Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23413 |
|---|---|
| ensemblid | ENSG00000107130.10 |
| hgncid | 3953 |
| symbol | NCS1 |
| name | neuronal calcium sensor 1 |
| refseq_nuc | NM_014286.4 |
| refseq_prot | NP_055101.2 |
| ensembl_nuc | ENST00000372398.6 |
| ensembl_prot | ENSP00000361475.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 130172404 |
| end | 130237303 |
| strand | + |
| ver | v1.2 |
| region | chr9:130172404-130237303 |
| region5000 | chr9:130167404-130242303 |
| regionname0 | NCS1_chr9_130172404_130237303 |
| regionname5000 | NCS1_chr9_130167404_130242303 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 190 | 348 | 90 | 80 | 114 | 16 | 46 | 80 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 573 | 239 | 53 | 46 | 90 | 11 | 37 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| c0002 | 0/0 | 573 | 106 | 37 | 34 | 23 | 5 | 7 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| c0003 | 0/0 | 573 | 2 | 0 | 0 | 0 | 0 | 2 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| c0004 | 0/0 | 573 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4594 | 36 | 0 | 9 | 25 | 2 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0002 | 0/0 | 4594 | 15 | 0 | 5 | 0 | 4 | 6 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0003 | 0/0 | 4593 | 13 | 0 | 1 | 6 | 3 | 3 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0004 | 0/0 | 4595 | 10 | 0 | 5 | 4 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0005 | 0/0 | 4594 | 7 | 0 | 0 | 4 | 0 | 3 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0006 | 0/0 | 4592 | 6 | 0 | 0 | 6 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0007 | 0/0 | 4593 | 6 | 0 | 0 | 3 | 0 | 3 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0008 | 0/0 | 4593 | 5 | 0 | 2 | 3 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0009 | 0/0 | 4594 | 4 | 0 | 3 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0010 | 0/0 | 4594 | 4 | 0 | 2 | 1 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0011 | 0/0 | 4595 | 4 | 0 | 4 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0012 | 0/0 | 4594 | 4 | 0 | 2 | 0 | 0 | 2 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0013 | 0/0 | 4593 | 4 | 0 | 0 | 4 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0014 | 0/0 | 4594 | 4 | 0 | 0 | 4 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0015 | 1/0 | 4592 | 4 | 0 | 0 | 2 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0016 | 0/0 | 4594 | 4 | 0 | 2 | 2 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0017 | 0/0 | 4593 | 4 | 1 | 0 | 2 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0018 | 0/0 | 4595 | 3 | 2 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0019 | 0/0 | 4594 | 3 | 0 | 0 | 3 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0020 | 0/0 | 4595 | 3 | 0 | 0 | 2 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0021 | 0/0 | 4593 | 3 | 3 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0022 | 0/0 | 4592 | 3 | 1 | 1 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0023 | 0/0 | 4593 | 3 | 1 | 2 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0024 | 0/0 | 4595 | 3 | 1 | 1 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0025 | 0/0 | 4594 | 3 | 0 | 3 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0026 | 0/0 | 4594 | 2 | 0 | 0 | 2 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0027 | 0/0 | 4593 | 2 | 2 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0028 | 0/0 | 4593 | 2 | 2 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0029 | 0/0 | 4594 | 2 | 2 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0030 | 0/0 | 4595 | 2 | 0 | 0 | 0 | 2 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0031 | 0/0 | 4594 | 2 | 0 | 2 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0032 | 0/0 | 4594 | 2 | 1 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0033 | 0/0 | 4594 | 2 | 0 | 2 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0034 | 0/0 | 4592 | 2 | 0 | 0 | 2 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0035 | 0/0 | 4593 | 2 | 0 | 0 | 2 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0036 | 0/0 | 4593 | 2 | 0 | 2 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0037 | 0/0 | 4593 | 2 | 0 | 0 | 2 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0038 | 0/0 | 4594 | 2 | 0 | 0 | 2 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0039 | 0/0 | 4593 | 2 | 0 | 2 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0040 | 0/0 | 4592 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0041 | 0/0 | 4593 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0042 | 0/0 | 4594 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0043 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0044 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0045 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0046 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0047 | 0/0 | 4593 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0048 | 0/0 | 4595 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0049 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0050 | 0/0 | 4594 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0051 | 0/0 | 4594 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0052 | 0/0 | 4594 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0053 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0054 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0055 | 0/0 | 4595 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0056 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0057 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0058 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0059 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0060 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0061 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0062 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0063 | 0/0 | 4596 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0064 | 0/0 | 4595 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0065 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0066 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0067 | 0/0 | 4593 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0068 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0069 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0070 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0071 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0072 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0073 | 0/0 | 4593 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0074 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0075 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0076 | 0/0 | 4592 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0077 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0078 | 0/0 | 4595 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0079 | 0/0 | 4594 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0080 | 0/0 | 4595 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0081 | 0/0 | 4595 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0082 | 0/0 | 4595 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0083 | 0/0 | 4595 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0084 | 0/0 | 4595 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0085 | 0/0 | 4595 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0086 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0087 | 0/0 | 4593 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0088 | 0/0 | 4594 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0089 | 0/0 | 4594 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0090 | 0/0 | 4594 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0091 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0092 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0093 | 0/0 | 4594 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0094 | 0/0 | 4594 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0095 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0096 | 0/0 | 4593 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0097 | 0/0 | 4594 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0098 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0099 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0100 | 0/0 | 4594 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0101 | 0/0 | 4594 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0102 | 0/0 | 4595 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0103 | 0/0 | 4594 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0104 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0105 | 0/0 | 4594 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0106 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0107 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0108 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0109 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0110 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0111 | 0/0 | 4594 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0112 | 0/0 | 4593 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0113 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0114 | 0/0 | 4594 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0115 | 0/0 | 4592 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0116 | 0/0 | 4594 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0117 | 0/0 | 4593 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0118 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0119 | 0/0 | 4593 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0120 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0121 | 0/0 | 4592 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0122 | 0/0 | 4594 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0123 | 0/0 | 4592 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0124 | 0/0 | 4593 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0125 | 0/0 | 4593 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0126 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0127 | 0/0 | 4594 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0128 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0129 | 0/0 | 4593 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0130 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0131 | 0/0 | 4592 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0132 | 0/0 | 4593 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0133 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0134 | 0/0 | 4592 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0135 | 0/0 | 4592 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0136 | 0/0 | 4593 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0137 | 0/0 | 4592 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0138 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0139 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0140 | 0/0 | 4593 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0141 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0142 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0143 | 0/0 | 4592 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0144 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0145 | 0/0 | 4592 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0146 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0147 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0148 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0149 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0150 | 0/0 | 4592 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0151 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0152 | 0/0 | 4594 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0153 | 0/0 | 4592 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0154 | 0/0 | 4594 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0155 | 0/0 | 4592 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0156 | 0/0 | 4593 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0157 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0158 | 0/0 | 4593 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0159 | 0/0 | 4593 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0160 | 0/0 | 4593 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0161 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0162 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0163 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0164 | 0/0 | 4592 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0165 | 0/0 | 4592 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0166 | 0/0 | 4592 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0167 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0168 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0169 | 0/0 | 4594 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0170 | 0/0 | 4594 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0171 | 0/0 | 4592 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0172 | 0/0 | 4593 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0173 | 0/0 | 4594 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0174 | 0/0 | 4594 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0175 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0176 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0177 | 0/0 | 4594 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0178 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0179 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0180 | 0/0 | 4593 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0181 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0182 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0183 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0184 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0185 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0186 | 0/0 | 4594 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0187 | 0/0 | 4594 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0188 | 0/0 | 4595 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0189 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0190 | 0/0 | 4594 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0191 | 0/0 | 4594 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0192 | 0/0 | 4594 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0193 | 0/0 | 4594 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0194 | 0/0 | 4594 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0195 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0196 | 0/0 | 4594 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0197 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0198 | 0/1 | 4593 | 1 | 0 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0199 | 0/0 | 4592 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0200 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| t0201 | 0/0 | 4594 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 573 | 239 | 53 | 46 | 90 | 11 | 37 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002 | 0/0 | 573 | 106 | 37 | 34 | 23 | 5 | 7 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0003 | 0/0 | 573 | 2 | 0 | 0 | 0 | 0 | 2 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0004 | 0/0 | 573 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5166 | 20 | 0 | 2 | 17 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0002 | 0/0 | 5166 | 12 | 0 | 3 | 0 | 3 | 6 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0003 | 0/0 | 5165 | 10 | 0 | 0 | 6 | 2 | 2 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0004 | 0/0 | 5167 | 9 | 0 | 4 | 4 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0005 | 0/0 | 5166 | 7 | 0 | 0 | 4 | 0 | 3 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0006 | 0/0 | 5164 | 6 | 0 | 0 | 6 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0007 | 0/0 | 5165 | 3 | 0 | 0 | 2 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0008 | 0/0 | 5165 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0009 | 0/0 | 5166 | 3 | 0 | 3 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0010 | 0/0 | 5166 | 2 | 0 | 0 | 1 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0013 | 0/0 | 5165 | 4 | 0 | 0 | 4 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0014 | 0/0 | 5166 | 4 | 0 | 0 | 4 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0015 | 1/0 | 5164 | 4 | 0 | 0 | 2 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0016 | 0/0 | 5166 | 3 | 0 | 1 | 2 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0017 | 0/0 | 5165 | 2 | 0 | 0 | 1 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0019 | 0/0 | 5166 | 3 | 0 | 0 | 3 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0020 | 0/0 | 5167 | 3 | 0 | 0 | 2 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0022 | 0/0 | 5164 | 3 | 1 | 1 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0023 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0024 | 0/0 | 5167 | 2 | 1 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0025 | 0/0 | 5166 | 3 | 0 | 3 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0026 | 0/0 | 5166 | 2 | 0 | 0 | 2 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0027 | 0/0 | 5165 | 2 | 2 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0028 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0029 | 0/0 | 5166 | 2 | 2 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0030 | 0/0 | 5167 | 2 | 0 | 0 | 0 | 2 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0031 | 0/0 | 5166 | 2 | 0 | 2 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0032 | 0/0 | 5166 | 2 | 1 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0033 | 0/0 | 5166 | 2 | 0 | 2 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0034 | 0/0 | 5164 | 2 | 0 | 0 | 2 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0035 | 0/0 | 5165 | 2 | 0 | 0 | 2 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0036 | 0/0 | 5165 | 2 | 0 | 2 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0037 | 0/0 | 5165 | 2 | 0 | 0 | 2 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0039 | 0/0 | 5165 | 2 | 0 | 2 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0041 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0042 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0043 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0044 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0045 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0046 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0047 | 0/0 | 5165 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0048 | 0/0 | 5167 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0049 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0050 | 0/0 | 5166 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0051 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0052 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0053 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0059 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0060 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0061 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0064 | 0/0 | 5167 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0066 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0067 | 0/0 | 5165 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0068 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0069 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0070 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0071 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0074 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0075 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0076 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0077 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0078 | 0/0 | 5167 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0079 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0080 | 0/0 | 5167 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0081 | 0/0 | 5167 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0082 | 0/0 | 5167 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0083 | 0/0 | 5167 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0084 | 0/0 | 5167 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0085 | 0/0 | 5167 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0089 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0090 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0091 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0092 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0094 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0095 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0096 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0098 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0099 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0101 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0102 | 0/0 | 5167 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0103 | 0/0 | 5166 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0104 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0105 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0106 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0107 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0108 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0110 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0114 | 0/0 | 5166 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0115 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0117 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0118 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0119 | 0/0 | 5165 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0120 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0121 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0122 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0124 | 0/0 | 5165 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0129 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0130 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0131 | 0/0 | 5164 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0132 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0134 | 0/0 | 5164 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0135 | 0/0 | 5164 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0136 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0138 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0140 | 0/0 | 5165 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0142 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0146 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0151 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0152 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0153 | 0/0 | 5164 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0154 | 0/0 | 5166 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0156 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0158 | 0/0 | 5165 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0159 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0160 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0162 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0165 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0166 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0167 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0168 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0169 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0170 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0176 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0177 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0178 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0179 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0181 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0182 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0183 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0186 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0187 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0188 | 0/0 | 5167 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0189 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0190 | 0/0 | 5166 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0191 | 0/0 | 5166 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0192 | 0/0 | 5166 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0193 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0195 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0196 | 0/0 | 5166 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0197 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0198 | 0/1 | 5165 | 1 | 0 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0200 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0001t0201 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0001 | 0/0 | 5166 | 16 | 0 | 7 | 8 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0002 | 0/0 | 5166 | 3 | 0 | 2 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0003 | 0/0 | 5165 | 3 | 0 | 1 | 0 | 1 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0004 | 0/0 | 5167 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0007 | 0/0 | 5165 | 3 | 0 | 0 | 1 | 0 | 2 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0008 | 0/0 | 5165 | 3 | 0 | 2 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0009 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0010 | 0/0 | 5166 | 2 | 0 | 2 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0011 | 0/0 | 5167 | 4 | 0 | 4 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0012 | 0/0 | 5166 | 2 | 0 | 2 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0016 | 0/0 | 5166 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0017 | 0/0 | 5165 | 2 | 1 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0018 | 0/0 | 5167 | 3 | 2 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0021 | 0/0 | 5165 | 3 | 3 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0023 | 0/0 | 5165 | 2 | 0 | 2 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0024 | 0/0 | 5167 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0028 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0038 | 0/0 | 5166 | 2 | 0 | 0 | 2 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0040 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0054 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0055 | 0/0 | 5167 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0056 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0057 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0058 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0062 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0063 | 0/0 | 5168 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0065 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0072 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0073 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0086 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0087 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0088 | 0/0 | 5166 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0093 | 0/0 | 5166 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0097 | 0/0 | 5166 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0100 | 0/0 | 5166 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0109 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0111 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0112 | 0/0 | 5165 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0113 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0116 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0123 | 0/0 | 5164 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0125 | 0/0 | 5165 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0126 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0127 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0128 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0133 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0137 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0139 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0141 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0143 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0144 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0145 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0147 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0148 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0149 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0150 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0155 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0157 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0161 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0163 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0164 | 0/0 | 5164 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0171 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0172 | 0/0 | 5165 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0173 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0174 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0175 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0180 | 0/0 | 5165 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0184 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0185 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0194 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0002t0199 | 0/0 | 5164 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0003t0012 | 0/0 | 5166 | 2 | 0 | 0 | 0 | 0 | 2 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| a0001c0004t0008 | 0/0 | 5165 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | copy fasta | chr9 | 130167404 | 130242303 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0006g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0007g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0009g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0009g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0009g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0010g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0010g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0013g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0013g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0013g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0013g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0014g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0014g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0014g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0014g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0015g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0015g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0015g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0015g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0016g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0016g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0016g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0017g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0017g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0019g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0019g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0019g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0020g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0020g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0020g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0022g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0022g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0022g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0023g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0024g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0024g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0025g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0025g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0025g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0026g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0026g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0027g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0027g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0028g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0029g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0029g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0030g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0030g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0031g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0031g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0032g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0032g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0033g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0033g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0034g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0034g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0035g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0035g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0036g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0036g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0037g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0037g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0039g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0039g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0041g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0042g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0043g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0044g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0045g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0046g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0047g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0048g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0049g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0050g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0051g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0052g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0053g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0059g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0060g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0061g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0064g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0066g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0067g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0068g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0069g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0070g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0071g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0074g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0075g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0076g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0077g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0078g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0079g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0080g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0081g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0082g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0083g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0084g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0085g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0089g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0090g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0091g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0092g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0094g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0095g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0096g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0098g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0099g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0101g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0102g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0103g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0104g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0105g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0106g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0107g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0108g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0110g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0114g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0115g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0117g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0118g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0119g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0120g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0121g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0122g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0124g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0129g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0130g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0131g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0132g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0134g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0135g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0136g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0138g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0140g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0142g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0146g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0151g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0152g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0153g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0154g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0156g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0158g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0159g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0160g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0162g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0165g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0166g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0167g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0168g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0169g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0170g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0176g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0177g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0178g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0179g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0181g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0182g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0183g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0186g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0187g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0188g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0189g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0190g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0191g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0192g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0193g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0195g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0196g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0197g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0198g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0200g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0001t0201g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0007g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0007g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0007g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0008g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0008g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0008g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0009g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0010g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0010g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0011g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0011g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0011g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0011g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0012g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0012g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0016g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0017g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0017g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0018g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0018g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0018g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0021g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0021g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0021g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0023g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0023g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0024g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0028g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0038g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0038g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0040g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0054g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0055g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0056g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0057g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0058g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0062g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0063g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0065g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0072g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0073g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0086g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0087g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0088g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0093g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0097g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0100g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0109g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0111g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0112g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0113g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0116g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0123g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0125g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0126g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0127g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0128g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0133g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0137g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0139g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0141g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0143g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0144g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0145g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0147g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0148g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0149g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0150g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0155g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0157g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0161g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0163g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0164g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0171g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0172g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0173g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0174g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0175g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0180g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0184g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0185g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0194g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0002t0199g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0003t0012g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0003t0012g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| a0001c0004t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0194 | g0025 | EUR | GBR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0066 | EUR | GBR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0135 | EUR | GBR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00140 | hp2 | a0001 | c0002 | t0087 | g0072 | EUR | GBR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0150 | EUR | FIN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0024 | EUR | FIN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00323 | hp2 | a0001 | c0001 | t0030 | g0038 | EUR | FIN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00408 | hp1 | a0001 | c0001 | t0037 | g0252 | EAS | CHS | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00423 | hp1 | a0001 | c0001 | t0102 | g0121 | EAS | CHS | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00438 | hp1 | a0001 | c0001 | t0037 | g0152 | EAS | CHS | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00438 | hp2 | a0001 | c0001 | t0007 | g0221 | EAS | CHS | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0197 | EAS | CHS | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00544 | hp2 | a0001 | c0001 | t0042 | g0052 | EAS | CHS | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00597 | hp1 | a0001 | c0001 | t0080 | g0151 | EAS | CHS | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00597 | hp2 | a0001 | c0001 | t0140 | g0236 | EAS | CHS | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00639 | hp1 | a0001 | c0001 | t0189 | g0216 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00639 | hp2 | a0001 | c0002 | t0008 | g0114 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00642 | hp1 | a0001 | c0001 | t0168 | g0107 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00735 | hp1 | a0001 | c0001 | t0092 | g0134 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00735 | hp2 | a0001 | c0001 | t0190 | g0081 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00738 | hp1 | a0001 | c0001 | t0032 | g0195 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00741 | hp1 | a0001 | c0002 | t0133 | g0047 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG00741 | hp2 | a0001 | c0002 | t0199 | g0110 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01069 | hp1 | a0001 | c0001 | t0154 | g0340 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01069 | hp2 | a0001 | c0001 | t0036 | g0288 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01070 | hp1 | a0001 | c0001 | t0192 | g0171 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01070 | hp2 | a0001 | c0001 | t0009 | g0093 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01071 | hp1 | a0001 | c0001 | t0036 | g0266 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01071 | hp2 | a0001 | c0001 | t0009 | g0084 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01074 | hp1 | a0001 | c0001 | t0106 | g0056 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0143 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01081 | hp1 | a0001 | c0002 | t0004 | g0124 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01081 | hp2 | a0001 | c0001 | t0025 | g0188 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01099 | hp1 | a0001 | c0002 | t0086 | g0213 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01099 | hp2 | a0001 | c0001 | t0039 | g0148 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01109 | hp1 | a0001 | c0001 | t0050 | g0308 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01109 | hp2 | a0001 | c0002 | t0018 | g0296 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0095 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01167 | hp2 | a0001 | c0001 | t0114 | g0290 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01168 | hp1 | a0001 | c0002 | t0093 | g0212 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01168 | hp2 | a0001 | c0001 | t0031 | g0091 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01169 | hp1 | a0001 | c0001 | t0031 | g0090 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0096 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0079 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01175 | hp2 | a0001 | c0002 | t0097 | g0039 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01192 | hp1 | a0001 | c0001 | t0009 | g0068 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01192 | hp2 | a0001 | c0001 | t0039 | g0106 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01243 | hp1 | a0001 | c0001 | t0022 | g0191 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01243 | hp2 | a0001 | c0001 | t0103 | g0137 | AMR | PUR | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01255 | hp1 | a0001 | c0001 | t0110 | g0030 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01255 | hp2 | a0001 | c0001 | t0196 | g0230 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0229 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01257 | hp1 | a0001 | c0001 | t0118 | g0231 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01257 | hp2 | a0001 | c0001 | t0033 | g0029 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01258 | hp1 | a0001 | c0001 | t0033 | g0031 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0268 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01261 | hp1 | a0001 | c0002 | t0003 | g0069 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01261 | hp2 | a0001 | c0001 | t0025 | g0113 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01358 | hp1 | a0001 | c0001 | t0025 | g0178 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01358 | hp2 | a0001 | c0002 | t0011 | g0217 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01361 | hp1 | a0001 | c0002 | t0185 | g0144 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01361 | hp2 | a0001 | c0001 | t0130 | g0175 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01433 | hp1 | a0001 | c0002 | t0010 | g0120 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01515 | hp1 | a0001 | c0001 | t0010 | g0282 | EUR | IBS | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0036 | EUR | IBS | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0087 | EUR | IBS | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0037 | EUR | IBS | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01884 | hp1 | a0001 | c0001 | t0146 | g0333 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01884 | hp2 | a0001 | c0002 | t0157 | g0173 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01891 | hp1 | a0001 | c0001 | t0061 | g0232 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01891 | hp2 | a0001 | c0001 | t0201 | g0338 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01928 | hp1 | a0001 | c0002 | t0008 | g0041 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01928 | hp2 | a0001 | c0001 | t0024 | g0067 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01934 | hp1 | a0001 | c0002 | t0011 | g0128 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0255 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01952 | hp1 | a0001 | c0001 | t0091 | g0015 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01975 | hp1 | a0001 | c0001 | t0104 | g0065 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01978 | hp1 | a0001 | c0002 | t0011 | g0071 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01978 | hp2 | a0001 | c0002 | t0023 | g0054 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01981 | hp1 | a0001 | c0002 | t0012 | g0012 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01981 | hp2 | a0001 | c0001 | t0191 | g0179 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01993 | hp1 | a0001 | c0001 | t0197 | g0260 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01993 | hp2 | a0001 | c0002 | t0012 | g0125 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02004 | hp1 | a0001 | c0001 | t0016 | g0123 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02004 | hp2 | a0001 | c0002 | t0100 | g0122 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02027 | hp1 | a0001 | c0001 | t0081 | g0241 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02027 | hp2 | a0001 | c0001 | t0067 | g0240 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02055 | hp1 | a0001 | c0002 | t0063 | g0235 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02055 | hp2 | a0001 | c0001 | t0074 | g0305 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02056 | hp1 | a0001 | c0001 | t0034 | g0102 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02056 | hp2 | a0001 | c0001 | t0010 | g0098 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02071 | hp1 | a0001 | c0001 | t0153 | g0160 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02071 | hp2 | a0001 | c0002 | t0123 | g0222 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02074 | hp1 | a0001 | c0001 | t0020 | g0133 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02074 | hp2 | a0001 | c0002 | t0164 | g0215 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02083 | hp2 | a0001 | c0001 | t0015 | g0163 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02135 | hp2 | a0001 | c0001 | t0016 | g0265 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02145 | hp1 | a0001 | c0001 | t0183 | g0103 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02145 | hp2 | a0001 | c0001 | t0107 | g0101 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02148 | hp1 | a0001 | c0002 | t0011 | g0061 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02165 | hp1 | a0001 | c0001 | t0008 | g0167 | EAS | CDX | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | CDX | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02258 | hp1 | a0001 | c0002 | t0184 | g0334 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02258 | hp2 | a0001 | c0002 | t0018 | g0245 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02273 | hp1 | a0001 | c0001 | t0077 | g0281 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02273 | hp2 | a0001 | c0002 | t0023 | g0059 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02280 | hp1 | a0001 | c0001 | t0053 | g0314 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02280 | hp2 | a0001 | c0002 | t0171 | g0300 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02293 | hp2 | a0001 | c0002 | t0016 | g0019 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02300 | hp2 | a0001 | c0002 | t0175 | g0043 | AMR | PEL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02451 | hp1 | a0001 | c0001 | t0024 | g0094 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02451 | hp2 | a0001 | c0002 | t0161 | g0309 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02523 | hp1 | a0001 | c0001 | t0169 | g0169 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | KHV | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02572 | hp1 | a0001 | c0001 | t0045 | g0345 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02572 | hp2 | a0001 | c0002 | t0147 | g0234 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02602 | hp1 | a0001 | c0001 | t0129 | g0297 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02602 | hp2 | a0001 | c0001 | t0096 | g0063 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02615 | hp1 | a0001 | c0002 | t0018 | g0299 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02615 | hp2 | a0001 | c0002 | t0055 | g0293 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02622 | hp1 | a0001 | c0001 | t0049 | g0328 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02622 | hp2 | a0001 | c0001 | t0181 | g0330 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02630 | hp1 | a0001 | c0001 | t0108 | g0303 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02630 | hp2 | a0001 | c0002 | t0126 | g0153 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02647 | hp1 | a0001 | c0001 | t0028 | g0320 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02647 | hp2 | a0001 | c0001 | t0059 | g0304 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02698 | hp1 | a0001 | c0001 | t0134 | g0165 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02698 | hp2 | a0001 | c0002 | t0073 | g0028 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02717 | hp1 | a0001 | c0002 | t0155 | g0344 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02717 | hp2 | a0001 | c0002 | t0143 | g0316 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02723 | hp1 | a0001 | c0001 | t0165 | g0346 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02723 | hp2 | a0001 | c0001 | t0120 | g0075 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02738 | hp2 | a0001 | c0001 | t0186 | g0242 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02809 | hp1 | a0001 | c0002 | t0150 | g0342 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02809 | hp2 | a0001 | c0001 | t0179 | g0155 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02818 | hp1 | a0001 | c0002 | t0141 | g0020 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02818 | hp2 | a0001 | c0001 | t0142 | g0326 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02886 | hp1 | a0001 | c0002 | t0021 | g0306 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02886 | hp2 | a0001 | c0001 | t0070 | g0324 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02895 | hp1 | a0001 | c0001 | t0027 | g0335 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02895 | hp2 | a0001 | c0001 | t0060 | g0302 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02897 | hp1 | a0001 | c0002 | t0057 | g0159 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02897 | hp2 | a0001 | c0001 | t0027 | g0336 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02922 | hp1 | a0001 | c0002 | t0148 | g0130 | AFR | ESN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02922 | hp2 | a0001 | c0001 | t0029 | g0325 | AFR | ESN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02965 | hp1 | a0001 | c0001 | t0029 | g0156 | AFR | ESN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02965 | hp2 | a0001 | c0001 | t0121 | g0076 | AFR | ESN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02970 | hp1 | a0001 | c0001 | t0044 | g0337 | AFR | ESN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02970 | hp2 | a0001 | c0001 | t0043 | g0327 | AFR | ESN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02976 | hp1 | a0001 | c0002 | t0062 | g0298 | AFR | ESN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02976 | hp2 | a0001 | c0002 | t0163 | g0323 | AFR | ESN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03041 | hp1 | a0001 | c0001 | t0064 | g0196 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03041 | hp2 | a0001 | c0002 | t0137 | g0158 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03098 | hp1 | a0001 | c0002 | t0144 | g0115 | AFR | MSL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03098 | hp2 | a0001 | c0001 | t0023 | g0104 | AFR | MSL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03130 | hp1 | a0001 | c0001 | t0166 | g0329 | AFR | ESN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03130 | hp2 | a0001 | c0002 | t0021 | g0034 | AFR | ESN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03139 | hp1 | a0001 | c0001 | t0068 | g0295 | AFR | ESN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03139 | hp2 | a0001 | c0001 | t0167 | g0064 | AFR | ESN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03195 | hp1 | a0001 | c0001 | t0195 | g0322 | AFR | ESN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03195 | hp2 | a0001 | c0002 | t0017 | g0317 | AFR | ESN | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03209 | hp1 | a0001 | c0002 | t0054 | g0199 | AFR | MSL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03209 | hp2 | a0001 | c0002 | t0128 | g0294 | AFR | MSL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03225 | hp1 | a0001 | c0002 | t0139 | g0343 | AFR | MSL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03225 | hp2 | a0001 | c0001 | t0032 | g0319 | AFR | MSL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03239 | hp1 | a0001 | c0001 | t0015 | g0203 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03239 | hp2 | a0001 | c0001 | t0052 | g0147 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03453 | hp1 | a0001 | c0002 | t0056 | g0311 | AFR | MSL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03453 | hp2 | a0001 | c0001 | t0022 | g0347 | AFR | MSL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03486 | hp1 | a0001 | c0002 | t0065 | g0205 | AFR | MSL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03486 | hp2 | a0001 | c0002 | t0113 | g0292 | AFR | MSL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03490 | hp1 | a0001 | c0002 | t0007 | g0177 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03490 | hp2 | a0001 | c0003 | t0012 | g0016 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0202 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03492 | hp1 | a0001 | c0002 | t0007 | g0186 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0189 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03540 | hp1 | a0001 | c0001 | t0151 | g0332 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03540 | hp2 | a0001 | c0001 | t0071 | g0233 | AFR | GWD | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03579 | hp1 | a0001 | c0002 | t0021 | g0312 | AFR | MSL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03579 | hp2 | a0001 | c0001 | t0138 | g0273 | AFR | MSL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03654 | hp1 | a0001 | c0001 | t0048 | g0085 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03669 | hp1 | a0001 | c0001 | t0051 | g0049 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03669 | hp2 | a0001 | c0001 | t0084 | g0180 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03688 | hp1 | a0001 | c0001 | t0160 | g0172 | SAS | STU | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | STU | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03704 | hp1 | a0001 | c0001 | t0159 | g0198 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03704 | hp2 | a0001 | c0001 | t0188 | g0287 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03710 | hp2 | a0001 | c0002 | t0009 | g0092 | SAS | PJL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0027 | SAS | BEB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03831 | hp2 | a0001 | c0001 | t0136 | g0117 | SAS | BEB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03834 | hp1 | a0001 | c0001 | t0089 | g0194 | SAS | BEB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03834 | hp2 | a0001 | c0001 | t0041 | g0201 | SAS | BEB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03927 | hp1 | a0001 | c0001 | t0078 | g0132 | SAS | BEB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0118 | SAS | BEB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03942 | hp1 | a0001 | c0001 | t0017 | g0116 | SAS | BEB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0086 | SAS | BEB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0279 | SAS | STU | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG04115 | hp2 | a0001 | c0001 | t0079 | g0267 | SAS | STU | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG04184 | hp1 | a0001 | c0001 | t0020 | g0100 | SAS | BEB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG04184 | hp2 | a0001 | c0001 | t0022 | g0161 | SAS | BEB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG04199 | hp1 | a0001 | c0002 | t0173 | g0051 | SAS | STU | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG04199 | hp2 | a0001 | c0001 | t0105 | g0078 | SAS | STU | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG04204 | hp1 | a0001 | c0003 | t0012 | g0014 | SAS | STU | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG04204 | hp2 | a0001 | c0001 | t0094 | g0111 | SAS | STU | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG04228 | hp1 | a0001 | c0001 | t0117 | g0105 | SAS | STU | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG04228 | hp2 | a0001 | c0001 | t0132 | g0109 | SAS | STU | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18522 | hp1 | a0001 | c0001 | t0182 | g0331 | AFR | YRI | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18522 | hp2 | a0001 | c0001 | t0076 | g0310 | AFR | YRI | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18612 | hp1 | a0001 | c0001 | t0170 | g0256 | EAS | CHB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18612 | hp2 | a0001 | c0001 | t0034 | g0248 | EAS | CHB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18747 | hp1 | a0001 | c0002 | t0038 | g0219 | EAS | CHB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18747 | hp2 | a0001 | c0002 | t0174 | g0057 | EAS | CHB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18906 | hp1 | a0001 | c0002 | t0028 | g0154 | AFR | YRI | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18906 | hp2 | a0001 | c0002 | t0145 | g0315 | AFR | YRI | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18942 | hp1 | a0001 | c0001 | t0013 | g0261 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18942 | hp2 | a0001 | c0001 | t0014 | g0258 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18945 | hp1 | a0001 | c0001 | t0158 | g0140 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0228 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18948 | hp1 | a0001 | c0001 | t0016 | g0184 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18948 | hp2 | a0001 | c0002 | t0008 | g0286 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18953 | hp1 | a0001 | c0001 | t0026 | g0082 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18953 | hp2 | a0001 | c0001 | t0082 | g0208 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18959 | hp1 | a0001 | c0002 | t0180 | g0257 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18959 | hp2 | a0001 | c0001 | t0101 | g0055 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18961 | hp1 | a0001 | c0001 | t0047 | g0247 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18961 | hp2 | a0001 | c0001 | t0124 | g0249 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18963 | hp1 | a0001 | c0002 | t0125 | g0002 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18963 | hp2 | a0001 | c0002 | t0112 | g0182 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18966 | hp1 | a0001 | c0004 | t0008 | g0223 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18966 | hp2 | a0001 | c0002 | t0024 | g0220 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18967 | hp1 | a0001 | c0001 | t0026 | g0004 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18969 | hp1 | a0001 | c0002 | t0116 | g0060 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18970 | hp1 | a0001 | c0001 | t0035 | g0270 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18970 | hp2 | a0001 | c0001 | t0193 | g0192 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18971 | hp2 | a0001 | c0002 | t0017 | g0074 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18974 | hp1 | a0001 | c0001 | t0014 | g0243 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18975 | hp1 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18975 | hp2 | a0001 | c0001 | t0135 | g0277 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18980 | hp2 | a0001 | c0001 | t0020 | g0237 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0099 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18983 | hp1 | a0001 | c0001 | t0131 | g0009 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18984 | hp1 | a0001 | c0001 | t0085 | g0138 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18985 | hp2 | a0001 | c0002 | t0007 | g0005 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0119 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18986 | hp2 | a0001 | c0001 | t0019 | g0088 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18995 | hp2 | a0001 | c0001 | t0119 | g0077 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18999 | hp1 | a0001 | c0001 | t0006 | g0131 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA18999 | hp2 | a0001 | c0001 | t0017 | g0253 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19000 | hp1 | a0001 | c0001 | t0014 | g0044 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19000 | hp2 | a0001 | c0001 | t0019 | g0080 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0262 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19006 | hp2 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19010 | hp1 | a0001 | c0001 | t0035 | g0271 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19010 | hp2 | a0001 | c0002 | t0127 | g0126 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19011 | hp1 | a0001 | c0001 | t0090 | g0275 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19011 | hp2 | a0001 | c0001 | t0006 | g0284 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19030 | hp1 | a0001 | c0001 | t0066 | g0263 | AFR | LWK | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19030 | hp2 | a0001 | c0001 | t0095 | g0341 | AFR | LWK | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19057 | hp2 | a0001 | c0001 | t0006 | g0204 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19064 | hp1 | a0001 | c0001 | t0177 | g0017 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19064 | hp2 | a0001 | c0001 | t0006 | g0348 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19065 | hp1 | a0001 | c0001 | t0019 | g0145 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19066 | hp1 | a0001 | c0001 | t0015 | g0238 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19066 | hp2 | a0001 | c0002 | t0038 | g0209 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19068 | hp1 | a0001 | c0001 | t0122 | g0251 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19074 | hp2 | a0001 | c0001 | t0014 | g0289 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19077 | hp1 | a0001 | c0001 | t0013 | g0224 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19077 | hp2 | a0001 | c0002 | t0111 | g0026 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19085 | hp2 | a0001 | c0001 | t0152 | g0185 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19088 | hp1 | a0001 | c0001 | t0013 | g0272 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19088 | hp2 | a0001 | c0001 | t0013 | g0244 | EAS | JPT | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19240 | hp1 | a0001 | c0001 | t0162 | g0301 | AFR | YRI | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA19240 | hp2 | a0001 | c0001 | t0176 | g0035 | AFR | YRI | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA20129 | hp1 | a0001 | c0001 | t0046 | g0166 | AFR | ASW | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA20129 | hp2 | a0001 | c0001 | t0098 | g0174 | AFR | ASW | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA20752 | hp1 | a0001 | c0001 | t0187 | g0200 | EUR | TSI | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0139 | EUR | TSI | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA20805 | hp1 | a0001 | c0001 | t0030 | g0176 | EUR | TSI | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0218 | EUR | TSI | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA20905 | hp1 | a0001 | c0001 | t0156 | g0089 | SAS | GIH | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA20905 | hp2 | a0001 | c0002 | t0172 | g0050 | SAS | GIH | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01123 | hp1 | a0001 | c0002 | t0088 | g0259 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG01123 | hp2 | a0001 | c0002 | t0010 | g0149 | AMR | CLM | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02109 | hp1 | a0001 | c0002 | t0040 | g0033 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02109 | hp2 | a0001 | c0002 | t0149 | g0207 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02486 | hp1 | a0001 | c0001 | t0099 | g0307 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02486 | hp2 | a0001 | c0001 | t0075 | g0318 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02559 | hp1 | a0001 | c0001 | t0069 | g0321 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG02559 | hp2 | a0001 | c0002 | t0109 | g0339 | AFR | ACB | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03471 | hp1 | a0001 | c0001 | t0200 | g0168 | AFR | MSL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| HG03471 | hp2 | a0001 | c0001 | t0115 | g0313 | AFR | MSL | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA20300 | hp1 | a0001 | c0001 | t0178 | g0157 | AFR | USA | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA20300 | hp2 | a0001 | c0001 | t0083 | g0170 | AFR | USA | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA21309 | hp1 | a0001 | c0002 | t0058 | g0264 | AFR | LWK | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| NA21309 | hp2 | a0001 | c0002 | t0072 | g0193 | AFR | LWK | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0198 | g0141 | REF | REF | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0015 | g0206 | REF | REF | NCS1_chr9_130167404_130242303 | NCS1 | chr9 | 130167404 | 130242303 |
| 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 |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:130217913
|
G | A | 1 | a0001c0004 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.171G>A | p.Pro57Pro | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/8 | 431/5164 | 171/573 | 57/190 | chr9 | 130217913 | ||
| chr9:130219727
|
C | T | 1 | a0001c0003 | 2 | HG03490.hp2 HG04204.hp1 |
splice_region_variant&synonymous_variant | LOW | c.231C>T | p.Asp77Asp | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/8 | 491/5164 | 231/573 | 77/190 | chr9 | 130219727 | ||
| chr9:130226430
|
T | G | 1 | a0001c0002 | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
synonymous_variant | LOW | c.516T>G | p.Gly172Gly | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/8 | 776/5164 | 516/573 | 172/190 | chr9 | 130226430 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:130172483
|
C | A | 1 | a0001c0002t0040 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-181C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/8 | 181 | chr9 | 130172483 | |||||
| chr9:130172594
|
G | C | 1 | a0001c0001t0041 | 1 | HG03834.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/8 | 70 | chr9 | 130172594 | |||||
| chr9:130172617
|
C | A | 1 | a0001c0001t0042 | 1 | HG00544.hp2 | 5_prime_UTR_variant | MODIFIER | c.-47C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/8 | 47 | chr9 | 130172617 | |||||
| chr9:130233045
|
C | T | 2 | a0001c0001t0200a0001c0001t0201 | 2 | HG01891.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*73C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 6558 | chr9 | 130233045 | |||||
| chr9:130233053
|
G | A | 1 | a0001c0001t0043 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*81G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 6566 | chr9 | 130233053 | |||||
| chr9:130233091
|
C | T | 1 | a0001c0002t0199 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 6604 | chr9 | 130233091 | |||||
| chr9:130233107
|
G | T | 4 | a0001c0001t0039a0001c0001t0196a0001c0001t0197others(1): Show | 5 | HG01099.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*135G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 6620 | chr9 | 130233107 | |||||
| chr9:130233150
|
C | T | 1 | a0001c0001t0195 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*178C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 6663 | chr9 | 130233150 | |||||
| chr9:130233253
|
G | A | 1 | a0001c0001t0044 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*281G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 6766 | chr9 | 130233253 | |||||
| chr9:130233273
|
C | T | 1 | a0001c0002t0194 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*301C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 6786 | chr9 | 130233273 | |||||
| chr9:130233425
|
G | A | 22 | a0001c0001t0045a0001c0001t0046a0001c0001t0047others(19): Show | 24 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*453G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 6938 | chr9 | 130233425 | |||||
| chr9:130233445
|
C | T | 2 | a0001c0001t0193a0001c0002t0038 | 3 | NA18747.hp1 NA18970.hp2 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*473C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 6958 | chr9 | 130233445 | |||||
| chr9:130233489
|
G | A | 79 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(76): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*517G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7002 | chr9 | 130233489 | |||||
| chr9:130233567
|
A | AT | 3 | a0001c0001t0064a0001c0002t0018a0001c0002t0063 | 5 | HG01109.hp2 HG02055.hp1 HG02258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*603dupT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7089 | INFO_REALIGN_3_PRIME | chr9 | 130233567 | ||||
| chr9:130233613
|
G | GT | 77 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(74): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*650dupT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7136 | INFO_REALIGN_3_PRIME | chr9 | 130233613 | ||||
| chr9:130233714
|
C | T | 1 | a0001c0002t0185 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*742C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7227 | chr9 | 130233714 | |||||
| chr9:130233797
|
A | T | 11 | a0001c0001t0107a0001c0001t0108a0001c0001t0178others(8): Show | 11 | HG01070.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*825A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7310 | chr9 | 130233797 | |||||
| chr9:130233798
|
T | G | 1 | a0001c0002t0109 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*826T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7311 | chr9 | 130233798 | |||||
| chr9:130233861
|
G | A | 2 | a0001c0001t0033a0001c0001t0110 | 3 | HG01255.hp1 HG01257.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*889G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7374 | chr9 | 130233861 | |||||
| chr9:130233901
|
A | G | 1 | a0001c0001t0177 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*929A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7414 | chr9 | 130233901 | |||||
| chr9:130233906
|
C | T | 1 | a0001c0001t0176 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*934C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7419 | chr9 | 130233906 | |||||
| chr9:130233981
|
G | A | 6 | a0001c0001t0030a0001c0001t0078a0001c0002t0038others(3): Show | 8 | HG00323.hp2 HG03486.hp2 HG03927.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1009G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7494 | chr9 | 130233981 | |||||
| chr9:130234023
|
C | T | 9 | a0001c0001t0023a0001c0001t0077a0001c0002t0023others(6): Show | 10 | HG01978.hp2 HG02273.hp1 HG02273.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1051C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7536 | chr9 | 130234023 | |||||
| chr9:130234040
|
C | T | 6 | a0001c0001t0029a0001c0001t0043a0001c0001t0074others(3): Show | 7 | HG02055.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1068C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7553 | chr9 | 130234040 | |||||
| chr9:130234058
|
G | A | 1 | a0001c0002t0172 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1086G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7571 | chr9 | 130234058 | |||||
| chr9:130234144
|
C | T | 1 | a0001c0002t0171 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1172C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7657 | chr9 | 130234144 | |||||
| chr9:130234178
|
G | A | 4 | a0001c0001t0030a0001c0001t0079a0001c0002t0172others(1): Show | 5 | HG00323.hp2 HG00741.hp2 HG04115.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1206G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7691 | chr9 | 130234178 | |||||
| chr9:130234231
|
G | A | 1 | a0001c0001t0074 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1259G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7744 | chr9 | 130234231 | |||||
| chr9:130234345
|
A | G | 1 | a0001c0001t0170 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1373A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7858 | chr9 | 130234345 | |||||
| chr9:130234367
|
C | T | 1 | a0001c0001t0169 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1395C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7880 | chr9 | 130234367 | |||||
| chr9:130234368
|
G | T | 101 | a0001c0001t0005a0001c0001t0016a0001c0001t0017others(98): Show | 125 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1396G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7881 | chr9 | 130234368 | |||||
| chr9:130234389
|
T | C | 22 | a0001c0001t0046a0001c0001t0050a0001c0001t0068others(19): Show | 24 | HG01109.hp1 HG01167.hp2 HG01884.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1417T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7902 | chr9 | 130234389 | |||||
| chr9:130234391
|
C | T | 1 | a0001c0001t0108 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1419C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7904 | chr9 | 130234391 | |||||
| chr9:130234408
|
C | A | 1 | a0001c0002t0116 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1436C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7921 | chr9 | 130234408 | |||||
| chr9:130234463
|
C | T | 1 | a0001c0001t0099 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1491C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 7976 | chr9 | 130234463 | |||||
| chr9:130234546
|
T | C | 1 | a0001c0001t0200 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1574T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8059 | chr9 | 130234546 | |||||
| chr9:130234596
|
A | G | 3 | a0001c0001t0106a0001c0001t0168a0001c0002t0199 | 3 | HG00642.hp1 HG00741.hp2 HG01074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1624A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8109 | chr9 | 130234596 | |||||
| chr9:130234667
|
C | T | 3 | a0001c0001t0036a0001c0001t0098a0001c0001t0191 | 4 | HG01069.hp2 HG01071.hp1 HG01981.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1695C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8180 | chr9 | 130234667 | |||||
| chr9:130234758
|
A | G | 9 | a0001c0001t0053a0001c0001t0061a0001c0001t0070others(6): Show | 13 | HG01109.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1786A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8271 | chr9 | 130234758 | |||||
| chr9:130234856
|
C | A | 24 | a0001c0001t0019a0001c0001t0027a0001c0001t0034others(21): Show | 29 | HG00642.hp1 HG01257.hp1 HG01981.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1884C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8369 | chr9 | 130234856 | |||||
| chr9:130234858
|
G | A | 15 | a0001c0001t0019a0001c0001t0034a0001c0001t0035others(12): Show | 19 | HG00642.hp1 HG01257.hp1 HG01981.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1886G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8371 | chr9 | 130234858 | |||||
| chr9:130234980
|
G | A | 1 | a0001c0001t0151 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2008G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8493 | chr9 | 130234980 | |||||
| chr9:130234992
|
T | C | 21 | a0001c0001t0006a0001c0001t0019a0001c0001t0034others(18): Show | 30 | HG00642.hp1 HG01257.hp1 HG01981.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2020T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8505 | chr9 | 130234992 | |||||
| chr9:130235104
|
C | T | 4 | a0001c0001t0076a0001c0001t0165a0001c0001t0166others(1): Show | 4 | HG02109.hp1 HG02723.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2132C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8617 | chr9 | 130235104 | |||||
| chr9:130235120
|
A | AC | 55 | a0001c0001t0001a0001c0001t0004a0001c0001t0013others(52): Show | 117 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*2155dupC | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8641 | INFO_REALIGN_3_PRIME | chr9 | 130235120 | ||||
| chr9:130235128
|
T | C | 3 | a0001c0001t0046a0001c0001t0151a0001c0002t0126 | 3 | HG02630.hp2 HG03540.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2156T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8641 | chr9 | 130235128 | |||||
| chr9:130235190
|
G | A | 6 | a0001c0002t0055a0001c0002t0057a0001c0002t0058others(3): Show | 6 | HG02559.hp2 HG02615.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2218G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8703 | chr9 | 130235190 | |||||
| chr9:130235212
|
C | G | 1 | a0001c0001t0035 | 2 | NA18970.hp1 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2240C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8725 | chr9 | 130235212 | |||||
| chr9:130235241
|
C | T | 1 | a0001c0002t0097 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2269C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8754 | chr9 | 130235241 | |||||
| chr9:130235347
|
G | A | 2 | a0001c0002t0109a0001c0002t0113 | 2 | HG02559.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2375G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 8860 | chr9 | 130235347 | |||||
| chr9:130235496
|
C | T | 128 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(125): Show | 241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
3_prime_UTR_variant | MODIFIER | c.*2524C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9009 | chr9 | 130235496 | |||||
| chr9:130235594
|
G | A | 5 | a0001c0002t0057a0001c0002t0058a0001c0002t0109others(2): Show | 5 | HG02559.hp2 HG02717.hp1 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2622G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9107 | chr9 | 130235594 | |||||
| chr9:130235616
|
C | T | 1 | a0001c0001t0085 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2644C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9129 | chr9 | 130235616 | |||||
| chr9:130235642
|
G | T | 4 | a0001c0001t0006a0001c0001t0124a0001c0001t0153others(1): Show | 9 | HG02071.hp1 NA18945.hp2 NA18961.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2670G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9155 | chr9 | 130235642 | |||||
| chr9:130235783
|
T | G | 1 | a0001c0001t0081 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2811T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9296 | chr9 | 130235783 | |||||
| chr9:130235840
|
G | A | 1 | a0001c0001t0129 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2868G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9353 | chr9 | 130235840 | |||||
| chr9:130235861
|
C | T | 55 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(52): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2889C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9374 | chr9 | 130235861 | |||||
| chr9:130235870
|
T | C | 5 | a0001c0001t0117a0001c0001t0118a0001c0001t0186others(2): Show | 5 | HG01257.hp1 HG02738.hp2 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2898T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9383 | chr9 | 130235870 | |||||
| chr9:130235920
|
G | A | 3 | a0001c0001t0106a0001c0001t0189a0001c0002t0199 | 3 | HG00639.hp1 HG00741.hp2 HG01074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2948G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9433 | chr9 | 130235920 | |||||
| chr9:130236000
|
C | T | 1 | a0001c0001t0096 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3028C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9513 | chr9 | 130236000 | |||||
| chr9:130236080
|
T | C | 129 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(126): Show | 240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*3108T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9593 | chr9 | 130236080 | |||||
| chr9:130236247
|
G | C | 6 | a0001c0001t0066a0001c0001t0068a0001c0001t0108others(3): Show | 6 | HG02258.hp1 HG02630.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3275G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9760 | chr9 | 130236247 | |||||
| chr9:130236278
|
G | C | 41 | a0001c0001t0019a0001c0001t0027a0001c0001t0034others(38): Show | 51 | HG00099.hp1 HG00597.hp1 HG00642.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3306G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9791 | chr9 | 130236278 | |||||
| chr9:130236290
|
T | C | 1 | a0001c0002t0072 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3318T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9803 | chr9 | 130236290 | |||||
| chr9:130236376
|
G | C | 3 | a0001c0002t0057a0001c0002t0109a0001c0002t0113 | 3 | HG02559.hp2 HG02897.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3404G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9889 | chr9 | 130236376 | |||||
| chr9:130236408
|
C | T | 1 | a0001c0001t0091 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3436C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 9921 | chr9 | 130236408 | |||||
| chr9:130236546
|
C | T | 1 | a0001c0001t0104 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3574C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10059 | chr9 | 130236546 | |||||
| chr9:130236547
|
T | C | 1 | a0001c0001t0104 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3575T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10060 | chr9 | 130236547 | |||||
| chr9:130236548
|
C | CT | 178 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(175): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*3592dupT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10078 | INFO_REALIGN_3_PRIME | chr9 | 130236548 | ||||
| chr9:130236548
|
C | T | 1 | a0001c0001t0104 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3576C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10061 | chr9 | 130236548 | |||||
| chr9:130236665
|
C | T | 1 | a0001c0001t0104 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3693C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10178 | chr9 | 130236665 | |||||
| chr9:130236750
|
T | C | 1 | a0001c0001t0198 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3778T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10263 | chr9 | 130236750 | |||||
| chr9:130236763
|
G | A | 2 | a0001c0001t0170a0001c0002t0127 | 2 | NA18612.hp1 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3791G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10276 | chr9 | 130236763 | |||||
| chr9:130236895
|
G | A | 3 | a0001c0001t0031a0001c0001t0096a0001c0002t0088 | 4 | HG01123.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3923G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10408 | chr9 | 130236895 | |||||
| chr9:130236903
|
C | T | 121 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(118): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*3931C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10416 | chr9 | 130236903 | |||||
| chr9:130236944
|
A | G | 8 | a0001c0001t0006a0001c0001t0131a0001c0001t0153others(5): Show | 13 | HG02071.hp1 HG02071.hp2 HG02717.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3972A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10457 | chr9 | 130236944 | |||||
| chr9:130237010
|
C | T | 1 | a0001c0001t0176 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4038C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10523 | chr9 | 130237010 | |||||
| chr9:130237011
|
G | A | 1 | a0001c0002t0157 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4039G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10524 | chr9 | 130237011 | |||||
| chr9:130237026
|
G | C | 2 | a0001c0001t0138a0001c0002t0113 | 2 | HG03486.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4054G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10539 | chr9 | 130237026 | |||||
| chr9:130237089
|
G | A | 3 | a0001c0001t0048a0001c0001t0083a0001c0001t0117 | 3 | HG03654.hp1 HG04228.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4117G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10602 | chr9 | 130237089 | |||||
| chr9:130237179
|
G | C | 86 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(83): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*4207G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10692 | chr9 | 130237179 | |||||
| chr9:130237282
|
C | T | 1 | a0001c0001t0069 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4310C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 8/8 | 10795 | chr9 | 130237282 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:130172758
|
C | A | 25 | a0001c0001t0003g0022a0001c0001t0004g0010a0001c0001t0026g0004others(22): Show | 25 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.64+31C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130172758 | ||||||
| chr9:130172777
|
A | ACCGCCC | 19 | a0001c0001t0022g0347a0001c0001t0027g0335a0001c0001t0027g0336others(16): Show | 19 | HG01069.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+65_64+70dupGCCC others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130172777 | |||||
| chr9:130172781
|
C | T | 1 | a0001c0001t0006g0348 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.64+54C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130172781 | ||||||
| chr9:130172786
|
G | C | 1 | a0001c0002t0111g0026 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.64+59G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130172786 | ||||||
| chr9:130172792
|
G | C | 1 | a0001c0001t0005g0027 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.64+65G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130172792 | ||||||
| chr9:130172842
|
C | A | 6 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+115C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130172842 | ||||||
| chr9:130172844
|
T | C | 1 | a0001c0002t0111g0026 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.64+117T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130172844 | ||||||
| chr9:130172847
|
C | T | 6 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+120C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130172847 | ||||||
| chr9:130172881
|
C | A | 2 | a0001c0001t0176g0035a0001c0002t0021g0034 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.64+154C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130172881 | ||||||
