0022a0001c0004t0002g0026a0002c0003t0001g0003others(11): Show | 15 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.113+6017C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817669 | ||||||
| chr2:168817672
|
T | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.113+6020T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817672 | ||||||
| chr2:168817869
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(170): Show | 181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.113+6217A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817869 | ||||||
| chr2:168818145
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(279): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.114-6489T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818145 | ||||||
| chr2:168818153
|
A | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(279): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.114-6481A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818153 | ||||||
| chr2:168818180
|
T | G | 18 | a0001c0001t0001g0004a0001c0001t0001g0286a0001c0001t0001g0287others(15): Show | 20 | HG00558.hp2 HG00673.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.114-6454T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818180 | ||||||
| chr2:168818206
|
T | G | 8 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(5): Show | 8 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.114-6428T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818206 | ||||||
| chr2:168818254
|
C | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.114-6380C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818254 | ||||||
| chr2:168818296
|
G | C | 72 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0068others(69): Show | 75 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.114-6338G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818296 | ||||||
| chr2:168818547
|
C | G | 9 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(6): Show | 9 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.114-6087C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818547 | ||||||
| chr2:168818598
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0273a0001c0001t0002g0045others(1): Show | 5 | HG01891.hp1 HG02615.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-6036G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818598 | ||||||
| chr2:168818600
|
G | A | 1 | a0002c0003t0001g0017 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.114-6034G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818600 | ||||||
| chr2:168818615
|
T | C | 1 | a0001c0009t0001g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.114-6019T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818615 | ||||||
| chr2:168818841
|
A | AT | 227 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(224): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.114-5786dupT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168818841 | |||||
| chr2:168818952
|
AAT | A | 20 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(17): Show | 21 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.114-5675_114-5674d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168818952 | |||||
| chr2:168819046
|
G | GA | 302 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(299): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.114-5581dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168819046 | |||||
| chr2:168819056
|
C | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(223): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.114-5578C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819056 | ||||||
| chr2:168819083
|
G | A | 1 | a0002c0003t0001g0009 | 2 | HG01516.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.114-5551G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819083 | ||||||
| chr2:168819109
|
T | C | 13 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(10): Show | 15 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.114-5525T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819109 | ||||||
| chr2:168819251
|
G | A | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.114-5383G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819251 | ||||||
| chr2:168819347
|
C | T | 2 | a0001c0007t0001g0213a0001c0007t0001g0214 | 2 | HG02074.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.114-5287C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819347 | ||||||
| chr2:168819377
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.114-5257A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819377 | ||||||
| chr2:168819454
|
C | G | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.114-5180C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819454 | ||||||
| chr2:168819535
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(220): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.114-5099G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819535 | ||||||
| chr2:168819575
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.114-5059T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819575 | ||||||
| chr2:168819843
|
G | T | 2 | a0002c0003t0001g0252a0002c0003t0001g0253 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.114-4791G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819843 | ||||||
| chr2:168819900
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.114-4734A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819900 | ||||||
| chr2:168819957
|
C | G | 1 | a0001c0001t0001g0144 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.114-4677C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819957 | ||||||
| chr2:168819965
|
C | T | 3 | a0001c0001t0001g0047a0001c0010t0001g0048a0001c0010t0001g0049 | 3 | HG02809.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.114-4669C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819965 | ||||||
| chr2:168820011
|
T | C | 310 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(307): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.114-4623T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820011 | ||||||
| chr2:168820071
|
G | T | 2 | a0001c0005t0003g0262a0001c0005t0003g0263 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.114-4563G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820071 | ||||||
| chr2:168820241
|
C | T | 86 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0162others(83): Show | 89 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.114-4393C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820241 | ||||||
| chr2:168820258
|
G | A | 5 | a0001c0001t0001g0047a0001c0001t0001g0215a0001c0001t0002g0217others(2): Show | 5 | HG02145.hp1 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-4376G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820258 | ||||||
| chr2:168820276
|
T | A | 1 | a0001c0001t0001g0146 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.114-4358T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820276 | ||||||
| chr2:168820374
|
G | A | 14 | a0001c0001t0002g0022a0001c0004t0002g0026a0002c0003t0001g0003others(11): Show | 15 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.114-4260G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820374 | ||||||
| chr2:168820718
|
C | CA | 169 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(166): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.114-3903dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168820718 | |||||
| chr2:168820718
|
C | CAA | 100 | a0001c0001t0001g0075a0001c0001t0001g0082a0001c0001t0001g0083others(97): Show | 103 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.114-3904_114-3903d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168820718 | |||||
| chr2:168820718
|
C | CAAA | 12 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0215others(9): Show | 13 | HG01891.hp1 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.114-3905_114-3903d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168820718 | |||||
| chr2:168820734
|
C | T | 3 | a0001c0009t0001g0260a0002c0003t0001g0252a0002c0003t0001g0253 | 3 | HG02647.hp1 HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.114-3900C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820734 | ||||||
| chr2:168820760
|
A | AC | 4 | a0001c0001t0001g0052a0001c0001t0001g0060a0001c0004t0002g0294others(1): Show | 4 | HG00673.hp2 HG00733.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-3870dupC | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168820760 | |||||
| chr2:168820778
|
C | A | 1 | a0002c0003t0001g0147 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.114-3856C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820778 | ||||||
| chr2:168820788
|
C | T | 1 | a0002c0003t0001g0017 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.114-3846C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820788 | ||||||
| chr2:168820835
|
G | A | 1 | a0001c0005t0003g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.114-3799G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820835 | ||||||
| chr2:168820918
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.114-3716T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820918 | ||||||
| chr2:168820943
|
C | T | 1 | a0002c0003t0001g0147 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.114-3691C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820943 | ||||||
| chr2:168820948
|
A | T | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.114-3686A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820948 | ||||||
| chr2:168821010
|
G | T | 2 | a0001c0004t0002g0255a0001c0005t0003g0254 | 2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.114-3624G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168821010 | ||||||
| chr2:168821687
|
C | T | 82 | a0001c0001t0001g0192a0001c0001t0001g0201a0001c0001t0001g0212others(79): Show | 85 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.114-2947C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168821687 | ||||||
| chr2:168821688
|
G | A | 20 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(17): Show | 21 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.114-2946G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168821688 | ||||||
| chr2:168821702
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | NA18960.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.114-2932G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168821702 | ||||||
| chr2:168821863
|
C | T | 4 | a0001c0001t0002g0050a0001c0009t0001g0260a0002c0003t0001g0252others(1): Show | 4 | HG02647.hp1 HG03041.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-2771C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168821863 | ||||||
| chr2:168821982
|
T | C | 1 | a0002c0003t0001g0252 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.114-2652T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168821982 | ||||||
| chr2:168822051
|
C | T | 4 | a0001c0001t0001g0063a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | NA18948.hp2 NA18992.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-2583C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822051 | ||||||
| chr2:168822171
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(225): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.114-2463T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822171 | ||||||
| chr2:168822182
|
T | C | 4 | a0001c0001t0001g0060a0001c0004t0002g0061a0001c0004t0002g0255others(1): Show | 4 | HG00733.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-2452T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822182 | ||||||
| chr2:168822195
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.114-2439T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822195 | ||||||
| chr2:168822347
|
GA | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.114-2277delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168822347 | |||||
| chr2:168822418
|
A | G | 1 | a0001c0002t0002g0210 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.114-2216A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822418 | ||||||
| chr2:168822491
|
A | G | 1 | a0002c0003t0001g0076 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.114-2143A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822491 | ||||||
| chr2:168822540
|
A | G | 2 | a0002c0003t0001g0252a0002c0003t0001g0253 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.114-2094A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822540 | ||||||
| chr2:168822675
|
C | T | 1 | a0001c0004t0002g0209 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.114-1959C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822675 | ||||||
| chr2:168822971
|
C | G | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG06807.hp1 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.114-1663C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822971 | ||||||
| chr2:168822972
|
A | C | 1 | a0001c0001t0002g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.114-1662A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822972 | ||||||
| chr2:168823085
|
T | G | 12 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0082others(9): Show | 12 | HG01943.hp1 HG02056.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-1549T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823085 | ||||||
| chr2:168823174
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(299): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.114-1460A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823174 | ||||||
| chr2:168823217
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 7 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.114-1417T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823217 | ||||||
| chr2:168823238
|
G | A | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.114-1396G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823238 | ||||||
| chr2:168823251
|
T | CGTGATCC others(127): Show |
1 | a0001c0002t0002g0308 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.114-1384_114-1383i others(136): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823251 | ||||||
| chr2:168823279
|
A | G | 1 | a0001c0004t0002g0255 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.114-1355A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823279 | ||||||
| chr2:168823307
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | HG02056.hp1 HG02071.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.114-1327C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823307 | ||||||
| chr2:168823347
|
A | C | 1 | a0001c0002t0002g0303 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.114-1287A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823347 | ||||||
| chr2:168823569
|
G | A | 17 | a0001c0001t0002g0022a0001c0004t0002g0026a0001c0005t0003g0015others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.114-1065G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823569 | ||||||
| chr2:168823577
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0273 | 3 | HG01891.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.114-1057A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823577 | ||||||
| chr2:168823612
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(226): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.114-1022C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823612 | ||||||
| chr2:168823847
|
C | T | 1 | a0001c0001t0002g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.114-787C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823847 | ||||||
| chr2:168823869
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.114-765G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823869 | ||||||
| chr2:168824173
|
T | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02602.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.114-461T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168824173 | ||||||
| chr2:168824267
|
A | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(234): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.114-367A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168824267 | ||||||
| chr2:168824456
|
G | A | 1 | a0004c0014t0001g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.114-178G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168824456 | ||||||
| chr2:168824610
|
A | G | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.114-24A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168824610 | ||||||
| chr2:168824725
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA20129.hp2 | splice_region_variant&intron_variant | LOW | c.197+8T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168824725 | ||||||
| chr2:168824760
|
T | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0273a0001c0001t0002g0045others(1): Show | 5 | HG01891.hp1 HG02615.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.197+43T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168824760 | ||||||
| chr2:168824768
|
T | TTTTGTTT others(1): Show |
60 | a0001c0001t0001g0004a0001c0001t0001g0192a0001c0001t0001g0201others(57): Show | 64 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.197+67_197+74dupGT others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 168824768 | |||||
| chr2:168824768
|
T | TTTTGTTT others(5): Show |
153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.197+63_197+74dupGT others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 168824768 | |||||
| chr2:168824768
|
T | TTTTGTTT others(9): Show |
14 | a0001c0001t0001g0062a0001c0001t0001g0082a0001c0001t0001g0090others(11): Show | 14 | HG01993.hp2 HG02056.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.197+59_197+74dupGT others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 168824768 | |||||
| chr2:168824768
|
T | TTTTGTTT others(13): Show |
1 | a0001c0001t0001g0088 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.197+55_197+74dupGT others(18): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 168824768 | |||||