| chr9:130172987
|
G | T | 2 | a0001c0001t0022g0347a0001c0001t0165g0346 | 2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.64+260G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130172987 | ||||||
| chr9:130172989
|
A | G | 138 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(135): Show | 138 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.64+262A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130172989 | ||||||
| chr9:130173035
|
G | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.64+308G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130173035 | ||||||
| chr9:130173062
|
G | A | 1 | a0001c0001t0030g0038 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.64+335G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130173062 | ||||||
| chr9:130173090
|
G | A | 101 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(98): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.64+363G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130173090 | ||||||
| chr9:130173199
|
T | TG | 89 | a0001c0001t0001g0239a0001c0001t0001g0246a0001c0001t0001g0254others(86): Show | 89 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.64+483dupG | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130173199 | |||||
| chr9:130173199
|
T | TGG | 54 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0058others(51): Show | 54 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+482_64+483dupGG | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130173199 | |||||
| chr9:130173199
|
T | TGGG | 29 | a0001c0001t0001g0048a0001c0001t0004g0045a0001c0001t0014g0044others(26): Show | 29 | HG00642.hp2 HG00741.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.64+481_64+483dupGG others(1): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130173199 | |||||
| chr9:130173208
|
G | T | 1 | a0001c0001t0001g0291 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.64+481G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130173208 | ||||||
| chr9:130173335
|
G | A | 190 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(187): Show | 190 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.64+608G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130173335 | ||||||
| chr9:130173387
|
C | CGGGCTGC others(14): Show |
1 | a0001c0001t0033g0029 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.64+661_64+681dupGG others(19): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130173387 | |||||
| chr9:130173405
|
A | C | 11 | a0001c0001t0028g0320a0001c0001t0029g0325a0001c0001t0032g0319others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+678A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130173405 | ||||||
| chr9:130173423
|
G | A | 69 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(66): Show | 69 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(66): Show |
intron_variant | MODIFIER | c.64+696G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130173423 | ||||||
| chr9:130173634
|
A | C | 144 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(141): Show | 144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.64+907A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130173634 | ||||||
| chr9:130173672
|
T | C | 251 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.64+945T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130173672 | ||||||
| chr9:130173688
|
G | A | 1 | a0001c0001t0022g0347 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.64+961G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130173688 | ||||||
| chr9:130173717
|
G | C | 53 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0062others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.64+990G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130173717 | ||||||
| chr9:130173832
|
C | T | 1 | a0001c0002t0145g0315 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64+1105C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130173832 | ||||||
| chr9:130173853
|
C | T | 165 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(162): Show | 165 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.64+1126C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130173853 | ||||||
| chr9:130174244
|
G | A | 22 | a0001c0001t0022g0347a0001c0001t0027g0335a0001c0001t0027g0336others(19): Show | 22 | HG01069.hp1 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.64+1517G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130174244 | ||||||
| chr9:130174269
|
C | T | 1 | a0001c0002t0113g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64+1542C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130174269 | ||||||
| chr9:130174312
|
C | T | 1 | a0001c0001t0176g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.64+1585C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130174312 | ||||||
| chr9:130174339
|
CA | C | 5 | a0001c0001t0044g0337a0001c0001t0151g0332a0001c0002t0139g0343others(2): Show | 5 | HG02717.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+1613delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130174339 | ||||||
| chr9:130174343
|
ATTAGCAC others(1): Show |
A | 5 | a0001c0001t0044g0337a0001c0001t0151g0332a0001c0002t0139g0343others(2): Show | 5 | HG02717.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+1618_64+1625del others(8): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130174343 | |||||
| chr9:130174525
|
T | C | 188 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(185): Show | 188 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.64+1798T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130174525 | ||||||
| chr9:130174637
|
C | T | 2 | a0001c0001t0120g0075a0001c0001t0121g0076 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.64+1910C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130174637 | ||||||
| chr9:130174704
|
G | T | 2 | a0001c0001t0004g0095a0001c0001t0004g0096 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.64+1977G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130174704 | ||||||
| chr9:130174726
|
G | A | 103 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.64+1999G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130174726 | ||||||
| chr9:130174742
|
C | T | 21 | a0001c0001t0002g0073a0001c0001t0002g0211a0001c0001t0002g0214others(18): Show | 21 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.64+2015C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130174742 | ||||||
| chr9:130174790
|
C | CA | 62 | a0001c0001t0001g0162a0001c0001t0002g0036a0001c0001t0002g0037others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.64+2080dupA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130174790 | |||||
| chr9:130174790
|
C | CAA | 8 | a0001c0001t0006g0131a0001c0001t0020g0133a0001c0001t0078g0132others(5): Show | 8 | HG01175.hp1 HG01952.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+2079_64+2080dup others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130174790 | |||||
| chr9:130174790
|
C | CAAAAAAA | 6 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+2074_64+2080dup others(7): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130174790 | |||||
| chr9:130174790
|
C | CAAAAAAA others(3): Show |
1 | a0001c0002t0113g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64+2071_64+2080dup others(10): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130174790 | |||||
| chr9:130174790
|
C | CAAAAAAA others(4): Show |
19 | a0001c0001t0004g0229a0001c0001t0013g0261a0001c0001t0014g0258others(16): Show | 19 | HG01069.hp2 HG01123.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+2070_64+2080dup others(11): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130174790 | |||||
| chr9:130174790
|
C | CAAAAAAA others(5): Show |
78 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.64+2069_64+2080dup others(12): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130174790 | |||||
| chr9:130174790
|
C | CAAAAAAA others(6): Show |
51 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0058others(48): Show | 51 | HG00438.hp2 HG00597.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.64+2068_64+2080dup others(13): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130174790 | |||||
| chr9:130174790
|
C | CAAAAAAA others(7): Show |
11 | a0001c0001t0001g0127a0001c0001t0014g0044a0001c0001t0042g0052others(8): Show | 11 | HG00544.hp2 HG01175.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+2067_64+2080dup others(14): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130174790 | |||||
| chr9:130174790
|
C | CAAAAAAA others(8): Show |
2 | a0001c0002t0172g0050a0001c0002t0173g0051 | 2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.64+2066_64+2080dup others(15): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130174790 | |||||
| chr9:130174857
|
G | A | 6 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+2130G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130174857 | ||||||
| chr9:130175210
|
G | A | 1 | a0001c0002t0161g0309 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.64+2483G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130175210 | ||||||
| chr9:130175254
|
T | C | 190 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(187): Show | 190 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.64+2527T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130175254 | ||||||
| chr9:130175270
|
C | G | 57 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0058others(54): Show | 57 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.64+2543C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130175270 | ||||||
| chr9:130175356
|
G | A | 1 | a0001c0001t0014g0243 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.64+2629G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130175356 | ||||||
| chr9:130175359
|
C | T | 1 | a0001c0002t0001g0021 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.64+2632C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130175359 | ||||||
| chr9:130175414
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.64+2687A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130175414 | ||||||
| chr9:130175431
|
G | A | 28 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.64+2704G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130175431 | ||||||
| chr9:130175438
|
C | T | 6 | a0001c0001t0027g0335a0001c0001t0027g0336a0001c0001t0166g0329others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+2711C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130175438 | ||||||
| chr9:130175569
|
A | G | 29 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0058others(26): Show | 29 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.64+2842A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130175569 | ||||||
| chr9:130175585
|
A | C | 28 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0058others(25): Show | 28 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.64+2858A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130175585 | ||||||
| chr9:130175628
|
G | C | 1 | a0001c0001t0020g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64+2901G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130175628 | ||||||
| chr9:130175856
|
G | A | 6 | a0001c0001t0027g0335a0001c0001t0027g0336a0001c0001t0166g0329others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+3129G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130175856 | ||||||
| chr9:130176042
|
C | CAACAGGG others(8): Show |
1 | a0001c0001t0005g0262 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.64+3316_64+3330dup others(15): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176042 | |||||
| chr9:130176083
|
C | T | 2 | a0001c0001t0037g0152a0001c0001t0080g0151 | 2 | HG00438.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.64+3356C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176083 | ||||||
| chr9:130176138
|
T | TTTCTTTC others(271): Show |
1 | a0001c0002t0001g0210 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.64+3413_64+3414ins others(278): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
T | TTTCTTTC others(24): Show |
1 | a0001c0001t0107g0101 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64+3413_64+3414ins others(31): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
T | TTTTC | 10 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0020g0100others(7): Show | 10 | HG00140.hp1 HG00438.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+3467_64+3470dup others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
T | TTTTCTTT others(1): Show |
13 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0005g0189others(10): Show | 13 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+3463_64+3470dup others(8): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
T | TTTTCTTT others(5): Show |
9 | a0001c0001t0001g0181a0001c0001t0002g0112a0001c0001t0004g0183others(6): Show | 9 | HG00423.hp2 HG01433.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+3459_64+3470dup others(12): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
T | TTTTCTTT others(9): Show |
7 | a0001c0001t0002g0073a0001c0001t0098g0174a0001c0001t0132g0109others(4): Show | 7 | HG00741.hp2 HG01358.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+3455_64+3470dup others(16): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
T | TTTTCTTT others(13): Show |
8 | a0001c0001t0016g0123a0001c0001t0023g0104a0001c0001t0039g0106others(5): Show | 8 | HG01192.hp2 HG02004.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+3451_64+3470dup others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
T | TTTTCTTT others(17): Show |
2 | a0001c0001t0183g0103a0001c0001t0200g0168 | 2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+3447_64+3470dup others(24): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
T | TTTTCTTT others(21): Show |
2 | a0001c0001t0002g0214a0001c0001t0134g0165 | 2 | HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.64+3443_64+3470dup others(28): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
T | TTTTCTTT others(25): Show |
1 | a0001c0002t0093g0212 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.64+3439_64+3470dup others(32): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
T | TTTTCTTT others(29): Show |
1 | a0001c0002t0087g0072 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.64+3435_64+3470dup others(36): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
T | TTTTCTTT others(37): Show |
1 | a0001c0001t0002g0211 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.64+3427_64+3470dup others(44): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
TTTTC | T | 13 | a0001c0001t0003g0066a0001c0001t0003g0097a0001c0001t0019g0088others(10): Show | 13 | HG00099.hp2 HG01074.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+3467_64+3470del others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
TTTTCTTT others(1): Show |
T | 9 | a0001c0001t0002g0037a0001c0001t0005g0146a0001c0001t0009g0068others(6): Show | 9 | HG01070.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+3463_64+3470del others(8): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
TTTTCTTT others(5): Show |
T | 2 | a0001c0001t0020g0133a0001c0001t0030g0038 | 2 | HG00323.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.64+3459_64+3470del others(12): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
TTTTCTTT others(13): Show |
T | 2 | a0001c0001t0001g0032a0001c0001t0002g0150 | 2 | HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.64+3451_64+3470del others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
TTTTCTTT others(17): Show |
T | 1 | a0001c0001t0176g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.64+3447_64+3470del others(24): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
TTTTCTTT others(21): Show |
T | 2 | a0001c0001t0120g0075a0001c0001t0121g0076 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.64+3443_64+3470del others(28): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176138
|
TTTTCTTT others(25): Show |
T | 1 | a0001c0002t0062g0298 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64+3439_64+3470del others(32): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176138 | |||||
| chr9:130176140
|
T | A | 2 | a0001c0002t0017g0317a0001c0002t0143g0316 | 2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.64+3413T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176140 | ||||||
| chr9:130176142
|
C | T | 123 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(120): Show | 123 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.64+3415C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176142 | ||||||
| chr9:130176155
|
TTTCTTTC others(24): Show |
T | 24 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0058others(21): Show | 24 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.64+3431_64+3461del others(31): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176155 | |||||
| chr9:130176156
|
TTCTTTCT others(23): Show |
T | 4 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0014g0044others(1): Show | 4 | HG02148.hp1 NA18985.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+3431_64+3460del others(30): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176156 | |||||
| chr9:130176156
|
TTCTTTCT others(27): Show |
T | 2 | a0001c0002t0017g0317a0001c0002t0143g0316 | 2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.64+3431_64+3464del others(34): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176156 | |||||
| chr9:130176159
|
TTTCTTTC others(28): Show |
T | 3 | a0001c0001t0053g0314a0001c0001t0099g0307a0001c0002t0021g0306 | 3 | HG02280.hp1 HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.64+3435_64+3469del others(35): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176159 | |||||
| chr9:130176160
|
TTCTTTCT others(27): Show |
T | 3 | a0001c0001t0050g0308a0001c0001t0061g0232a0001c0001t0114g0290 | 3 | HG01109.hp1 HG01167.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.64+3435_64+3468del others(34): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176160 | |||||
| chr9:130176163
|
TTTCTTTC others(24): Show |
T | 13 | a0001c0001t0059g0304a0001c0001t0060g0302a0001c0001t0074g0305others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+3439_64+3469del others(31): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176163 | |||||
| chr9:130176164
|
TTCTTTCT others(15): Show |
T | 1 | a0001c0001t0033g0029 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.64+3439_64+3460del others(22): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176164 | |||||
| chr9:130176164
|
TTCTTTCT others(23): Show |
T | 1 | a0001c0002t0145g0315 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64+3439_64+3468del others(30): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176164 | |||||
| chr9:130176165
|
TCTTTCTT others(14): Show |
T | 4 | a0001c0001t0033g0031a0001c0001t0110g0030a0001c0002t0040g0033others(1): Show | 4 | HG01255.hp1 HG01258.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+3439_64+3459del others(21): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176165 | ||||||
| chr9:130176167
|
TTTCTTTC others(8): Show |
T | 1 | a0001c0002t0001g0024 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.64+3443_64+3457del others(15): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176167 | |||||
| chr9:130176167
|
TTTCTTTC others(20): Show |
T | 3 | a0001c0001t0129g0297a0001c0002t0021g0034a0001c0002t0148g0130 | 3 | HG02602.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.64+3443_64+3469del others(27): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176167 | |||||
| chr9:130176168
|
TTCTTTCT others(7): Show |
T | 119 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(116): Show | 119 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.64+3443_64+3456del others(14): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176168 | |||||
| chr9:130176168
|
TTCTTTCT others(11): Show |
T | 1 | a0001c0002t0194g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.64+3443_64+3460del others(18): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176168 | |||||
| chr9:130176168
|
TTCTTTCT others(19): Show |
T | 3 | a0001c0001t0068g0295a0001c0002t0055g0293a0001c0002t0128g0294 | 3 | HG02615.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.64+3443_64+3468del others(26): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176168 | |||||
| chr9:130176171
|
TTTCTTTC others(16): Show |
T | 1 | a0001c0002t0113g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64+3447_64+3469del others(23): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176171 | |||||
| chr9:130176172
|
TTCTTTCT others(3): Show |
T | 2 | a0001c0001t0013g0244a0001c0001t0013g0272 | 2 | NA19088.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.64+3447_64+3456del others(10): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176172 | |||||
| chr9:130176186
|
C | T | 123 | a0001c0001t0001g0032a0001c0001t0001g0225a0001c0001t0001g0226others(120): Show | 123 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.64+3459C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176186 | ||||||
| chr9:130176187
|
T | TTTCTTTC others(273): Show |
1 | a0001c0001t0102g0121 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.64+3470_64+3471ins others(280): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176187 | |||||
| chr9:130176190
|
C | CTTTCTTT others(7): Show |
2 | a0001c0001t0016g0184a0001c0001t0152g0185 | 2 | NA18948.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.64+3470_64+3471ins others(14): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176190 | |||||
| chr9:130176190
|
C | T | 35 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(32): Show | 35 | HG00099.hp1 HG00544.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.64+3463C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176190 | ||||||
| chr9:130176191
|
TTTC | T | 114 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(111): Show | 114 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.64+3467_64+3469del others(3): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176191 | |||||
| chr9:130176192
|
TTC | T | 10 | a0001c0001t0026g0004a0001c0001t0045g0345a0001c0001t0067g0240others(7): Show | 10 | HG01981.hp1 HG02027.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+3467_64+3468del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176192 | |||||
| chr9:130176194
|
C | CTTTCTTT others(6): Show |
1 | a0001c0001t0025g0113 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.64+3470_64+3471ins others(13): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176194 | |||||
| chr9:130176194
|
C | CTTTCTTT others(10): Show |
1 | a0001c0001t0005g0099 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.64+3470_64+3471ins others(17): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176194 | |||||
| chr9:130176194
|
C | CTTTCTTT others(14): Show |
1 | a0001c0001t0189g0216 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.64+3470_64+3471ins others(21): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176194 | |||||
| chr9:130176194
|
C | T | 37 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(34): Show | 37 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.64+3467C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176194 | ||||||
| chr9:130176195
|
T | TTTCTTTC others(4): Show |
5 | a0001c0001t0022g0161a0001c0001t0025g0178a0001c0001t0080g0151others(2): Show | 5 | HG00597.hp1 HG01358.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+3470_64+3471ins others(11): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176195 | |||||
| chr9:130176195
|
T | TTTCTTTC others(8): Show |
1 | a0001c0001t0002g0108 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.64+3470_64+3471ins others(15): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176195 | |||||
| chr9:130176195
|
T | TTTCTTTC others(12): Show |
1 | a0001c0001t0192g0171 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.64+3470_64+3471ins others(19): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176195 | |||||
| chr9:130176195
|
T | TTTCTTTC others(20): Show |
1 | a0001c0002t0086g0213 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.64+3470_64+3471ins others(27): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176195 | |||||
| chr9:130176195
|
T | TTTCTTTC others(24): Show |
1 | a0001c0001t0015g0163 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.64+3470_64+3471ins others(31): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176195 | |||||
| chr9:130176196
|
T | TTCTTTCT others(3): Show |
4 | a0001c0001t0030g0176a0001c0001t0130g0175a0001c0002t0004g0124others(1): Show | 4 | HG01081.hp1 HG01361.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+3470_64+3471ins others(10): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176196 | |||||
| chr9:130176196
|
T | TTCTTTCT others(7): Show |
3 | a0001c0001t0002g0070a0001c0001t0160g0172a0001c0001t0168g0107 | 3 | HG00642.hp1 HG02738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.64+3470_64+3471ins others(14): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176196 | |||||
| chr9:130176196
|
T | TTCTTTCT others(11): Show |
2 | a0001c0001t0001g0162a0001c0001t0083g0170 | 2 | HG02135.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.64+3470_64+3471ins others(18): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176196 | |||||
| chr9:130176196
|
T | TTCTTTCT others(15): Show |
2 | a0001c0001t0008g0167a0001c0001t0046g0166 | 2 | HG02165.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.64+3470_64+3471ins others(22): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176196 | |||||
| chr9:130176196
|
T | TTCTTTCT others(19): Show |
2 | a0001c0001t0001g0164a0001c0001t0010g0098 | 2 | HG00408.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.64+3470_64+3471ins others(26): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176196 | |||||
| chr9:130176196
|
T | TTCTTTCT others(23): Show |
1 | a0001c0001t0006g0348 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.64+3470_64+3471ins others(30): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176196 | |||||
| chr9:130176197
|
T | TCTTTCTT others(10): Show |
1 | a0001c0001t0169g0169 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.64+3470_64+3471ins others(17): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176197 | ||||||
| chr9:130176197
|
T | TCTTTCTT others(30): Show |
1 | a0001c0001t0034g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.64+3470_64+3471ins others(37): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176197 | ||||||
| chr9:130176198
|
T | C | 1 | a0001c0001t0102g0121 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.64+3471T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176198 | ||||||
| chr9:130176199
|
T | C | 1 | a0001c0001t0005g0197 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.64+3472T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176199 | ||||||
| chr9:130176210
|
G | T | 3 | a0001c0001t0034g0102a0001c0001t0102g0121a0001c0002t0001g0210 | 3 | HG00423.hp1 HG02056.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.64+3483G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176210 | ||||||
| chr9:130176379
|
A | G | 2 | a0001c0001t0186g0242a0001c0001t0188g0287 | 2 | HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.64+3652A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176379 | ||||||
| chr9:130176491
|
CGGCCTTA others(28): Show |
C | 1 | a0001c0002t0001g0210 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.64+3766_64+3800del others(35): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130176491 | |||||
| chr9:130176622
|
A | G | 2 | a0001c0001t0003g0087a0001c0001t0024g0094 | 2 | HG01517.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.64+3895A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176622 | ||||||
| chr9:130176690
|
C | T | 2 | a0001c0002t0017g0317a0001c0002t0143g0316 | 2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.64+3963C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176690 | ||||||
| chr9:130176691
|
G | A | 1 | a0001c0001t0046g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.64+3964G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176691 | ||||||
| chr9:130176696
|
C | T | 54 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(51): Show | 54 | HG00544.hp2 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.64+3969C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176696 | ||||||
| chr9:130176839
|
G | C | 1 | a0001c0001t0201g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+4112G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176839 | ||||||
| chr9:130176977
|
C | A | 1 | a0001c0002t0097g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.64+4250C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130176977 | ||||||
| chr9:130177143
|
C | A | 1 | a0001c0002t0086g0213 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.64+4416C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130177143 | ||||||
| chr9:130177160
|
C | T | 64 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0062others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.64+4433C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130177160 | ||||||
| chr9:130177207
|
G | A | 6 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+4480G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130177207 | ||||||
| chr9:130177259
|
A | T | 6 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+4532A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130177259 | ||||||
| chr9:130177352
|
A | G | 10 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(7): Show | 10 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+4625A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130177352 | ||||||
| chr9:130177354
|
G | A | 6 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+4627G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130177354 | ||||||
| chr9:130177453
|
A | C | 26 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0127others(23): Show | 26 | HG00741.hp1 HG01074.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.64+4726A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130177453 | ||||||
| chr9:130177454
|
GGA | G | 6 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+4731_64+4732del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130177454 | |||||
| chr9:130177507
|
G | A | 6 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+4780G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130177507 | ||||||
| chr9:130177513
|
G | C | 104 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.64+4786G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130177513 | ||||||
| chr9:130177633
|
TA | T | 3 | a0001c0002t0021g0034a0001c0002t0113g0292a0001c0002t0148g0130 | 3 | HG02922.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64+4907delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130177633 | ||||||
| chr9:130177728
|
C | T | 181 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0127others(178): Show | 181 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.64+5001C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130177728 | ||||||
| chr9:130177863
|
C | T | 2 | a0001c0001t0120g0075a0001c0001t0121g0076 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.64+5136C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130177863 | ||||||
| chr9:130177884
|
C | T | 1 | a0001c0001t0024g0067 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.64+5157C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130177884 | ||||||
| chr9:130177922
|
C | T | 6 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+5195C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130177922 | ||||||
| chr9:130178083
|
G | A | 1 | a0001c0001t0176g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.64+5356G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178083 | ||||||
| chr9:130178198
|
A | G | 1 | a0001c0001t0082g0208 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.64+5471A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178198 | ||||||
| chr9:130178258
|
T | C | 2 | a0001c0001t0022g0347a0001c0001t0165g0346 | 2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.64+5531T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178258 | ||||||
| chr9:130178270
|
G | C | 1 | a0001c0001t0078g0132 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.64+5543G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178270 | ||||||
| chr9:130178322
|
T | G | 3 | a0001c0002t0021g0034a0001c0002t0113g0292a0001c0002t0148g0130 | 3 | HG02922.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64+5595T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178322 | ||||||
| chr9:130178414
|
A | G | 113 | a0001c0001t0001g0032a0001c0001t0001g0225a0001c0001t0001g0226others(110): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.64+5687A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178414 | ||||||
| chr9:130178417
|
C | T | 1 | a0001c0002t0113g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64+5690C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178417 | ||||||
| chr9:130178454
|
C | T | 133 | a0001c0001t0001g0032a0001c0001t0001g0225a0001c0001t0001g0226others(130): Show | 133 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.64+5727C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178454 | ||||||
| chr9:130178455
|
G | A | 2 | a0001c0002t0017g0317a0001c0002t0143g0316 | 2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.64+5728G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178455 | ||||||
| chr9:130178499
|
C | T | 6 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+5772C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178499 | ||||||
| chr9:130178540
|
G | C | 3 | a0001c0001t0076g0310a0001c0002t0056g0311a0001c0002t0062g0298 | 3 | HG02976.hp1 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.64+5813G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178540 | ||||||
| chr9:130178620
|
A | G | 2 | a0001c0002t0017g0317a0001c0002t0143g0316 | 2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.64+5893A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178620 | ||||||
| chr9:130178625
|
T | C | 104 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.64+5898T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178625 | ||||||
| chr9:130178699
|
C | T | 1 | a0001c0001t0183g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64+5972C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178699 | ||||||
| chr9:130178700
|
G | A | 1 | a0001c0001t0176g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.64+5973G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178700 | ||||||
| chr9:130178768
|
C | T | 110 | a0001c0001t0001g0032a0001c0001t0001g0225a0001c0001t0001g0226others(107): Show | 110 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.64+6041C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178768 | ||||||
| chr9:130178787
|
GAC | G | 110 | a0001c0001t0001g0032a0001c0001t0001g0225a0001c0001t0001g0226others(107): Show | 110 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.64+6062_64+6063del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178787 | |||||
| chr9:130178834
|
T | TCCCTC | 64 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(61): Show | 64 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.64+6150_64+6154dup others(5): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178834 | |||||
| chr9:130178834
|
T | TCCCTCCC others(3): Show |
31 | a0001c0001t0001g0274a0001c0001t0003g0022a0001c0001t0004g0010others(28): Show | 31 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+6145_64+6154dup others(10): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178834 | |||||
| chr9:130178834
|
T | TCCCTCCC others(8): Show |
2 | a0001c0001t0176g0035a0001c0002t0161g0309 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.64+6140_64+6154dup others(15): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178834 | |||||
| chr9:130178834
|
TCCCTC | T | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0062others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.64+6150_64+6154del others(5): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178834 | |||||
| chr9:130178834
|
TCCCTCCC others(3): Show |
T | 30 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0127others(27): Show | 30 | HG00741.hp1 HG01074.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.64+6145_64+6154del others(10): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178834 | |||||
| chr9:130178834
|
TCCCTCCC others(8): Show |
T | 2 | a0001c0001t0074g0305a0001c0001t0115g0313 | 2 | HG02055.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+6140_64+6154del others(15): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178834 | |||||
| chr9:130178834
|
TCCCTCCC others(13): Show |
T | 2 | a0001c0002t0056g0311a0001c0002t0062g0298 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.64+6135_64+6154del others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178834 | |||||
| chr9:130178851
|
C | CTTCT | 21 | a0001c0001t0022g0347a0001c0001t0027g0335a0001c0001t0027g0336others(18): Show | 21 | HG01069.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.64+6124_64+6125ins others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178851 | ||||||
| chr9:130178852
|
C | T | 21 | a0001c0001t0022g0347a0001c0001t0027g0335a0001c0001t0027g0336others(18): Show | 21 | HG01069.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.64+6125C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178852 | ||||||
| chr9:130178866
|
C | CCTCCCCT others(8): Show |
2 | a0001c0002t0021g0034a0001c0002t0148g0130 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.64+6153_64+6154ins others(15): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178866 | |||||
| chr9:130178866
|
C | CCTCCCCT others(3): Show |
1 | a0001c0002t0113g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64+6148_64+6149ins others(10): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178866 | |||||
| chr9:130178877
|
C | T | 3 | a0001c0001t0059g0304a0001c0001t0060g0302a0001c0001t0108g0303 | 3 | HG02630.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.64+6150C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178877 | ||||||
| chr9:130178880
|
C | T | 3 | a0001c0001t0059g0304a0001c0001t0060g0302a0001c0001t0108g0303 | 3 | HG02630.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.64+6153C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178880 | ||||||
| chr9:130178881
|
C | T | 3 | a0001c0001t0059g0304a0001c0001t0060g0302a0001c0001t0108g0303 | 3 | HG02630.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.64+6154C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178881 | ||||||
| chr9:130178882
|
T | C | 6 | a0001c0001t0050g0308a0001c0001t0053g0314a0001c0001t0061g0232others(3): Show | 6 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+6155T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178882 | ||||||
| chr9:130178883
|
T | C | 3 | a0001c0001t0059g0304a0001c0001t0060g0302a0001c0001t0108g0303 | 3 | HG02630.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.64+6156T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178883 | ||||||
| chr9:130178885
|
T | C | 9 | a0001c0001t0050g0308a0001c0001t0053g0314a0001c0001t0059g0304others(6): Show | 9 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+6158T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178885 | ||||||
| chr9:130178886
|
T | C | 9 | a0001c0001t0050g0308a0001c0001t0053g0314a0001c0001t0059g0304others(6): Show | 9 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+6159T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178886 | ||||||
| chr9:130178887
|
T | C | 1 | a0001c0001t0114g0290 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.64+6160T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178887 | ||||||
| chr9:130178888
|
C | T | 6 | a0001c0001t0050g0308a0001c0001t0053g0314a0001c0001t0061g0232others(3): Show | 6 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+6161C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178888 | ||||||
| chr9:130178890
|
C | T | 5 | a0001c0001t0050g0308a0001c0001t0053g0314a0001c0001t0061g0232others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+6163C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178890 | ||||||
| chr9:130178891
|
C | T | 5 | a0001c0001t0050g0308a0001c0001t0053g0314a0001c0001t0061g0232others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+6164C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178891 | ||||||
| chr9:130178893
|
C | T | 3 | a0001c0002t0021g0034a0001c0002t0113g0292a0001c0002t0148g0130 | 3 | HG02922.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64+6166C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178893 | ||||||
| chr9:130178893
|
CCCCTG | C | 9 | a0001c0001t0074g0305a0001c0001t0076g0310a0001c0001t0115g0313others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+6171_64+6175del others(5): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178893 | |||||
| chr9:130178898
|
G | C | 14 | a0001c0001t0050g0308a0001c0001t0053g0314a0001c0001t0059g0304others(11): Show | 14 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+6171G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178898 | ||||||
| chr9:130178903
|
C | CCCCCTCC others(4): Show |
1 | a0001c0001t0020g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.64+6179_64+6180ins others(11): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178903 | |||||
| chr9:130178903
|
C | CCCCTCCC others(3): Show |
61 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0062others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.64+6203_64+6212dup others(10): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178903 | |||||
| chr9:130178903
|
C | CCCCTT | 5 | a0001c0001t0129g0297a0001c0001t0162g0301a0001c0002t0055g0293others(2): Show | 5 | HG02280.hp2 HG02602.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+6180_64+6181ins others(5): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178903 | |||||
| chr9:130178903
|
C | T | 3 | a0001c0001t0059g0304a0001c0001t0060g0302a0001c0001t0108g0303 | 3 | HG02630.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.64+6176C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178903 | ||||||
| chr9:130178903
|
CCCCTCCC others(3): Show |
C | 1 | a0001c0002t0003g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.64+6203_64+6212del others(10): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178903 | |||||
| chr9:130178908
|
C | G | 110 | a0001c0001t0001g0032a0001c0001t0001g0225a0001c0001t0001g0226others(107): Show | 110 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.64+6181C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178908 | ||||||
| chr9:130178913
|
T | C | 110 | a0001c0001t0001g0032a0001c0001t0001g0225a0001c0001t0001g0226others(107): Show | 110 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.64+6186T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178913 | ||||||
| chr9:130178940
|
T | C | 109 | a0001c0001t0001g0032a0001c0001t0001g0225a0001c0001t0001g0226others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.64+6213T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178940 | ||||||
| chr9:130178941
|
CT | C | 8 | a0001c0001t0001g0127a0001c0001t0002g0211a0001c0001t0005g0146others(5): Show | 8 | HG01168.hp1 HG01256.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+6225delT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178941 | |||||
| chr9:130178941
|
CTT | C | 6 | a0001c0001t0023g0104a0001c0001t0046g0166a0001c0001t0107g0101others(3): Show | 6 | HG02145.hp1 HG02145.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+6224_64+6225del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130178941 | |||||
| chr9:130178942
|
T | C | 1 | a0001c0002t0008g0286 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.64+6215T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178942 | ||||||
| chr9:130178994
|
G | T | 110 | a0001c0001t0001g0032a0001c0001t0001g0225a0001c0001t0001g0226others(107): Show | 110 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.64+6267G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130178994 | ||||||
| chr9:130179016
|
T | C | 113 | a0001c0001t0001g0032a0001c0001t0001g0225a0001c0001t0001g0226others(110): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.64+6289T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179016 | ||||||
| chr9:130179026
|
C | G | 1 | a0001c0002t0093g0212 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.64+6299C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179026 | ||||||
| chr9:130179059
|
C | T | 1 | a0001c0001t0168g0107 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.64+6332C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179059 | ||||||
| chr9:130179102
|
T | A | 1 | a0001c0001t0001g0187 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.64+6375T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179102 | ||||||
| chr9:130179135
|
A | G | 1 | a0001c0002t0128g0294 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64+6408A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179135 | ||||||
| chr9:130179219
|
C | T | 23 | a0001c0001t0050g0308a0001c0001t0053g0314a0001c0001t0059g0304others(20): Show | 23 | HG01109.hp1 HG01109.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.64+6492C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179219 | ||||||
| chr9:130179262
|
G | C | 1 | a0001c0001t0168g0107 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.64+6535G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179262 | ||||||
| chr9:130179310
|
A | G | 2 | a0001c0001t0120g0075a0001c0001t0121g0076 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.64+6583A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179310 | ||||||
| chr9:130179361
|
G | A | 3 | a0001c0002t0021g0034a0001c0002t0113g0292a0001c0002t0148g0130 | 3 | HG02922.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64+6634G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179361 | ||||||
| chr9:130179371
|
T | C | 1 | a0001c0001t0190g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+6644T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179371 | ||||||
| chr9:130179420
|
C | T | 6 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+6693C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179420 | ||||||
| chr9:130179504
|
T | G | 3 | a0001c0002t0054g0199a0001c0002t0144g0115a0001c0002t0157g0173 | 3 | HG01884.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.64+6777T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179504 | ||||||
| chr9:130179505
|
C | T | 1 | a0001c0001t0089g0194 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.64+6778C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179505 | ||||||
| chr9:130179564
|
T | C | 1 | a0001c0001t0071g0233 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64+6837T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179564 | ||||||
| chr9:130179697
|
T | C | 1 | a0001c0001t0071g0233 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64+6970T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179697 | ||||||
| chr9:130179715
|
T | C | 6 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+6988T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179715 | ||||||