| chr2:168824833
|
G | T | 5 | a0003c0006t0001g0276a0003c0006t0001g0277a0003c0006t0001g0278others(2): Show | 5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.197+116G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168824833 | ||||||
| chr2:168824888
|
C | T | 2 | a0001c0004t0002g0044a0001c0004t0002g0234 | 2 | HG01074.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.197+171C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168824888 | ||||||
| chr2:168824915
|
G | A | 2 | a0001c0002t0002g0163a0001c0002t0002g0164 | 2 | HG01109.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.197+198G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168824915 | ||||||
| chr2:168824916
|
G | C | 2 | a0001c0002t0002g0163a0001c0002t0002g0164 | 2 | HG01109.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.197+199G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168824916 | ||||||
| chr2:168825019
|
A | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.197+302A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168825019 | ||||||
| chr2:168825239
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 186 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.197+522G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168825239 | ||||||
| chr2:168825397
|
G | A | 2 | a0001c0001t0002g0016a0001c0005t0003g0002 | 3 | HG01884.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.197+680G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168825397 | ||||||
| chr2:168825668
|
TA | T | 5 | a0001c0005t0003g0077a0001c0005t0003g0078a0001c0005t0003g0079others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+952delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168825668 | ||||||
| chr2:168825745
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.197+1028T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168825745 | ||||||
| chr2:168825867
|
A | G | 5 | a0003c0006t0001g0276a0003c0006t0001g0277a0003c0006t0001g0278others(2): Show | 5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.197+1150A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168825867 | ||||||
| chr2:168826200
|
C | T | 33 | a0001c0001t0001g0192a0001c0001t0001g0201a0001c0001t0001g0212others(30): Show | 35 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.197+1483C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826200 | ||||||
| chr2:168826220
|
G | GAGAGGTA others(1): Show |
27 | a0001c0001t0001g0192a0001c0001t0001g0201a0001c0001t0001g0212others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.197+1505_197+1506i others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 168826220 | |||||
| chr2:168826220
|
G | GAGGGGTG others(1): Show |
270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(267): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.197+1512_197+1519d others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 168826220 | |||||
| chr2:168826221
|
A | AGAGGTAT | 4 | a0002c0003t0001g0009a0002c0003t0001g0011a0002c0003t0001g0258others(1): Show | 6 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.197+1505_197+1506i others(9): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 168826221 | |||||
| chr2:168826354
|
A | T | 2 | a0001c0002t0002g0156a0001c0007t0001g0155 | 2 | HG00438.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.197+1637A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826354 | ||||||
| chr2:168826446
|
T | C | 81 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0067others(78): Show | 84 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.198-1712T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826446 | ||||||
| chr2:168826456
|
T | C | 112 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0067others(109): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.198-1702T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826456 | ||||||
| chr2:168826479
|
T | C | 1 | a0001c0001t0002g0100 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.198-1679T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826479 | ||||||
| chr2:168826527
|
C | T | 1 | a0001c0004t0002g0058 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.198-1631C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826527 | ||||||
| chr2:168826551
|
G | A | 31 | a0001c0001t0001g0192a0001c0001t0001g0201a0001c0001t0001g0212others(28): Show | 33 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.198-1607G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826551 | ||||||
| chr2:168826698
|
G | A | 2 | a0001c0001t0002g0016a0001c0005t0003g0002 | 3 | HG01884.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.198-1460G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826698 | ||||||
| chr2:168826915
|
C | T | 8 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0090others(5): Show | 8 | HG01943.hp1 HG02056.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.198-1243C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826915 | ||||||
| chr2:168827041
|
G | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02074.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.198-1117G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827041 | ||||||
| chr2:168827141
|
C | G | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.198-1017C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827141 | ||||||
| chr2:168827160
|
C | G | 1 | a0004c0014t0001g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.198-998C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827160 | ||||||
| chr2:168827241
|
A | G | 1 | a0003c0006t0002g0266 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.198-917A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827241 | ||||||
| chr2:168827417
|
G | A | 45 | a0001c0001t0001g0192a0001c0001t0001g0201a0001c0001t0001g0212others(42): Show | 48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.198-741G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827417 | ||||||
| chr2:168827471
|
A | G | 1 | a0004c0014t0001g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.198-687A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827471 | ||||||
| chr2:168827598
|
C | T | 8 | a0001c0004t0002g0234a0001c0005t0003g0012a0001c0005t0003g0246others(5): Show | 9 | HG01255.hp2 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-560C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827598 | ||||||
| chr2:168827606
|
C | T | 5 | a0003c0006t0001g0276a0003c0006t0001g0277a0003c0006t0001g0278others(2): Show | 5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.198-552C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827606 | ||||||
| chr2:168827632
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18997.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.198-526G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827632 | ||||||
| chr2:168827713
|
G | A | 1 | a0001c0004t0002g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.198-445G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827713 | ||||||
| chr2:168827947
|
A | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.198-211A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827947 | ||||||
| chr2:168827952
|
G | C | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.198-206G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827952 | ||||||
| chr2:168827960
|
G | A | 1 | a0001c0004t0002g0239 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.198-198G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827960 | ||||||
| chr2:168828123
|
A | G | 18 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(15): Show | 19 | HG00423.hp1 HG00673.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-35A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168828123 | ||||||
| chr2:168828240
|
C | G | 8 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0090others(5): Show | 8 | HG01943.hp1 HG02056.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.260+20C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 4/15 | chr2 | 168828240 | ||||||
| chr2:168828761
|
A | G | 1 | a0002c0003t0001g0147 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.342+260A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168828761 | ||||||
| chr2:168828762
|
A | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(215): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.342+261A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168828762 | ||||||
| chr2:168828776
|
A | G | 1 | a0001c0002t0002g0303 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.342+275A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168828776 | ||||||
| chr2:168828819
|
T | C | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.342+318T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168828819 | ||||||
| chr2:168829246
|
A | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.342+745A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168829246 | ||||||
| chr2:168829343
|
G | A | 1 | a0001c0002t0002g0166 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.342+842G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168829343 | ||||||
| chr2:168829477
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.342+976C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168829477 | ||||||
| chr2:168829518
|
G | A | 3 | a0001c0001t0002g0050a0002c0003t0001g0252a0002c0003t0001g0253 | 3 | HG02647.hp1 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.342+1017G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168829518 | ||||||
| chr2:168829520
|
T | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 297 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.342+1019T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168829520 | ||||||
| chr2:168829619
|
C | T | 7 | a0001c0005t0003g0012a0001c0005t0003g0246a0001c0005t0003g0247others(4): Show | 8 | HG01255.hp2 HG01884.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.342+1118C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168829619 | ||||||
| chr2:168829789
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.342+1288A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168829789 | ||||||
| chr2:168830049
|
C | T | 99 | a0001c0001t0001g0201a0001c0001t0001g0212a0001c0001t0002g0281others(96): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.343-1423C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830049 | ||||||
| chr2:168830148
|
G | A | 2 | a0003c0006t0001g0310a0003c0006t0001g0311 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.343-1324G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830148 | ||||||
| chr2:168830293
|
T | C | 1 | a0001c0007t0006g0167 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.343-1179T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830293 | ||||||
| chr2:168830547
|
G | T | 1 | a0001c0002t0002g0191 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.343-925G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830547 | ||||||
| chr2:168830637
|
A | G | 1 | a0001c0004t0002g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.343-835A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830637 | ||||||
| chr2:168830701
|
T | C | 5 | a0003c0006t0001g0276a0003c0006t0001g0277a0003c0006t0001g0278others(2): Show | 5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-771T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830701 | ||||||
| chr2:168830831
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 149 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.343-641C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830831 | ||||||
| chr2:168830849
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 90 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.343-623G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830849 | ||||||
| chr2:168830909
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.343-563A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830909 | ||||||
| chr2:168831170
|
A | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.343-302A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168831170 | ||||||
| chr2:168831247
|
A | C | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.343-225A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168831247 | ||||||
| chr2:168831558
|
G | T | 1 | a0001c0004t0002g0058 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.405+24G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168831558 | ||||||
| chr2:168831645
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.405+111T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168831645 | ||||||
| chr2:168831869
|
A | G | 2 | a0003c0006t0002g0266a0004c0014t0001g0235 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.405+335A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168831869 | ||||||
| chr2:168832189
|
AATTTAGT others(7): Show |
A | 11 | a0001c0001t0001g0036a0001c0001t0001g0192a0001c0005t0003g0034others(8): Show | 11 | HG01123.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.405+658_405+671del others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 168832189 | |||||
| chr2:168832209
|
G | A | 1 | a0003c0006t0002g0266 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.405+675G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168832209 | ||||||
| chr2:168832237
|
G | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 208 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.405+703G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168832237 | ||||||
| chr2:168832370
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.405+836G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168832370 | ||||||
| chr2:168832532
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.405+998G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168832532 | ||||||
| chr2:168832760
|
G | T | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.405+1226G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168832760 | ||||||
| chr2:168832822
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.405+1288A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168832822 | ||||||
| chr2:168832837
|
A | G | 77 | a0001c0001t0001g0201a0001c0001t0001g0212a0001c0001t0002g0281others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.405+1303A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168832837 | ||||||
| chr2:168833022
|
T | C | 33 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0068others(30): Show | 34 | HG00642.hp2 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.406-1205T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833022 | ||||||
| chr2:168833131
|
G | A | 12 | a0001c0009t0001g0260a0001c0009t0001g0267a0003c0006t0001g0274others(9): Show | 12 | HG01261.hp2 HG02572.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.406-1096G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833131 | ||||||
| chr2:168833166
|
C | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(163): Show | 175 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.406-1061C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833166 | ||||||
| chr2:168833220
|
G | A | 19 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(16): Show | 20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.406-1007G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833220 | ||||||
| chr2:168833261
|
G | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 208 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.406-966G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833261 | ||||||
| chr2:168833267
|
C | G | 3 | a0003c0006t0001g0274a0003c0006t0001g0310a0003c0006t0001g0311 | 3 | HG02572.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.406-960C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833267 | ||||||
| chr2:168833396
|
C | G | 1 | a0001c0001t0001g0092 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.406-831C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833396 | ||||||
| chr2:168833425
|
C | G | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.406-802C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833425 | ||||||
| chr2:168833532
|
T | C | 1 | a0002c0003t0001g0018 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.406-695T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833532 | ||||||
| chr2:168833579
|
C | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(285): Show | 299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.406-648C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833579 | ||||||
| chr2:168833705
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.406-522G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833705 | ||||||
| chr2:168833748
|
G | T | 2 | a0003c0006t0001g0310a0003c0006t0001g0311 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.406-479G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833748 | ||||||
| chr2:168833816
|
CA | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 208 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.406-408delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 168833816 | |||||
| chr2:168833899
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.406-328T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833899 | ||||||
| chr2:168833912
|
A | G | 1 | a0001c0004t0002g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.406-315A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833912 | ||||||
| chr2:168834001
|
G | A | 1 | a0002c0003t0001g0023 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.406-226G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168834001 | ||||||
| chr2:168834118
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.406-109A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168834118 | ||||||
| chr2:168834219
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(182): Show | 195 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