| chr9:130179784
|
T | A | 115 | a0001c0001t0001g0032a0001c0001t0001g0225a0001c0001t0001g0226others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.64+7057T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179784 | ||||||
| chr9:130179894
|
C | A | 1 | a0001c0001t0138g0273 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.64+7167C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179894 | ||||||
| chr9:130179964
|
G | A | 1 | a0001c0001t0020g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.64+7237G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130179964 | ||||||
| chr9:130179995
|
TTATC | T | 44 | a0001c0001t0001g0164a0001c0001t0001g0239a0001c0001t0003g0022others(41): Show | 44 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(41): Show |
intron_variant | MODIFIER | c.64+7321_64+7324del others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130179995 | |||||
| chr9:130179995
|
TTATCTAT others(1): Show |
T | 113 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0129others(110): Show | 113 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.64+7317_64+7324del others(8): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130179995 | |||||
| chr9:130179995
|
TTATCTAT others(5): Show |
T | 159 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0127others(156): Show | 159 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.64+7313_64+7324del others(12): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130179995 | |||||
| chr9:130179995
|
TTATCTAT others(9): Show |
T | 19 | a0001c0001t0001g0246a0001c0001t0016g0184a0001c0001t0016g0265others(16): Show | 19 | HG00423.hp1 HG02135.hp2 HG02523.hp1 others(16): Show |
intron_variant | MODIFIER | c.64+7309_64+7324del others(16): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130179995 | |||||
| chr9:130179995
|
TTATCTAT others(13): Show |
T | 9 | a0001c0001t0060g0302a0001c0001t0076g0310a0001c0002t0021g0034others(6): Show | 9 | HG02109.hp1 HG02809.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+7305_64+7324del others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130179995 | |||||
| chr9:130180003
|
C | T | 1 | a0001c0002t0113g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64+7276C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180003 | ||||||
| chr9:130180010
|
T | C | 1 | a0001c0001t0071g0233 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64+7283T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180010 | ||||||
| chr9:130180064
|
C | T | 2 | a0001c0001t0120g0075a0001c0001t0121g0076 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.64+7337C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180064 | ||||||
| chr9:130180097
|
C | T | 1 | a0001c0001t0190g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+7370C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180097 | ||||||
| chr9:130180117
|
C | T | 20 | a0001c0001t0022g0347a0001c0001t0027g0335a0001c0001t0027g0336others(17): Show | 20 | HG01069.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.64+7390C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180117 | ||||||
| chr9:130180128
|
G | A | 6 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+7401G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180128 | ||||||
| chr9:130180185
|
C | T | 3 | a0001c0002t0021g0034a0001c0002t0113g0292a0001c0002t0148g0130 | 3 | HG02922.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64+7458C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180185 | ||||||
| chr9:130180187
|
C | G | 1 | a0001c0001t0043g0327 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.64+7460C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180187 | ||||||
| chr9:130180262
|
A | G | 2 | a0001c0001t0120g0075a0001c0001t0121g0076 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.64+7535A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180262 | ||||||
| chr9:130180293
|
C | T | 2 | a0001c0001t0006g0131a0001c0001t0007g0083 | 2 | NA18975.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.64+7566C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180293 | ||||||
| chr9:130180299
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.64+7572G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180299 | ||||||
| chr9:130180314
|
G | A | 1 | a0001c0001t0138g0273 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.64+7587G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180314 | ||||||
| chr9:130180326
|
G | A | 2 | a0001c0001t0120g0075a0001c0001t0121g0076 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.64+7599G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180326 | ||||||
| chr9:130180422
|
A | G | 2 | a0001c0001t0035g0270a0001c0001t0047g0247 | 2 | NA18961.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.64+7695A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180422 | ||||||
| chr9:130180482
|
T | C | 1 | a0001c0001t0020g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.64+7755T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180482 | ||||||
| chr9:130180487
|
G | A | 1 | a0001c0002t0113g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64+7760G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180487 | ||||||
| chr9:130180515
|
G | A | 129 | a0001c0001t0001g0032a0001c0001t0001g0225a0001c0001t0001g0226others(126): Show | 129 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.64+7788G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180515 | ||||||
| chr9:130180530
|
G | T | 1 | a0001c0001t0071g0233 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64+7803G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180530 | ||||||
| chr9:130180679
|
C | A | 1 | a0001c0002t0010g0149 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.64+7952C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180679 | ||||||
| chr9:130180687
|
A | G | 3 | a0001c0001t0071g0233a0001c0002t0017g0317a0001c0002t0143g0316 | 3 | HG02717.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.64+7960A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180687 | ||||||
| chr9:130180761
|
G | A | 9 | a0001c0001t0050g0308a0001c0001t0053g0314a0001c0001t0061g0232others(6): Show | 9 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+8034G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180761 | ||||||
| chr9:130180764
|
T | C | 137 | a0001c0001t0001g0032a0001c0001t0001g0225a0001c0001t0001g0226others(134): Show | 137 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.64+8037T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180764 | ||||||
| chr9:130180773
|
G | C | 3 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0104g0065 | 3 | HG01167.hp1 HG01169.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.64+8046G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180773 | ||||||
| chr9:130180803
|
A | G | 186 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0058others(183): Show | 186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.64+8076A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180803 | ||||||
| chr9:130180834
|
T | C | 1 | a0001c0001t0176g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.64+8107T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180834 | ||||||
| chr9:130180879
|
C | T | 20 | a0001c0001t0022g0347a0001c0001t0027g0335a0001c0001t0027g0336others(17): Show | 20 | HG01069.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.64+8152C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130180879 | ||||||
| chr9:130181106
|
A | C | 2 | a0001c0001t0006g0131a0001c0001t0146g0333 | 2 | HG01884.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.64+8379A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181106 | ||||||
| chr9:130181291
|
C | A | 1 | a0001c0001t0132g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.64+8564C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181291 | ||||||
| chr9:130181411
|
T | C | 1 | a0001c0002t0065g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64+8684T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181411 | ||||||
| chr9:130181413
|
C | T | 1 | a0001c0001t0071g0233 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64+8686C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181413 | ||||||
| chr9:130181472
|
G | T | 2 | a0001c0002t0017g0317a0001c0002t0143g0316 | 2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.64+8745G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181472 | ||||||
| chr9:130181506
|
TG | T | 162 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0058others(159): Show | 162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.64+8784delG | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130181506 | |||||
| chr9:130181551
|
A | T | 1 | a0001c0001t0105g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.64+8824A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181551 | ||||||
| chr9:130181574
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.64+8847C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181574 | ||||||
| chr9:130181608
|
C | T | 2 | a0001c0001t0068g0295a0001c0001t0095g0341 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.64+8881C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181608 | ||||||
| chr9:130181630
|
T | C | 181 | a0001c0001t0001g0032a0001c0001t0001g0225a0001c0001t0001g0226others(178): Show | 181 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.64+8903T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181630 | ||||||
| chr9:130181691
|
G | A | 2 | a0001c0002t0017g0317a0001c0002t0143g0316 | 2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.64+8964G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181691 | ||||||
| chr9:130181725
|
C | T | 21 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0127others(18): Show | 21 | HG00741.hp1 HG01074.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.64+8998C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181725 | ||||||
| chr9:130181766
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.64+9039G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181766 | ||||||
| chr9:130181801
|
G | A | 21 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0127others(18): Show | 21 | HG00741.hp1 HG01074.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.64+9074G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181801 | ||||||
| chr9:130181817
|
A | G | 2 | a0001c0001t0059g0304a0001c0001t0060g0302 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.64+9090A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181817 | ||||||
| chr9:130181929
|
G | T | 1 | a0001c0002t0001g0003 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.64+9202G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181929 | ||||||
| chr9:130181930
|
T | G | 1 | a0001c0002t0001g0003 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.64+9203T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181930 | ||||||
| chr9:130181931
|
G | T | 1 | a0001c0002t0001g0003 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.64+9204G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181931 | ||||||
| chr9:130181971
|
G | A | 2 | a0001c0001t0131g0009a0001c0002t0001g0008 | 2 | NA18973.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.64+9244G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130181971 | ||||||
| chr9:130182033
|
A | G | 3 | a0001c0001t0089g0194a0001c0001t0134g0165a0001c0002t0065g0205 | 3 | HG02698.hp1 HG03486.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.64+9306A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182033 | ||||||
| chr9:130182102
|
C | G | 5 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(2): Show | 5 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+9375C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182102 | ||||||
| chr9:130182266
|
T | C | 140 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0002g0036others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.64+9539T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182266 | ||||||
| chr9:130182322
|
T | C | 1 | a0001c0001t0077g0281 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.64+9595T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182322 | ||||||
| chr9:130182329
|
C | T | 1 | a0001c0002t0017g0317 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.64+9602C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182329 | ||||||
| chr9:130182369
|
C | T | 3 | a0001c0001t0001g0162a0001c0001t0004g0183a0001c0001t0006g0348 | 3 | HG02040.hp2 HG02135.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.64+9642C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182369 | ||||||
| chr9:130182373
|
C | T | 69 | a0001c0001t0001g0058a0001c0001t0002g0036a0001c0001t0002g0037others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.64+9646C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182373 | ||||||
| chr9:130182520
|
C | T | 1 | a0001c0001t0023g0104 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.64+9793C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182520 | ||||||
| chr9:130182523
|
C | T | 4 | a0001c0001t0003g0269a0001c0001t0003g0280a0001c0001t0014g0243others(1): Show | 4 | NA18967.hp2 NA18974.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+9796C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182523 | ||||||
| chr9:130182615
|
C | T | 1 | a0001c0001t0052g0147 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64+9888C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182615 | ||||||
| chr9:130182627
|
G | A | 1 | a0001c0001t0035g0270 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.64+9900G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182627 | ||||||
| chr9:130182684
|
G | A | 1 | a0001c0002t0093g0212 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.64+9957G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182684 | ||||||
| chr9:130182752
|
C | T | 1 | a0001c0001t0085g0138 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.64+10025C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182752 | ||||||
| chr9:130182856
|
A | G | 1 | a0001c0001t0176g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.64+10129A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182856 | ||||||
| chr9:130182897
|
A | T | 1 | a0001c0002t0112g0182 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.64+10170A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182897 | ||||||
| chr9:130182912
|
A | G | 23 | a0001c0001t0001g0048a0001c0001t0002g0150a0001c0001t0003g0269others(20): Show | 23 | HG00280.hp1 HG00423.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.64+10185A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182912 | ||||||
| chr9:130182987
|
G | A | 24 | a0001c0001t0001g0129a0001c0001t0001g0162a0001c0001t0001g0187others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.64+10260G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130182987 | ||||||
| chr9:130183056
|
C | T | 1 | a0001c0001t0118g0231 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.64+10329C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183056 | ||||||
| chr9:130183152
|
G | T | 1 | a0001c0001t0003g0279 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.64+10425G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183152 | ||||||
| chr9:130183227
|
C | T | 1 | a0001c0001t0034g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.64+10500C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183227 | ||||||
| chr9:130183285
|
C | T | 16 | a0001c0001t0001g0048a0001c0001t0101g0055a0001c0001t0106g0056others(13): Show | 16 | HG00741.hp1 HG01074.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.64+10558C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183285 | ||||||
| chr9:130183306
|
T | TG | 38 | a0001c0001t0001g0053a0001c0001t0001g0129a0001c0001t0001g0162others(35): Show | 38 | HG00423.hp2 HG00639.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.64+10588dupG | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130183306 | |||||
| chr9:130183308
|
G | GC | 38 | a0001c0001t0002g0214a0001c0001t0003g0087a0001c0001t0024g0094others(35): Show | 38 | HG00423.hp1 HG01069.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.64+10581_64+10582i others(3): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183308 | ||||||
| chr9:130183309
|
G | A | 1 | a0001c0002t0088g0259 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.64+10582G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183309 | ||||||
| chr9:130183309
|
G | GC | 16 | a0001c0001t0032g0195a0001c0001t0049g0328a0001c0001t0050g0308others(13): Show | 16 | HG00639.hp2 HG00738.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.64+10582_64+10583i others(3): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183309 | ||||||
| chr9:130183310
|
G | T | 8 | a0001c0001t0044g0337a0001c0001t0095g0341a0001c0001t0108g0303others(5): Show | 8 | HG02109.hp1 HG02280.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+10583G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183310 | ||||||
| chr9:130183312
|
G | T | 132 | a0001c0001t0001g0032a0001c0001t0001g0127a0001c0001t0001g0164others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.64+10585G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183312 | ||||||
| chr9:130183313
|
G | A | 104 | a0001c0001t0001g0032a0001c0001t0001g0127a0001c0001t0001g0164others(101): Show | 104 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.64+10586G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183313 | ||||||
| chr9:130183449
|
G | A | 6 | a0001c0001t0001g0048a0001c0002t0001g0042a0001c0002t0023g0054others(3): Show | 6 | HG01978.hp2 HG02273.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+10722G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183449 | ||||||
| chr9:130183463
|
G | A | 2 | a0001c0001t0167g0064a0001c0002t0055g0293 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.64+10736G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183463 | ||||||
| chr9:130183554
|
C | T | 1 | a0001c0001t0001g0048 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.64+10827C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183554 | ||||||
| chr9:130183630
|
C | A | 1 | a0001c0001t0010g0282 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.64+10903C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183630 | ||||||
| chr9:130183667
|
TTC | T | 80 | a0001c0001t0001g0048a0001c0001t0002g0214a0001c0001t0003g0022others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.64+10948_64+10949d others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130183667 | |||||
| chr9:130183667
|
TTCTC | T | 16 | a0001c0001t0028g0320a0001c0001t0029g0156a0001c0001t0029g0325others(13): Show | 16 | HG02486.hp2 HG02559.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.64+10946_64+10949d others(6): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130183667 | |||||
| chr9:130183712
|
CCTTCCTT others(16): Show |
C | 17 | a0001c0001t0001g0048a0001c0001t0042g0052a0001c0001t0101g0055others(14): Show | 17 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.64+11005_64+11027d others(25): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130183712 | |||||
| chr9:130183745
|
TTCTTTC | T | 4 | a0001c0001t0032g0195a0001c0001t0134g0165a0001c0002t0008g0114others(1): Show | 4 | HG00639.hp2 HG00738.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+11036_64+11041d others(8): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130183745 | |||||
| chr9:130183779
|
C | A | 1 | a0001c0001t0090g0275 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.64+11052C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183779 | ||||||
| chr9:130183837
|
T | A | 6 | a0001c0001t0005g0197a0001c0001t0006g0119a0001c0001t0006g0204others(3): Show | 6 | HG00544.hp1 HG00597.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+11110T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183837 | ||||||
| chr9:130183841
|
G | A | 1 | a0001c0001t0117g0105 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.64+11114G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183841 | ||||||
| chr9:130183849
|
G | A | 2 | a0001c0001t0005g0027a0001c0001t0010g0282 | 2 | HG01515.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.64+11122G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183849 | ||||||
| chr9:130183850
|
C | A | 1 | a0001c0001t0121g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.64+11123C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183850 | ||||||
| chr9:130183882
|
C | T | 3 | a0001c0001t0138g0273a0001c0001t0146g0333a0001c0001t0154g0340 | 3 | HG01069.hp1 HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.64+11155C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183882 | ||||||
| chr9:130183903
|
G | A | 1 | a0001c0002t0161g0309 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.64+11176G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183903 | ||||||
| chr9:130183935
|
G | A | 2 | a0001c0001t0131g0009a0001c0002t0143g0316 | 2 | HG02717.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.64+11208G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130183935 | ||||||
| chr9:130184053
|
A | G | 50 | a0001c0001t0002g0214a0001c0001t0003g0022a0001c0001t0037g0252others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.64+11326A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184053 | ||||||
| chr9:130184106
|
G | A | 1 | a0001c0002t0174g0057 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.64+11379G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184106 | ||||||
| chr9:130184264
|
A | G | 1 | a0001c0001t0182g0331 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.64+11537A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184264 | ||||||
| chr9:130184307
|
G | GACCC | 3 | a0001c0002t0057g0159a0001c0002t0128g0294a0001c0002t0149g0207 | 3 | HG02109.hp2 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.64+11583_64+11586d others(6): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130184307 | |||||
| chr9:130184336
|
G | T | 104 | a0001c0001t0001g0048a0001c0001t0002g0214a0001c0001t0003g0022others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.64+11609G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184336 | ||||||
| chr9:130184365
|
T | C | 26 | a0001c0001t0001g0048a0001c0001t0042g0052a0001c0001t0090g0275others(23): Show | 26 | HG00544.hp2 HG00642.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.64+11638T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184365 | ||||||
| chr9:130184472
|
G | A | 2 | a0001c0001t0071g0233a0001c0001t0115g0313 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.64+11745G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184472 | ||||||
| chr9:130184510
|
C | T | 14 | a0001c0001t0028g0320a0001c0001t0029g0156a0001c0001t0029g0325others(11): Show | 14 | HG02486.hp2 HG02559.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+11783C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184510 | ||||||
| chr9:130184586
|
C | T | 1 | a0001c0002t0055g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+11859C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184586 | ||||||
| chr9:130184729
|
G | A | 59 | a0001c0001t0002g0214a0001c0001t0003g0022a0001c0001t0028g0320others(56): Show | 59 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.64+12002G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184729 | ||||||
| chr9:130184772
|
C | T | 1 | a0001c0002t0040g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.64+12045C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184772 | ||||||
| chr9:130184794
|
A | AT | 237 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0058others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.64+12079dupT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130184794 | |||||
| chr9:130184893
|
G | T | 219 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0058others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.64+12166G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184893 | ||||||
| chr9:130184942
|
C | T | 1 | a0001c0001t0003g0022 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.64+12215C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184942 | ||||||
| chr9:130184959
|
G | A | 1 | a0001c0001t0015g0203 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.64+12232G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184959 | ||||||
| chr9:130184984
|
A | G | 1 | a0001c0001t0037g0152 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.64+12257A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184984 | ||||||
| chr9:130184996
|
T | C | 238 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0058others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.64+12269T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130184996 | ||||||
| chr9:130185194
|
A | C | 341 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.64+12467A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185194 | ||||||
| chr9:130185239
|
T | G | 2 | a0001c0001t0022g0347a0001c0001t0165g0346 | 2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.64+12512T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185239 | ||||||
| chr9:130185241
|
T | C | 226 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0058others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.64+12514T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185241 | ||||||
| chr9:130185252
|
C | T | 1 | a0001c0002t0112g0182 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.64+12525C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185252 | ||||||
| chr9:130185303
|
T | C | 326 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(323): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.64+12576T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185303 | ||||||
| chr9:130185330
|
C | A | 1 | a0001c0001t0074g0305 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.64+12603C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185330 | ||||||
| chr9:130185332
|
A | G | 1 | a0001c0001t0130g0175 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.64+12605A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185332 | ||||||
| chr9:130185422
|
C | T | 1 | a0001c0002t0001g0003 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.64+12695C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185422 | ||||||
| chr9:130185423
|
T | C | 1 | a0001c0002t0001g0003 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.64+12696T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185423 | ||||||
| chr9:130185424
|
C | T | 1 | a0001c0002t0001g0003 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.64+12697C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185424 | ||||||
| chr9:130185436
|
G | A | 1 | a0001c0002t0184g0334 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+12709G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185436 | ||||||
| chr9:130185488
|
G | T | 1 | a0001c0002t0088g0259 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.64+12761G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185488 | ||||||
| chr9:130185522
|
C | T | 2 | a0001c0001t0074g0305a0001c0001t0176g0035 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.64+12795C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185522 | ||||||
| chr9:130185586
|
G | A | 3 | a0001c0002t0057g0159a0001c0002t0128g0294a0001c0002t0149g0207 | 3 | HG02109.hp2 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.64+12859G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185586 | ||||||
| chr9:130185789
|
G | A | 3 | a0001c0001t0061g0232a0001c0001t0114g0290a0001c0001t0151g0332 | 3 | HG01167.hp2 HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.64+13062G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185789 | ||||||
| chr9:130185804
|
C | T | 2 | a0001c0002t0021g0034a0001c0002t0148g0130 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.64+13077C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185804 | ||||||
| chr9:130185830
|
A | G | 1 | a0001c0001t0071g0233 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64+13103A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185830 | ||||||
| chr9:130185864
|
T | C | 336 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(333): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.64+13137T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185864 | ||||||
| chr9:130185876
|
C | A | 3 | a0001c0002t0057g0159a0001c0002t0128g0294a0001c0002t0149g0207 | 3 | HG02109.hp2 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.64+13149C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185876 | ||||||
| chr9:130185900
|
T | C | 1 | a0001c0002t0065g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64+13173T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185900 | ||||||
| chr9:130185942
|
C | T | 2 | a0001c0001t0071g0233a0001c0001t0115g0313 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.64+13215C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185942 | ||||||
| chr9:130185949
|
T | G | 4 | a0001c0001t0090g0275a0001c0001t0159g0198a0001c0001t0168g0107others(1): Show | 4 | HG00642.hp1 HG01123.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+13222T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185949 | ||||||
| chr9:130185963
|
G | T | 3 | a0001c0001t0001g0181a0001c0001t0006g0228a0001c0004t0008g0223 | 3 | HG00423.hp2 NA18945.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.64+13236G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130185963 | ||||||
| chr9:130186003
|
G | A | 6 | a0001c0001t0167g0064a0001c0002t0017g0317a0001c0002t0021g0034others(3): Show | 6 | HG02615.hp2 HG02922.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+13276G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130186003 | ||||||
| chr9:130186045
|
T | C | 324 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.64+13318T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130186045 | ||||||
| chr9:130186046
|
G | A | 218 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0058others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.64+13319G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130186046 | ||||||
| chr9:130186171
|
G | A | 1 | a0001c0001t0061g0232 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64+13444G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130186171 | ||||||
| chr9:130186205
|
A | G | 4 | a0001c0001t0090g0275a0001c0001t0159g0198a0001c0001t0168g0107others(1): Show | 4 | HG00642.hp1 HG01123.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+13478A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130186205 | ||||||
| chr9:130186271
|
T | C | 261 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.64+13544T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130186271 | ||||||
| chr9:130186398
|
T | C | 1 | a0001c0001t0120g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64+13671T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130186398 | ||||||
| chr9:130186561
|
C | T | 2 | a0001c0001t0004g0139a0001c0001t0032g0195 | 2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.64+13834C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130186561 | ||||||
| chr9:130186570
|
TC | T | 4 | a0001c0002t0021g0312a0001c0002t0056g0311a0001c0002t0062g0298others(1): Show | 4 | HG01884.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+13845delC | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130186570 | |||||
| chr9:130186598
|
C | A | 1 | a0001c0001t0041g0201 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+13871C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130186598 | ||||||
| chr9:130186722
|
G | C | 2 | a0001c0001t0146g0333a0001c0001t0154g0340 | 2 | HG01069.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.64+13995G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130186722 | ||||||
| chr9:130186754
|
G | T | 6 | a0001c0001t0167g0064a0001c0002t0017g0317a0001c0002t0021g0034others(3): Show | 6 | HG02615.hp2 HG02922.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+14027G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130186754 | ||||||
| chr9:130186818
|
C | T | 2 | a0001c0001t0001g0291a0001c0001t0004g0010 | 2 | NA18971.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.64+14091C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130186818 | ||||||
| chr9:130186819
|
C | T | 1 | a0001c0002t0143g0316 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.64+14092C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130186819 | ||||||
| chr9:130186956
|
G | A | 1 | a0001c0001t0140g0236 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.65-14002G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130186956 | ||||||
| chr9:130187148
|
G | A | 3 | a0001c0001t0066g0263a0001c0002t0018g0245a0001c0002t0063g0235 | 3 | HG02055.hp1 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.65-13810G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130187148 | ||||||
| chr9:130187176
|
G | C | 3 | a0001c0001t0066g0263a0001c0002t0018g0245a0001c0002t0063g0235 | 3 | HG02055.hp1 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.65-13782G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130187176 | ||||||
| chr9:130187197
|
C | T | 1 | a0001c0002t0163g0323 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.65-13761C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130187197 | ||||||
| chr9:130187236
|
C | T | 1 | a0001c0002t0123g0222 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.65-13722C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130187236 | ||||||
| chr9:130187266
|
A | C | 324 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.65-13692A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130187266 | ||||||
| chr9:130187266
|
A | T | 2 | a0001c0001t0096g0063a0001c0001t0103g0137 | 2 | HG01243.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.65-13692A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130187266 | ||||||
| chr9:130187327
|
G | A | 22 | a0001c0001t0001g0048a0001c0001t0042g0052a0001c0001t0101g0055others(19): Show | 22 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.65-13631G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130187327 | ||||||
| chr9:130187399
|
G | A | 1 | a0001c0001t0006g0284 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.65-13559G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130187399 | ||||||
| chr9:130187550
|
C | T | 218 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0058others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.65-13408C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130187550 | ||||||
| chr9:130187585
|
G | A | 218 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0058others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.65-13373G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130187585 | ||||||
| chr9:130187640
|
A | G | 324 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.65-13318A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130187640 | ||||||
| chr9:130187669
|
T | C | 335 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(332): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.65-13289T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130187669 | ||||||
| chr9:130187723
|
G | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.65-13235G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130187723 | ||||||
| chr9:130187796
|
TC | T | 4 | a0001c0001t0090g0275a0001c0001t0159g0198a0001c0001t0168g0107others(1): Show | 4 | HG00642.hp1 HG01123.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-13160delC | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130187796 | |||||
| chr9:130187859
|
A | G | 2 | a0001c0001t0071g0233a0001c0001t0115g0313 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.65-13099A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130187859 | ||||||
| chr9:130188005
|
A | G | 13 | a0001c0001t0001g0162a0001c0001t0003g0285a0001c0001t0004g0183others(10): Show | 13 | HG00438.hp1 HG02040.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-12953A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130188005 | ||||||
| chr9:130188022
|
G | A | 1 | a0001c0001t0136g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.65-12936G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130188022 | ||||||
| chr9:130188079
|
A | G | 324 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.65-12879A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130188079 | ||||||
| chr9:130188303
|
C | T | 2 | a0001c0001t0186g0242a0001c0001t0188g0287 | 2 | HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.65-12655C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130188303 | ||||||
| chr9:130188327
|
C | T | 1 | a0001c0002t0184g0334 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.65-12631C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130188327 | ||||||
| chr9:130188423
|
CT | C | 73 | a0001c0001t0001g0291a0001c0001t0002g0214a0001c0001t0003g0022others(70): Show | 73 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.65-12519delT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130188423 | |||||
| chr9:130188480
|
T | TGGCTCGA others(4): Show |
265 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.65-12474_65-12464d others(13): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130188480 | |||||
| chr9:130188596
|
C | T | 2 | a0001c0002t0021g0034a0001c0002t0148g0130 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-12362C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130188596 | ||||||
| chr9:130188654
|
C | T | 1 | a0001c0001t0108g0303 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.65-12304C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130188654 | ||||||
| chr9:130188842
|
G | A | 2 | a0001c0001t0028g0320a0001c0001t0070g0324 | 2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.65-12116G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130188842 | ||||||
| chr9:130188914
|
G | C | 19 | a0001c0001t0001g0048a0001c0001t0047g0247a0001c0001t0101g0055others(16): Show | 19 | HG01978.hp2 HG02273.hp2 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.65-12044G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130188914 | ||||||
| chr9:130188952
|
G | C | 1 | a0001c0002t0184g0334 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.65-12006G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130188952 | ||||||
| chr9:130188993
|
A | T | 1 | a0001c0001t0130g0175 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.65-11965A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130188993 | ||||||
| chr9:130189084
|
C | G | 1 | a0001c0001t0083g0170 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.65-11874C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189084 | ||||||
| chr9:130189103
|
G | A | 1 | a0001c0001t0121g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.65-11855G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189103 | ||||||
| chr9:130189456
|
T | C | 4 | a0001c0002t0021g0312a0001c0002t0056g0311a0001c0002t0062g0298others(1): Show | 4 | HG01884.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-11502T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189456 | ||||||
| chr9:130189592
|
A | G | 1 | a0001c0001t0121g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.65-11366A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189592 | ||||||
| chr9:130189699
|
G | A | 26 | a0001c0001t0001g0048a0001c0001t0003g0022a0001c0001t0047g0247others(23): Show | 26 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.65-11259G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189699 | ||||||
| chr9:130189858
|
C | CAAAAA | 6 | a0001c0001t0106g0056a0001c0002t0001g0003a0001c0002t0001g0007others(3): Show | 6 | HG01074.hp1 NA18963.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-11082_65-11078d others(7): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189858 | |||||
| chr9:130189858
|
C | CAAAAAA | 8 | a0001c0002t0001g0006a0001c0002t0001g0042a0001c0002t0001g0046others(5): Show | 8 | HG00741.hp1 HG01175.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-11083_65-11078d others(8): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189858 | |||||
| chr9:130189858
|
CA | C | 9 | a0001c0001t0003g0087a0001c0001t0003g0097a0001c0001t0017g0116others(6): Show | 9 | HG01069.hp2 HG01261.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-11078delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189858 | |||||
| chr9:130189858
|
CAA | C | 16 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0164others(13): Show | 16 | HG00408.hp2 HG01069.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-11079_65-11078d others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189858 | |||||
| chr9:130189858
|
CAAA | C | 20 | a0001c0001t0001g0162a0001c0001t0001g0291a0001c0001t0004g0010others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.65-11080_65-11078d others(5): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189858 | |||||
| chr9:130189858
|
CAAAA | C | 6 | a0001c0001t0001g0226a0001c0001t0004g0096a0001c0001t0170g0256others(3): Show | 6 | HG01169.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-11081_65-11078d others(6): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189858 | |||||
| chr9:130189858
|
CAAAAA | C | 13 | a0001c0001t0006g0348a0001c0001t0010g0098a0001c0001t0022g0161others(10): Show | 13 | HG01243.hp1 HG02056.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-11082_65-11078d others(7): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189858 | |||||
| chr9:130189874
|
AAAAAAAT others(6): Show |
A | 1 | a0001c0002t0010g0149 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.65-11082_65-11070d others(15): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189874 | |||||
| chr9:130189875
|
A | AATATATA others(25): Show |
1 | a0001c0001t0044g0337 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.65-11082_65-11081i others(34): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189875 | |||||
| chr9:130189875
|
A | T | 3 | a0001c0001t0025g0113a0001c0001t0146g0333a0001c0001t0191g0179 | 3 | HG01261.hp2 HG01884.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.65-11083A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189875 | ||||||
| chr9:130189876
|
AAAAAT | A | 71 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0073others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.65-11080_65-11076d others(7): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189876 | |||||
| chr9:130189876
|
AAAAATAT others(6): Show |
A | 8 | a0001c0002t0002g0218a0001c0002t0004g0124a0001c0002t0011g0061others(5): Show | 8 | HG01081.hp1 HG01358.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-11080_65-11068d others(15): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189876 | |||||
| chr9:130189877
|
A | AATATATA others(7): Show |
1 | a0001c0001t0114g0290 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.65-11080_65-11079i others(16): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189877 | |||||
| chr9:130189877
|
A | AATATATA others(11): Show |
1 | a0001c0001t0061g0232 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.65-11080_65-11079i others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189877 | |||||
| chr9:130189877
|
A | T | 17 | a0001c0001t0003g0097a0001c0001t0017g0116a0001c0001t0025g0113others(14): Show | 17 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.65-11081A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189877 | ||||||
| chr9:130189877
|
AAAAT | A | 10 | a0001c0001t0001g0053a0001c0001t0001g0225a0001c0001t0001g0278others(7): Show | 10 | HG01106.hp2 HG01928.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-11079_65-11076d others(6): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189877 | |||||
| chr9:130189877
|
AAAATAT | A | 15 | a0001c0001t0001g0187a0001c0001t0001g0227a0001c0001t0006g0284others(12): Show | 15 | HG00280.hp2 HG00423.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.65-11079_65-11074d others(8): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189877 | |||||
| chr9:130189878
|
AAATAT | A | 52 | a0001c0001t0001g0058a0001c0001t0001g0181a0001c0001t0001g0190others(49): Show | 52 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.65-11078_65-11074d others(7): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189878 | |||||
| chr9:130189879
|
A | AAAAAAAA others(47): Show |
1 | a0001c0002t0058g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.65-11078_65-11077i others(56): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AAAAAAAA others(21): Show |
1 | a0001c0002t0018g0245 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.65-11078_65-11077i others(30): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AAAAAAAA others(23): Show |
1 | a0001c0002t0063g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.65-11078_65-11077i others(32): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0159g0198 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.65-11078_65-11077i others(34): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AAAAAAAA others(30): Show |
2 | a0001c0001t0066g0263a0001c0001t0168g0107 | 2 | HG00642.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.65-11078_65-11077i others(39): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0003g0022 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.65-11078_65-11077i others(29): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0117g0105 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.65-11078_65-11077i others(31): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AAAAAAAA others(21): Show |
1 | a0001c0002t0028g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.65-11078_65-11077i others(30): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AAAAAAAA others(27): Show |
1 | a0001c0002t0088g0259 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.65-11078_65-11077i others(36): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AAAAAAAA others(6): Show |
2 | a0001c0002t0056g0311a0001c0002t0157g0173 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.65-11078_65-11077i others(15): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AAAAAAAT others(6): Show |
1 | a0001c0002t0021g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.65-11078_65-11077i others(15): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AAAAAAAT others(8): Show |
1 | a0001c0001t0138g0273 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.65-11078_65-11077i others(17): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AAAAAAAT others(14): Show |
1 | a0001c0001t0201g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-11078_65-11077i others(23): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AAAAAATA others(7): Show |
1 | a0001c0002t0062g0298 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.65-11078_65-11077i others(16): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AAAAAATA others(9): Show |
1 | a0001c0001t0115g0313 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.65-11078_65-11077i others(18): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | AATATATA others(7): Show |
1 | a0001c0002t0065g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.65-11062_65-11049d others(16): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0151g0332 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65-11079_65-11078i others(15): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189879 | ||||||
| chr9:130189879
|
A | T | 38 | a0001c0001t0001g0129a0001c0001t0003g0087a0001c0001t0003g0097others(35): Show | 38 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.65-11079A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189879 | ||||||
| chr9:130189879
|
AATAT | A | 11 | a0001c0001t0002g0070a0001c0001t0019g0080a0001c0001t0022g0347others(8): Show | 11 | HG02071.hp2 HG02486.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-11052_65-11049d others(6): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189879
|
AATATAT | A | 9 | a0001c0001t0043g0327a0001c0001t0135g0277a0001c0002t0001g0018others(6): Show | 9 | HG00323.hp1 HG00642.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-11054_65-11049d others(8): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130189879 | |||||
| chr9:130189880
|
ATAT | A | 9 | a0001c0001t0001g0032a0001c0001t0007g0118a0001c0001t0026g0004others(6): Show | 9 | HG01255.hp1 HG01257.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-11077_65-11075d others(5): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189880 | ||||||
| chr9:130189880
|
ATATAT | A | 21 | a0001c0001t0003g0276a0001c0001t0003g0280a0001c0001t0005g0027others(18): Show | 21 | HG01515.hp1 HG02027.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.65-11077_65-11073d others(7): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189880 | ||||||
| chr9:130189881
|
T | A | 14 | a0001c0001t0121g0076a0001c0001t0176g0035a0001c0002t0001g0001others(11): Show | 14 | HG00741.hp1 HG01175.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.65-11077T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189881 | ||||||
| chr9:130189883
|
T | A | 4 | a0001c0001t0121g0076a0001c0002t0001g0046a0001c0002t0021g0034others(1): Show | 4 | HG02922.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-11075T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189883 | ||||||
| chr9:130189885
|
T | A | 6 | a0001c0001t0022g0347a0001c0001t0121g0076a0001c0002t0057g0159others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-11073T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189885 | ||||||
| chr9:130189887
|
T | A | 11 | a0001c0001t0022g0347a0001c0001t0035g0271a0001c0001t0041g0201others(8): Show | 11 | HG02109.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.65-11071T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189887 | ||||||
| chr9:130189889
|
T | A | 5 | a0001c0001t0071g0233a0001c0002t0057g0159a0001c0002t0128g0294others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-11069T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189889 | ||||||
| chr9:130189891
|
T | A | 4 | a0001c0002t0057g0159a0001c0002t0128g0294a0001c0002t0149g0207others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-11067T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189891 | ||||||
| chr9:130189893
|
T | A | 4 | a0001c0002t0057g0159a0001c0002t0128g0294a0001c0002t0149g0207others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-11065T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189893 | ||||||
| chr9:130189897
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0016g0265 | 2 | HG02135.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.65-11061T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189897 | ||||||
| chr9:130189904
|
A | G | 1 | a0001c0001t0201g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-11054A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189904 | ||||||
| chr9:130189929
|
C | T | 1 | a0001c0002t0009g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.65-11029C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189929 | ||||||
| chr9:130189952
|
T | C | 346 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(343): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.65-11006T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130189952 | ||||||
| chr9:130190008
|
G | C | 2 | a0001c0001t0115g0313a0001c0001t0138g0273 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.65-10950G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130190008 | ||||||
| chr9:130190032
|
A | AAG | 187 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0129others(184): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.65-10894_65-10893d others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130190032 | |||||
| chr9:130190032
|
A | AAGAG | 18 | a0001c0001t0001g0058a0001c0001t0002g0150a0001c0001t0002g0214others(15): Show | 18 | HG00280.hp1 HG00544.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.65-10896_65-10893d others(6): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130190032 | |||||
| chr9:130190032
|
A | AAGAGAG | 10 | a0001c0001t0001g0127a0001c0001t0001g0162a0001c0001t0001g0274others(7): Show | 10 | HG00438.hp1 HG01952.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.65-10898_65-10893d others(8): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130190032 | |||||
| chr9:130190032
|
A | AAGAGAGA others(3): Show |
34 | a0001c0001t0014g0243a0001c0001t0037g0252a0001c0001t0078g0132others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(31): Show |
intron_variant | MODIFIER | c.65-10902_65-10893d others(12): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130190032 | |||||
| chr9:130190032
|
A | AAGAGAGA others(5): Show |
14 | a0001c0001t0022g0347a0001c0001t0029g0156a0001c0001t0039g0148others(11): Show | 14 | HG01099.hp2 HG01255.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-10904_65-10893d others(14): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130190032 | |||||
| chr9:130190032
|
A | AAGAGAGA others(7): Show |
4 | a0001c0001t0075g0318a0001c0002t0009g0092a0001c0002t0093g0212others(1): Show | 4 | HG01168.hp1 HG01361.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-10906_65-10893d others(16): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130190032 | |||||
| chr9:130190032
|
A | AAGAGAGA others(9): Show |
6 | a0001c0001t0029g0325a0001c0001t0032g0319a0001c0001t0076g0310others(3): Show | 6 | HG02818.hp2 HG02922.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-10908_65-10893d others(18): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130190032 | |||||
| chr9:130190032
|
A | AAGAGAGA others(11): Show |
2 | a0001c0001t0069g0321a0001c0001t0179g0155 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.65-10910_65-10893d others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130190032 | |||||
| chr9:130190032
|
AAG | A | 37 | a0001c0001t0001g0048a0001c0001t0003g0022a0001c0001t0046g0166others(34): Show | 37 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.65-10894_65-10893d others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130190032 | |||||
| chr9:130190032
|
AAGAGAG | A | 3 | a0001c0001t0071g0233a0001c0002t0109g0339a0001c0002t0145g0315 | 3 | HG02559.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.65-10898_65-10893d others(8): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130190032 | |||||
| chr9:130190215
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.65-10743A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130190215 | ||||||
| chr9:130190328
|
CAG | C | 3 | a0001c0001t0005g0189a0001c0001t0005g0202a0001c0001t0079g0267 | 3 | HG03491.hp2 HG03492.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.65-10628_65-10627d others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130190328 | |||||
| chr9:130190420
|
T | C | 1 | a0001c0002t0003g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.65-10538T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130190420 | ||||||
| chr9:130190770
|
C | T | 1 | a0001c0001t0044g0337 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.65-10188C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130190770 | ||||||
| chr9:130190825
|
C | A | 2 | a0001c0001t0028g0320a0001c0001t0070g0324 | 2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.65-10133C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130190825 | ||||||
| chr9:130191094
|
A | T | 3 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0104g0065 | 3 | HG01167.hp1 HG01169.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.65-9864A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191094 | ||||||
| chr9:130191095
|
G | T | 1 | a0001c0001t0132g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.65-9863G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191095 | ||||||
| chr9:130191115
|
C | G | 5 | a0001c0001t0167g0064a0001c0001t0176g0035a0001c0002t0017g0317others(2): Show | 5 | HG02922.hp1 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-9843C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191115 | ||||||
| chr9:130191162
|
C | T | 8 | a0001c0001t0001g0226a0001c0001t0005g0197a0001c0001t0006g0119others(5): Show | 8 | HG00544.hp1 HG00597.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-9796C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191162 | ||||||
| chr9:130191167
|
C | T | 5 | a0001c0001t0044g0337a0001c0001t0074g0305a0001c0001t0120g0075others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-9791C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191167 | ||||||
| chr9:130191244
|
C | T | 1 | a0001c0002t0023g0054 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.65-9714C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191244 | ||||||
| chr9:130191263
|
G | A | 1 | a0001c0001t0121g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.65-9695G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191263 | ||||||
| chr9:130191369
|
T | TC | 9 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(6): Show | 9 | NA18963.hp1 NA18969.hp1 NA18980.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-9587dupC | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130191369 | |||||
| chr9:130191469
|
C | T | 2 | a0001c0001t0071g0233a0001c0001t0162g0301 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.65-9489C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191469 | ||||||
| chr9:130191605
|
C | T | 21 | a0001c0001t0001g0048a0001c0001t0047g0247a0001c0001t0106g0056others(18): Show | 21 | HG00741.hp1 HG01074.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.65-9353C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191605 | ||||||
| chr9:130191679
|
C | T | 1 | a0001c0002t0100g0122 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.65-9279C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191679 | ||||||
| chr9:130191695
|
C | T | 1 | a0001c0002t0123g0222 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.65-9263C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191695 | ||||||
| chr9:130191709
|
G | A | 5 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0159g0198others(2): Show | 5 | HG00642.hp1 HG01123.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-9249G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191709 | ||||||
| chr9:130191725
|
G | A | 1 | a0001c0001t0030g0176 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.65-9233G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191725 | ||||||
| chr9:130191773
|
C | G | 3 | a0001c0001t0005g0197a0001c0001t0006g0119a0001c0001t0006g0204 | 3 | HG00544.hp1 NA18986.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.65-9185C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191773 | ||||||
| chr9:130191814
|
C | T | 14 | a0001c0001t0001g0181a0001c0001t0001g0225a0001c0001t0001g0227others(11): Show | 14 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-9144C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191814 | ||||||
| chr9:130191868
|
T | A | 1 | a0001c0002t0194g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.65-9090T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191868 | ||||||
| chr9:130191883
|
G | A | 1 | a0001c0002t0017g0317 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.65-9075G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191883 | ||||||
| chr9:130191988
|
G | A | 2 | a0001c0001t0115g0313a0001c0001t0138g0273 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.65-8970G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130191988 | ||||||
| chr9:130192017
|
C | T | 1 | a0001c0004t0008g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.65-8941C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130192017 | ||||||
| chr9:130192076
|
G | T | 1 | a0001c0001t0029g0325 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.65-8882G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130192076 | ||||||
| chr9:130192187
|
G | T | 5 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0159g0198others(2): Show | 5 | HG00642.hp1 HG01123.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-8771G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130192187 | ||||||
| chr9:130192323
|
G | A | 189 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0058others(186): Show | 189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.65-8635G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130192323 | ||||||
| chr9:130192389
|
G | A | 1 | a0001c0002t0010g0120 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.65-8569G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130192389 | ||||||
| chr9:130192543
|
C | T | 1 | a0001c0001t0041g0201 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.65-8415C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130192543 | ||||||
| chr9:130192560
|
C | T | 5 | a0001c0001t0044g0337a0001c0001t0074g0305a0001c0001t0120g0075others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-8398C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130192560 | ||||||
| chr9:130192565
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.65-8393G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130192565 | ||||||
| chr9:130192718
|
C | A | 3 | a0001c0001t0060g0302a0001c0001t0064g0196a0001c0001t0200g0168 | 3 | HG02895.hp2 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-8240C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130192718 | ||||||
| chr9:130192729
|
C | T | 1 | a0001c0001t0134g0165 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.65-8229C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130192729 | ||||||
| chr9:130192745
|
G | T | 4 | a0001c0001t0001g0058a0001c0001t0004g0142a0001c0001t0010g0098others(1): Show | 4 | HG01928.hp2 HG02056.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-8213G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130192745 | ||||||
| chr9:130192893
|
G | A | 71 | a0001c0001t0001g0162a0001c0001t0003g0285a0001c0001t0004g0183others(68): Show | 71 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.65-8065G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130192893 | ||||||
| chr9:130192972
|
A | C | 6 | a0001c0001t0022g0347a0001c0001t0066g0263a0001c0001t0165g0346others(3): Show | 6 | HG02055.hp1 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-7986A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130192972 | ||||||
| chr9:130192975
|
G | A | 1 | a0001c0001t0044g0337 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.65-7983G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130192975 | ||||||
| chr9:130193010
|
C | G | 2 | a0001c0001t0071g0233a0001c0001t0162g0301 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.65-7948C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193010 | ||||||
| chr9:130193017
|
C | T | 1 | a0001c0001t0092g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.65-7941C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193017 | ||||||
| chr9:130193034
|
C | G | 18 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(15): Show | 18 | HG00741.hp1 HG01175.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.65-7924C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193034 | ||||||
| chr9:130193040
|
C | T | 3 | a0001c0001t0176g0035a0001c0002t0021g0034a0001c0002t0148g0130 | 3 | HG02922.hp1 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.65-7918C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193040 | ||||||
| chr9:130193101
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.65-7857G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193101 | ||||||
| chr9:130193174
|
C | T | 216 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.65-7784C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193174 | ||||||
| chr9:130193207
|
G | C | 73 | a0001c0001t0003g0022a0001c0001t0014g0243a0001c0001t0022g0347others(70): Show | 73 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.65-7751G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193207 | ||||||
| chr9:130193273
|
C | G | 4 | a0001c0001t0044g0337a0001c0001t0120g0075a0001c0002t0109g0339others(1): Show | 4 | HG02559.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-7685C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193273 | ||||||
| chr9:130193288
|
G | A | 3 | a0001c0001t0016g0184a0001c0001t0131g0009a0001c0001t0152g0185 | 3 | NA18948.hp1 NA18983.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.65-7670G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193288 | ||||||
| chr9:130193431
|
C | T | 2 | a0001c0001t0023g0104a0001c0001t0182g0331 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.65-7527C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193431 | ||||||
| chr9:130193452
|
T | G | 1 | a0001c0002t0001g0013 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.65-7506T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193452 | ||||||
| chr9:130193560
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.65-7398C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193560 | ||||||
| chr9:130193770
|
G | A | 1 | a0001c0001t0007g0118 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.65-7188G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193770 | ||||||
| chr9:130193842
|
G | T | 1 | a0001c0002t0010g0120 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.65-7116G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193842 | ||||||
| chr9:130193846
|
G | A | 2 | a0001c0001t0071g0233a0001c0001t0162g0301 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.65-7112G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193846 | ||||||
| chr9:130193883
|
G | C | 2 | a0001c0001t0167g0064a0001c0002t0017g0317 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.65-7075G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193883 | ||||||
| chr9:130193950
|
G | A | 57 | a0001c0001t0014g0243a0001c0001t0020g0100a0001c0001t0037g0252others(54): Show | 57 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.65-7008G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193950 | ||||||
| chr9:130193995
|
C | T | 1 | a0001c0001t0015g0203 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.65-6963C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130193995 | ||||||
| chr9:130194040
|
C | G | 4 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0014g0258others(1): Show | 4 | NA18942.hp2 NA18944.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-6918C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194040 | ||||||
| chr9:130194069
|
G | A | 2 | a0001c0001t0167g0064a0001c0002t0017g0317 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.65-6889G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194069 | ||||||
| chr9:130194081
|
G | A | 1 | a0001c0001t0162g0301 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.65-6877G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194081 | ||||||
| chr9:130194112
|
C | T | 4 | a0001c0001t0044g0337a0001c0001t0120g0075a0001c0002t0109g0339others(1): Show | 4 | HG02559.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-6846C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194112 | ||||||
| chr9:130194225
|
C | T | 8 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0115g0313others(5): Show | 8 | HG02559.hp2 HG02723.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-6733C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194225 | ||||||
| chr9:130194337
|
G | T | 1 | a0001c0001t0003g0285 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.65-6621G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194337 | ||||||
| chr9:130194343
|
A | AGGCTGTG others(19): Show |
66 | a0001c0001t0014g0243a0001c0001t0020g0100a0001c0001t0037g0252others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.65-6605_65-6580dup others(26): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130194343 | |||||
| chr9:130194348
|
G | A | 1 | a0001c0001t0130g0175 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.65-6610G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194348 | ||||||
| chr9:130194518
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.65-6440C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194518 | ||||||
| chr9:130194522
|
C | A | 8 | a0001c0001t0002g0136a0001c0001t0002g0150a0001c0001t0003g0066others(5): Show | 8 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-6436C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194522 | ||||||
| chr9:130194522
|
C | G | 51 | a0001c0001t0014g0243a0001c0001t0020g0100a0001c0001t0037g0252others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.65-6436C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194522 | ||||||
| chr9:130194523
|
C | T | 1 | a0001c0001t0200g0168 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.65-6435C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194523 | ||||||
| chr9:130194557
|
C | T | 2 | a0001c0001t0071g0233a0001c0001t0162g0301 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.65-6401C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194557 | ||||||
| chr9:130194820
|
G | A | 2 | a0001c0001t0071g0233a0001c0001t0162g0301 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.65-6138G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194820 | ||||||
| chr9:130194876
|
C | T | 5 | a0001c0001t0095g0341a0001c0001t0099g0307a0001c0001t0107g0101others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-6082C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194876 | ||||||
| chr9:130194935
|
G | A | 50 | a0001c0001t0014g0243a0001c0001t0020g0100a0001c0001t0037g0252others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.65-6023G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130194935 | ||||||
| chr9:130195178
|
C | T | 3 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0002t0088g0259 | 3 | HG01123.hp1 HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.65-5780C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130195178 | ||||||
| chr9:130195244
|
A | G | 193 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0129others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.65-5714A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130195244 | ||||||
| chr9:130195258
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.65-5700A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130195258 | ||||||
| chr9:130195318
|
G | A | 1 | a0001c0001t0151g0332 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65-5640G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130195318 | ||||||
| chr9:130195435
|
G | GT | 22 | a0001c0001t0001g0162a0001c0001t0022g0347a0001c0001t0025g0113others(19): Show | 22 | HG01261.hp2 HG01978.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.65-5509dupT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130195435 | |||||
| chr9:130195435
|
G | T | 1 | a0001c0002t0004g0124 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.65-5523G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130195435 | ||||||
| chr9:130195548
|
G | A | 2 | a0001c0002t0017g0074a0001c0002t0164g0215 | 2 | HG02074.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.65-5410G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130195548 | ||||||
| chr9:130195598
|
A | G | 4 | a0001c0001t0059g0304a0001c0001t0060g0302a0001c0001t0064g0196others(1): Show | 4 | HG02647.hp2 HG02895.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-5360A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130195598 | ||||||
| chr9:130195647
|
C | T | 1 | a0001c0001t0121g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.65-5311C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130195647 | ||||||
| chr9:130195715
|
C | T | 1 | a0001c0002t0109g0339 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.65-5243C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130195715 | ||||||
| chr9:130195752
|
T | G | 6 | a0001c0001t0046g0166a0001c0001t0066g0263a0001c0001t0121g0076others(3): Show | 6 | HG02055.hp1 HG02258.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-5206T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130195752 | ||||||
| chr9:130195820
|
C | T | 1 | a0001c0002t0173g0051 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.65-5138C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130195820 | ||||||
| chr9:130195905
|
G | C | 1 | a0001c0002t0199g0110 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.65-5053G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130195905 | ||||||
| chr9:130196026
|
C | T | 243 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.65-4932C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130196026 | ||||||
| chr9:130196269
|
A | G | 4 | a0001c0001t0001g0127a0001c0001t0014g0044a0001c0001t0082g0208others(1): Show | 4 | HG02523.hp1 NA18953.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-4689A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130196269 | ||||||
| chr9:130196401
|
A | C | 1 | a0001c0001t0007g0221 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.65-4557A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130196401 | ||||||
| chr9:130196464
|
C | T | 5 | a0001c0001t0115g0313a0001c0001t0138g0273a0001c0001t0146g0333others(2): Show | 5 | HG01069.hp1 HG01884.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-4494C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130196464 | ||||||
| chr9:130196476
|
C | T | 1 | a0001c0001t0151g0332 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65-4482C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130196476 | ||||||
| chr9:130196572
|
C | T | 7 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0186g0242others(4): Show | 7 | HG01123.hp1 HG02738.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-4386C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130196572 | ||||||
| chr9:130196584
|
C | T | 10 | a0001c0001t0044g0337a0001c0001t0066g0263a0001c0001t0071g0233others(7): Show | 10 | HG02055.hp1 HG02258.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.65-4374C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130196584 | ||||||
| chr9:130196670
|
C | T | 26 | a0001c0001t0025g0113a0001c0001t0025g0178a0001c0001t0025g0188others(23): Show | 26 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.65-4288C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130196670 | ||||||
| chr9:130196671
|
G | A | 24 | a0001c0001t0022g0347a0001c0001t0028g0320a0001c0001t0029g0156others(21): Show | 24 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.65-4287G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130196671 | ||||||
| chr9:130196681
|
G | A | 32 | a0001c0001t0003g0022a0001c0001t0025g0113a0001c0001t0025g0178others(29): Show | 32 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.65-4277G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130196681 | ||||||
| chr9:130196721
|
G | T | 6 | a0001c0001t0066g0263a0001c0001t0167g0064a0001c0001t0176g0035others(3): Show | 6 | HG02055.hp1 HG02258.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-4237G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130196721 | ||||||
| chr9:130196897
|
C | T | 1 | a0001c0002t0008g0041 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.65-4061C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130196897 | ||||||
| chr9:130196932
|
G | A | 1 | a0001c0001t0045g0345 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.65-4026G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130196932 | ||||||
| chr9:130197039
|
C | T | 328 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(325): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.65-3919C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130197039 | ||||||
| chr9:130197177
|
G | A | 7 | a0001c0001t0166g0329a0001c0002t0028g0154a0001c0002t0040g0033others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-3781G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130197177 | ||||||
| chr9:130197192
|
G | A | 6 | a0001c0001t0066g0263a0001c0001t0167g0064a0001c0001t0176g0035others(3): Show | 6 | HG02055.hp1 HG02258.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-3766G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130197192 | ||||||
| chr9:130197250
|
C | T | 1 | a0001c0001t0201g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-3708C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130197250 | ||||||
| chr9:130197484
|
C | T | 2 | a0001c0002t0007g0177a0001c0002t0007g0186 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.65-3474C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130197484 | ||||||
| chr9:130197596
|
C | G | 1 | a0001c0001t0003g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.65-3362C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130197596 | ||||||
| chr9:130197737
|
C | A | 2 | a0001c0002t0097g0039a0001c0002t0133g0047 | 2 | HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.65-3221C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130197737 | ||||||
| chr9:130197740
|
A | C | 70 | a0001c0001t0014g0243a0001c0001t0016g0184a0001c0001t0037g0252others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-3218A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130197740 | ||||||
| chr9:130197755
|
G | T | 3 | a0001c0001t0027g0335a0001c0001t0027g0336a0001c0001t0181g0330 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.65-3203G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130197755 | ||||||
| chr9:130197852
|
A | G | 2 | a0001c0001t0044g0337a0001c0001t0071g0233 | 2 | HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.65-3106A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130197852 | ||||||
| chr9:130197890
|
G | A | 2 | a0001c0001t0120g0075a0001c0002t0113g0292 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.65-3068G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130197890 | ||||||
| chr9:130197912
|
C | T | 210 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(207): Show | 210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.65-3046C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130197912 | ||||||
| chr9:130197967
|
GA | G | 275 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.65-2974delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130197967 | |||||
| chr9:130198023
|
G | T | 1 | a0001c0001t0030g0176 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.65-2935G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130198023 | ||||||
| chr9:130198035
|
C | G | 25 | a0001c0001t0025g0113a0001c0001t0025g0178a0001c0001t0025g0188others(22): Show | 25 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.65-2923C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130198035 | ||||||
| chr9:130198180
|
G | A | 2 | a0001c0001t0120g0075a0001c0002t0113g0292 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.65-2778G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130198180 | ||||||
| chr9:130198238
|
T | A | 3 | a0001c0001t0059g0304a0001c0001t0060g0302a0001c0001t0064g0196 | 3 | HG02647.hp2 HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.65-2720T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130198238 | ||||||
| chr9:130198316
|
G | A | 6 | a0001c0001t0001g0226a0001c0001t0005g0197a0001c0001t0006g0119others(3): Show | 6 | HG00544.hp1 HG02135.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-2642G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130198316 | ||||||
| chr9:130198319
|
G | C | 2 | a0001c0001t0132g0109a0001c0001t0200g0168 | 2 | HG03471.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.65-2639G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130198319 | ||||||
| chr9:130198347
|
G | T | 209 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(206): Show | 209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.65-2611G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130198347 | ||||||
| chr9:130198372
|
G | A | 4 | a0001c0002t0021g0312a0001c0002t0056g0311a0001c0002t0062g0298others(1): Show | 4 | HG01884.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-2586G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130198372 | ||||||
| chr9:130198419
|
T | C | 284 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.65-2539T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130198419 | ||||||
| chr9:130198449
|
C | T | 1 | a0001c0001t0176g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.65-2509C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130198449 | ||||||
| chr9:130198604
|
A | G | 3 | a0001c0002t0054g0199a0001c0002t0137g0158a0001c0002t0144g0115 | 3 | HG03041.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.65-2354A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130198604 | ||||||
| chr9:130198982
|
C | T | 1 | a0001c0001t0106g0056 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.65-1976C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130198982 | ||||||
| chr9:130199098
|
CT | C | 265 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.65-1847delT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130199098 | |||||
| chr9:130199098
|
CTT | C | 49 | a0001c0001t0001g0058a0001c0001t0002g0036a0001c0001t0002g0037others(46): Show | 49 | HG00323.hp2 HG00597.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.65-1848_65-1847del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130199098 | |||||
| chr9:130199179
|
C | T | 1 | a0001c0001t0003g0276 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.65-1779C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130199179 | ||||||
| chr9:130199274
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.65-1684T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130199274 | ||||||
| chr9:130199345
|
G | A | 1 | a0001c0001t0168g0107 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.65-1613G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130199345 | ||||||
| chr9:130199463
|
G | A | 2 | a0001c0001t0002g0108a0001c0001t0002g0112 | 2 | HG03688.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.65-1495G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130199463 | ||||||
| chr9:130199481
|
A | T | 17 | a0001c0001t0022g0347a0001c0001t0028g0320a0001c0001t0029g0156others(14): Show | 17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.65-1477A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130199481 | ||||||
| chr9:130199488
|
G | A | 1 | a0001c0001t0022g0161 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.65-1470G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130199488 | ||||||
| chr9:130199528
|
G | A | 26 | a0001c0001t0025g0113a0001c0001t0025g0178a0001c0001t0025g0188others(23): Show | 26 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.65-1430G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130199528 | ||||||
| chr9:130199845
|
T | C | 26 | a0001c0001t0025g0113a0001c0001t0025g0178a0001c0001t0025g0188others(23): Show | 26 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.65-1113T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130199845 | ||||||
| chr9:130199897
|
G | GTTCA | 7 | a0001c0001t0001g0032a0001c0001t0002g0211a0001c0001t0031g0090others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-1033_65-1030dup others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130199897 | |||||
| chr9:130199897
|
G | GTTCATTC others(1): Show |
96 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0129others(93): Show | 96 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.65-1037_65-1030dup others(8): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130199897 | |||||
| chr9:130199897
|
G | GTTCATTC others(5): Show |
122 | a0001c0001t0001g0048a0001c0001t0001g0127a0001c0001t0001g0162others(119): Show | 122 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.65-1041_65-1030dup others(12): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130199897 | |||||
| chr9:130199897
|
G | GTTCATTC others(9): Show |
10 | a0001c0001t0001g0190a0001c0001t0003g0283a0001c0001t0006g0204others(7): Show | 10 | HG01175.hp2 HG01515.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-1045_65-1030dup others(16): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130199897 | |||||
| chr9:130199897
|
G | GTTCATTC others(13): Show |
1 | a0001c0002t0157g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.65-1049_65-1030dup others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130199897 | |||||
| chr9:130199922
|
T | TTCATTCA others(4): Show |
1 | a0001c0001t0033g0031 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.65-1030_65-1029ins others(11): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 130199922 | |||||
| chr9:130199967
|
G | A | 2 | a0001c0001t0115g0313a0001c0001t0138g0273 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.65-991G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130199967 | ||||||
| chr9:130200221
|
G | A | 208 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(205): Show | 208 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.65-737G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130200221 | ||||||
| chr9:130200249
|
A | C | 14 | a0001c0002t0021g0034a0001c0002t0021g0306a0001c0002t0054g0199others(11): Show | 14 | HG02280.hp2 HG02451.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-709A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130200249 | ||||||
| chr9:130200362
|
C | G | 66 | a0001c0001t0001g0058a0001c0001t0014g0243a0001c0001t0016g0184others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.65-596C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130200362 | ||||||
| chr9:130200413
|
C | T | 1 | a0001c0001t0106g0056 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.65-545C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130200413 | ||||||
| chr9:130200438
|
A | G | 290 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.65-520A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130200438 | ||||||
| chr9:130200522
|
A | T | 285 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.65-436A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130200522 | ||||||
| chr9:130200537
|
T | C | 286 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.65-421T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130200537 | ||||||
| chr9:130200590
|
A | G | 9 | a0001c0001t0044g0337a0001c0001t0066g0263a0001c0001t0071g0233others(6): Show | 9 | HG02055.hp1 HG02258.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-368A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130200590 | ||||||
| chr9:130200834
|
C | T | 2 | a0001c0002t0056g0311a0001c0002t0062g0298 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.65-124C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130200834 | ||||||
| chr9:130200836
|
T | G | 290 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.65-122T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130200836 | ||||||
| chr9:130200850
|
G | A | 323 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.65-108G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | chr9 | 130200850 | ||||||
| chr9:130201071
|
T | C | 323 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.89+89T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130201071 | ||||||
| chr9:130201072
|
C | G | 7 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0186g0242others(4): Show | 7 | HG01123.hp1 HG02738.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.89+90C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130201072 | ||||||
| chr9:130201342
|
C | T | 1 | a0001c0002t0009g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.89+360C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130201342 | ||||||
| chr9:130201419
|
T | A | 323 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.89+437T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130201419 | ||||||
| chr9:130201574
|
G | A | 1 | a0001c0002t0112g0182 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.89+592G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130201574 | ||||||
| chr9:130201811
|
G | T | 8 | a0001c0001t0166g0329a0001c0002t0028g0154a0001c0002t0040g0033others(5): Show | 8 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.89+829G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130201811 | ||||||
| chr9:130201813
|
G | A | 1 | a0001c0001t0004g0010 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.89+831G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130201813 | ||||||
| chr9:130201815
|
C | G | 1 | a0001c0001t0067g0240 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.89+833C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130201815 | ||||||
| chr9:130201839
|
C | G | 23 | a0001c0001t0002g0070a0001c0001t0002g0108a0001c0001t0002g0112others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.89+857C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130201839 | ||||||
| chr9:130201889
|
T | G | 1 | a0001c0002t0113g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.89+907T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130201889 | ||||||
| chr9:130201988
|
G | A | 2 | a0001c0002t0009g0092a0001c0002t0185g0144 | 2 | HG01361.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.89+1006G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130201988 | ||||||
| chr9:130202205
|
C | T | 3 | a0001c0001t0005g0197a0001c0001t0006g0119a0001c0001t0006g0204 | 3 | HG00544.hp1 NA18986.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.89+1223C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130202205 | ||||||
| chr9:130202354
|
A | G | 126 | a0001c0001t0003g0022a0001c0001t0014g0243a0001c0001t0016g0184others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.89+1372A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130202354 | ||||||
| chr9:130202579
|
GT | G | 316 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.89+1613delT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130202579 | |||||
| chr9:130202662
|
C | T | 1 | a0001c0002t0147g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.89+1680C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130202662 | ||||||
| chr9:130202666
|
G | A | 1 | a0001c0001t0193g0192 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.89+1684G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130202666 | ||||||
| chr9:130202768
|
C | T | 4 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.89+1786C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130202768 | ||||||
| chr9:130202908
|
G | A | 1 | a0001c0002t0113g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.89+1926G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130202908 | ||||||
| chr9:130202949
|
C | G | 1 | a0001c0001t0032g0195 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.89+1967C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130202949 | ||||||
| chr9:130203046
|
A | ATG | 15 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0166g0329others(12): Show | 15 | HG01123.hp1 HG01361.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.89+2098_89+2099dup others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130203046 | |||||
| chr9:130203046
|
A | ATGTGTG | 3 | a0001c0002t0018g0245a0001c0002t0058g0264a0001c0002t0063g0235 | 3 | HG02055.hp1 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.89+2094_89+2099dup others(6): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130203046 | |||||
| chr9:130203046
|
A | ATGTGTGT others(11): Show |
1 | a0001c0001t0071g0233 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.89+2082_89+2099dup others(18): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130203046 | |||||
| chr9:130203046
|
A | ATGTGTGT others(15): Show |
1 | a0001c0001t0044g0337 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.89+2078_89+2099dup others(22): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130203046 | |||||
| chr9:130203046
|
A | ATGTGTGT others(23): Show |
1 | a0001c0001t0176g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89+2070_89+2099dup others(30): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130203046 | |||||
| chr9:130203046
|
ATG | A | 34 | a0001c0001t0001g0129a0001c0001t0002g0036a0001c0001t0002g0037others(31): Show | 34 | HG00735.hp1 HG01192.hp2 HG01515.hp2 others(31): Show |
intron_variant | MODIFIER | c.89+2098_89+2099del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130203046 | |||||
| chr9:130203046
|
ATGTG | A | 214 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(211): Show | 214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.89+2096_89+2099del others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130203046 | |||||
| chr9:130203046
|
ATGTGTGT others(1): Show |
A | 3 | a0001c0002t0011g0217a0001c0002t0127g0126a0001c0002t0180g0257 | 3 | HG01358.hp2 NA18959.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.89+2092_89+2099del others(8): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130203046 | |||||
| chr9:130203065
|
T | C | 26 | a0001c0001t0025g0113a0001c0001t0025g0178a0001c0001t0025g0188others(23): Show | 26 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.89+2083T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203065 | ||||||
| chr9:130203098
|
A | ATG | 4 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.89+2129_89+2130dup others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130203098 | |||||
| chr9:130203122
|
GTA | G | 16 | a0001c0001t0001g0129a0001c0001t0001g0162a0001c0001t0002g0108others(13): Show | 16 | HG00738.hp2 HG01256.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.89+2154_89+2155del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130203122 | |||||
| chr9:130203135
|
TA | T | 83 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0127others(80): Show | 83 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.89+2154delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203135 | ||||||
| chr9:130203136
|
A | T | 10 | a0001c0001t0002g0073a0001c0001t0002g0108a0001c0001t0002g0112others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.89+2154A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203136 | ||||||
| chr9:130203136
|
AT | A | 112 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0274others(109): Show | 112 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.89+2169delT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130203136 | |||||
| chr9:130203136
|
ATT | A | 12 | a0001c0001t0002g0070a0001c0001t0002g0150a0001c0001t0003g0066others(9): Show | 12 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.89+2168_89+2169del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130203136 | |||||
| chr9:130203137
|
T | TA | 30 | a0001c0001t0003g0022a0001c0001t0046g0166a0001c0001t0117g0105others(27): Show | 30 | HG00741.hp1 HG01123.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.89+2155_89+2156ins others(1): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203137 | ||||||