splice_region_variant&intron_variant | LOW | c.406-8T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168834219 | ||||||
| chr2:168834406
|
G | A | 1 | a0001c0002t0002g0205 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.504+81G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834406 | ||||||
| chr2:168834479
|
C | A | 1 | a0001c0002t0002g0168 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.504+154C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834479 | ||||||
| chr2:168834490
|
T | C | 19 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(16): Show | 20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.504+165T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834490 | ||||||
| chr2:168834490
|
T | TGC | 5 | a0001c0005t0003g0015a0002c0003t0001g0009a0002c0003t0001g0018others(2): Show | 6 | HG01099.hp1 HG01496.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+182_504+183dup others(2): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834490 | |||||
| chr2:168834493
|
GCGCGCGC others(15): Show |
G | 1 | a0002c0003t0001g0306 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.504+170_504+191del others(22): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834493 | |||||
| chr2:168834493
|
GCGCGCGC others(17): Show |
G | 18 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(15): Show | 19 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.504+170_504+193del others(24): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834493 | |||||
| chr2:168834497
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.504+172G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834497 | ||||||
| chr2:168834499
|
G | GCACACAC others(5): Show |
7 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(4): Show | 8 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.504+175_504+176ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834499 | |||||
| chr2:168834499
|
G | GCACACAC others(7): Show |
1 | a0001c0004t0002g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.504+175_504+176ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834499 | |||||
| chr2:168834499
|
G | GCGCACAC others(9): Show |
3 | a0003c0006t0001g0276a0003c0006t0001g0279a0003c0013t0003g0275 | 3 | HG01261.hp2 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.504+177_504+178ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834499 | |||||
| chr2:168834499
|
G | GCGCGCAC others(9): Show |
1 | a0004c0014t0001g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.504+179_504+180ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834499 | |||||
| chr2:168834500
|
C | T | 2 | a0001c0001t0001g0060a0001c0004t0002g0061 | 2 | HG00733.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.504+175C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834500 | ||||||
| chr2:168834501
|
G | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(13): Show | 17 | HG01070.hp1 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.504+176G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834501 | ||||||
| chr2:168834501
|
G | GCACACAC others(3): Show |
5 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 5 | HG00438.hp1 HG01261.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.504+177_504+178ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834501 | |||||
| chr2:168834501
|
G | GCACACAC others(5): Show |
41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(38): Show | 46 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.504+177_504+178ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834501 | |||||
| chr2:168834501
|
G | GCACACAC others(7): Show |
10 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0273others(7): Show | 11 | HG01168.hp2 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.504+177_504+178ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834501 | |||||
| chr2:168834501
|
G | GCACACAC others(9): Show |
1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.504+177_504+178ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834501 | |||||
| chr2:168834502
|
C | A | 1 | a0001c0007t0001g0071 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.504+177C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834502 | ||||||
| chr2:168834503
|
G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(153): Show | 165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.504+178G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834503 | ||||||
| chr2:168834503
|
G | GCACA | 3 | a0001c0008t0003g0219a0001c0008t0003g0220a0001c0008t0003g0221 | 3 | HG02451.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.504+179_504+180ins others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834503 | |||||
| chr2:168834503
|
G | GCACACAC others(3): Show |
1 | a0003c0006t0001g0274 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.504+179_504+180ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834503 | |||||
| chr2:168834503
|
G | GCACACAC others(9): Show |
1 | a0003c0006t0002g0266 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.504+179_504+180ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834503 | |||||
| chr2:168834505
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(162): Show | 173 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.504+180G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834505 | ||||||
| chr2:168834505
|
G | GCACACAC others(7): Show |
1 | a0001c0005t0003g0034 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.504+181_504+182ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834505 | |||||
| chr2:168834505
|
G | GCAGCGCG others(12): Show |
1 | a0001c0002t0002g0169 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.504+181_504+182ins others(19): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834505 | |||||
| chr2:168834507
|
G | A | 133 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0047others(130): Show | 136 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.504+182G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834507 | ||||||
| chr2:168834507
|
G | GCACACAC others(3): Show |
4 | a0001c0002t0002g0170a0001c0002t0002g0191a0001c0002t0002g0308others(1): Show | 4 | HG00408.hp1 HG01168.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+208_504+217dup others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCAGCGCG others(20): Show |
1 | a0001c0005t0003g0262 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.504+184_504+185ins others(27): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCACAC others(3): Show |
3 | a0001c0002t0002g0207a0001c0002t0002g0232a0001c0004t0002g0283 | 3 | HG00621.hp1 HG03704.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.504+183_504+184ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCACAC others(5): Show |
8 | a0001c0001t0001g0270a0001c0002t0002g0173a0001c0002t0002g0174others(5): Show | 8 | HG01070.hp1 HG01074.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.504+183_504+184ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCACAC others(7): Show |
3 | a0001c0001t0001g0036a0001c0004t0002g0230a0001c0004t0002g0255 | 3 | HG01175.hp2 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.504+183_504+184ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCACAC others(9): Show |
1 | a0001c0005t0003g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+183_504+184ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCAC others(3): Show |
4 | a0001c0001t0001g0201a0001c0002t0002g0159a0001c0002t0002g0182others(1): Show | 4 | HG02071.hp2 HG02602.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+183_504+184ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCAC others(5): Show |
7 | a0001c0002t0002g0179a0001c0002t0002g0180a0001c0002t0002g0181others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.504+183_504+184ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCAC others(7): Show |
12 | a0001c0002t0002g0177a0001c0002t0002g0178a0001c0002t0002g0205others(9): Show | 12 | HG00323.hp1 HG02015.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.504+183_504+184ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCAC others(9): Show |
1 | a0001c0002t0002g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.504+183_504+184ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCAC others(11): Show |
1 | a0001c0002t0002g0208 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.504+183_504+184ins others(18): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCAC others(13): Show |
1 | a0001c0002t0002g0175 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.504+183_504+184ins others(20): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCGC others(3): Show |
1 | a0001c0004t0002g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.504+183_504+184ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCGC others(5): Show |
6 | a0001c0002t0002g0073a0001c0002t0002g0161a0001c0002t0002g0187others(3): Show | 6 | HG00738.hp1 HG03688.hp2 NA19054.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+183_504+184ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCGC others(7): Show |
8 | a0001c0002t0002g0072a0001c0002t0002g0156a0001c0002t0002g0164others(5): Show | 8 | HG00438.hp2 HG01256.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.504+183_504+184ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCGC others(9): Show |
2 | a0001c0002t0002g0163a0001c0002t0002g0166 | 2 | HG01109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.504+183_504+184ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCGC others(11): Show |
1 | a0001c0002t0002g0183 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.504+183_504+184ins others(18): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCGC others(7): Show |
2 | a0001c0001t0001g0212a0001c0002t0002g0168 | 2 | HG00673.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.504+183_504+184ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCGC others(9): Show |
1 | a0001c0002t0002g0190 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.504+183_504+184ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCGC others(11): Show |
1 | a0001c0002t0002g0189 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.504+183_504+184ins others(18): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCGC others(5): Show |
1 | a0001c0005t0003g0272 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.504+183_504+184ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCGC others(19): Show |
1 | a0001c0001t0001g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.504+183_504+184ins others(26): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
G | GCGCGCGC others(21): Show |
1 | a0001c0005t0003g0263 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.504+183_504+184ins others(28): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834507
|
GCA | G | 10 | a0001c0004t0002g0026a0002c0003t0001g0003a0002c0003t0001g0017others(7): Show | 11 | HG00099.hp1 HG01069.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.504+216_504+217del others(2): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | |||||
| chr2:168834509
|
A | ACACACAC others(3): Show |
3 | a0001c0001t0001g0280a0001c0001t0002g0045a0001c0001t0002g0046 | 3 | HG02615.hp1 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.504+193_504+194ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834509 | |||||
| chr2:168834509
|
A | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0055others(39): Show | 46 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.504+184A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834509 | ||||||
| chr2:168834511
|
A | ACACACAC others(5): Show |
2 | a0001c0001t0001g0105a0001c0001t0001g0293 | 2 | HG03831.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.504+195_504+196ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834511 | |||||
| chr2:168834511
|
A | ACACACAC others(1): Show |
4 | a0001c0001t0001g0215a0001c0001t0002g0217a0001c0001t0004g0216others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+193_504+194ins others(8): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834511 | |||||
| chr2:168834511
|
A | ACACACAC others(3): Show |
47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0059others(44): Show | 48 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.504+193_504+194ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834511 | |||||
| chr2:168834511
|
A | ACACACG | 4 | a0001c0001t0001g0047a0001c0009t0001g0267a0001c0010t0001g0048others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+191_504+192ins others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834511 | |||||
| chr2:168834511
|
A | G | 1 | a0001c0004t0002g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.504+186A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834511 | ||||||
| chr2:168834513
|
A | ACACACGC others(1): Show |
8 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0139others(5): Show | 8 | HG02056.hp2 HG03209.hp1 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.504+193_504+194ins others(8): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834513 | |||||
| chr2:168834517
|
A | ACGCGCAC others(3): Show |
1 | a0001c0001t0001g0091 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.504+193_504+194ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834517 | |||||
| chr2:168834541
|
A | ACACACAC others(4): Show |
1 | a0001c0004t0002g0241 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.504+217_504+218ins others(11): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834541 | |||||
| chr2:168834541
|
A | ACACACAC others(11): Show |
1 | a0001c0001t0002g0245 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.504+217_504+218ins others(18): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834541 | |||||
| chr2:168834541
|
A | ACACACAC others(7): Show |
2 | a0001c0001t0001g0060a0001c0001t0002g0101 | 2 | HG00733.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.504+217_504+218ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834541 | |||||
| chr2:168834541
|
A | ACACACAC others(5): Show |
7 | a0001c0001t0001g0145a0001c0001t0002g0064a0001c0001t0002g0102others(4): Show | 7 | HG00642.hp2 HG00735.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+217_504+218ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834541 | |||||
| chr2:168834541
|
A | ACACACAC others(3): Show |
5 | a0001c0001t0001g0240a0001c0005t0003g0246a0001c0005t0003g0247others(2): Show | 5 | HG01255.hp2 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.504+217_504+218ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834541 | |||||
| chr2:168834541
|
A | ACACACAC others(1): Show |
10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0002g0022others(7): Show | 11 | HG01358.hp2 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.504+217_504+218ins others(8): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834541 | |||||
| chr2:168834541
|
A | ACACACC | 4 | a0001c0001t0001g0244a0001c0001t0002g0021a0001c0001t0002g0066others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+217_504+218ins others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834541 | |||||
| chr2:168834541
|
A | C | 21 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(18): Show | 22 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.504+216A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834541 | ||||||
| chr2:168834542
|
C | CACACACA others(6): Show |
1 | a0001c0002t0002g0172 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.504+217_504+218ins others(13): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834542 | ||||||
| chr2:168834600
|
G | GC | 11 | a0001c0001t0001g0036a0001c0001t0001g0192a0001c0005t0003g0034others(8): Show | 11 | HG01123.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.504+278dupC | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834600 | |||||
| chr2:168834677
|
A | G | 8 | a0001c0005t0003g0012a0001c0005t0003g0246a0001c0005t0003g0247others(5): Show | 9 | HG01255.hp2 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.504+352A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834677 | ||||||
| chr2:168834762
|
A | G | 9 | a0001c0001t0001g0063a0001c0001t0001g0082a0001c0001t0001g0088others(6): Show | 9 | HG01943.hp1 HG02056.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.504+437A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834762 | ||||||
| chr2:168834773
|
A | C | 1 | a0001c0001t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.504+448A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834773 | ||||||
| chr2:168834802
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.504+477A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834802 | ||||||
| chr2:168835030
|
C | G | 9 | a0001c0001t0001g0063a0001c0001t0001g0082a0001c0001t0001g0088others(6): Show | 9 | HG01943.hp1 HG02056.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.504+705C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835030 | ||||||
| chr2:168835208
|
G | A | 5 | a0003c0006t0001g0276a0003c0006t0001g0277a0003c0006t0001g0278others(2): Show | 5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.504+883G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835208 | ||||||
| chr2:168835235
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.504+910C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835235 | ||||||
| chr2:168835241
|
A | AT | 18 | a0001c0001t0001g0005a0001c0001t0001g0036a0001c0001t0001g0051others(15): Show | 19 | HG01123.hp1 HG01516.hp1 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.504+925dupT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168835241 | |||||
| chr2:168835265
|
G | C | 1 | a0001c0001t0002g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.504+940G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835265 | ||||||
| chr2:168835299
|
G | A | 3 | a0003c0006t0001g0274a0003c0006t0001g0310a0003c0006t0001g0311 | 3 | HG02572.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.504+974G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835299 | ||||||