| chr9:130203137
|
T | TATA | 10 | a0001c0001t0025g0113a0001c0001t0025g0178a0001c0001t0025g0188others(7): Show | 10 | HG00639.hp1 HG00735.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.89+2155_89+2156ins others(3): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203137 | ||||||
| chr9:130203138
|
T | A | 63 | a0001c0001t0015g0203a0001c0001t0022g0347a0001c0001t0028g0320others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.89+2156T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203138 | ||||||
| chr9:130203139
|
T | A | 69 | a0001c0001t0001g0291a0001c0001t0004g0010a0001c0001t0017g0116others(66): Show | 69 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.89+2157T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203139 | ||||||
| chr9:130203140
|
T | A | 51 | a0001c0001t0009g0068a0001c0001t0009g0084a0001c0001t0009g0093others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.89+2158T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203140 | ||||||
| chr9:130203141
|
T | A | 5 | a0001c0002t0001g0042a0001c0002t0023g0054a0001c0002t0023g0059others(2): Show | 5 | HG01978.hp2 HG02273.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.89+2159T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203141 | ||||||
| chr9:130203142
|
T | A | 7 | a0001c0001t0022g0347a0001c0001t0044g0337a0001c0001t0121g0076others(4): Show | 7 | HG01069.hp1 HG01884.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.89+2160T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203142 | ||||||
| chr9:130203316
|
A | G | 4 | a0001c0001t0066g0263a0001c0002t0018g0245a0001c0002t0058g0264others(1): Show | 4 | HG02055.hp1 HG02258.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.89+2334A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203316 | ||||||
| chr9:130203507
|
G | T | 2 | a0001c0001t0031g0090a0001c0001t0031g0091 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.89+2525G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203507 | ||||||
| chr9:130203551
|
G | C | 4 | a0001c0001t0019g0080a0001c0001t0019g0088a0001c0001t0019g0145others(1): Show | 4 | NA18984.hp1 NA18986.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.89+2569G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203551 | ||||||
| chr9:130203723
|
G | A | 3 | a0001c0001t0121g0076a0001c0001t0146g0333a0001c0001t0154g0340 | 3 | HG01069.hp1 HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.89+2741G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203723 | ||||||
| chr9:130203810
|
G | C | 1 | a0001c0001t0032g0195 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.89+2828G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203810 | ||||||
| chr9:130203967
|
T | C | 312 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(309): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.89+2985T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203967 | ||||||
| chr9:130203980
|
A | T | 3 | a0001c0001t0022g0191a0001c0001t0129g0297a0001c0001t0130g0175 | 3 | HG01243.hp1 HG01361.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.89+2998A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203980 | ||||||
| chr9:130203990
|
T | C | 71 | a0001c0001t0014g0243a0001c0001t0016g0184a0001c0001t0039g0106others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.89+3008T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130203990 | ||||||
| chr9:130204141
|
C | T | 200 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(197): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.89+3159C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130204141 | ||||||
| chr9:130204268
|
A | T | 304 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(301): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.89+3286A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130204268 | ||||||
| chr9:130204321
|
C | T | 6 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075others(3): Show | 6 | HG02723.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.89+3339C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130204321 | ||||||
| chr9:130204327
|
C | T | 1 | a0001c0002t0123g0222 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.89+3345C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130204327 | ||||||
| chr9:130204688
|
G | T | 304 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(301): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.89+3706G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130204688 | ||||||
| chr9:130204713
|
T | C | 5 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075others(2): Show | 5 | HG02723.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.89+3731T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130204713 | ||||||
| chr9:130204749
|
G | A | 4 | a0001c0001t0005g0197a0001c0001t0006g0119a0001c0001t0006g0204others(1): Show | 4 | HG00544.hp1 NA18961.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.89+3767G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130204749 | ||||||
| chr9:130204782
|
C | T | 1 | a0001c0002t0073g0028 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.89+3800C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130204782 | ||||||
| chr9:130204817
|
A | G | 6 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075others(3): Show | 6 | HG02723.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.89+3835A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130204817 | ||||||
| chr9:130204824
|
G | A | 6 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075others(3): Show | 6 | HG02723.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.89+3842G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130204824 | ||||||
| chr9:130204841
|
G | A | 4 | a0001c0001t0005g0197a0001c0001t0006g0119a0001c0001t0006g0204others(1): Show | 4 | HG00544.hp1 NA18961.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.89+3859G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130204841 | ||||||
| chr9:130204865
|
G | A | 6 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075others(3): Show | 6 | HG02723.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.89+3883G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130204865 | ||||||
| chr9:130204917
|
A | G | 200 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(197): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.89+3935A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130204917 | ||||||
| chr9:130205009
|
G | A | 297 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.89+4027G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130205009 | ||||||
| chr9:130205121
|
A | G | 310 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.89+4139A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130205121 | ||||||
| chr9:130205244
|
G | A | 6 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075others(3): Show | 6 | HG02723.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.89+4262G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130205244 | ||||||
| chr9:130205308
|
G | C | 3 | a0001c0001t0049g0328a0001c0001t0050g0308a0001c0001t0053g0314 | 3 | HG01109.hp1 HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.89+4326G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130205308 | ||||||
| chr9:130205352
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.89+4370G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130205352 | ||||||
| chr9:130205418
|
C | T | 1 | a0001c0001t0026g0004 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.89+4436C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130205418 | ||||||
| chr9:130205483
|
G | T | 1 | a0001c0001t0052g0147 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.89+4501G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130205483 | ||||||
| chr9:130205536
|
A | AG | 25 | a0001c0001t0025g0113a0001c0001t0025g0178a0001c0001t0025g0188others(22): Show | 25 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.89+4555dupG | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130205536 | |||||
| chr9:130205537
|
G | GA | 253 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.89+4573dupA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130205537 | |||||
| chr9:130205537
|
G | GAA | 15 | a0001c0001t0001g0226a0001c0001t0002g0037a0001c0001t0002g0062others(12): Show | 15 | HG00438.hp1 HG01106.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.89+4572_89+4573dup others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130205537 | |||||
| chr9:130205537
|
GA | G | 6 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075others(3): Show | 6 | HG02723.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.89+4573delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130205537 | |||||
| chr9:130205560
|
G | A | 11 | a0001c0001t0166g0329a0001c0002t0021g0312a0001c0002t0028g0154others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.89+4578G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130205560 | ||||||
| chr9:130205653
|
T | C | 3 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075 | 3 | HG02723.hp2 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.89+4671T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130205653 | ||||||
| chr9:130205677
|
G | GA | 12 | a0001c0001t0001g0127a0001c0001t0002g0108a0001c0001t0002g0136others(9): Show | 12 | HG00438.hp2 HG00544.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.89+4709dupA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130205677 | |||||
| chr9:130205677
|
GA | G | 25 | a0001c0001t0025g0113a0001c0001t0025g0178a0001c0001t0025g0188others(22): Show | 25 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.89+4709delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130205677 | |||||
| chr9:130205680
|
A | G | 1 | a0001c0001t0022g0347 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.89+4698A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130205680 | ||||||
| chr9:130205833
|
TA | T | 13 | a0001c0001t0031g0091a0001c0001t0064g0196a0001c0001t0166g0329others(10): Show | 13 | HG01168.hp2 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.89+4865delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130205833 | |||||
| chr9:130206081
|
C | T | 1 | a0001c0002t0024g0220 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.89+5099C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130206081 | ||||||
| chr9:130206205
|
T | G | 6 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075others(3): Show | 6 | HG02723.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.89+5223T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130206205 | ||||||
| chr9:130206222
|
A | G | 4 | a0001c0001t0001g0032a0001c0001t0033g0029a0001c0001t0033g0031others(1): Show | 4 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.89+5240A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130206222 | ||||||
| chr9:130206226
|
C | T | 5 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075others(2): Show | 5 | HG02723.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.89+5244C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130206226 | ||||||
| chr9:130206233
|
G | A | 310 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.89+5251G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130206233 | ||||||
| chr9:130206355
|
G | A | 304 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(301): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.89+5373G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130206355 | ||||||
| chr9:130206381
|
G | A | 17 | a0001c0001t0022g0347a0001c0001t0028g0320a0001c0001t0029g0156others(14): Show | 17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.89+5399G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130206381 | ||||||
| chr9:130206391
|
TTTTC | T | 5 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075others(2): Show | 5 | HG02723.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.89+5421_89+5424del others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130206391 | |||||
| chr9:130206403
|
CT | C | 8 | a0001c0001t0005g0146a0001c0001t0005g0262a0001c0001t0014g0044others(5): Show | 8 | HG00544.hp2 HG01167.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.89+5441delT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130206403 | |||||
| chr9:130206403
|
CTT | C | 191 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(188): Show | 191 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.89+5440_89+5441del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130206403 | |||||
| chr9:130206403
|
CTTT | C | 102 | a0001c0001t0003g0022a0001c0001t0014g0243a0001c0001t0016g0184others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.89+5439_89+5441del others(3): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130206403 | |||||
| chr9:130206409
|
T | C | 5 | a0001c0001t0046g0166a0001c0001t0183g0103a0001c0002t0018g0299others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.89+5427T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130206409 | ||||||
| chr9:130206410
|
T | C | 1 | a0001c0002t0145g0315 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.89+5428T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130206410 | ||||||
| chr9:130206534
|
G | A | 2 | a0001c0001t0002g0108a0001c0001t0002g0112 | 2 | HG03688.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.89+5552G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130206534 | ||||||
| chr9:130206763
|
G | A | 11 | a0001c0001t0166g0329a0001c0002t0021g0312a0001c0002t0028g0154others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.89+5781G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130206763 | ||||||
| chr9:130206805
|
C | A | 113 | a0001c0001t0003g0022a0001c0001t0014g0243a0001c0001t0016g0184others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.89+5823C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130206805 | ||||||
| chr9:130206948
|
G | A | 33 | a0001c0001t0003g0022a0001c0001t0025g0113a0001c0001t0025g0178others(30): Show | 33 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.89+5966G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130206948 | ||||||
| chr9:130207053
|
T | C | 5 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075others(2): Show | 5 | HG02723.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.89+6071T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130207053 | ||||||
| chr9:130207096
|
A | T | 4 | a0001c0001t0066g0263a0001c0002t0018g0245a0001c0002t0058g0264others(1): Show | 4 | HG02055.hp1 HG02258.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.89+6114A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130207096 | ||||||
| chr9:130207127
|
C | T | 1 | a0001c0001t0162g0301 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.89+6145C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130207127 | ||||||
| chr9:130207298
|
C | T | 1 | a0001c0002t0003g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.89+6316C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130207298 | ||||||
| chr9:130207306
|
C | G | 321 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.89+6324C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130207306 | ||||||
| chr9:130207456
|
C | T | 1 | a0001c0001t0003g0279 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.89+6474C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130207456 | ||||||
| chr9:130207459
|
G | A | 4 | a0001c0001t0066g0263a0001c0002t0018g0245a0001c0002t0058g0264others(1): Show | 4 | HG02055.hp1 HG02258.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.89+6477G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130207459 | ||||||
| chr9:130207463
|
C | T | 1 | a0001c0002t0185g0144 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.89+6481C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130207463 | ||||||
| chr9:130207691
|
C | T | 102 | a0001c0001t0003g0022a0001c0001t0014g0243a0001c0001t0016g0184others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.89+6709C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130207691 | ||||||
| chr9:130207731
|
G | A | 1 | a0001c0001t0120g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.89+6749G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130207731 | ||||||
| chr9:130207738
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.89+6756G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130207738 | ||||||
| chr9:130207772
|
G | A | 1 | a0001c0001t0176g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89+6790G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130207772 | ||||||
| chr9:130207950
|
T | A | 1 | a0001c0001t0013g0261 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.89+6968T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130207950 | ||||||
| chr9:130208042
|
A | T | 6 | a0001c0001t0029g0325a0001c0001t0032g0319a0001c0001t0069g0321others(3): Show | 6 | HG02486.hp2 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.89+7060A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208042 | ||||||
| chr9:130208053
|
G | C | 321 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.89+7071G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208053 | ||||||
| chr9:130208238
|
G | A | 1 | a0001c0001t0003g0269 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.89+7256G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208238 | ||||||
| chr9:130208311
|
G | T | 2 | a0001c0001t0001g0226a0001c0001t0016g0265 | 2 | HG02135.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.89+7329G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208311 | ||||||
| chr9:130208403
|
C | T | 1 | a0001c0001t0176g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89+7421C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208403 | ||||||
| chr9:130208428
|
A | T | 4 | a0001c0001t0183g0103a0001c0002t0018g0299a0001c0002t0065g0205others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.89+7446A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208428 | ||||||
| chr9:130208441
|
G | A | 1 | a0001c0001t0037g0152 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.89+7459G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208441 | ||||||
| chr9:130208460
|
G | A | 101 | a0001c0001t0014g0243a0001c0001t0016g0184a0001c0001t0025g0113others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.89+7478G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208460 | ||||||
| chr9:130208467
|
C | T | 2 | a0001c0002t0028g0154a0001c0002t0040g0033 | 2 | HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.89+7485C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208467 | ||||||
| chr9:130208478
|
C | A | 3 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075 | 3 | HG02723.hp2 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.89+7496C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208478 | ||||||
| chr9:130208658
|
T | G | 321 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.89+7676T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208658 | ||||||
| chr9:130208666
|
C | G | 1 | a0001c0001t0030g0038 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.89+7684C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208666 | ||||||
| chr9:130208679
|
C | A | 1 | a0001c0002t0112g0182 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.89+7697C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208679 | ||||||
| chr9:130208705
|
T | C | 1 | a0001c0001t0176g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89+7723T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208705 | ||||||
| chr9:130208717
|
G | A | 1 | a0001c0001t0099g0307 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89+7735G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208717 | ||||||
| chr9:130208781
|
C | T | 26 | a0001c0001t0025g0113a0001c0001t0025g0178a0001c0001t0025g0188others(23): Show | 26 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.89+7799C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208781 | ||||||
| chr9:130208791
|
C | T | 10 | a0001c0001t0003g0022a0001c0001t0044g0337a0001c0001t0071g0233others(7): Show | 10 | HG01123.hp1 HG02723.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+7809C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208791 | ||||||
| chr9:130208793
|
G | T | 3 | a0001c0001t0162g0301a0001c0001t0201g0338a0001c0002t0109g0339 | 3 | HG01891.hp2 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.89+7811G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208793 | ||||||
| chr9:130208800
|
C | T | 26 | a0001c0001t0025g0113a0001c0001t0025g0178a0001c0001t0025g0188others(23): Show | 26 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.89+7818C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208800 | ||||||
| chr9:130208876
|
CTG | C | 10 | a0001c0001t0003g0022a0001c0001t0044g0337a0001c0001t0071g0233others(7): Show | 10 | HG01123.hp1 HG02723.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+7911_89+7912del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130208876 | |||||
| chr9:130208882
|
G | C | 1 | a0001c0001t0162g0301 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.89+7900G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208882 | ||||||
| chr9:130208951
|
G | A | 208 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(205): Show | 208 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.89+7969G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208951 | ||||||
| chr9:130208954
|
G | A | 5 | a0001c0001t0115g0313a0001c0001t0121g0076a0001c0001t0138g0273others(2): Show | 5 | HG01069.hp1 HG01884.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.89+7972G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130208954 | ||||||
| chr9:130209138
|
G | C | 5 | a0001c0001t0166g0329a0001c0002t0057g0159a0001c0002t0128g0294others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.89+8156G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209138 | ||||||
| chr9:130209140
|
C | T | 2 | a0001c0002t0028g0154a0001c0002t0040g0033 | 2 | HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.89+8158C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209140 | ||||||
| chr9:130209156
|
G | A | 2 | a0001c0002t0007g0177a0001c0002t0007g0186 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.89+8174G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209156 | ||||||
| chr9:130209182
|
G | C | 3 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075 | 3 | HG02723.hp2 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.89+8200G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209182 | ||||||
| chr9:130209393
|
G | A | 1 | a0001c0001t0092g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.89+8411G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209393 | ||||||
| chr9:130209395
|
G | A | 1 | a0001c0001t0176g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89+8413G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209395 | ||||||
| chr9:130209541
|
G | A | 29 | a0001c0001t0025g0113a0001c0001t0025g0178a0001c0001t0025g0188others(26): Show | 29 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.90-8291G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209541 | ||||||
| chr9:130209552
|
G | T | 208 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(205): Show | 208 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.90-8280G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209552 | ||||||
| chr9:130209766
|
C | T | 7 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0186g0242others(4): Show | 7 | HG01123.hp1 HG02738.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.90-8066C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209766 | ||||||
| chr9:130209773
|
G | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0006g0348others(5): Show | 8 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.90-8059G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209773 | ||||||
| chr9:130209877
|
C | T | 208 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(205): Show | 208 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.90-7955C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209877 | ||||||
| chr9:130209886
|
C | T | 1 | a0001c0002t0001g0255 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.90-7946C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209886 | ||||||
| chr9:130209943
|
C | A | 5 | a0001c0001t0166g0329a0001c0002t0057g0159a0001c0002t0128g0294others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.90-7889C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209943 | ||||||
| chr9:130209970
|
G | A | 1 | a0001c0002t0109g0339 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.90-7862G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209970 | ||||||
| chr9:130209984
|
C | G | 1 | a0001c0001t0026g0004 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.90-7848C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130209984 | ||||||
| chr9:130210078
|
C | T | 2 | a0001c0002t0021g0034a0001c0002t0148g0130 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.90-7754C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130210078 | ||||||
| chr9:130210227
|
C | T | 10 | a0001c0001t0003g0022a0001c0001t0044g0337a0001c0001t0071g0233others(7): Show | 10 | HG01123.hp1 HG02723.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-7605C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130210227 | ||||||
| chr9:130210246
|
A | C | 8 | a0001c0002t0021g0312a0001c0002t0028g0154a0001c0002t0040g0033others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.90-7586A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130210246 | ||||||
| chr9:130210340
|
A | G | 3 | a0001c0001t0044g0337a0001c0001t0071g0233a0001c0001t0120g0075 | 3 | HG02723.hp2 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.90-7492A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130210340 | ||||||
| chr9:130210400
|
G | GA | 89 | a0001c0001t0003g0022a0001c0001t0014g0243a0001c0001t0016g0184others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.90-7417dupA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130210400 | |||||
| chr9:130210400
|
G | GAA | 24 | a0001c0001t0025g0178a0001c0001t0025g0188a0001c0001t0187g0200others(21): Show | 24 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.90-7418_90-7417dup others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130210400 | |||||
| chr9:130210527
|
C | A | 1 | a0001c0001t0193g0192 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.90-7305C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130210527 | ||||||
| chr9:130210550
|
T | C | 321 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.90-7282T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130210550 | ||||||
| chr9:130210843
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0117g0105a0001c0002t0111g0026 | 2 | HG04228.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.90-6985_90-6976dup others(10): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130210843 | |||||
| chr9:130210995
|
T | C | 321 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.90-6837T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130210995 | ||||||
| chr9:130210999
|
C | T | 1 | a0001c0001t0005g0027 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.90-6833C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130210999 | ||||||
| chr9:130211010
|
A | AT | 49 | a0001c0001t0001g0129a0001c0001t0001g0187a0001c0001t0025g0113others(46): Show | 49 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.90-6801dupT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130211010 | |||||
| chr9:130211010
|
A | ATT | 253 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.90-6802_90-6801dup others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130211010 | |||||
| chr9:130211010
|
A | ATTT | 16 | a0001c0001t0001g0274a0001c0001t0001g0278a0001c0001t0002g0062others(13): Show | 16 | HG01106.hp1 HG01361.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.90-6803_90-6801dup others(3): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130211010 | |||||
| chr9:130211010
|
ATTT | A | 9 | a0001c0001t0003g0022a0001c0001t0044g0337a0001c0001t0071g0233others(6): Show | 9 | HG01123.hp1 HG02723.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.90-6803_90-6801del others(3): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130211010 | |||||
| chr9:130211061
|
C | T | 3 | a0001c0001t0134g0165a0001c0001t0159g0198a0001c0001t0168g0107 | 3 | HG00642.hp1 HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.90-6771C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130211061 | ||||||
| chr9:130211088
|
G | A | 321 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.90-6744G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130211088 | ||||||
| chr9:130211265
|
T | C | 1 | a0001c0001t0153g0160 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.90-6567T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130211265 | ||||||
| chr9:130211283
|
A | G | 11 | a0001c0001t0003g0022a0001c0001t0044g0337a0001c0001t0071g0233others(8): Show | 11 | HG01123.hp1 HG02723.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.90-6549A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130211283 | ||||||
| chr9:130211433
|
C | T | 7 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0186g0242others(4): Show | 7 | HG01123.hp1 HG02738.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.90-6399C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130211433 | ||||||
| chr9:130211499
|
G | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0006g0348others(5): Show | 8 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.90-6333G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130211499 | ||||||
| chr9:130211618
|
C | T | 26 | a0001c0001t0025g0113a0001c0001t0025g0178a0001c0001t0025g0188others(23): Show | 26 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.90-6214C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130211618 | ||||||
| chr9:130211652
|
G | A | 2 | a0001c0002t0001g0001a0001c0002t0001g0006 | 2 | NA19012.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.90-6180G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130211652 | ||||||
| chr9:130211709
|
G | A | 212 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(209): Show | 212 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.90-6123G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130211709 | ||||||
| chr9:130211709
|
G | C | 5 | a0001c0001t0066g0263a0001c0002t0018g0245a0001c0002t0055g0293others(2): Show | 5 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.90-6123G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130211709 | ||||||
| chr9:130211970
|
C | A | 2 | a0001c0002t0072g0193a0001c0002t0113g0292 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.90-5862C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130211970 | ||||||
| chr9:130212020
|
G | A | 1 | a0001c0001t0201g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.90-5812G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212020 | ||||||
| chr9:130212031
|
A | ACCATGTG others(8): Show |
25 | a0001c0001t0025g0113a0001c0001t0025g0178a0001c0001t0025g0188others(22): Show | 25 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.90-5796_90-5782dup others(15): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130212031 | |||||
| chr9:130212050
|
T | C | 225 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(222): Show | 225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.90-5782T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212050 | ||||||
| chr9:130212118
|
C | T | 7 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0186g0242others(4): Show | 7 | HG01123.hp1 HG02738.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.90-5714C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212118 | ||||||
| chr9:130212135
|
T | A | 4 | a0001c0001t0001g0225a0001c0001t0004g0045a0001c0001t0067g0240others(1): Show | 4 | HG02027.hp2 HG02083.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-5697T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212135 | ||||||
| chr9:130212253
|
C | T | 3 | a0001c0001t0022g0347a0001c0001t0165g0346a0001c0002t0147g0234 | 3 | HG02572.hp2 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.90-5579C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212253 | ||||||
| chr9:130212375
|
C | T | 96 | a0001c0001t0014g0243a0001c0001t0016g0184a0001c0001t0025g0113others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.90-5457C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212375 | ||||||
| chr9:130212433
|
A | G | 1 | a0001c0001t0006g0348 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.90-5399A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212433 | ||||||
| chr9:130212441
|
G | C | 225 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(222): Show | 225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.90-5391G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212441 | ||||||
| chr9:130212461
|
C | T | 1 | a0001c0001t0190g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.90-5371C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212461 | ||||||
| chr9:130212532
|
C | A | 1 | a0001c0002t0017g0317 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.90-5300C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212532 | ||||||
| chr9:130212532
|
C | T | 8 | a0001c0001t0115g0313a0001c0001t0121g0076a0001c0001t0138g0273others(5): Show | 8 | HG01069.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.90-5300C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212532 | ||||||
| chr9:130212535
|
G | A | 5 | a0001c0001t0166g0329a0001c0002t0057g0159a0001c0002t0128g0294others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.90-5297G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212535 | ||||||
| chr9:130212608
|
G | A | 6 | a0001c0002t0021g0312a0001c0002t0028g0154a0001c0002t0040g0033others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.90-5224G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212608 | ||||||
| chr9:130212645
|
C | T | 67 | a0001c0001t0001g0058a0001c0001t0002g0036a0001c0001t0002g0037others(64): Show | 67 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.90-5187C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212645 | ||||||
| chr9:130212717
|
A | G | 324 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.90-5115A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212717 | ||||||
| chr9:130212765
|
T | C | 8 | a0001c0001t0115g0313a0001c0001t0121g0076a0001c0001t0138g0273others(5): Show | 8 | HG01069.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.90-5067T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212765 | ||||||
| chr9:130212779
|
A | G | 2 | a0001c0002t0072g0193a0001c0002t0113g0292 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.90-5053A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212779 | ||||||
| chr9:130212785
|
T | A | 263 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(260): Show | 263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.90-5047T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212785 | ||||||
| chr9:130212878
|
C | T | 1 | a0001c0004t0008g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.90-4954C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212878 | ||||||
| chr9:130212903
|
A | T | 1 | a0001c0001t0020g0237 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.90-4929A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212903 | ||||||
| chr9:130212961
|
G | T | 224 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(221): Show | 224 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.90-4871G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212961 | ||||||
| chr9:130212983
|
C | A | 1 | a0001c0001t0035g0270 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.90-4849C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130212983 | ||||||
| chr9:130213301
|
G | A | 1 | a0001c0001t0117g0105 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.90-4531G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213301 | ||||||
| chr9:130213309
|
G | A | 205 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(202): Show | 205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.90-4523G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213309 | ||||||
| chr9:130213377
|
T | A | 324 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.90-4455T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213377 | ||||||
| chr9:130213411
|
G | C | 1 | a0001c0002t0086g0213 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.90-4421G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213411 | ||||||
| chr9:130213423
|
C | T | 1 | a0001c0001t0007g0221 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.90-4409C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213423 | ||||||
| chr9:130213427
|
C | T | 3 | a0001c0001t0027g0335a0001c0001t0027g0336a0001c0001t0181g0330 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.90-4405C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213427 | ||||||
| chr9:130213487
|
G | A | 9 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(6): Show | 9 | NA18963.hp1 NA18969.hp1 NA18980.hp1 others(6): Show |
intron_variant | MODIFIER | c.90-4345G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213487 | ||||||
| chr9:130213526
|
G | A | 62 | a0001c0001t0014g0243a0001c0001t0016g0184a0001c0001t0140g0236others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.90-4306G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213526 | ||||||
| chr9:130213526
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.90-4306G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213526 | ||||||
| chr9:130213586
|
T | C | 7 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0186g0242others(4): Show | 7 | HG01123.hp1 HG02738.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.90-4246T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213586 | ||||||
| chr9:130213650
|
A | G | 62 | a0001c0001t0014g0243a0001c0001t0016g0184a0001c0001t0140g0236others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.90-4182A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213650 | ||||||
| chr9:130213739
|
C | T | 1 | a0001c0001t0082g0208 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.90-4093C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213739 | ||||||
| chr9:130213775
|
C | T | 1 | a0001c0001t0044g0337 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.90-4057C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213775 | ||||||
| chr9:130213858
|
C | T | 9 | a0001c0001t0001g0274a0001c0001t0115g0313a0001c0001t0121g0076others(6): Show | 9 | HG01069.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.90-3974C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213858 | ||||||
| chr9:130213996
|
T | C | 329 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(326): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.90-3836T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130213996 | ||||||
| chr9:130214045
|
C | T | 3 | a0001c0001t0061g0232a0001c0001t0114g0290a0001c0001t0151g0332 | 3 | HG01167.hp2 HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.90-3787C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130214045 | ||||||
| chr9:130214171
|
A | C | 263 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(260): Show | 263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.90-3661A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130214171 | ||||||
| chr9:130214204
|
G | A | 1 | a0001c0001t0046g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.90-3628G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130214204 | ||||||
| chr9:130214236
|
G | C | 1 | a0001c0001t0003g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.90-3596G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130214236 | ||||||
| chr9:130214260
|
G | A | 61 | a0001c0001t0014g0243a0001c0001t0016g0184a0001c0001t0140g0236others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.90-3572G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130214260 | ||||||
| chr9:130214315
|
C | T | 1 | a0001c0001t0045g0345 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.90-3517C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130214315 | ||||||
| chr9:130214408
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.90-3424G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130214408 | ||||||
| chr9:130214535
|
G | C | 1 | a0001c0001t0075g0318 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.90-3297G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130214535 | ||||||
| chr9:130214549
|
G | A | 4 | a0001c0002t0054g0199a0001c0002t0126g0153a0001c0002t0137g0158others(1): Show | 4 | HG02630.hp2 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.90-3283G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130214549 | ||||||
| chr9:130214568
|
G | A | 7 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0186g0242others(4): Show | 7 | HG01123.hp1 HG02738.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.90-3264G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130214568 | ||||||
| chr9:130214576
|
G | T | 197 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(194): Show | 197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.90-3256G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130214576 | ||||||
| chr9:130214670
|
C | G | 39 | a0001c0001t0003g0022a0001c0001t0025g0113a0001c0001t0025g0178others(36): Show | 39 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.90-3162C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130214670 | ||||||
| chr9:130214670
|
C | T | 1 | a0001c0001t0201g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.90-3162C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130214670 | ||||||
| chr9:130215159
|
T | C | 328 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(325): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.90-2673T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130215159 | ||||||
| chr9:130215491
|
G | A | 1 | a0001c0002t0171g0300 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.90-2341G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130215491 | ||||||
| chr9:130215505
|
C | G | 1 | a0001c0001t0020g0237 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.90-2327C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130215505 | ||||||
| chr9:130215505
|
C | T | 7 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0186g0242others(4): Show | 7 | HG01123.hp1 HG02738.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.90-2327C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130215505 | ||||||
| chr9:130215514
|
C | T | 3 | a0001c0001t0162g0301a0001c0001t0201g0338a0001c0002t0109g0339 | 3 | HG01891.hp2 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.90-2318C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130215514 | ||||||
| chr9:130215539
|
G | A | 8 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0179g0155others(5): Show | 8 | HG01123.hp1 HG02738.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.90-2293G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130215539 | ||||||
| chr9:130215585
|
C | T | 6 | a0001c0001t0001g0226a0001c0001t0005g0197a0001c0001t0006g0119others(3): Show | 6 | HG00544.hp1 HG02135.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.90-2247C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130215585 | ||||||
| chr9:130215586
|
A | G | 328 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(325): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.90-2246A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130215586 | ||||||
| chr9:130215614
|
C | G | 1 | a0001c0001t0105g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.90-2218C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130215614 | ||||||
| chr9:130215908
|
C | A | 1 | a0001c0001t0006g0131 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.90-1924C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130215908 | ||||||
| chr9:130215938
|
C | T | 1 | a0001c0002t0008g0114 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.90-1894C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130215938 | ||||||
| chr9:130215965
|
C | G | 3 | a0001c0001t0009g0068a0001c0001t0009g0084a0001c0001t0009g0093 | 3 | HG01070.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.90-1867C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130215965 | ||||||
| chr9:130216120
|
A | G | 296 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.90-1712A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216120 | ||||||
| chr9:130216178
|
G | C | 11 | a0001c0001t0166g0329a0001c0002t0021g0312a0001c0002t0056g0311others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.90-1654G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216178 | ||||||
| chr9:130216188
|
C | T | 1 | a0001c0001t0003g0283 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.90-1644C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216188 | ||||||
| chr9:130216197
|
C | T | 1 | a0001c0001t0042g0052 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.90-1635C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216197 | ||||||
| chr9:130216198
|
G | A | 78 | a0001c0001t0003g0022a0001c0001t0014g0243a0001c0001t0016g0184others(75): Show | 78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.90-1634G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216198 | ||||||
| chr9:130216221
|
G | A | 1 | a0001c0001t0077g0281 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.90-1611G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216221 | ||||||
| chr9:130216281
|
C | T | 4 | a0001c0002t0010g0149a0001c0002t0087g0072a0001c0002t0100g0122others(1): Show | 4 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-1551C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216281 | ||||||
| chr9:130216409
|
C | T | 2 | a0001c0002t0055g0293a0001c0002t0058g0264 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.90-1423C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216409 | ||||||
| chr9:130216418
|
T | C | 7 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0186g0242others(4): Show | 7 | HG01123.hp1 HG02738.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.90-1414T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216418 | ||||||
| chr9:130216464
|
C | T | 2 | a0001c0001t0031g0090a0001c0001t0031g0091 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.90-1368C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216464 | ||||||
| chr9:130216481
|
C | T | 5 | a0001c0001t0166g0329a0001c0002t0057g0159a0001c0002t0128g0294others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.90-1351C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216481 | ||||||
| chr9:130216572
|
T | C | 60 | a0001c0001t0014g0243a0001c0001t0016g0184a0001c0001t0140g0236others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.90-1260T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216572 | ||||||
| chr9:130216592
|
T | G | 60 | a0001c0001t0014g0243a0001c0001t0016g0184a0001c0001t0140g0236others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.90-1240T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216592 | ||||||