| chr2:168835396
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.504+1071A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835396 | ||||||
| chr2:168835448
|
T | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.504+1123T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835448 | ||||||
| chr2:168835460
|
C | A | 6 | a0001c0002t0002g0072a0001c0002t0002g0073a0001c0002t0002g0161others(3): Show | 6 | NA18943.hp1 NA18951.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+1135C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835460 | ||||||
| chr2:168835472
|
C | T | 1 | a0001c0009t0001g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.504+1147C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835472 | ||||||
| chr2:168835859
|
G | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 131 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.504+1534G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835859 | ||||||
| chr2:168835927
|
T | C | 2 | a0001c0001t0002g0019a0001c0001t0002g0020 | 2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.504+1602T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835927 | ||||||
| chr2:168836050
|
A | C | 4 | a0001c0002t0002g0072a0001c0002t0002g0073a0001c0002t0002g0161others(1): Show | 4 | NA18970.hp1 NA19054.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+1725A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836050 | ||||||
| chr2:168836132
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.504+1807C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836132 | ||||||
| chr2:168836155
|
A | T | 1 | a0001c0007t0001g0214 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.504+1830A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836155 | ||||||
| chr2:168836207
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.504+1882A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836207 | ||||||
| chr2:168836298
|
A | C | 2 | a0001c0005t0003g0262a0001c0005t0003g0263 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.504+1973A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836298 | ||||||
| chr2:168836530
|
C | A | 1 | a0001c0002t0002g0185 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.504+2205C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836530 | ||||||
| chr2:168836538
|
A | T | 2 | a0001c0001t0002g0019a0001c0001t0002g0020 | 2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.504+2213A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836538 | ||||||
| chr2:168836599
|
C | G | 3 | a0001c0009t0001g0260a0003c0006t0002g0266a0004c0014t0001g0235 | 3 | HG02976.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.504+2274C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836599 | ||||||
| chr2:168836631
|
C | G | 2 | a0001c0009t0001g0260a0004c0014t0001g0235 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.504+2306C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836631 | ||||||
| chr2:168836734
|
A | T | 1 | a0001c0001t0001g0288 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.504+2409A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836734 | ||||||
| chr2:168836904
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(197): Show | 210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.504+2579T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836904 | ||||||
| chr2:168836980
|
T | A | 54 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0068others(51): Show | 56 | HG00423.hp1 HG00642.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.504+2655T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836980 | ||||||
| chr2:168837027
|
A | G | 57 | a0001c0001t0001g0270a0001c0002t0002g0010a0001c0002t0002g0072others(54): Show | 58 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.504+2702A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837027 | ||||||
| chr2:168837164
|
C | A | 4 | a0003c0006t0001g0274a0003c0006t0001g0278a0003c0006t0001g0310others(1): Show | 4 | HG02572.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+2839C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837164 | ||||||
| chr2:168837298
|
A | G | 19 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(16): Show | 20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.504+2973A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837298 | ||||||
| chr2:168837300
|
C | CT | 86 | a0001c0001t0001g0055a0001c0001t0001g0090a0001c0001t0001g0092others(83): Show | 87 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.504+3002dupT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168837300 | |||||
| chr2:168837300
|
C | CTT | 31 | a0001c0002t0002g0154a0001c0002t0002g0156a0001c0002t0002g0170others(28): Show | 34 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.504+3001_504+3002d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168837300 | |||||
| chr2:168837300
|
CT | C | 16 | a0001c0001t0001g0131a0001c0001t0001g0268a0001c0001t0001g0269others(13): Show | 16 | HG01496.hp2 HG02886.hp2 HG02896.hp1 others(13): Show |
intron_variant | MODIFIER | c.504+3002delT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168837300 | |||||
| chr2:168837371
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.504+3046G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837371 | ||||||
| chr2:168837372
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.504+3047C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837372 | ||||||
| chr2:168837378
|
C | T | 36 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0068others(33): Show | 37 | HG00642.hp2 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.504+3053C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837378 | ||||||
| chr2:168837414
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.504+3089A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837414 | ||||||
| chr2:168837530
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.504+3205C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837530 | ||||||
| chr2:168837552
|
G | A | 1 | a0001c0002t0002g0308 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.504+3227G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837552 | ||||||
| chr2:168837601
|
G | A | 1 | a0003c0006t0001g0274 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.504+3276G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837601 | ||||||
| chr2:168837673
|
T | G | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.504+3348T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837673 | ||||||
| chr2:168837784
|
C | T | 14 | a0001c0001t0001g0036a0001c0001t0001g0192a0001c0005t0003g0034others(11): Show | 14 | HG01123.hp1 HG01516.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.504+3459C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837784 | ||||||
| chr2:168837867
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.504+3542A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837867 | ||||||
| chr2:168837921
|
G | C | 73 | a0001c0001t0001g0212a0001c0001t0002g0281a0001c0001t0002g0282others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.504+3596G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837921 | ||||||
| chr2:168837951
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.504+3626T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837951 | ||||||
| chr2:168838221
|
A | C | 2 | a0001c0001t0001g0105a0001c0001t0001g0128 | 2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.504+3896A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838221 | ||||||
| chr2:168838250
|
C | A | 1 | a0001c0001t0001g0047 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.504+3925C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838250 | ||||||
| chr2:168838415
|
T | G | 1 | a0001c0002t0002g0205 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.504+4090T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838415 | ||||||
| chr2:168838486
|
C | T | 11 | a0001c0009t0001g0260a0003c0006t0001g0274a0003c0006t0001g0276others(8): Show | 11 | HG01261.hp2 HG02572.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.504+4161C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838486 | ||||||
| chr2:168838521
|
C | T | 73 | a0001c0001t0001g0212a0001c0001t0001g0280a0001c0001t0002g0281others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.504+4196C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838521 | ||||||
| chr2:168838529
|
C | A | 19 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(16): Show | 20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.504+4204C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838529 | ||||||
| chr2:168838529
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.504+4204C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838529 | ||||||
| chr2:168838573
|
A | G | 19 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(16): Show | 20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.504+4248A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838573 | ||||||
| chr2:168838603
|
G | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(121): Show | 132 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.504+4278G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838603 | ||||||
| chr2:168838606
|
A | G | 15 | a0001c0001t0001g0036a0001c0001t0001g0192a0001c0005t0003g0034others(12): Show | 15 | HG01123.hp1 HG01261.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.504+4281A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838606 | ||||||
| chr2:168838686
|
G | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 208 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.505-4306G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838686 | ||||||
| chr2:168838786
|
A | ACT | 5 | a0003c0006t0001g0276a0003c0006t0001g0277a0003c0006t0001g0278others(2): Show | 5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-4203_505-4202d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168838786 | |||||
| chr2:168838789
|
C | CT | 184 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(181): Show | 194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.505-4188dupT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168838789 | |||||
| chr2:168838789
|
C | T | 3 | a0001c0004t0002g0264a0001c0009t0001g0260a0004c0014t0001g0235 | 3 | HG03041.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.505-4203C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838789 | ||||||
| chr2:168839020
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.505-3972G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839020 | ||||||
| chr2:168839048
|
G | T | 1 | a0001c0001t0001g0117 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.505-3944G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839048 | ||||||
| chr2:168839065
|
G | A | 8 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(5): Show | 8 | HG00423.hp1 HG02027.hp2 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.505-3927G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839065 | ||||||
| chr2:168839141
|
C | G | 19 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(16): Show | 20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.505-3851C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839141 | ||||||
| chr2:168839184
|
G | T | 2 | a0001c0010t0001g0048a0001c0010t0001g0049 | 2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.505-3808G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839184 | ||||||
| chr2:168839253
|
C | G | 1 | a0001c0001t0002g0084 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.505-3739C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839253 | ||||||
| chr2:168839448
|
G | C | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.505-3544G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839448 | ||||||
| chr2:168839540
|
A | G | 1 | a0001c0005t0003g0034 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.505-3452A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839540 | ||||||
| chr2:168839569
|
A | G | 1 | a0001c0004t0002g0195 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.505-3423A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839569 | ||||||
| chr2:168839680
|
G | T | 3 | a0001c0005t0003g0015a0001c0010t0001g0048a0001c0010t0001g0049 | 3 | HG02809.hp1 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.505-3312G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839680 | ||||||
| chr2:168839695
|
C | T | 6 | a0001c0001t0001g0215a0001c0001t0004g0216a0001c0001t0004g0218others(3): Show | 6 | HG02145.hp1 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-3297C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839695 | ||||||
| chr2:168839813
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.505-3179G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839813 | ||||||
| chr2:168839840
|
C | T | 2 | a0002c0003t0001g0252a0002c0003t0001g0253 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.505-3152C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839840 | ||||||
| chr2:168839884
|
C | CA | 46 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0083others(43): Show | 47 | HG00621.hp2 HG00673.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.505-3091dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168839884 | |||||
| chr2:168839884
|
C | CAA | 17 | a0001c0001t0001g0036a0001c0001t0001g0067a0001c0001t0001g0106others(14): Show | 17 | HG00423.hp1 HG01261.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.505-3092_505-3091d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168839884 | |||||
| chr2:168839884
|
C | CAAA | 12 | a0001c0001t0001g0192a0001c0001t0001g0268a0001c0001t0001g0269others(9): Show | 12 | HG01123.hp1 HG01496.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.505-3093_505-3091d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168839884 | |||||
| chr2:168839900
|
A | T | 1 | a0002c0003t0001g0030 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.505-3092A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839900 | ||||||
| chr2:168839901
|
AT | A | 26 | a0001c0001t0001g0047a0001c0001t0001g0085a0001c0001t0001g0107others(23): Show | 26 | HG01168.hp2 HG01884.hp1 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.505-3090delT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839901 | ||||||
| chr2:168839901
|
ATAT | A | 16 | a0001c0001t0002g0282a0001c0002t0002g0168a0001c0002t0002g0204others(13): Show | 16 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.505-3090_505-3088d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839901 | ||||||
| chr2:168839902
|
T | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(235): Show | 250 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.505-3090T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839902 | ||||||
| chr2:168839904
|
T | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(214): Show | 227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.505-3088T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839904 | ||||||
| chr2:168839906
|
T | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(202): Show | 215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.505-3086T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839906 | ||||||
| chr2:168839908
|
T | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(184): Show | 196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.505-3084T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839908 | ||||||
| chr2:168839910
|
T | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 189 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.505-3082T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839910 | ||||||
| chr2:168839912
|
T | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.505-3080T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839912 | ||||||
| chr2:168839914
|
T | A | 22 | a0001c0001t0001g0047a0001c0001t0001g0144a0001c0001t0001g0162others(19): Show | 23 | HG00735.hp1 HG01167.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.505-3078T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839914 | ||||||
| chr2:168839921
|
A | G | 1 | a0001c0007t0001g0213 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.505-3071A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839921 | ||||||
| chr2:168839921
|
ATG | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(16): Show | 21 | HG01175.hp1 HG01884.hp2 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.505-3053_505-3052d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168839921 | |||||
| chr2:168839921
|
ATGTG | A | 51 | a0001c0001t0001g0212a0001c0002t0002g0010a0001c0002t0002g0072others(48): Show | 52 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.505-3055_505-3052d others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168839921 | |||||
| chr2:168839923
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(213): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.505-3069G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839923 | ||||||
| chr2:168839925
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(227): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.505-3067G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839925 | ||||||
| chr2:168839927
|
G | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 213 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.505-3065G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839927 | ||||||
| chr2:168839929
|
G | A | 4 | a0003c0006t0001g0276a0003c0006t0001g0277a0003c0006t0001g0278others(1): Show | 4 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-3063G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839929 | ||||||
| chr2:168840245
|
T | C | 1 | a0001c0012t0001g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.505-2747T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840245 | ||||||
| chr2:168840337
|