| chr9:130216630
|
C | T | 261 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(258): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.90-1202C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216630 | ||||||
| chr9:130216631
|
G | A | 1 | a0001c0001t0025g0188 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.90-1201G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216631 | ||||||
| chr9:130216715
|
C | CA | 13 | a0001c0001t0002g0037a0001c0001t0002g0136a0001c0001t0003g0269others(10): Show | 13 | HG00597.hp1 HG00738.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.90-1101dupA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130216715 | |||||
| chr9:130216715
|
CA | C | 8 | a0001c0001t0003g0022a0001c0001t0024g0094a0001c0001t0117g0105others(5): Show | 8 | HG01123.hp1 HG02451.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.90-1101delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130216715 | |||||
| chr9:130216741
|
G | A | 60 | a0001c0001t0014g0243a0001c0001t0016g0184a0001c0001t0140g0236others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.90-1091G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216741 | ||||||
| chr9:130216808
|
C | T | 2 | a0001c0001t0183g0103a0001c0002t0109g0339 | 2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.90-1024C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216808 | ||||||
| chr9:130216809
|
A | G | 329 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(326): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.90-1023A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216809 | ||||||
| chr9:130216842
|
T | C | 1 | a0001c0001t0094g0111 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.90-990T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216842 | ||||||
| chr9:130216852
|
C | G | 2 | a0001c0002t0055g0293a0001c0002t0058g0264 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.90-980C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216852 | ||||||
| chr9:130216867
|
C | T | 2 | a0001c0003t0012g0014a0001c0003t0012g0016 | 2 | HG03490.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.90-965C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216867 | ||||||
| chr9:130216870
|
T | C | 2 | a0001c0002t0056g0311a0001c0002t0062g0298 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.90-962T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216870 | ||||||
| chr9:130216883
|
G | A | 1 | a0001c0001t0186g0242 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.90-949G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216883 | ||||||
| chr9:130216961
|
T | C | 1 | a0001c0001t0007g0118 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.90-871T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216961 | ||||||
| chr9:130216962
|
TG | T | 67 | a0001c0001t0003g0022a0001c0001t0014g0243a0001c0001t0016g0184others(64): Show | 67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.90-867delG | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 130216962 | |||||
| chr9:130216994
|
A | G | 1 | a0001c0001t0007g0118 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.90-838A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130216994 | ||||||
| chr9:130217204
|
G | A | 19 | a0001c0001t0022g0347a0001c0001t0028g0320a0001c0001t0029g0156others(16): Show | 19 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.90-628G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130217204 | ||||||
| chr9:130217214
|
A | G | 328 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(325): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.90-618A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130217214 | ||||||
| chr9:130217227
|
G | A | 1 | a0001c0001t0002g0150 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.90-605G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130217227 | ||||||
| chr9:130217257
|
G | A | 60 | a0001c0001t0014g0243a0001c0001t0016g0184a0001c0001t0140g0236others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.90-575G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130217257 | ||||||
| chr9:130217312
|
C | T | 1 | a0001c0002t0194g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.90-520C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130217312 | ||||||
| chr9:130217596
|
G | A | 1 | a0001c0001t0044g0337 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.90-236G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130217596 | ||||||
| chr9:130217600
|
C | T | 1 | a0001c0001t0140g0236 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.90-232C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130217600 | ||||||
| chr9:130217646
|
G | A | 1 | a0001c0001t0044g0337 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.90-186G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130217646 | ||||||
| chr9:130217756
|
G | A | 206 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(203): Show | 206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.90-76G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130217756 | ||||||
| chr9:130217768
|
T | G | 1 | a0001c0002t0097g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.90-64T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 2/7 | chr9 | 130217768 | ||||||
| chr9:130218025
|
C | T | 1 | a0001c0001t0176g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.228+55C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218025 | ||||||
| chr9:130218045
|
T | C | 7 | a0001c0001t0166g0329a0001c0002t0028g0154a0001c0002t0040g0033others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.228+75T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218045 | ||||||
| chr9:130218056
|
G | A | 5 | a0001c0001t0066g0263a0001c0002t0018g0245a0001c0002t0055g0293others(2): Show | 5 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.228+86G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218056 | ||||||
| chr9:130218087
|
C | T | 2 | a0001c0001t0002g0108a0001c0001t0002g0112 | 2 | HG03688.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.228+117C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218087 | ||||||
| chr9:130218147
|
T | C | 2 | a0001c0001t0031g0090a0001c0001t0031g0091 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.228+177T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218147 | ||||||
| chr9:130218151
|
GAC | G | 3 | a0001c0001t0005g0099a0001c0001t0047g0247a0001c0001t0080g0151 | 3 | HG00597.hp1 NA18961.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.228+187_228+188del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 130218151 | |||||
| chr9:130218214
|
C | T | 7 | a0001c0001t0166g0329a0001c0002t0028g0154a0001c0002t0040g0033others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.228+244C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218214 | ||||||
| chr9:130218223
|
T | C | 1 | a0001c0002t0141g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.228+253T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218223 | ||||||
| chr9:130218323
|
C | G | 60 | a0001c0001t0014g0243a0001c0001t0016g0184a0001c0001t0140g0236others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.228+353C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218323 | ||||||
| chr9:130218369
|
A | G | 1 | a0001c0002t0113g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.228+399A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218369 | ||||||
| chr9:130218589
|
A | G | 6 | a0001c0001t0115g0313a0001c0001t0120g0075a0001c0001t0121g0076others(3): Show | 6 | HG01069.hp1 HG01884.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.228+619A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218589 | ||||||
| chr9:130218595
|
AT | A | 61 | a0001c0001t0014g0243a0001c0001t0016g0184a0001c0001t0140g0236others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.228+639delT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 130218595 | |||||
| chr9:130218651
|
G | A | 2 | a0001c0001t0003g0279a0001c0001t0160g0172 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.228+681G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218651 | ||||||
| chr9:130218730
|
T | C | 60 | a0001c0001t0014g0243a0001c0001t0016g0184a0001c0001t0140g0236others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.228+760T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218730 | ||||||
| chr9:130218940
|
A | C | 1 | a0001c0001t0029g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.229-785A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218940 | ||||||
| chr9:130218951
|
C | T | 7 | a0001c0001t0166g0329a0001c0002t0028g0154a0001c0002t0040g0033others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.229-774C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218951 | ||||||
| chr9:130218976
|
C | T | 25 | a0001c0001t0025g0113a0001c0001t0025g0178a0001c0001t0025g0188others(22): Show | 25 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.229-749C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130218976 | ||||||
| chr9:130219043
|
A | G | 1 | a0001c0002t0058g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.229-682A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219043 | ||||||
| chr9:130219098
|
T | A | 1 | a0001c0001t0048g0085 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.229-627T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219098 | ||||||
| chr9:130219127
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.229-598C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219127 | ||||||
| chr9:130219150
|
A | G | 1 | a0001c0001t0067g0240 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.229-575A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219150 | ||||||
| chr9:130219191
|
G | A | 4 | a0001c0001t0183g0103a0001c0002t0018g0299a0001c0002t0065g0205others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-534G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219191 | ||||||
| chr9:130219234
|
C | T | 7 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0186g0242others(4): Show | 7 | HG01123.hp1 HG02738.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.229-491C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219234 | ||||||
| chr9:130219271
|
G | A | 2 | a0001c0001t0004g0095a0001c0001t0004g0096 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.229-454G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219271 | ||||||
| chr9:130219332
|
C | T | 2 | a0001c0001t0006g0228a0001c0001t0090g0275 | 2 | NA18945.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.229-393C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219332 | ||||||
| chr9:130219339
|
G | A | 17 | a0001c0001t0022g0347a0001c0001t0028g0320a0001c0001t0029g0156others(14): Show | 17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.229-386G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219339 | ||||||
| chr9:130219467
|
C | T | 3 | a0001c0001t0005g0099a0001c0001t0047g0247a0001c0001t0080g0151 | 3 | HG00597.hp1 NA18961.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.229-258C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219467 | ||||||
| chr9:130219523
|
C | T | 7 | a0001c0001t0166g0329a0001c0002t0028g0154a0001c0002t0040g0033others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.229-202C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219523 | ||||||
| chr9:130219572
|
G | T | 1 | a0001c0001t0002g0136 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.229-153G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219572 | ||||||
| chr9:130219586
|
C | T | 1 | a0001c0002t0017g0317 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.229-139C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219586 | ||||||
| chr9:130219654
|
G | A | 1 | a0001c0002t0125g0002 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.229-71G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219654 | ||||||
| chr9:130219659
|
G | A | 1 | a0001c0001t0023g0104 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.229-66G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219659 | ||||||
| chr9:130219687
|
C | T | 7 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0186g0242others(4): Show | 7 | HG01123.hp1 HG02738.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.229-38C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219687 | ||||||
| chr9:130219711
|
C | T | 6 | a0001c0002t0001g0018a0001c0002t0001g0021a0001c0002t0001g0023others(3): Show | 6 | HG00323.hp1 HG00642.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.229-14C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 3/7 | chr9 | 130219711 | ||||||
| chr9:130219872
|
G | A | 6 | a0001c0001t0003g0022a0001c0001t0117g0105a0001c0001t0186g0242others(3): Show | 6 | HG02738.hp2 HG03491.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.307+69G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130219872 | ||||||
| chr9:130219906
|
G | A | 1 | a0001c0001t0071g0233 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.307+103G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130219906 | ||||||
| chr9:130220125
|
G | A | 3 | a0001c0001t0005g0189a0001c0001t0005g0202a0001c0001t0079g0267 | 3 | HG03491.hp2 HG03492.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.307+322G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220125 | ||||||
| chr9:130220212
|
G | A | 3 | a0001c0001t0121g0076a0001c0001t0146g0333a0001c0001t0154g0340 | 3 | HG01069.hp1 HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.307+409G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220212 | ||||||
| chr9:130220217
|
C | T | 6 | a0001c0001t0115g0313a0001c0001t0120g0075a0001c0001t0121g0076others(3): Show | 6 | HG01069.hp1 HG01884.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.307+414C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220217 | ||||||
| chr9:130220233
|
A | G | 1 | a0001c0001t0193g0192 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.307+430A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220233 | ||||||
| chr9:130220400
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.307+597A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220400 | ||||||
| chr9:130220466
|
C | T | 1 | a0001c0001t0026g0004 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.307+663C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220466 | ||||||
| chr9:130220517
|
C | T | 2 | a0001c0002t0021g0312a0001c0002t0157g0173 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.307+714C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220517 | ||||||
| chr9:130220542
|
C | T | 1 | a0001c0001t0162g0301 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.307+739C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220542 | ||||||
| chr9:130220550
|
C | T | 1 | a0001c0001t0151g0332 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.307+747C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220550 | ||||||
| chr9:130220634
|
C | G | 2 | a0001c0002t0055g0293a0001c0002t0058g0264 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.307+831C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220634 | ||||||
| chr9:130220634
|
C | T | 1 | a0001c0001t0176g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.307+831C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220634 | ||||||
| chr9:130220722
|
C | A | 1 | a0001c0001t0004g0139 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.307+919C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220722 | ||||||
| chr9:130220753
|
CT | C | 23 | a0001c0001t0001g0225a0001c0001t0002g0037a0001c0001t0002g0211others(20): Show | 23 | HG01256.hp1 HG01257.hp2 HG01517.hp2 others(20): Show |
intron_variant | MODIFIER | c.307+964delT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130220753 | |||||
| chr9:130220819
|
T | C | 2 | a0001c0002t0056g0311a0001c0002t0062g0298 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.307+1016T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220819 | ||||||
| chr9:130220836
|
T | C | 2 | a0001c0003t0012g0014a0001c0003t0012g0016 | 2 | HG03490.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.307+1033T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220836 | ||||||
| chr9:130220889
|
G | A | 1 | a0001c0001t0013g0261 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.307+1086G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220889 | ||||||
| chr9:130220913
|
A | G | 2 | a0001c0001t0005g0189a0001c0001t0005g0202 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.307+1110A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220913 | ||||||
| chr9:130220984
|
T | A | 1 | a0001c0002t0023g0054 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.307+1181T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220984 | ||||||
| chr9:130220984
|
T | G | 328 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(325): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.307+1181T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220984 | ||||||
| chr9:130220990
|
G | A | 2 | a0001c0001t0003g0280a0001c0001t0035g0271 | 2 | NA18984.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.307+1187G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220990 | ||||||
| chr9:130220994
|
C | T | 2 | a0001c0002t0021g0312a0001c0002t0157g0173 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.307+1191C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130220994 | ||||||
| chr9:130221055
|
G | A | 1 | a0001c0002t0017g0317 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.307+1252G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221055 | ||||||
| chr9:130221264
|
T | A | 4 | a0001c0001t0183g0103a0001c0002t0018g0299a0001c0002t0065g0205others(1): Show | 4 | HG02145.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-1386T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221264 | ||||||
| chr9:130221335
|
A | AAT | 3 | a0001c0001t0044g0337a0001c0002t0028g0154a0001c0002t0040g0033 | 3 | HG02109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.308-1301_308-1300d others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221335 | |||||
| chr9:130221349
|
TAA | T | 11 | a0001c0001t0166g0329a0001c0002t0021g0312a0001c0002t0038g0209others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.308-1298_308-1297d others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221349 | |||||
| chr9:130221377
|
CAT | C | 7 | a0001c0001t0026g0082a0001c0002t0001g0042a0001c0002t0023g0054others(4): Show | 7 | HG01978.hp2 HG02273.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.308-1237_308-1236d others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221377 | |||||
| chr9:130221377
|
CATAT | C | 11 | a0001c0001t0002g0108a0001c0001t0002g0214a0001c0001t0019g0145others(8): Show | 11 | HG00642.hp1 HG02109.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.308-1239_308-1236d others(6): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221377 | |||||
| chr9:130221377
|
CATATAT | C | 15 | a0001c0001t0002g0073a0001c0001t0004g0010a0001c0001t0015g0203others(12): Show | 15 | HG00597.hp1 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.308-1241_308-1236d others(8): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221377 | |||||
| chr9:130221377
|
CATATATA others(1): Show |
C | 20 | a0001c0001t0002g0070a0001c0001t0004g0139a0001c0001t0010g0098others(17): Show | 20 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.308-1243_308-1236d others(10): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221377 | |||||
| chr9:130221377
|
CATATATA others(3): Show |
C | 13 | a0001c0001t0003g0097a0001c0001t0003g0279a0001c0001t0005g0099others(10): Show | 13 | HG01169.hp1 HG01243.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.308-1245_308-1236d others(12): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221377 | |||||
| chr9:130221377
|
CATATATA others(5): Show |
C | 28 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0002g0211others(25): Show | 28 | HG00408.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.308-1247_308-1236d others(14): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221377 | |||||
| chr9:130221377
|
CATATATA others(7): Show |
C | 33 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0190others(30): Show | 33 | HG00280.hp2 HG00423.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.308-1249_308-1236d others(16): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221377 | |||||
| chr9:130221377
|
CATATATA others(9): Show |
C | 11 | a0001c0001t0002g0136a0001c0001t0002g0150a0001c0001t0027g0335others(8): Show | 11 | HG00280.hp1 HG00738.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.308-1251_308-1236d others(18): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221377 | |||||
| chr9:130221377
|
CATATATA others(11): Show |
C | 2 | a0001c0001t0009g0068a0001c0001t0048g0085 | 2 | HG01192.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.308-1253_308-1236d others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221377 | |||||
| chr9:130221377
|
CATATATA others(13): Show |
C | 4 | a0001c0001t0009g0084a0001c0001t0009g0093a0001c0001t0030g0176others(1): Show | 4 | HG01070.hp2 HG01071.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-1255_308-1236d others(22): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221377 | |||||
| chr9:130221389
|
TATATATA others(23): Show |
T | 1 | a0001c0002t0157g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.308-1259_308-1230d others(32): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221389 | |||||
| chr9:130221389
|
TATATATA others(25): Show |
T | 4 | a0001c0002t0011g0128a0001c0002t0011g0217a0001c0002t0073g0028others(1): Show | 4 | HG01358.hp2 HG01934.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-1259_308-1228d others(34): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221389 | |||||
| chr9:130221391
|
TATATATA others(23): Show |
T | 1 | a0001c0002t0021g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.308-1257_308-1228d others(32): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221391 | |||||
| chr9:130221391
|
TATATATA others(25): Show |
T | 14 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0040others(11): Show | 14 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.308-1257_308-1226d others(34): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221391 | |||||
| chr9:130221391
|
TATATATA others(27): Show |
T | 1 | a0001c0002t0012g0012 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.308-1257_308-1224d others(36): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221391 | |||||
| chr9:130221393
|
TATATATA others(23): Show |
T | 1 | a0001c0002t0100g0122 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.308-1255_308-1226d others(32): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221393 | |||||
| chr9:130221393
|
TATATATA others(25): Show |
T | 19 | a0001c0002t0001g0018a0001c0002t0001g0210a0001c0002t0002g0218others(16): Show | 19 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.308-1255_308-1224d others(34): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221393 | |||||
| chr9:130221393
|
TATATATA others(31): Show |
T | 1 | a0001c0002t0155g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.308-1255_308-1218d others(40): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221393 | |||||
| chr9:130221395
|
T | G | 1 | a0001c0001t0134g0165 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.308-1255T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221395 | ||||||
| chr9:130221395
|
TATATATA others(23): Show |
T | 1 | a0001c0002t0008g0041 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.308-1253_308-1224d others(32): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221395 | |||||
| chr9:130221395
|
TATATATA others(25): Show |
T | 13 | a0001c0002t0001g0008a0001c0002t0001g0024a0001c0002t0001g0255others(10): Show | 13 | HG00323.hp1 HG01123.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.308-1253_308-1222d others(34): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221395 | |||||
| chr9:130221397
|
T | G | 1 | a0001c0001t0134g0165 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.308-1253T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221397 | ||||||
| chr9:130221397
|
TATATATA others(11): Show |
T | 3 | a0001c0001t0016g0265a0001c0001t0022g0347a0001c0001t0165g0346 | 3 | HG02135.hp2 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.308-1251_308-1234d others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221397 | |||||
| chr9:130221397
|
TATATATA others(13): Show |
T | 1 | a0001c0002t0055g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.308-1251_308-1232d others(22): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221397 | |||||
| chr9:130221397
|
TATATATA others(19): Show |
T | 2 | a0001c0002t0057g0159a0001c0002t0184g0334 | 2 | HG02258.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.308-1251_308-1226d others(28): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221397 | |||||
| chr9:130221397
|
TATATATA others(23): Show |
T | 1 | a0001c0002t0001g0013 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.308-1251_308-1222d others(32): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221397 | |||||
| chr9:130221397
|
TATATATA others(25): Show |
T | 7 | a0001c0002t0003g0135a0001c0002t0008g0114a0001c0002t0017g0074others(4): Show | 7 | HG00140.hp1 HG00639.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.308-1251_308-1220d others(34): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221397 | |||||
| chr9:130221399
|
T | C | 1 | a0001c0001t0026g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.308-1251T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221399 | ||||||
| chr9:130221399
|
T | G | 6 | a0001c0001t0134g0165a0001c0001t0183g0103a0001c0002t0001g0006others(3): Show | 6 | HG01109.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-1251T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221399 | ||||||
| chr9:130221399
|
TATATATA others(9): Show |
T | 4 | a0001c0001t0003g0066a0001c0001t0016g0184a0001c0002t0072g0193others(1): Show | 4 | HG00099.hp2 HG02572.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-1249_308-1234d others(18): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221399 | |||||
| chr9:130221399
|
TATATATA others(11): Show |
T | 3 | a0001c0001t0032g0319a0001c0001t0069g0321a0001c0001t0076g0310 | 3 | HG02559.hp1 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.308-1249_308-1232d others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221399 | |||||
| chr9:130221399
|
TATATATA others(19): Show |
T | 3 | a0001c0001t0166g0329a0001c0002t0128g0294a0001c0002t0149g0207 | 3 | HG02109.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.308-1249_308-1224d others(28): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221399 | |||||
| chr9:130221401
|
T | C | 1 | a0001c0001t0085g0138 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.308-1249T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221401 | ||||||
| chr9:130221401
|
T | G | 12 | a0001c0001t0020g0133a0001c0001t0080g0151a0001c0001t0092g0134others(9): Show | 12 | HG00597.hp1 HG00735.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.308-1249T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221401 | ||||||
| chr9:130221401
|
TATATATA others(7): Show |
T | 19 | a0001c0001t0001g0181a0001c0001t0001g0187a0001c0001t0006g0204others(16): Show | 19 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.308-1247_308-1234d others(16): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221401 | |||||
| chr9:130221401
|
TATATATA others(9): Show |
T | 2 | a0001c0001t0095g0341a0001c0001t0107g0101 | 2 | HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.308-1247_308-1232d others(18): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221401 | |||||
| chr9:130221401
|
TATATATA others(11): Show |
T | 5 | a0001c0001t0028g0320a0001c0001t0068g0295a0001c0001t0070g0324others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-1247_308-1230d others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221401 | |||||
| chr9:130221401
|
TATATATA others(13): Show |
T | 1 | a0001c0001t0051g0049 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.308-1247_308-1228d others(22): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221401 | |||||
| chr9:130221403
|
T | G | 26 | a0001c0001t0002g0062a0001c0001t0004g0139a0001c0001t0019g0145others(23): Show | 26 | HG00597.hp1 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.308-1247T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221403 | ||||||
| chr9:130221403
|
TATATATA others(5): Show |
T | 7 | a0001c0001t0001g0127a0001c0001t0001g0164a0001c0001t0001g0291others(4): Show | 7 | HG00408.hp2 HG00438.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.308-1245_308-1234d others(14): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221403 | |||||
| chr9:130221403
|
TATATATA others(7): Show |
T | 22 | a0001c0001t0001g0129a0001c0001t0001g0162a0001c0001t0001g0239others(19): Show | 22 | HG00438.hp1 HG01256.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.308-1245_308-1232d others(16): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221403 | |||||
| chr9:130221403
|
TATATATA others(9): Show |
T | 4 | a0001c0001t0001g0254a0001c0001t0043g0327a0001c0001t0046g0166others(1): Show | 4 | HG02970.hp2 HG03540.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-1245_308-1230d others(18): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221403 | |||||
| chr9:130221403
|
TATATATA others(11): Show |
T | 4 | a0001c0001t0029g0156a0001c0001t0029g0325a0001c0001t0075g0318others(1): Show | 4 | HG02486.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-1245_308-1228d others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221403 | |||||
| chr9:130221405
|
T | G | 39 | a0001c0001t0002g0062a0001c0001t0002g0108a0001c0001t0002g0214others(36): Show | 39 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.308-1245T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221405 | ||||||
| chr9:130221405
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0084g0180 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.308-1243_308-1234d others(12): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221405 | |||||
| chr9:130221405
|
TATATATA others(5): Show |
T | 7 | a0001c0001t0003g0283a0001c0001t0118g0231a0001c0001t0146g0333others(4): Show | 7 | HG01069.hp1 HG01257.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.308-1243_308-1232d others(14): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221405 | |||||
| chr9:130221405
|
TATATATA others(7): Show |
T | 11 | a0001c0001t0001g0246a0001c0001t0003g0285a0001c0001t0005g0189others(8): Show | 11 | HG00544.hp1 HG02523.hp1 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.308-1243_308-1230d others(16): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221405 | |||||
| chr9:130221405
|
TATATATA others(11): Show |
T | 3 | a0001c0001t0082g0208a0001c0001t0158g0140a0001c0001t0179g0155 | 3 | HG02809.hp2 NA18945.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.308-1243_308-1226d others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221405 | |||||
| chr9:130221407
|
T | G | 54 | a0001c0001t0002g0062a0001c0001t0002g0073a0001c0001t0002g0108others(51): Show | 54 | HG00597.hp1 HG00639.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.308-1243T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221407 | ||||||
| chr9:130221407
|
TATATATA others(5): Show |
T | 4 | a0001c0001t0005g0027a0001c0001t0016g0123a0001c0001t0121g0076others(1): Show | 4 | HG02004.hp1 HG02965.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-1241_308-1230d others(14): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221407 | |||||
| chr9:130221407
|
TATATATA others(7): Show |
T | 2 | a0001c0001t0001g0226a0001c0001t0013g0261 | 2 | NA18942.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.308-1241_308-1228d others(16): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221407 | |||||
| chr9:130221407
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0108g0303 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.308-1241_308-1226d others(18): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221407 | |||||
| chr9:130221407
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0142g0326 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.308-1241_308-1224d others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221407 | |||||
| chr9:130221409
|
T | G | 67 | a0001c0001t0002g0062a0001c0001t0002g0070a0001c0001t0002g0073others(64): Show | 67 | HG00597.hp1 HG00639.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.308-1241T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221409 | ||||||
| chr9:130221411
|
T | G | 94 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0002g0036others(91): Show | 94 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.308-1239T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221411 | ||||||
| chr9:130221411
|
T | TAGAGAGA others(3): Show |
1 | a0001c0001t0138g0273 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.308-1238_308-1237i others(12): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221411 | |||||
| chr9:130221413
|
T | G | 129 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0058others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.308-1237T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221413 | ||||||
| chr9:130221413
|
T | TATATATA others(11): Show |
1 | a0001c0002t0065g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.308-1236_308-1235i others(20): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221413 | |||||
| chr9:130221441
|
G | A | 14 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0011others(11): Show | 14 | HG01978.hp2 HG02273.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.308-1209G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221441 | ||||||
| chr9:130221441
|
G | GAA | 3 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0133g0047 | 3 | HG00741.hp1 NA18980.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.308-1208_308-1207i others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221441 | |||||
| chr9:130221447
|
G | A | 1 | a0001c0002t0017g0317 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.308-1203G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221447 | ||||||
| chr9:130221451
|
G | A | 1 | a0001c0002t0065g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.308-1199G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221451 | ||||||
| chr9:130221451
|
GA | G | 9 | a0001c0001t0003g0097a0001c0001t0009g0068a0001c0001t0025g0113others(6): Show | 9 | HG00597.hp1 HG00738.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.308-1196delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221451 | |||||
| chr9:130221521
|
G | A | 1 | a0001c0001t0044g0337 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.308-1129G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221521 | ||||||
| chr9:130221581
|
G | A | 4 | a0001c0002t0010g0149a0001c0002t0087g0072a0001c0002t0100g0122others(1): Show | 4 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-1069G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221581 | ||||||
| chr9:130221632
|
C | A | 345 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(342): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.308-1018C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221632 | ||||||
| chr9:130221771
|
C | T | 1 | a0001c0001t0034g0248 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.308-879C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221771 | ||||||
| chr9:130221771
|
CACATAAA others(105): Show |
C | 3 | a0001c0002t0017g0317a0001c0002t0072g0193a0001c0002t0113g0292 | 3 | HG03195.hp2 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.308-784_308-673del | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221771 | |||||
| chr9:130221776
|
A | AAATATAA others(97): Show |
1 | a0001c0002t0057g0159 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.308-803_308-802ins others(104): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221776 | |||||
| chr9:130221806
|
T | C | 6 | a0001c0002t0054g0199a0001c0002t0055g0293a0001c0002t0056g0311others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-844T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221806 | ||||||
| chr9:130221811
|
A | AAATATAA others(62): Show |
4 | a0001c0001t0166g0329a0001c0002t0128g0294a0001c0002t0149g0207others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-803_308-802ins others(69): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221811 | |||||
| chr9:130221811
|
A | AATATAAA others(229): Show |
1 | a0001c0002t0157g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.308-838_308-837ins others(236): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221811 | |||||
| chr9:130221811
|
A | AATATAAA others(263): Show |
1 | a0001c0002t0021g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.308-838_308-837ins others(270): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221811 | |||||
| chr9:130221841
|
T | C | 6 | a0001c0002t0054g0199a0001c0002t0055g0293a0001c0002t0056g0311others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-809T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221841 | ||||||
| chr9:130221845
|
TA | T | 70 | a0001c0001t0005g0027a0001c0001t0010g0282a0001c0001t0034g0248others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.308-802delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221845 | |||||
| chr9:130221859
|
GTATATAT others(37): Show |
G | 17 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(14): Show | 17 | HG00741.hp1 HG01978.hp2 HG02273.hp2 others(14): Show |
intron_variant | MODIFIER | c.308-784_308-741del others(44): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221859 | |||||
| chr9:130221876
|
T | C | 2 | a0001c0002t0054g0199a0001c0002t0062g0298 | 2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.308-774T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221876 | ||||||
| chr9:130221881
|
A | AAATATAA others(21): Show |
7 | a0001c0001t0044g0337a0001c0001t0166g0329a0001c0002t0057g0159others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.308-768_308-767ins others(28): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AAATATAA others(228): Show |
1 | a0001c0002t0054g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.308-768_308-767ins others(235): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AAATATAA others(263): Show |
1 | a0001c0002t0055g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.308-768_308-767ins others(270): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AAATATAA others(158): Show |
2 | a0001c0002t0058g0264a0001c0002t0147g0234 | 2 | HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.308-768_308-767ins others(165): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AAATATAA others(262): Show |
2 | a0001c0002t0056g0311a0001c0002t0062g0298 | 2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.308-768_308-767ins others(269): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AAATATAA others(158): Show |
1 | a0001c0002t0018g0299 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.308-768_308-767ins others(165): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AAATATAA others(157): Show |
8 | a0001c0001t0002g0073a0001c0001t0013g0261a0001c0001t0016g0265others(5): Show | 8 | HG02135.hp2 HG02145.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.308-768_308-767ins others(164): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(54): Show |
3 | a0001c0001t0115g0313a0001c0001t0120g0075a0001c0001t0138g0273 | 3 | HG02723.hp2 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.308-766_308-765ins others(61): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(227): Show |
1 | a0001c0001t0136g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.308-766_308-765ins others(234): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(88): Show |
12 | a0001c0001t0003g0279a0001c0001t0005g0027a0001c0001t0010g0282others(9): Show | 12 | HG00597.hp2 HG01069.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.308-766_308-765ins others(95): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(123): Show |
1 | a0001c0001t0060g0302 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.308-766_308-765ins others(130): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(158): Show |
1 | a0001c0001t0119g0077 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.308-766_308-765ins others(165): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(216): Show |
1 | a0001c0002t0137g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.308-766_308-765ins others(223): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(251): Show |
1 | a0001c0002t0144g0115 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.308-766_308-765ins others(258): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(186): Show |
1 | a0001c0002t0126g0153 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.308-766_308-765ins others(193): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(122): Show |
92 | a0001c0001t0001g0048a0001c0001t0001g0127a0001c0001t0001g0162others(89): Show | 92 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.308-766_308-765ins others(129): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(157): Show |
54 | a0001c0001t0001g0053a0001c0001t0002g0036a0001c0001t0002g0037others(51): Show | 54 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.308-766_308-765ins others(164): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(192): Show |
5 | a0001c0001t0006g0228a0001c0001t0023g0104a0001c0001t0090g0275others(2): Show | 5 | HG03098.hp2 NA18522.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-766_308-765ins others(199): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(156): Show |
52 | a0001c0001t0001g0274a0001c0001t0003g0276a0001c0001t0003g0283others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.308-766_308-765ins others(163): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(191): Show |
21 | a0001c0001t0001g0032a0001c0001t0003g0087a0001c0001t0004g0010others(18): Show | 21 | HG01069.hp2 HG01070.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.308-766_308-765ins others(198): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(226): Show |
2 | a0001c0001t0001g0129a0001c0001t0006g0131 | 2 | NA18999.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.308-766_308-765ins others(233): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(190): Show |
24 | a0001c0001t0022g0347a0001c0001t0050g0308a0001c0001t0114g0290others(21): Show | 24 | HG00741.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.308-766_308-765ins others(197): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(225): Show |
3 | a0001c0001t0001g0058a0001c0001t0002g0214a0001c0001t0015g0203 | 3 | HG02148.hp2 HG02735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.308-766_308-765ins others(232): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(327): Show |
1 | a0001c0002t0001g0040 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.308-766_308-765ins others(334): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(224): Show |
9 | a0001c0001t0028g0320a0001c0001t0032g0319a0001c0001t0061g0232others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.308-766_308-765ins others(231): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(259): Show |
2 | a0001c0001t0020g0133a0001c0001t0024g0067 | 2 | HG01928.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.308-766_308-765ins others(266): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(258): Show |
7 | a0001c0001t0029g0156a0001c0001t0029g0325a0001c0001t0068g0295others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.308-766_308-765ins others(265): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(292): Show |
5 | a0001c0001t0043g0327a0001c0001t0178g0157a0001c0001t0179g0155others(2): Show | 5 | HG02809.hp2 HG02970.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-766_308-765ins others(299): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(326): Show |
2 | a0001c0002t0038g0209a0001c0002t0112g0182 | 2 | NA18963.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.308-766_308-765ins others(333): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221881
|
A | AATATAAA others(360): Show |
2 | a0001c0002t0038g0219a0001c0002t0093g0212 | 2 | HG01168.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.308-766_308-765ins others(367): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221881 | |||||
| chr9:130221885
|
C | T | 1 | a0001c0002t0163g0323 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.308-765C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221885 | ||||||
| chr9:130221887
|
TA | T | 20 | a0001c0001t0002g0250a0001c0001t0003g0279a0001c0001t0003g0283others(17): Show | 20 | HG01168.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.308-760delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221887 | |||||
| chr9:130221888
|
A | ATTATGTA others(121): Show |
1 | a0001c0002t0163g0323 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.308-762_308-761ins others(128): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221888 | ||||||
| chr9:130221901
|
GTA | G | 14 | a0001c0001t0022g0347a0001c0001t0028g0320a0001c0001t0029g0156others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.308-742_308-741del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221901 | |||||
| chr9:130221909
|
A | G | 4 | a0001c0002t0054g0199a0001c0002t0055g0293a0001c0002t0056g0311others(1): Show | 4 | HG02615.hp2 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-741A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221909 | ||||||
| chr9:130221922
|
TA | T | 8 | a0001c0001t0183g0103a0001c0002t0001g0040a0001c0002t0018g0299others(5): Show | 8 | HG01168.hp1 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.308-725delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221922 | |||||
| chr9:130221936
|
GTA | G | 206 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(203): Show | 206 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.308-707_308-706del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221936 | |||||
| chr9:130221938
|
A | ATATAAAT others(24): Show |
5 | a0001c0001t0035g0271a0001c0001t0051g0049a0001c0001t0052g0147others(2): Show | 5 | HG02027.hp2 HG02273.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-708_308-707ins others(31): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221938 | |||||
| chr9:130221938
|
A | ATATAAAT others(57): Show |
1 | a0001c0001t0003g0097 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.308-708_308-707ins others(64): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221938 | |||||
| chr9:130221938
|
A | ATATAAAT others(90): Show |
2 | a0001c0001t0004g0095a0001c0001t0004g0096 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.308-708_308-707ins others(97): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221938 | |||||
| chr9:130221938
|
A | ATATATAA others(26): Show |
7 | a0001c0001t0019g0080a0001c0001t0030g0176a0001c0001t0121g0076others(4): Show | 7 | HG01069.hp1 HG01884.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.308-642_308-610dup others(33): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221938 | |||||
| chr9:130221938
|
A | ATATATAA others(299): Show |
1 | a0001c0002t0109g0339 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.308-691_308-690ins others(306): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221938 | |||||
| chr9:130221938
|
A | ATATATAA others(295): Show |
2 | a0001c0002t0028g0154a0001c0002t0040g0033 | 2 | HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.308-691_308-690ins others(302): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221938 | |||||
| chr9:130221940
|
A | C | 1 | a0001c0002t0001g0040 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.308-710A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221940 | ||||||
| chr9:130221944
|
A | G | 9 | a0001c0001t0066g0263a0001c0002t0018g0245a0001c0002t0054g0199others(6): Show | 9 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.308-706A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130221944 | ||||||
| chr9:130221957
|
TA | T | 3 | a0001c0002t0001g0040a0001c0002t0093g0212a0001c0002t0144g0115 | 3 | HG01168.hp1 HG02300.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.308-690delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221957 | |||||
| chr9:130221958
|
A | AATATAAA others(60): Show |
3 | a0001c0002t0126g0153a0001c0002t0137g0158a0001c0002t0145g0315 | 3 | HG02630.hp2 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.308-691_308-690ins others(67): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221958 | |||||
| chr9:130221958
|
A | AATATAAA others(94): Show |
6 | a0001c0002t0008g0114a0001c0002t0021g0034a0001c0002t0021g0306others(3): Show | 6 | HG00639.hp2 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.308-691_308-690ins others(101): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221958 | |||||
| chr9:130221958
|
A | AATATAAA others(128): Show |
9 | a0001c0002t0002g0218a0001c0002t0003g0069a0001c0002t0003g0086others(6): Show | 9 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(6): Show |
intron_variant | MODIFIER | c.308-691_308-690ins others(135): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221958 | |||||
| chr9:130221958
|
A | AATATAAA others(162): Show |
25 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(22): Show | 25 | HG00323.hp1 HG00642.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.308-691_308-690ins others(169): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221958 | |||||
| chr9:130221958
|
A | AATATAAA others(196): Show |
3 | a0001c0002t0009g0092a0001c0002t0073g0028a0001c0002t0185g0144 | 3 | HG01361.hp1 HG02698.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.308-691_308-690ins others(203): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221958 | |||||
| chr9:130221958
|
A | AATATAAA others(196): Show |
2 | a0001c0002t0011g0128a0001c0002t0180g0257 | 2 | HG01934.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.308-691_308-690ins others(203): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221958 | |||||
| chr9:130221958
|
A | AATATAAA others(162): Show |
3 | a0001c0002t0004g0124a0001c0002t0011g0217a0001c0002t0024g0220 | 3 | HG01081.hp1 HG01358.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.308-691_308-690ins others(169): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221958 | |||||
| chr9:130221958
|
A | AATATAAA others(128): Show |
2 | a0001c0002t0010g0149a0001c0002t0139g0343 | 2 | HG01123.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.308-691_308-690ins others(135): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221958 | |||||
| chr9:130221958
|
A | AATATAAA others(94): Show |
2 | a0001c0002t0100g0122a0001c0002t0143g0316 | 2 | HG02004.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.308-691_308-690ins others(101): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221958 | |||||
| chr9:130221958
|
A | AATATAAA others(162): Show |
2 | a0001c0002t0002g0079a0001c0002t0002g0143 | 2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.308-691_308-690ins others(169): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221958 | |||||
| chr9:130221971
|
G | GTA | 42 | a0001c0001t0115g0313a0001c0001t0120g0075a0001c0001t0138g0273others(39): Show | 42 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.308-674_308-673dup others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221971 | |||||
| chr9:130221973
|
A | ATC | 27 | a0001c0002t0001g0040a0001c0002t0002g0079a0001c0002t0002g0143others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.308-676_308-675ins others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221973 | |||||
| chr9:130221990
|
TA | T | 60 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.308-657delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221990 | |||||
| chr9:130221991
|
A | AATATAAA others(94): Show |
1 | a0001c0002t0155g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.308-658_308-657ins others(101): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221991 | |||||
| chr9:130221991
|
A | AATATAAA others(162): Show |
1 | a0001c0002t0163g0323 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.308-658_308-657ins others(169): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130221991 | |||||
| chr9:130222004
|
G | GTA | 19 | a0001c0002t0001g0018a0001c0002t0001g0021a0001c0002t0001g0023others(16): Show | 19 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.308-641_308-640dup others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222004 | |||||
| chr9:130222006
|
A | ATC | 43 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0040others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.308-643_308-642ins others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222006 | |||||
| chr9:130222039
|
ATC | A | 3 | a0001c0001t0183g0103a0001c0002t0018g0299a0001c0002t0065g0205 | 3 | HG02145.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.308-609_308-608del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222039 | |||||
| chr9:130222041
|
C | A | 4 | a0001c0002t0001g0210a0001c0002t0017g0074a0001c0002t0123g0222others(1): Show | 4 | HG02071.hp2 HG02074.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-609C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222041 | ||||||
| chr9:130222046
|
AAT | A | 324 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.308-596_308-595del others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222046 | |||||
| chr9:130222048
|
T | TATATACA others(24): Show |
5 | a0001c0001t0166g0329a0001c0002t0057g0159a0001c0002t0128g0294others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.308-597_308-596ins others(31): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222048 | |||||
| chr9:130222067
|
A | G | 4 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026others(1): Show | 4 | NA18747.hp1 NA18963.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-583A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222067 | ||||||
| chr9:130222085
|
T | TATACATA others(22): Show |
3 | a0001c0001t0183g0103a0001c0002t0018g0299a0001c0002t0065g0205 | 3 | HG02145.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.308-562_308-561ins others(29): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222085 | |||||
| chr9:130222090
|
A | G | 2 | a0001c0002t0028g0154a0001c0002t0040g0033 | 2 | HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.308-560A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222090 | ||||||
| chr9:130222091
|
T | C | 73 | a0001c0001t0166g0329a0001c0002t0001g0008a0001c0002t0001g0013others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.308-559T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222091 | ||||||
| chr9:130222096
|
G | GTGTATAT others(21): Show |
2 | a0001c0002t0028g0154a0001c0002t0040g0033 | 2 | HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.308-551_308-550ins others(28): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222096 | |||||
| chr9:130222102
|
A | G | 196 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(193): Show | 196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.308-548A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222102 | ||||||
| chr9:130222111
|
T | C | 1 | a0001c0002t0147g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.308-539T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222111 | ||||||
| chr9:130222112
|
A | G | 6 | a0001c0001t0166g0329a0001c0002t0057g0159a0001c0002t0128g0294others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.308-538A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222112 | ||||||
| chr9:130222113
|
C | T | 6 | a0001c0001t0166g0329a0001c0002t0057g0159a0001c0002t0128g0294others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.308-537C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222113 | ||||||
| chr9:130222114
|
G | A | 6 | a0001c0001t0166g0329a0001c0002t0057g0159a0001c0002t0128g0294others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.308-536G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222114 | ||||||
| chr9:130222114
|
G | GTA | 284 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.308-526_308-525dup others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222114 | |||||
| chr9:130222114
|
G | GTATATAT others(25): Show |
3 | a0001c0001t0003g0279a0001c0001t0191g0179a0001c0002t0163g0323 | 3 | HG01981.hp2 HG02976.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.308-525_308-524ins others(32): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222114 | |||||
| chr9:130222116
|
A | ATATATAT others(19): Show |
2 | a0001c0002t0021g0312a0001c0002t0157g0173 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.308-524_308-499dup others(26): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222116 | |||||
| chr9:130222124
|
A | ATATATG | 4 | a0001c0001t0183g0103a0001c0002t0018g0299a0001c0002t0065g0205others(1): Show | 4 | HG02145.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-525_308-524ins others(6): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222124 | |||||
| chr9:130222124
|
A | ATATG | 5 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026others(2): Show | 5 | HG00741.hp2 NA18747.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-525_308-524ins others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222124 | |||||
| chr9:130222126
|
G | A | 21 | a0001c0001t0005g0197a0001c0001t0006g0119a0001c0001t0006g0204others(18): Show | 21 | HG00544.hp1 HG00741.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.308-524G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222126 | ||||||
| chr9:130222128
|
G | A | 5 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026others(2): Show | 5 | HG00741.hp2 NA18747.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-522G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222128 | ||||||
| chr9:130222128
|
G | GTA | 5 | a0001c0001t0166g0329a0001c0002t0057g0159a0001c0002t0128g0294others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.308-511_308-510dup others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222128 | |||||
| chr9:130222128
|
G | GTGTATA | 4 | a0001c0001t0005g0197a0001c0001t0006g0119a0001c0001t0006g0204others(1): Show | 4 | HG00544.hp1 NA18961.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-521_308-520ins others(6): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222128 | |||||
| chr9:130222130
|
A | G | 17 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(14): Show | 17 | HG00741.hp1 HG01978.hp2 HG02273.hp2 others(14): Show |
intron_variant | MODIFIER | c.308-520A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222130 | ||||||
| chr9:130222134
|
ATATATAC others(1): Show |
A | 17 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(14): Show | 17 | HG00741.hp1 HG01978.hp2 HG02273.hp2 others(14): Show |
intron_variant | MODIFIER | c.308-509_308-502del others(8): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222134 | |||||
| chr9:130222142
|
G | GTA | 4 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026others(1): Show | 4 | NA18747.hp1 NA18963.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-498_308-497dup others(2): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 130222142 | |||||
| chr9:130222156
|
A | G | 1 | a0001c0002t0145g0315 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.308-494A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222156 | ||||||
| chr9:130222224
|
G | A | 1 | a0001c0001t0103g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.308-426G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222224 | ||||||
| chr9:130222294
|
A | G | 1 | a0001c0002t0109g0339 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.308-356A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222294 | ||||||
| chr9:130222350
|
G | C | 4 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026others(1): Show | 4 | NA18747.hp1 NA18963.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-300G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222350 | ||||||
| chr9:130222492
|
C | T | 6 | a0001c0002t0054g0199a0001c0002t0055g0293a0001c0002t0056g0311others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-158C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222492 | ||||||
| chr9:130222618
|
C | A | 1 | a0001c0002t0017g0317 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.308-32C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | chr9 | 130222618 | ||||||
| chr9:130222755
|
C | G | 1 | a0001c0002t0001g0024 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.396+17C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 5/7 | chr9 | 130222755 | ||||||
| chr9:130222832
|
T | C | 216 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(213): Show | 216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.396+94T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 5/7 | chr9 | 130222832 | ||||||
| chr9:130222979
|
GC | G | 188 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0127others(185): Show | 188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.397-102delC | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 5/7 | chr9 | 130222979 | ||||||
| chr9:130222980
|
C | G | 9 | a0001c0001t0001g0032a0001c0001t0001g0058a0001c0001t0001g0239others(6): Show | 9 | HG01433.hp2 HG02027.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.397-102C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 5/7 | chr9 | 130222980 | ||||||
| chr9:130222983
|
C | G | 198 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(195): Show | 198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.397-99C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 5/7 | chr9 | 130222983 | ||||||
| chr9:130223208
|
G | A | 8 | a0001c0001t0166g0329a0001c0002t0021g0034a0001c0002t0028g0154others(5): Show | 8 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.474+49G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130223208 | ||||||
| chr9:130223429
|
C | G | 17 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(14): Show | 17 | HG00741.hp1 HG01978.hp2 HG02273.hp2 others(14): Show |
intron_variant | MODIFIER | c.474+270C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130223429 | ||||||
| chr9:130223467
|
A | G | 6 | a0001c0002t0054g0199a0001c0002t0055g0293a0001c0002t0056g0311others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.474+308A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130223467 | ||||||
| chr9:130223532
|
A | T | 1 | a0001c0001t0003g0280 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.474+373A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130223532 | ||||||
| chr9:130223553
|
G | A | 1 | a0001c0001t0201g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.474+394G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130223553 | ||||||
| chr9:130223637
|
C | T | 3 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026 | 3 | NA18747.hp1 NA19066.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.474+478C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130223637 | ||||||
| chr9:130223780
|
G | C | 1 | a0001c0001t0015g0238 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.474+621G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130223780 | ||||||
| chr9:130223851
|
T | C | 2 | a0001c0001t0031g0090a0001c0001t0031g0091 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.474+692T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130223851 | ||||||
| chr9:130223932
|
T | C | 1 | a0001c0002t0023g0059 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.474+773T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130223932 | ||||||
| chr9:130223936
|
G | T | 328 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(325): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.474+777G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130223936 | ||||||
| chr9:130224003
|
T | C | 126 | a0001c0001t0022g0347a0001c0001t0028g0320a0001c0001t0029g0156others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.474+844T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224003 | ||||||
| chr9:130224020
|
G | A | 198 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(195): Show | 198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.474+861G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224020 | ||||||
| chr9:130224046
|
C | A | 1 | a0001c0001t0044g0337 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.474+887C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224046 | ||||||
| chr9:130224068
|
G | A | 9 | a0001c0001t0166g0329a0001c0002t0038g0209a0001c0002t0038g0219others(6): Show | 9 | HG02109.hp2 HG02258.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+909G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224068 | ||||||
| chr9:130224163
|
A | T | 1 | a0001c0001t0201g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.474+1004A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224163 | ||||||
| chr9:130224226
|
G | A | 2 | a0001c0002t0072g0193a0001c0002t0113g0292 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.474+1067G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224226 | ||||||
| chr9:130224292
|
T | TA | 23 | a0001c0001t0001g0058a0001c0001t0004g0095a0001c0001t0005g0146others(20): Show | 23 | HG00438.hp2 HG00735.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.474+1154dupA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 130224292 | |||||
| chr9:130224292
|
TA | T | 10 | a0001c0001t0001g0187a0001c0001t0002g0112a0001c0001t0003g0280others(7): Show | 10 | HG01069.hp1 HG01169.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.474+1154delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 130224292 | |||||
| chr9:130224292
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0002t0018g0296 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.474+1142_474+1154d others(15): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 130224292 | |||||
| chr9:130224391
|
C | CA | 101 | a0001c0001t0032g0195a0001c0001t0033g0029a0001c0001t0033g0031others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.474+1249dupA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 130224391 | |||||
| chr9:130224391
|
CA | C | 7 | a0001c0001t0001g0164a0001c0001t0001g0254a0001c0001t0019g0088others(4): Show | 7 | HG00408.hp2 HG03098.hp2 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.474+1249delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 130224391 | |||||
| chr9:130224450
|
C | T | 93 | a0001c0001t0001g0048a0001c0001t0001g0127a0001c0001t0001g0162others(90): Show | 93 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.474+1291C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224450 | ||||||
| chr9:130224494
|
G | C | 1 | a0001c0001t0084g0180 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.474+1335G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224494 | ||||||
| chr9:130224514
|
C | T | 2 | a0001c0002t0002g0218a0001c0002t0097g0039 | 2 | HG01175.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.474+1355C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224514 | ||||||
| chr9:130224544
|
G | T | 2 | a0001c0002t0137g0158a0001c0002t0144g0115 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.474+1385G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224544 | ||||||
| chr9:130224561
|
G | GAA | 9 | a0001c0001t0166g0329a0001c0002t0038g0209a0001c0002t0038g0219others(6): Show | 9 | HG02109.hp2 HG02258.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+1409_474+1410d others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 130224561 | |||||
| chr9:130224569
|
AT | A | 8 | a0001c0001t0044g0337a0001c0001t0176g0035a0001c0002t0008g0286others(5): Show | 8 | HG01884.hp2 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.474+1411delT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224569 | ||||||
| chr9:130224570
|
T | A | 321 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.474+1411T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224570 | ||||||
| chr9:130224575
|
T | A | 17 | a0001c0001t0166g0329a0001c0002t0021g0312a0001c0002t0038g0209others(14): Show | 17 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.474+1416T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224575 | ||||||
| chr9:130224754
|
C | G | 6 | a0001c0002t0054g0199a0001c0002t0055g0293a0001c0002t0056g0311others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.474+1595C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224754 | ||||||
| chr9:130224788
|
G | A | 14 | a0001c0001t0166g0329a0001c0002t0021g0312a0001c0002t0038g0209others(11): Show | 14 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.475-1601G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224788 | ||||||
| chr9:130224883
|
C | T | 3 | a0001c0001t0059g0304a0001c0001t0060g0302a0001c0001t0064g0196 | 3 | HG02647.hp2 HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.475-1506C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224883 | ||||||
| chr9:130224904
|
T | G | 6 | a0001c0002t0054g0199a0001c0002t0055g0293a0001c0002t0056g0311others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-1485T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130224904 | ||||||
| chr9:130225020
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.475-1369C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225020 | ||||||
| chr9:130225049
|
G | A | 1 | a0001c0002t0174g0057 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.475-1340G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225049 | ||||||
| chr9:130225140
|
C | T | 66 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.475-1249C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225140 | ||||||
| chr9:130225183
|
C | A | 5 | a0001c0001t0001g0291a0001c0001t0006g0284a0001c0001t0013g0272others(2): Show | 5 | NA19011.hp2 NA19066.hp1 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.475-1206C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225183 | ||||||
| chr9:130225207
|
C | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0164a0001c0001t0015g0163others(1): Show | 4 | HG00408.hp2 HG02071.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-1182C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225207 | ||||||
| chr9:130225419
|
C | T | 1 | a0001c0001t0103g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.475-970C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225419 | ||||||
| chr9:130225421
|
C | T | 8 | a0001c0002t0021g0312a0001c0002t0054g0199a0001c0002t0055g0293others(5): Show | 8 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.475-968C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225421 | ||||||
| chr9:130225447
|
C | T | 1 | a0001c0001t0022g0161 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.475-942C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225447 | ||||||
| chr9:130225454
|
G | A | 2 | a0001c0002t0021g0312a0001c0002t0157g0173 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-935G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225454 | ||||||
| chr9:130225571
|
G | A | 1 | a0001c0001t0034g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.475-818G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225571 | ||||||
| chr9:130225664
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.475-725C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225664 | ||||||
| chr9:130225689
|
T | C | 15 | a0001c0001t0166g0329a0001c0002t0021g0312a0001c0002t0038g0209others(12): Show | 15 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.475-700T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225689 | ||||||
| chr9:130225716
|
C | T | 1 | a0001c0001t0132g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.475-673C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225716 | ||||||
| chr9:130225737
|
A | G | 8 | a0001c0002t0021g0312a0001c0002t0054g0199a0001c0002t0055g0293others(5): Show | 8 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.475-652A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225737 | ||||||
| chr9:130225741
|
C | T | 18 | a0001c0001t0022g0347a0001c0001t0028g0320a0001c0001t0029g0156others(15): Show | 18 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.475-648C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225741 | ||||||
| chr9:130225752
|
T | G | 2 | a0001c0001t0001g0127a0001c0001t0014g0044 | 2 | NA18985.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.475-637T>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225752 | ||||||
| chr9:130225796
|
A | T | 1 | a0001c0002t0126g0153 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.475-593A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225796 | ||||||
| chr9:130225882
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.475-507A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130225882 | ||||||
| chr9:130226131
|
G | T | 4 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026others(1): Show | 4 | NA18747.hp1 NA18963.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-258G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 6/7 | chr9 | 130226131 | ||||||
| chr9:130226585
|
A | G | 1 | a0001c0002t0109g0339 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*17+81A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130226585 | ||||||
| chr9:130226636
|
AGCTGGGA others(7): Show |
A | 3 | a0001c0001t0096g0063a0001c0001t0098g0174a0001c0001t0103g0137 | 3 | HG01243.hp2 HG02602.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.*17+138_*17+151del others(14): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130226636 | |||||
| chr9:130226854
|
G | A | 4 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026others(1): Show | 4 | NA18747.hp1 NA18963.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.*17+350G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130226854 | ||||||
| chr9:130226882
|
G | A | 1 | a0001c0001t0037g0152 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.*17+378G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130226882 | ||||||
| chr9:130226904
|
T | C | 199 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(196): Show | 199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.*17+400T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130226904 | ||||||
| chr9:130227022
|
C | CA | 20 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0005g0099others(17): Show | 20 | HG01243.hp2 HG01515.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.*17+535dupA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130227022 | |||||
| chr9:130227034
|
A | C | 65 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(62): Show | 65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.*17+530A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227034 | ||||||
| chr9:130227035
|
A | AG | 4 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026others(1): Show | 4 | NA18747.hp1 NA18963.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.*17+531_*17+532ins others(1): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227035 | ||||||
| chr9:130227071
|
C | T | 1 | a0001c0002t0001g0011 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.*17+567C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227071 | ||||||
| chr9:130227116
|
G | C | 2 | a0001c0002t0072g0193a0001c0002t0113g0292 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.*17+612G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227116 | ||||||
| chr9:130227156
|
C | G | 1 | a0001c0002t0109g0339 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*17+652C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227156 | ||||||
| chr9:130227274
|
C | CT | 5 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0057g0159others(2): Show | 5 | HG02897.hp1 NA18747.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.*17+776dupT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130227274 | |||||
| chr9:130227317
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0014g0044 | 2 | NA18985.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.*17+813C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227317 | ||||||
| chr9:130227323
|
G | A | 1 | a0001c0002t0008g0286 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.*17+819G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227323 | ||||||
| chr9:130227444
|
A | G | 1 | a0001c0001t0048g0085 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.*17+940A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227444 | ||||||
| chr9:130227464
|
G | A | 1 | a0001c0002t0173g0051 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.*17+960G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227464 | ||||||
| chr9:130227575
|
C | T | 4 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026others(1): Show | 4 | NA18747.hp1 NA18963.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.*17+1071C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227575 | ||||||
| chr9:130227609
|
G | A | 1 | a0001c0002t0004g0124 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.*17+1105G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227609 | ||||||
| chr9:130227667
|
C | T | 1 | a0001c0002t0057g0159 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.*17+1163C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227667 | ||||||
| chr9:130227800
|
G | A | 2 | a0001c0001t0115g0313a0001c0001t0138g0273 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.*17+1296G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227800 | ||||||
| chr9:130227885
|
A | C | 2 | a0001c0001t0183g0103a0001c0002t0065g0205 | 2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.*17+1381A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227885 | ||||||
| chr9:130227892
|
C | G | 94 | a0001c0001t0001g0048a0001c0001t0001g0127a0001c0001t0001g0162others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.*17+1388C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130227892 | ||||||
| chr9:130228075
|
C | T | 3 | a0001c0001t0051g0049a0001c0001t0052g0147a0001c0001t0077g0281 | 3 | HG02273.hp1 HG03239.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.*17+1571C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130228075 | ||||||
| chr9:130228134
|
G | C | 104 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.*17+1630G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130228134 | ||||||
| chr9:130228136
|
G | A | 1 | a0001c0002t0057g0159 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.*17+1632G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130228136 | ||||||
| chr9:130228150
|
T | TA | 3 | a0001c0002t0017g0317a0001c0002t0021g0312a0001c0002t0157g0173 | 3 | HG01884.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*17+1648dupA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130228150 | |||||
| chr9:130228190
|
C | CT | 7 | a0001c0001t0044g0337a0001c0001t0201g0338a0001c0002t0038g0209others(4): Show | 7 | HG01891.hp2 HG02897.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.*17+1696dupT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130228190 | |||||
| chr9:130228349
|
TA | T | 11 | a0001c0002t0018g0245a0001c0002t0018g0296a0001c0002t0018g0299others(8): Show | 11 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.*17+1855delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130228349 | |||||
| chr9:130228359
|
A | T | 1 | a0001c0002t0017g0317 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.*17+1855A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130228359 | ||||||
| chr9:130228362
|
G | GT | 5 | a0001c0001t0005g0027a0001c0001t0107g0101a0001c0002t0021g0312others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.*17+1866dupT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130228362 | |||||
| chr9:130228362
|
G | T | 1 | a0001c0002t0017g0317 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.*17+1858G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130228362 | ||||||
| chr9:130228371
|
G | T | 1 | a0001c0002t0054g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.*17+1867G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130228371 | ||||||
| chr9:130228464
|
T | A | 8 | a0001c0002t0001g0040a0001c0002t0004g0124a0001c0002t0011g0061others(5): Show | 8 | HG01081.hp1 HG01358.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.*17+1960T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130228464 | ||||||
| chr9:130228476
|
G | A | 1 | a0001c0001t0098g0174 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*17+1972G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130228476 | ||||||
| chr9:130228551
|
C | A | 1 | a0001c0002t0147g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.*17+2047C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130228551 | ||||||
| chr9:130228655
|
T | C | 1 | a0001c0001t0001g0254 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.*17+2151T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130228655 | ||||||
| chr9:130228671
|
C | CT | 21 | a0001c0001t0027g0335a0001c0002t0001g0001a0001c0002t0001g0003others(18): Show | 21 | HG00741.hp1 HG01978.hp2 HG02273.hp2 others(18): Show |
intron_variant | MODIFIER | c.*17+2180dupT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130228671 | |||||
| chr9:130228672
|
T | C | 3 | a0001c0002t0017g0317a0001c0002t0021g0312a0001c0002t0157g0173 | 3 | HG01884.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*17+2168T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130228672 | ||||||
| chr9:130228733
|
T | C | 5 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0057g0159others(2): Show | 5 | HG02897.hp1 NA18747.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.*17+2229T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130228733 | ||||||
| chr9:130228897
|
T | A | 4 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026others(1): Show | 4 | NA18747.hp1 NA18963.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.*17+2393T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130228897 | ||||||
| chr9:130228996
|
T | TTAC | 4 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026others(1): Show | 4 | NA18747.hp1 NA18963.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.*17+2494_*17+2495i others(5): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130228996 | |||||
| chr9:130229013
|
T | A | 1 | a0001c0002t0065g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.*17+2509T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229013 | ||||||
| chr9:130229091
|
T | A | 1 | a0001c0002t0057g0159 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.*17+2587T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229091 | ||||||
| chr9:130229213
|
AT | A | 4 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026others(1): Show | 4 | NA18747.hp1 NA18963.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.*17+2711delT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130229213 | |||||
| chr9:130229265
|
C | CT | 35 | a0001c0001t0014g0044a0001c0002t0001g0001a0001c0002t0001g0003others(32): Show | 35 | HG00741.hp1 HG01109.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.*17+2776dupT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130229265 | |||||
| chr9:130229265
|
CT | C | 66 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.*17+2776delT | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130229265 | |||||
| chr9:130229315
|
C | T | 1 | a0001c0002t0109g0339 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*17+2811C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229315 | ||||||
| chr9:130229316
|
G | A | 2 | a0001c0001t0197g0260a0001c0002t0017g0317 | 2 | HG01993.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.*17+2812G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229316 | ||||||
| chr9:130229410
|
A | G | 1 | a0001c0002t0147g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.*17+2906A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229410 | ||||||
| chr9:130229416
|
G | A | 3 | a0001c0001t0007g0118a0001c0001t0041g0201a0001c0001t0156g0089 | 3 | HG03834.hp2 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.*17+2912G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229416 | ||||||
| chr9:130229434
|
T | C | 1 | a0001c0002t0056g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*17+2930T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229434 | ||||||
| chr9:130229439
|
G | A | 4 | a0001c0001t0001g0291a0001c0001t0006g0284a0001c0001t0013g0272others(1): Show | 4 | NA19011.hp2 NA19066.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.*17+2935G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229439 | ||||||
| chr9:130229500
|
A | G | 18 | a0001c0002t0017g0317a0001c0002t0018g0245a0001c0002t0018g0296others(15): Show | 18 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.*17+2996A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229500 | ||||||
| chr9:130229519
|
C | A | 1 | a0001c0001t0067g0240 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.*17+3015C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229519 | ||||||
| chr9:130229616
|
G | A | 17 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0006others(14): Show | 17 | HG00741.hp1 HG01978.hp2 HG02273.hp2 others(14): Show |
intron_variant | MODIFIER | c.*17+3112G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229616 | ||||||
| chr9:130229661
|
A | G | 13 | a0001c0002t0017g0317a0001c0002t0018g0245a0001c0002t0018g0296others(10): Show | 13 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.*17+3157A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229661 | ||||||
| chr9:130229782
|
C | T | 4 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026others(1): Show | 4 | NA18747.hp1 NA18963.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.*18-3208C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229782 | ||||||
| chr9:130229783
|
G | A | 194 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(191): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.*18-3207G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229783 | ||||||
| chr9:130229921
|
T | C | 4 | a0001c0002t0038g0209a0001c0002t0038g0219a0001c0002t0111g0026others(1): Show | 4 | NA18747.hp1 NA18963.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.*18-3069T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130229921 | ||||||
| chr9:130230210
|
G | A | 9 | a0001c0002t0018g0245a0001c0002t0018g0296a0001c0002t0018g0299others(6): Show | 9 | HG01109.hp2 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.*18-2780G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130230210 | ||||||
| chr9:130230251
|
C | T | 3 | a0001c0001t0121g0076a0001c0001t0146g0333a0001c0001t0154g0340 | 3 | HG01069.hp1 HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.*18-2739C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130230251 | ||||||
| chr9:130230282
|
C | T | 2 | a0001c0002t0072g0193a0001c0002t0113g0292 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.*18-2708C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130230282 | ||||||
| chr9:130230430
|
C | T | 1 | a0001c0001t0107g0101 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.*18-2560C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130230430 | ||||||
| chr9:130230711
|
T | TA | 71 | a0001c0001t0001g0129a0001c0001t0014g0044a0001c0001t0035g0271others(68): Show | 71 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.*18-2265dupA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130230711 | |||||
| chr9:130230711
|
TA | T | 7 | a0001c0001t0001g0187a0001c0001t0016g0184a0001c0001t0019g0088others(4): Show | 7 | HG01069.hp1 HG01257.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.*18-2265delA | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130230711 | |||||
| chr9:130230803
|
C | CT | 320 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(317): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.*18-2187_*18-2186i others(3): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130230803 | ||||||
| chr9:130230843
|
A | T | 1 | a0001c0002t0163g0323 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.*18-2147A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130230843 | ||||||
| chr9:130230883
|
A | G | 267 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.*18-2107A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130230883 | ||||||
| chr9:130230968
|
C | T | 1 | a0001c0001t0068g0295 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.*18-2022C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130230968 | ||||||
| chr9:130231089
|
G | T | 2 | a0001c0001t0183g0103a0001c0002t0065g0205 | 2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.*18-1901G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130231089 | ||||||
| chr9:130231219
|
C | T | 1 | a0001c0001t0020g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.*18-1771C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130231219 | ||||||
| chr9:130231287
|
G | A | 260 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.*18-1703G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130231287 | ||||||
| chr9:130231362
|
A | AC | 270 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.*18-1628_*18-1627i others(3): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130231362 | ||||||
| chr9:130231363
|
A | T | 270 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.*18-1627A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130231363 | ||||||
| chr9:130231364
|
C | CTT | 54 | a0001c0001t0001g0274a0001c0001t0044g0337a0001c0001t0115g0313others(51): Show | 54 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.*18-1624_*18-1623d others(4): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130231364 | |||||
| chr9:130231364
|
C | T | 270 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0053others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.*18-1626C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130231364 | ||||||
| chr9:130231375
|
T | A | 43 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(40): Show | 43 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.*18-1615T>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130231375 | ||||||
| chr9:130231390
|
T | C | 1 | a0001c0001t0013g0244 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.*18-1600T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130231390 | ||||||
| chr9:130231512
|
T | C | 2 | a0001c0002t0072g0193a0001c0002t0113g0292 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.*18-1478T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130231512 | ||||||
| chr9:130231627
|
G | A | 1 | a0001c0002t0003g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.*18-1363G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130231627 | ||||||
| chr9:130231776
|
C | A | 1 | a0001c0001t0101g0055 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.*18-1214C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130231776 | ||||||
| chr9:130231897
|
C | A | 9 | a0001c0001t0017g0253a0001c0001t0121g0076a0001c0001t0146g0333others(6): Show | 9 | HG01069.hp1 HG01884.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.*18-1093C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130231897 | ||||||
| chr9:130231972
|
G | T | 3 | a0001c0001t0022g0347a0001c0001t0165g0346a0001c0001t0166g0329 | 3 | HG02723.hp1 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.*18-1018G>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130231972 | ||||||
| chr9:130232003
|
G | C | 1 | a0001c0001t0101g0055 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.*18-987G>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130232003 | ||||||
| chr9:130232095
|
C | G | 3 | a0001c0001t0001g0181a0001c0001t0158g0140a0001c0004t0008g0223 | 3 | HG00423.hp2 NA18945.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.*18-895C>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130232095 | ||||||
| chr9:130232150
|
T | C | 1 | a0001c0001t0099g0307 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.*18-840T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130232150 | ||||||
| chr9:130232190
|
T | C | 1 | a0001c0001t0007g0221 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.*18-800T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130232190 | ||||||
| chr9:130232315
|
G | A | 5 | a0001c0001t0115g0313a0001c0001t0120g0075a0001c0001t0138g0273others(2): Show | 5 | HG01884.hp2 HG02723.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.*18-675G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130232315 | ||||||
| chr9:130232734
|
C | T | 1 | a0001c0002t0116g0060 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.*18-256C>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130232734 | ||||||
| chr9:130232751
|
A | T | 1 | a0001c0001t0022g0161 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.*18-239A>T | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130232751 | ||||||
| chr9:130232808
|
A | AC | 43 | a0001c0002t0001g0008a0001c0002t0001g0013a0001c0002t0001g0018others(40): Show | 43 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.*18-180dupC | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 130232808 | |||||
| chr9:130232808
|
A | C | 22 | a0001c0001t0002g0070a0001c0001t0002g0108a0001c0001t0002g0112others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.*18-182A>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130232808 | ||||||
| chr9:130232809
|
C | A | 33 | a0001c0001t0035g0271a0001c0001t0044g0337a0001c0001t0115g0313others(30): Show | 33 | HG00741.hp1 HG01884.hp2 HG01978.hp2 others(30): Show |
intron_variant | MODIFIER | c.*18-181C>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130232809 | ||||||
| chr9:130232826
|
T | C | 2 | a0001c0002t0002g0218a0001c0002t0097g0039 | 2 | HG01175.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.*18-164T>C | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130232826 | ||||||
| chr9:130232881
|
A | G | 48 | a0001c0001t0115g0313a0001c0001t0120g0075a0001c0001t0138g0273others(45): Show | 48 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.*18-109A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130232881 | ||||||
| chr9:130232921
|
G | A | 1 | a0001c0002t0113g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.*18-69G>A | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130232921 | ||||||
| chr9:130232956
|
A | G | 6 | a0001c0001t0115g0313a0001c0001t0120g0075a0001c0001t0138g0273others(3): Show | 6 | HG01884.hp2 HG02723.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.*18-34A>G | NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 7/7 | chr9 | 130232956 |