G | A | 19 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(16): Show | 20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.505-2655G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840337 | ||||||
| chr2:168840432
|
A | G | 10 | a0001c0001t0001g0055a0001c0001t0002g0019a0001c0001t0002g0020others(7): Show | 10 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.505-2560A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840432 | ||||||
| chr2:168840455
|
C | G | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(98): Show | 105 | HG00423.hp1 HG00642.hp2 HG00673.hp2 others(102): Show |
intron_variant | MODIFIER | c.505-2537C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840455 | ||||||
| chr2:168840462
|
G | A | 2 | a0002c0003t0001g0252a0002c0003t0001g0253 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.505-2530G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840462 | ||||||
| chr2:168840466
|
C | T | 19 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(16): Show | 20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.505-2526C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840466 | ||||||
| chr2:168840529
|
C | CAA | 6 | a0001c0001t0001g0036a0001c0001t0001g0060a0001c0001t0001g0152others(3): Show | 6 | HG00733.hp1 HG02109.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-2442_505-2441d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168840529 | |||||
| chr2:168840529
|
C | CAAA | 9 | a0001c0001t0001g0192a0001c0001t0001g0268a0001c0005t0003g0034others(6): Show | 9 | HG01123.hp1 HG01516.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.505-2443_505-2441d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168840529 | |||||
| chr2:168840529
|
CA | C | 92 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0051others(89): Show | 96 | HG00423.hp1 HG00642.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.505-2441delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168840529 | |||||
| chr2:168840529
|
CAA | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(152): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.505-2442_505-2441d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168840529 | |||||
| chr2:168840540
|
A | C | 3 | a0001c0001t0001g0309a0002c0003t0001g0252a0002c0003t0001g0253 | 3 | HG02647.hp1 NA18967.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.505-2452A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840540 | ||||||
| chr2:168840541
|
A | C | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0051others(59): Show | 66 | HG00423.hp1 HG00642.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.505-2451A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840541 | ||||||
| chr2:168840543
|
A | C | 2 | a0001c0004t0002g0200a0001c0004t0002g0239 | 2 | HG00140.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.505-2449A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840543 | ||||||
| chr2:168840546
|
A | AAC | 6 | a0001c0001t0001g0215a0001c0001t0004g0216a0001c0001t0004g0218others(3): Show | 6 | HG02145.hp1 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-2445_505-2444i others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168840546 | |||||
| chr2:168840546
|
A | C | 6 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0050others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-2446A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840546 | ||||||
| chr2:168840552
|
C | A | 3 | a0001c0001t0001g0036a0001c0005t0003g0035a0001c0005t0003g0037 | 3 | HG02109.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.505-2440C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840552 | ||||||
| chr2:168840572
|
G | T | 17 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0070others(14): Show | 21 | HG00280.hp1 HG00621.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.505-2420G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840572 | ||||||
| chr2:168840716
|
G | A | 8 | a0001c0001t0001g0055a0001c0001t0002g0019a0001c0001t0002g0020others(5): Show | 8 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.505-2276G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840716 | ||||||
| chr2:168840800
|
T | C | 2 | a0003c0006t0001g0310a0003c0006t0001g0311 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.505-2192T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840800 | ||||||
| chr2:168840826
|
C | T | 4 | a0003c0006t0001g0276a0003c0006t0001g0277a0003c0006t0001g0278others(1): Show | 4 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-2166C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840826 | ||||||
| chr2:168840918
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(208): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.505-2074T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840918 | ||||||
| chr2:168840945
|
T | G | 8 | a0001c0001t0002g0016a0001c0005t0003g0002a0001c0005t0003g0043others(5): Show | 9 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.505-2047T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840945 | ||||||
| chr2:168840985
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.505-2007G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840985 | ||||||
| chr2:168841023
|
T | C | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0051others(61): Show | 68 | HG00423.hp1 HG00642.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.505-1969T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841023 | ||||||
| chr2:168841040
|
C | T | 24 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0051others(21): Show | 27 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.505-1952C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841040 | ||||||
| chr2:168841151
|
C | T | 19 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0145others(16): Show | 19 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.505-1841C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841151 | ||||||
| chr2:168841235
|
C | CA | 24 | a0001c0002t0002g0154a0001c0002t0002g0159a0001c0002t0002g0163others(21): Show | 27 | HG00099.hp1 HG00323.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.505-1731dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | |||||
| chr2:168841235
|
C | CAA | 8 | a0001c0001t0001g0055a0001c0001t0002g0020a0001c0001t0002g0050others(5): Show | 8 | HG02257.hp1 HG02572.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.505-1732_505-1731d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | |||||
| chr2:168841235
|
C | CAAAAAAA others(8): Show |
2 | a0002c0003t0001g0252a0002c0003t0001g0253 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.505-1745_505-1731d others(17): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | |||||
| chr2:168841235
|
CAAAAAAA | C | 17 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0145others(14): Show | 17 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.505-1737_505-1731d others(9): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | |||||
| chr2:168841235
|
CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(2): Show | 6 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-1738_505-1731d others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | |||||
| chr2:168841235
|
CAAAAAAA others(2): Show |
C | 40 | a0001c0001t0001g0004a0001c0001t0001g0261a0001c0001t0001g0273others(37): Show | 43 | HG00423.hp1 HG00673.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.505-1739_505-1731d others(11): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | |||||
| chr2:168841235
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0289a0003c0006t0002g0266 | 2 | HG02976.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.505-1742_505-1731d others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | |||||
| chr2:168841235
|
CAAAAAAA others(6): Show |
C | 135 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.505-1743_505-1731d others(15): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | |||||
| chr2:168841293
|
AATAT | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.505-1689_505-1686d others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841293 | |||||
| chr2:168841301
|
T | G | 1 | a0001c0010t0001g0049 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.505-1691T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841301 | ||||||
| chr2:168841403
|
GC | G | 5 | a0001c0001t0001g0270a0003c0006t0001g0276a0003c0006t0001g0277others(2): Show | 5 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-1586delC | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841403 | |||||
| chr2:168841452
|
A | T | 73 | a0001c0001t0001g0212a0001c0001t0002g0281a0001c0001t0002g0282others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.505-1540A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841452 | ||||||
| chr2:168841559
|
C | A | 4 | a0001c0002t0002g0010a0001c0002t0002g0173a0001c0002t0002g0179others(1): Show | 5 | HG03490.hp2 HG03492.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.505-1433C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841559 | ||||||
| chr2:168841573
|
T | G | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0050others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-1419T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841573 | ||||||
| chr2:168841790
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0273 | 3 | HG01891.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.505-1202T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841790 | ||||||
| chr2:168841869
|
A | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(202): Show | 215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.505-1123A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841869 | ||||||
| chr2:168841883
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.505-1109G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841883 | ||||||
| chr2:168842106
|
G | A | 19 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(16): Show | 20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.505-886G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842106 | ||||||
| chr2:168842446
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0273 | 3 | HG01891.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.505-546T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842446 | ||||||
| chr2:168842613
|
A | G | 1 | a0001c0004t0002g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.505-379A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842613 | ||||||
| chr2:168842754
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.505-238A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842754 | ||||||
| chr2:168842821
|
T | C | 10 | a0001c0001t0001g0145a0001c0001t0001g0244a0001c0001t0002g0022others(7): Show | 10 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.505-171T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842821 | ||||||
| chr2:168842840
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(131): Show | 140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.505-152G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842840 | ||||||
| chr2:168842866
|
A | G | 1 | a0001c0005t0003g0080 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.505-126A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842866 | ||||||
| chr2:168842928
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.505-64A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842928 | ||||||
| chr2:168843200
|
A | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0051others(22): Show | 28 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.630+83A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843200 | ||||||
| chr2:168843280
|
C | T | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.630+163C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843280 | ||||||
| chr2:168843472
|
G | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0002g0021others(2): Show | 5 | HG01496.hp2 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.630+355G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843472 | ||||||
| chr2:168843491
|
C | T | 1 | a0001c0004t0002g0094 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.630+374C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843491 | ||||||
| chr2:168843620
|
A | G | 9 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0050others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.630+503A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843620 | ||||||
| chr2:168843665
|
G | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(208): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.630+548G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843665 | ||||||
| chr2:168843758
|
G | C | 1 | a0001c0004t0002g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.630+641G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843758 | ||||||
| chr2:168843953
|
T | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(288): Show | 302 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.630+836T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843953 | ||||||
| chr2:168844116
|
A | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0002g0021others(2): Show | 5 | HG01496.hp2 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.630+999A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844116 | ||||||
| chr2:168844235
|
C | T | 19 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(16): Show | 20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.630+1118C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844235 | ||||||
| chr2:168844328
|
C | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(108): Show | 117 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.630+1211C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844328 | ||||||
| chr2:168844393
|
T | TA | 109 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(106): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.630+1286dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168844393 | |||||
| chr2:168844393
|
T | TAA | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(97): Show | 104 | HG00423.hp1 HG00642.hp2 HG00673.hp2 others(101): Show |
intron_variant | MODIFIER | c.630+1285_630+1286d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168844393 | |||||
| chr2:168844536
|
A | T | 10 | a0001c0001t0001g0055a0001c0001t0002g0019a0001c0001t0002g0020others(7): Show | 10 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.630+1419A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844536 | ||||||
| chr2:168844544
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(208): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.630+1427A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844544 | ||||||
| chr2:168844684
|
C | G | 1 | a0001c0001t0002g0157 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.630+1567C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844684 | ||||||
| chr2:168844686
|
C | A | 2 | a0002c0003t0001g0252a0002c0003t0001g0253 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.630+1569C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844686 | ||||||
| chr2:168844686
|
C | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.630+1569C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844686 | ||||||
| chr2:168844729
|
G | A | 1 | a0001c0012t0001g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.630+1612G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844729 | ||||||
| chr2:168844729
|
G | C | 1 | a0003c0006t0002g0266 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.630+1612G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844729 | ||||||
| chr2:168844845
|
A | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(208): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.630+1728A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844845 | ||||||
| chr2:168844865
|
G | A | 2 | a0002c0003t0001g0252a0002c0003t0001g0253 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.630+1748G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844865 | ||||||
| chr2:168844875
|
G | GA | 189 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(186): Show | 199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.630+1771dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168844875 | |||||
| chr2:168844875
|
G | GAA | 15 | a0001c0001t0001g0036a0001c0001t0001g0192a0001c0005t0003g0034others(12): Show | 15 | HG01123.hp1 HG01261.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.630+1770_630+1771d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168844875 | |||||
| chr2:168844890
|
A | G | 1 | a0001c0002t0002g0175 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.630+1773A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844890 | ||||||
| chr2:168844902
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0273 | 3 | HG01891.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.630+1785C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844902 | ||||||
| chr2:168844936
|
G | A | 2 | a0002c0003t0001g0252a0002c0003t0001g0253 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.630+1819G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844936 | ||||||
| chr2:168844940
|
A | T | 18 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(15): Show | 18 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.630+1823A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844940 | ||||||
| chr2:168844950
|
A | G | 2 | a0002c0003t0001g0252a0002c0003t0001g0253 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.630+1833A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844950 | ||||||
| chr2:168844960
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.630+1843C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844960 | ||||||
| chr2:168844961
|
G | A | 1 | a0001c0004t0002g0158 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.630+1844G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844961 | ||||||
| chr2:168845089
|
G | GA | 211 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(208): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.630+1978dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168845089 | |||||
| chr2:168845128
|
G | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(208): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.630+2011G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845128 | ||||||
| chr2:168845129
|
G | A | 10 | a0001c0001t0001g0261a0001c0001t0002g0016a0001c0005t0003g0002others(7): Show | 11 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.630+2012G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845129 | ||||||
| chr2:168845407
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.630+2290G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845407 | ||||||
| chr2:168845503
|
T | C | 1 | a0003c0006t0002g0266 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.630+2386T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845503 | ||||||
| chr2:168845527
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 212 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.630+2410A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845527 | ||||||
| chr2:168845580
|
C | T | 2 | a0002c0003t0001g0252a0002c0003t0001g0253 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.630+2463C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845580 | ||||||
| chr2:168845601
|
A | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0096a0001c0001t0001g0125 | 3 | HG02056.hp1 NA19076.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.630+2484A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845601 | ||||||
| chr2:168845641
|
C | T | 18 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(15): Show | 18 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.630+2524C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845641 | ||||||
| chr2:168845753
|
T | C | 2 | a0002c0003t0001g0252a0002c0003t0001g0253 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.630+2636T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845753 | ||||||
| chr2:168845789
|
C | CCTT | 10 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0130others(7): Show | 10 | HG01358.hp2 HG01884.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.630+2673_630+2675d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168845789 | |||||
| chr2:168845790
|
C | CT | 17 | a0001c0001t0002g0069a0001c0002t0002g0072a0001c0002t0002g0073others(14): Show | 17 | HG00673.hp1 HG01074.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.630+2690dupT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168845790 | |||||
| chr2:168845790
|
C | CTTCT | 137 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.630+2675_630+2676i others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168845790 | |||||
| chr2:168845790
|
C | CTTCTT | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(41): Show | 46 | HG01261.hp1 HG01517.hp2 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.630+2675_630+2676i others(7): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168845790 | |||||
| chr2:168845790
|
C | CTTCTTT | 18 | a0001c0001t0001g0060a0001c0001t0001g0192a0001c0001t0002g0016others(15): Show | 19 | HG00733.hp1 HG01123.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.630+2675_630+2676i others(8): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168845790 | |||||
| chr2:168845830
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.630+2713A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845830 | ||||||
| chr2:168846125
|
T | C | 2 | a0001c0004t0002g0193a0001c0004t0002g0197 | 2 | HG01070.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.630+3008T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846125 | ||||||
| chr2:168846188
|
A | T | 4 | a0002c0003t0001g0009a0002c0003t0001g0011a0002c0003t0001g0258others(1): Show | 6 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.630+3071A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846188 | ||||||
| chr2:168846270
|
G | A | 3 | a0003c0006t0001g0274a0003c0006t0001g0310a0003c0006t0001g0311 | 3 | HG02572.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.630+3153G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846270 | ||||||
| chr2:168846285
|
G | A | 4 | a0001c0002t0002g0010a0001c0002t0002g0173a0001c0002t0002g0179others(1): Show | 5 | HG03490.hp2 HG03492.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.630+3168G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846285 | ||||||
| chr2:168846325
|
T | C | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0050others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+3208T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846325 | ||||||
| chr2:168846419
|
A | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(139): Show | 148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.630+3302A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846419 | ||||||
| chr2:168846486
|
T | C | 1 | a0001c0002t0002g0156 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.630+3369T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846486 | ||||||
| chr2:168846524
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(148): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.630+3407A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846524 | ||||||
| chr2:168846589
|
C | A | 7 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0050others(4): Show | 7 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.630+3472C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846589 | ||||||
| chr2:168846609
|
A | G | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0047others(33): Show | 40 | HG01255.hp2 HG01884.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.630+3492A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846609 | ||||||
| chr2:168846643
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.630+3526A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846643 | ||||||
| chr2:168846714
|
TTTTTAAA others(7): Show |
T | 3 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0090 | 3 | NA18962.hp2 NA18977.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.630+3599_630+3612d others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168846714 | |||||
| chr2:168846850
|
T | G | 1 | a0001c0001t0001g0127 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.630+3733T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846850 | ||||||
| chr2:168846920
|
C | G | 1 | a0001c0001t0001g0142 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.630+3803C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846920 | ||||||
| chr2:168846972
|
G | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(300): Show | 316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.630+3855G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846972 | ||||||
| chr2:168847150
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(125): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.631-3934C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847150 | ||||||
| chr2:168847241
|
T | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(123): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.631-3843T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847241 | ||||||
| chr2:168847366
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.631-3718C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847366 | ||||||
| chr2:168847386
|
T | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 212 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.631-3698T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847386 | ||||||
| chr2:168847403
|
GGAGCCTC others(11): Show |
G | 2 | a0001c0001t0001g0144a0001c0004t0002g0158 | 2 | HG02523.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.631-3668_631-3651d others(20): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168847403 | |||||
| chr2:168847464
|
G | A | 22 | a0001c0001t0001g0212a0001c0001t0002g0281a0001c0001t0002g0282others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.631-3620G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847464 | ||||||
| chr2:168847638
|
A | G | 3 | a0001c0002t0002g0166a0001c0002t0002g0176a0001c0004t0002g0224 | 3 | HG03669.hp1 HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.631-3446A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847638 | ||||||
| chr2:168847801
|
G | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0192 | 3 | HG01123.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.631-3283G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847801 | ||||||
| chr2:168847823
|
T | A | 1 | a0001c0001t0001g0111 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.631-3261T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847823 | ||||||
| chr2:168847906
|
T | C | 1 | a0001c0002t0002g0168 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.631-3178T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847906 | ||||||
| chr2:168847977
|
T | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(96): Show | 105 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.631-3107T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847977 | ||||||
| chr2:168848244
|
T | A | 17 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0045others(14): Show | 17 | HG00642.hp2 HG00735.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.631-2840T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848244 | ||||||
| chr2:168848333
|
T | G | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.631-2751T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848333 | ||||||
| chr2:168848336
|
C | T | 5 | a0001c0001t0001g0047a0001c0001t0001g0060a0001c0001t0001g0152others(2): Show | 5 | HG00733.hp1 HG02818.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.631-2748C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848336 | ||||||
| chr2:168848395
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0192 | 3 | HG01123.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.631-2689C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848395 | ||||||
| chr2:168848430
|
G | A | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.631-2654G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848430 | ||||||
| chr2:168848527
|
T | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(96): Show | 105 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.631-2557T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848527 | ||||||
| chr2:168848560
|
CA | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(96): Show | 105 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.631-2518delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168848560 | |||||
| chr2:168848594
|
A | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(121): Show | 130 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.631-2490A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848594 | ||||||
| chr2:168848806
|
T | C | 47 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(44): Show | 50 | HG01255.hp2 HG01261.hp1 HG01516.hp1 others(47): Show |
intron_variant | MODIFIER | c.631-2278T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848806 | ||||||
| chr2:168848819
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0128 | 2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.631-2265C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848819 | ||||||
| chr2:168848865
|
T | C | 1 | a0001c0001t0001g0304 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.631-2219T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848865 | ||||||
| chr2:168848867
|
G | A | 6 | a0001c0001t0001g0055a0003c0006t0001g0274a0003c0006t0001g0310others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.631-2217G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848867 | ||||||
| chr2:168848876
|
T | C | 6 | a0001c0001t0001g0055a0003c0006t0001g0274a0003c0006t0001g0310others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.631-2208T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848876 | ||||||
| chr2:168849054
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.631-2030C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849054 | ||||||
| chr2:168849059
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0192 | 3 | HG01123.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.631-2025C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849059 | ||||||
| chr2:168849165
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.631-1919C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849165 | ||||||
| chr2:168849203
|
C | T | 1 | a0003c0006t0002g0266 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.631-1881C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849203 | ||||||
| chr2:168849365
|
C | CT | 6 | a0001c0001t0001g0055a0003c0006t0001g0274a0003c0006t0001g0310others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.631-1711dupT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849365 | |||||
| chr2:168849372
|
T | C | 1 | a0001c0002t0002g0154 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.631-1712T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849372 | ||||||
| chr2:168849558
|
G | A | 5 | a0001c0001t0001g0036a0003c0006t0001g0276a0003c0006t0001g0277others(2): Show | 5 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.631-1526G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849558 | ||||||
| chr2:168849569
|
T | C | 141 | a0001c0001t0001g0005a0001c0001t0001g0047a0001c0001t0001g0051others(138): Show | 145 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.631-1515T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849569 | ||||||
| chr2:168849646
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0192 | 3 | HG01123.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.631-1438G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849646 | ||||||
| chr2:168849670
|
C | CA | 105 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(102): Show | 111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.631-1395dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849670 | |||||
| chr2:168849670
|
C | CAA | 30 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0095others(27): Show | 30 | HG00423.hp1 HG01109.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.631-1396_631-1395d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849670 | |||||
| chr2:168849670
|
C | CAAA | 131 | a0001c0001t0001g0005a0001c0001t0001g0047a0001c0001t0001g0051others(128): Show | 134 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.631-1397_631-1395d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849670 | |||||
| chr2:168849670
|
C | CAAAA | 13 | a0001c0001t0001g0153a0001c0001t0001g0270a0001c0001t0002g0016others(10): Show | 14 | HG00621.hp1 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.631-1398_631-1395d others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849670 | |||||
| chr2:168849748
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.631-1336G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849748 | ||||||
| chr2:168849905
|
G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(11): Show | 15 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.631-1179G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849905 | ||||||
| chr2:168849918
|
A | ATTTTG | 30 | a0001c0001t0001g0047a0001c0001t0001g0060a0001c0001t0001g0082others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.631-1162_631-1161i others(7): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849918 | |||||
| chr2:168849918
|
A | ATTTTGT | 82 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0002t0002g0010others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.631-1162_631-1161i others(8): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849918 | |||||
| chr2:168849919
|
T | TTTTG | 155 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.631-1162_631-1161i others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849919 | |||||
| chr2:168849923
|
T | G | 1 | a0001c0001t0001g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.631-1161T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849923 | ||||||
| chr2:168850024
|
TG | T | 8 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(5): Show | 8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.631-1059delG | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850024 | ||||||
| chr2:168850176
|
G | A | 3 | a0003c0006t0001g0274a0003c0006t0001g0310a0003c0006t0001g0311 | 3 | HG02572.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.631-908G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850176 | ||||||
| chr2:168850193
|
A | G | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0050others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-891A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850193 | ||||||
| chr2:168850557
|
A | G | 2 | a0001c0005t0003g0262a0001c0005t0003g0263 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.631-527A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850557 | ||||||
| chr2:168850596
|
A | AT | 16 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(13): Show | 16 | HG00438.hp1 HG00621.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.631-469dupT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168850596 | |||||
| chr2:168850596
|
AT | A | 8 | a0001c0001t0001g0051a0001c0001t0001g0288a0001c0001t0001g0304others(5): Show | 8 | HG00423.hp1 HG01943.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.631-469delT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168850596 | |||||
| chr2:168850596
|
ATT | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0052a0001c0001t0001g0053others(14): Show | 18 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.631-470_631-469del others(2): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168850596 | |||||
| chr2:168850597
|
T | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0192 | 3 | HG01123.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.631-487T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850597 | ||||||
| chr2:168850638
|
C | T | 1 | a0001c0002t0002g0302 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.631-446C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850638 | ||||||
| chr2:168850699
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.631-385G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850699 | ||||||
| chr2:168850752
|
A | AAATTCTC others(3): Show |
1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.631-318_631-309dup others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168850752 | |||||
| chr2:168850752
|
AAATTCTC others(3): Show |
A | 87 | a0001c0001t0001g0047a0001c0001t0001g0060a0001c0001t0001g0152others(84): Show | 88 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.631-318_631-309del others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168850752 | |||||
| chr2:168850812
|
T | C | 1 | a0001c0005t0003g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.631-272T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850812 | ||||||
| chr2:168850918
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(114): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.631-166C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850918 | ||||||
| chr2:168850945
|
T | C | 8 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(5): Show | 8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.631-139T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850945 | ||||||
| chr2:168851042
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.631-42A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168851042 | ||||||
| chr2:168851067
|
A | G | 5 | a0003c0006t0001g0274a0003c0006t0001g0310a0003c0006t0001g0311others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.631-17A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168851067 | ||||||
| chr2:168851267
|
T | C | 2 | a0001c0005t0003g0035a0001c0005t0003g0037 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.730-12T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 9/15 | chr2 | 168851267 | ||||||
| chr2:168851478
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.855+74T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851478 | ||||||
| chr2:168851503
|
A | C | 8 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(5): Show | 8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.855+99A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851503 | ||||||
| chr2:168851537
|
A | T | 5 | a0001c0001t0001g0036a0003c0006t0001g0276a0003c0006t0001g0277others(2): Show | 5 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.855+133A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851537 | ||||||
| chr2:168851643
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.855+239C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851643 | ||||||
| chr2:168851687
|
C | G | 1 | a0001c0005t0003g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.855+283C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851687 | ||||||
| chr2:168851710
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(15): Show | 19 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.855+306C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851710 | ||||||
| chr2:168851759
|
C | T | 1 | a0002c0003t0001g0030 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.855+355C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851759 | ||||||
| chr2:168851798
|
A | T | 21 | a0001c0001t0002g0016a0001c0001t0002g0021a0001c0001t0002g0022others(18): Show | 21 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.855+394A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851798 | ||||||
| chr2:168851812
|
A | G | 1 | a0001c0005t0003g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.855+408A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851812 | ||||||
| chr2:168851864
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(15): Show | 19 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.855+460C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851864 | ||||||
| chr2:168851980
|
C | T | 2 | a0002c0003t0001g0252a0002c0003t0001g0253 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.855+576C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851980 | ||||||
| chr2:168852374
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.855+970G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852374 | ||||||
| chr2:168852391
|
T | C | 2 | a0001c0001t0004g0216a0001c0001t0004g0218 | 2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.855+987T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852391 | ||||||
| chr2:168852432
|
T | C | 5 | a0001c0001t0001g0036a0003c0006t0001g0276a0003c0006t0001g0277others(2): Show | 5 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.855+1028T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852432 | ||||||
| chr2:168852503
|
C | T | 9 | a0001c0005t0003g0002a0001c0005t0003g0043a0001c0005t0003g0077others(6): Show | 10 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.855+1099C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852503 | ||||||
| chr2:168852504
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0268a0001c0001t0001g0273 | 4 | HG01891.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.855+1100T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852504 | ||||||
| chr2:168852563
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.855+1159C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852563 | ||||||
| chr2:168852594
|
C | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(277): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.855+1190C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852594 | ||||||
| chr2:168852687
|
C | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.855+1283C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852687 | ||||||
| chr2:168852954
|
G | A | 11 | a0001c0001t0001g0036a0001c0001t0002g0019a0001c0001t0002g0020others(8): Show | 11 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.855+1550G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852954 | ||||||
| chr2:168853172
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.855+1768G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853172 | ||||||
| chr2:168853247
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(115): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.855+1843G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853247 | ||||||
| chr2:168853484
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.856-1868G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853484 | ||||||
| chr2:168853648
|
C | T | 2 | a0002c0003t0001g0030a0002c0003t0001g0033 | 2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.856-1704C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853648 | ||||||
| chr2:168853674
|
G | C | 1 | a0001c0001t0001g0265 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.856-1678G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853674 | ||||||
| chr2:168853782
|
G | A | 2 | a0001c0002t0002g0169a0001c0002t0002g0190 | 2 | NA18948.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.856-1570G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853782 | ||||||
| chr2:168853867
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.856-1485A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853867 | ||||||
| chr2:168853928
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 7 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-1424C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853928 | ||||||
| chr2:168853943
|
C | A | 2 | a0002c0003t0001g0252a0002c0003t0001g0253 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.856-1409C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853943 | ||||||
| chr2:168854025
|
G | A | 30 | a0001c0005t0003g0002a0001c0005t0003g0012a0001c0005t0003g0015others(27): Show | 32 | HG01255.hp2 HG01261.hp1 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.856-1327G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854025 | ||||||
| chr2:168854028
|
C | T | 8 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(5): Show | 8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-1324C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854028 | ||||||
| chr2:168854097
|
G | A | 87 | a0001c0001t0001g0047a0001c0001t0001g0060a0001c0001t0001g0152others(84): Show | 88 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.856-1255G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854097 | ||||||
| chr2:168854349
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02602.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.856-1003C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854349 | ||||||
| chr2:168854390
|
C | T | 1 | a0001c0004t0002g0230 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.856-962C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854390 | ||||||
| chr2:168854467
|
TC | T | 8 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(5): Show | 8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-884delC | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854467 | ||||||
| chr2:168854608
|
T | G | 8 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(5): Show | 8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-744T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854608 | ||||||
| chr2:168854751
|
C | T | 2 | a0002c0003t0001g0003a0002c0003t0001g0025 | 3 | HG00099.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.856-601C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854751 | ||||||
| chr2:168854794
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(120): Show | 129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.856-558T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854794 | ||||||
| chr2:168854838
|
T | G | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.856-514T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854838 | ||||||
| chr2:168855486
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.964+26C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168855486 | ||||||
| chr2:168855558
|
G | A | 5 | a0001c0001t0001g0047a0001c0001t0001g0060a0001c0001t0001g0152others(2): Show | 5 | HG00733.hp1 HG02818.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.964+98G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168855558 | ||||||
| chr2:168855566
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.964+106T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168855566 | ||||||
| chr2:168855603
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(16): Show | 20 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.964+143A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168855603 | ||||||
| chr2:168855605
|
C | CA | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(206): Show | 216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.964+158dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855605 | |||||
| chr2:168855607
|
A | AC | 3 | a0001c0001t0001g0096a0001c0001t0001g0192a0001c0001t0001g0265 | 3 | HG01123.hp1 HG02056.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.964+147_964+148ins others(1): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168855607 | ||||||
| chr2:168855617
|
AAGT | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(9): Show | 13 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.964+160_964+162del others(3): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855617 | |||||
| chr2:168855638
|
C | CA | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(206): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.964+194dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855638 | |||||
| chr2:168855638
|
C | CAA | 47 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0192others(44): Show | 47 | HG00140.hp1 HG00423.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.964+193_964+194dup others(2): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855638 | |||||
| chr2:168855638
|
C | CAAA | 7 | a0001c0001t0001g0309a0001c0005t0003g0249a0001c0005t0003g0272others(4): Show | 7 | HG02074.hp2 HG02451.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+192_964+194dup others(3): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855638 | |||||
| chr2:168855638
|
C | CAAAA | 25 | a0001c0005t0003g0002a0001c0005t0003g0012a0001c0005t0003g0015others(22): Show | 27 | HG01255.hp2 HG01261.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.964+191_964+194dup others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855638 | |||||
| chr2:168855638
|
CAAAA | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(14): Show | 18 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.964+191_964+194del others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855638 | |||||
| chr2:168855890
|
T | TA | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0050others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+431dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855890 | |||||
| chr2:168855995
|
C | T | 8 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(5): Show | 8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.964+535C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168855995 | ||||||
| chr2:168856068
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.964+608C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168856068 | ||||||
| chr2:168856076
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(16): Show | 20 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.965-614A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168856076 | ||||||
| chr2:168856084
|
G | A | 58 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(55): Show | 61 | HG00423.hp1 HG01255.hp2 HG01261.hp1 others(58): Show |
intron_variant | MODIFIER | c.965-606G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168856084 | ||||||
| chr2:168856086
|
T | C | 31 | a0001c0005t0003g0002a0001c0005t0003g0012a0001c0005t0003g0015others(28): Show | 33 | HG01255.hp2 HG01261.hp1 HG01516.hp1 others(30): Show |
intron_variant | MODIFIER | c.965-604T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168856086 | ||||||
| chr2:168856420
|
C | T | 13 | a0002c0003t0001g0013a0002c0003t0001g0057a0002c0003t0001g0076others(10): Show | 14 | NA18945.hp1 NA18949.hp1 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.965-270C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168856420 | ||||||
| chr2:168856537
|
T | G | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.965-153T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168856537 | ||||||
| chr2:168856574
|
T | TA | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(149): Show | 160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.965-105dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168856574 | |||||
| chr2:168856823
|
G | T | 1 | a0001c0010t0001g0048 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1053+45G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168856823 | ||||||
| chr2:168856841
|
T | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(17): Show | 21 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.1053+63T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168856841 | ||||||
| chr2:168856901
|
G | C | 5 | a0001c0001t0001g0036a0003c0006t0001g0276a0003c0006t0001g0277others(2): Show | 5 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1053+123G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168856901 | ||||||
| chr2:168857010
|
G | A | 1 | a0001c0001t0002g0245 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1053+232G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857010 | ||||||
| chr2:168857068
|
G | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(19): Show | 23 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1053+290G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857068 | ||||||
| chr2:168857173
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1053+395C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857173 | ||||||
| chr2:168857299
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1053+521T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857299 | ||||||
| chr2:168857518
|
G | C | 2 | a0002c0003t0001g0027a0002c0003t0001g0032 | 2 | HG01928.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1053+740G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857518 | ||||||
| chr2:168857730
|
T | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(19): Show | 23 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1053+952T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857730 | ||||||
| chr2:168857840
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(150): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1053+1062T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857840 | ||||||
| chr2:168857881
|
T | C | 2 | a0001c0007t0001g0213a0001c0007t0001g0214 | 2 | HG02074.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1053+1103T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857881 | ||||||
| chr2:168857975
|
G | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(19): Show | 23 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1053+1197G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857975 | ||||||
| chr2:168858017
|
C | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(28): Show | 32 | HG00423.hp1 HG01123.hp1 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.1053+1239C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858017 | ||||||
| chr2:168858072
|
C | T | 9 | a0001c0001t0001g0192a0001c0001t0001g0287a0001c0001t0001g0288others(6): Show | 9 | HG00423.hp1 HG01123.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1053+1294C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858072 | ||||||
| chr2:168858167
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1054-1345A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858167 | ||||||
| chr2:168858172
|
T | G | 1 | a0001c0002t0002g0222 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1054-1340T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858172 | ||||||
| chr2:168858379
|
T | C | 1 | a0001c0004t0002g0243 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1054-1133T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858379 | ||||||
| chr2:168858383
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(119): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1054-1129T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858383 | ||||||
| chr2:168858522
|
G | T | 1 | a0001c0001t0001g0126 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1054-990G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858522 | ||||||
| chr2:168858817
|
G | A | 5 | a0003c0006t0001g0274a0003c0006t0001g0310a0003c0006t0001g0311others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054-695G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858817 | ||||||
| chr2:168859097
|
C | G | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1054-415C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168859097 | ||||||
| chr2:168859100
|
C | T | 9 | a0001c0001t0001g0192a0001c0001t0001g0287a0001c0001t0001g0288others(6): Show | 9 | HG00423.hp1 HG01123.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1054-412C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168859100 | ||||||
| chr2:168859176
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(120): Show | 129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1054-336A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168859176 | ||||||
| chr2:168859192
|
A | C | 15 | a0001c0001t0002g0016a0001c0001t0002g0021a0001c0001t0002g0022others(12): Show | 15 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1054-320A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168859192 | ||||||
| chr2:168859195
|
T | C | 1 | a0001c0002t0002g0225 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1054-317T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168859195 | ||||||
| chr2:168859207
|
T | A | 1 | a0001c0009t0001g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1054-305T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168859207 | ||||||
| chr2:168859357
|
AT | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(28): Show | 32 | HG00423.hp1 HG01123.hp1 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.1054-146delT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 168859357 | |||||
| chr2:168859371
|
C | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(29): Show | 33 | HG00423.hp1 HG01123.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.1054-141C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168859371 | ||||||
| chr2:168859762
|
TAAG | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(19): Show | 23 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1179+130_1179+132d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 168859762 | |||||
| chr2:168859823
|
A | G | 1 | a0002c0003t0001g0017 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1179+186A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168859823 | ||||||
| chr2:168859876
|
T | C | 1 | a0001c0002t0002g0010 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1179+239T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168859876 | ||||||
| chr2:168859906
|
C | A | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0050others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179+269C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168859906 | ||||||
| chr2:168860008
|
T | G | 5 | a0001c0001t0001g0036a0003c0006t0001g0276a0003c0006t0001g0277others(2): Show | 5 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+371T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860008 | ||||||
| chr2:168860151
|
A | G | 3 | a0001c0002t0002g0205a0001c0002t0002g0210a0001c0002t0002g0232 | 3 | HG00621.hp1 HG02015.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1179+514A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860151 | ||||||
| chr2:168860182
|
C | T | 8 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(5): Show | 8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1179+545C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860182 | ||||||
| chr2:168860222
|
T | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(19): Show | 23 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1180-573T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860222 | ||||||
| chr2:168860279
|
G | T | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1180-516G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860279 | ||||||
| chr2:168860396
|
C | T | 6 | a0001c0001t0001g0059a0001c0001t0001g0086a0001c0001t0001g0087others(3): Show | 6 | HG00423.hp2 NA18960.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1180-399C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860396 | ||||||
| chr2:168860446
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1180-349G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860446 | ||||||
| chr2:168860488
|
C | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.1180-307C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860488 | ||||||
| chr2:168860504
|
C | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0268a0001c0001t0001g0273 | 4 | HG01891.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-291C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860504 | ||||||
| chr2:168860596
|
G | A | 1 | a0002c0003t0001g0023 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1180-199G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860596 | ||||||
| chr2:168860613
|
G | A | 1 | a0001c0001t0002g0282 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1180-182G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860613 | ||||||
| chr2:168860652
|
C | T | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0050others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180-143C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860652 | ||||||
| chr2:168860669
|
T | TA | 158 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(155): Show | 166 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1180-114dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 168860669 | |||||
| chr2:168860680
|
AAGAAAAA others(6): Show |
A | 1 | a0001c0002t0002g0164 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1180-103_1180-91de others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 168860680 | |||||
| chr2:168860686
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1180-109A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860686 | ||||||
| chr2:168860689
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1180-106C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860689 | ||||||
| chr2:168860923
|
C | T | 1 | a0001c0002t0002g0302 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1294+14C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168860923 | ||||||
| chr2:168861031
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(185): Show | 196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1294+122T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861031 | ||||||
| chr2:168861050
|
A | T | 1 | a0001c0001t0002g0237 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1294+141A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861050 | ||||||
| chr2:168861061
|
C | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(15): Show | 19 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.1294+152C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861061 | ||||||
| chr2:168861114
|
C | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(275): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1294+205C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861114 | ||||||
| chr2:168861318
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1294+409T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861318 | ||||||
| chr2:168861408
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0139a0001c0001t0001g0140others(4): Show | 8 | HG00558.hp2 HG01257.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1294+499C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861408 | ||||||
| chr2:168861484
|
TA | T | 8 | a0001c0001t0001g0261a0001c0001t0001g0270a0001c0001t0001g0289others(5): Show | 8 | NA18961.hp1 NA18994.hp1 NA18994.hp2 others(5): Show |
intron_variant | MODIFIER | c.1295-462delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 168861484 | |||||
| chr2:168861590
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1295-370G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861590 | ||||||
| chr2:168861791
|
G | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(60): Show | 66 | HG00423.hp1 HG01123.hp1 HG01255.hp2 others(63): Show |
intron_variant | MODIFIER | c.1295-169G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861791 | ||||||
| chr2:168862123
|
G | C | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0050others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1384+74G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862123 | ||||||
| chr2:168862127
|
G | A | 4 | a0001c0005t0003g0012a0001c0005t0003g0065a0001c0005t0003g0248others(1): Show | 5 | HG01255.hp2 HG02258.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1384+78G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862127 | ||||||
| chr2:168862367
|
T | C | 4 | a0001c0002t0002g0010a0001c0002t0002g0173a0001c0002t0002g0179others(1): Show | 5 | HG03490.hp2 HG03492.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384+318T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862367 | ||||||
| chr2:168862385
|
C | CACAAG | 3 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116 | 3 | HG00140.hp2 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1384+338_1384+342d others(7): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168862385 | |||||
| chr2:168862392
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(240): Show | 252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.1384+343T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862392 | ||||||
| chr2:168862471
|
A | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(251): Show | 263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1384+422A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862471 | ||||||
| chr2:168862543
|
TGTAA | T | 102 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0020others(99): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1384+501_1384+504d others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168862543 | |||||
| chr2:168862554
|
G | T | 1 | a0001c0004t0002g0243 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1384+505G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862554 | ||||||
| chr2:168862569
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1384+520T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862569 | ||||||
| chr2:168862756
|
C | CTTCTTTA others(1): Show |
98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 103 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1384+708_1384+715d others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168862756 | |||||
| chr2:168862819
|
C | T | 8 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0304others(5): Show | 8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1384+770C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862819 | ||||||
| chr2:168862852
|
G | A | 3 | a0001c0001t0002g0022a0001c0001t0002g0242a0001c0001t0002g0281 | 3 | HG00642.hp2 HG01074.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1384+803G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862852 | ||||||
| chr2:168862990
|
T | G | 102 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0020others(99): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1384+941T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862990 | ||||||
| chr2:168863027
|
AAGAC | A | 278 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(275): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1384+984_1384+987d others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168863027 | |||||
| chr2:168863129
|
G | T | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1384+1080G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863129 | ||||||
| chr2:168863142
|
C | A | 5 | a0001c0001t0001g0215a0001c0001t0001g0261a0001c0010t0001g0048others(2): Show | 5 | HG02486.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1384+1093C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863142 | ||||||
| chr2:168863193
|
C | G | 256 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(253): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1384+1144C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863193 | ||||||
| chr2:168863296
|
A | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(278): Show | 291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.1384+1247A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863296 | ||||||
| chr2:168863363
|
T | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(256): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.1384+1314T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863363 | ||||||
| chr2:168863432
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1384+1383G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863432 | ||||||
| chr2:168863441
|
T | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(254): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1384+1392T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863441 | ||||||
| chr2:168863472
|
A | C | 1 | a0001c0007t0001g0071 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1385-1362A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863472 | ||||||
| chr2:168863485
|
G | A | 1 | a0001c0004t0002g0038 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1385-1349G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863485 | ||||||
| chr2:168863569
|
T | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 7 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1385-1265T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863569 | ||||||
| chr2:168863660
|
G | T | 6 | a0001c0001t0001g0055a0003c0006t0001g0274a0003c0006t0001g0310others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1385-1174G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863660 | ||||||
| chr2:168863669
|
TGTGA | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(275): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1385-1158_1385-115 others(8): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168863669 | |||||
| chr2:168863705
|
G | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(251): Show | 263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1385-1129G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863705 | ||||||
| chr2:168863903
|
C | T | 1 | a0001c0007t0001g0214 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1385-931C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863903 | ||||||
| chr2:168863917
|
A | ATT | 6 | a0001c0001t0001g0047a0001c0001t0001g0060a0001c0001t0001g0152others(3): Show | 6 | HG00733.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1385-907_1385-906d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168863917 | |||||
| chr2:168863921
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1385-913T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863921 | ||||||
| chr2:168863979
|
TAGCTCAC others(50): Show |
T | 2 | a0001c0002t0002g0205a0001c0002t0002g0232 | 2 | HG00621.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.1385-796_1385-740d others(59): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168863979 | |||||
| chr2:168863997
|
G | A | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0050others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1385-837G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863997 | ||||||
| chr2:168864226
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(10): Show | 14 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1385-608C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168864226 | ||||||
| chr2:168864229
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0192 | 2 | HG01123.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1385-605G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168864229 | ||||||
| chr2:168864285
|
GT | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(273): Show | 286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1385-538delT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168864285 | |||||
| chr2:168864430
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1385-404C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168864430 | ||||||
| chr2:168864506
|
GA | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(251): Show | 263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1385-325delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168864506 | |||||
| chr2:168864530
|
C | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(94): Show | 103 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1385-304C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168864530 | ||||||
| chr2:168864564
|
C | T | 1 | a0003c0006t0002g0266 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1385-270C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168864564 | ||||||
| chr2:168864565
|
G | A | 1 | a0001c0012t0001g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1385-269G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168864565 | ||||||
| chr2:168864640
|
T | G | 40 | a0001c0001t0001g0192a0001c0001t0001g0287a0001c0001t0001g0288others(37): Show | 42 | HG00423.hp1 HG01123.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.1385-194T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168864640 |