Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4690 |
|---|---|
| ensemblid | ENSG00000158092.7 |
| hgncid | 7664 |
| symbol | NCK1 |
| name | NCK adaptor protein 1 |
| refseq_nuc | NM_001291999.2 |
| refseq_prot | NP_001278928.1 |
| ensembl_nuc | ENST00000481752.6 |
| ensembl_prot | ENSP00000417273.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 136862208 |
| end | 136951606 |
| strand | + |
| ver | v1.2 |
| region | chr3:136862208-136951606 |
| region5000 | chr3:136857208-136956606 |
| regionname0 | NCK1_chr3_136862208_136951606 |
| regionname5000 | NCK1_chr3_136857208_136956606 |
| 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 | 377 | 220 | 59 | 41 | 71 | 11 | 36 | 51 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0002 | 0/0 | 377 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0003 | 0/0 | 377 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0004 | 0/0 | 377 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0005 | 0/0 | 377 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| 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 | 1134 | 219 | 59 | 41 | 70 | 11 | 36 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| c0002 | 0/0 | 1134 | 7 | 7 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| c0003 | 0/0 | 1134 | 3 | 0 | 3 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| c0004 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| c0005 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| c0006 | 0/0 | 1134 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| 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 | 0/1 | 3315 | 128 | 27 | 26 | 43 | 7 | 24 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0002 | 1/0 | 3318 | 57 | 19 | 11 | 14 | 4 | 8 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0003 | 0/0 | 3318 | 25 | 5 | 4 | 12 | 1 | 3 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0004 | 0/0 | 3315 | 4 | 4 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0005 | 0/0 | 3316 | 4 | 2 | 2 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0006 | 0/0 | 3318 | 3 | 3 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0007 | 0/0 | 3318 | 2 | 2 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0008 | 0/0 | 3318 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0009 | 0/0 | 3318 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0010 | 0/0 | 3315 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0011 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0012 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0013 | 0/0 | 3315 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0014 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0015 | 0/0 | 3315 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| t0016 | 0/0 | 3315 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| 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 | 1134 | 219 | 59 | 41 | 70 | 11 | 36 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0004 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0002c0002 | 0/0 | 1134 | 7 | 7 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0003c0003 | 0/0 | 1134 | 3 | 0 | 3 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0004c0005 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0005c0006 | 0/0 | 1134 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4448 | 124 | 27 | 23 | 42 | 7 | 24 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0001t0002 | 1/0 | 4451 | 52 | 15 | 11 | 14 | 3 | 8 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0001t0003 | 0/0 | 4451 | 25 | 5 | 4 | 12 | 1 | 3 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0001t0004 | 0/0 | 4448 | 4 | 4 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0001t0005 | 0/0 | 4449 | 4 | 2 | 2 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0001t0007 | 0/0 | 4451 | 2 | 2 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0001t0009 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0001t0010 | 0/0 | 4448 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0001t0011 | 0/0 | 4448 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0001t0012 | 0/0 | 4448 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0001t0013 | 0/0 | 4448 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0001t0014 | 0/0 | 4448 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0001t0015 | 0/0 | 4448 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0001t0016 | 0/0 | 4448 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0001c0004t0001 | 0/0 | 4448 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0002c0002t0002 | 0/0 | 4451 | 4 | 4 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0002c0002t0006 | 0/0 | 4451 | 3 | 3 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0003c0003t0001 | 0/0 | 4448 | 3 | 0 | 3 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0004c0005t0008 | 0/0 | 4451 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| a0005c0006t0002 | 0/0 | 4451 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | copy fasta | chr3 | 136857208 | 136956606 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0010g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0011g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0012g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0013g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0015g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0016g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0002c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0002c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0002c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0002c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0002c0002t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0002c0002t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0002c0002t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0003c0003t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0003c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0003c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0004c0005t0008g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0005c0006t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00099 | hp2 | a0005 | c0006 | t0002 | g0166 | EUR | GBR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0146 | EUR | GBR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0175 | EUR | FIN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01070 | hp2 | a0003 | c0003 | t0001 | g0022 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0183 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0184 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01261 | hp1 | a0003 | c0003 | t0001 | g0023 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0021 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0206 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01496 | hp1 | a0001 | c0001 | t0015 | g0019 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0223 | EUR | IBS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | IBS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0198 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02523 | hp1 | a0001 | c0004 | t0001 | g0115 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0085 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0181 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02683 | hp2 | a0001 | c0001 | t0010 | g0113 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0199 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0197 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02976 | hp1 | a0001 | c0001 | t0014 | g0020 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0228 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03139 | hp2 | a0002 | c0002 | t0006 | g0190 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03486 | hp1 | a0002 | c0002 | t0006 | g0201 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03516 | hp2 | a0001 | c0001 | t0016 | g0004 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0202 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0207 | SAS | STU | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | YRI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | YRI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18963 | hp1 | a0004 | c0005 | t0008 | g0127 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18967 | hp2 | a0001 | c0001 | t0011 | g0055 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | LWK | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | LWK | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | LWK | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19065 | hp1 | a0001 | c0001 | t0013 | g0131 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19240 | hp1 | a0002 | c0002 | t0006 | g0195 | AFR | YRI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ASW | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ASW | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | TSI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0147 | EUR | TSI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0210 | SAS | GIH | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0182 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | USA | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | USA | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | USA | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | USA | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0180 | AFR | LWK | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0079 | REF | REF | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0194 | REF | REF | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:136945634
|
C | G | 1 | a0005 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.278C>G | p.Ala93Gly | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/4 | 442/4451 | 278/1134 | 93/377 | chr3 | 136945634 | ||
| chr3:136945895
|
C | T | 1 | a0003 | 3 | HG01070.hp2 HG01261.hp1 HG01358.hp1 |
missense_variant | MODERATE | c.539C>T | p.Ala180Val | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/4 | 703/4451 | 539/1134 | 180/377 | chr3 | 136945895 | ||
| chr3:136946128
|
G | C | 1 | a0002 | 7 | HG02280.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
missense_variant | MODERATE | c.772G>C | p.Gly258Arg | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/4 | 936/4451 | 772/1134 | 258/377 | chr3 | 136946128 | ||
| chr3:136946267
|
A | G | 1 | a0004 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.911A>G | p.Asp304Gly | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/4 | 1075/4451 | 911/1134 | 304/377 | chr3 | 136946267 | ||
| chr3:136946268
|
T | A | 1 | a0004 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.912T>A | p.Asp304Glu | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/4 | 1076/4451 | 912/1134 | 304/377 | chr3 | 136946268 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:136945611
|
T | C | 1 | a0001c0004 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.255T>C | p.Ser85Ser | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/4 | 419/4451 | 255/1134 | 85/377 | chr3 | 136945611 | ||
| chr3:136946079
|
A | C | 1 | a0004c0005 | 1 | NA18963.hp1 | synonymous_variant | LOW | c.723A>C | p.Leu241Leu | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/4 | 887/4451 | 723/1134 | 241/377 | chr3 | 136946079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:136862230
|
C | T | 1 | a0001c0001t0016 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-142C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/4 | 65772 | chr3 | 136862230 | |||||
| chr3:136948563
|
T | C | 1 | a0001c0001t0003 | 25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*110T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 110 | chr3 | 136948563 | |||||
| chr3:136948826
|
T | C | 1 | a0002c0002t0006 | 3 | HG03139.hp2 HG03486.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*373T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 373 | chr3 | 136948826 | |||||
| chr3:136948883
|
GGA | G | 1 | a0001c0001t0005 | 4 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*434_*435delAG | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 434 | INFO_REALIGN_3_PRIME | chr3 | 136948883 | ||||
| chr3:136949079
|
A | G | 1 | a0001c0001t0004 | 4 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*626A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 626 | chr3 | 136949079 | |||||
| chr3:136949227
|
A | C | 1 | a0001c0001t0015 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*774A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 774 | chr3 | 136949227 | |||||
| chr3:136949418
|
TAA | T | 11 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(8): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*966_*967delAA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 966 | chr3 | 136949418 | |||||
| chr3:136949422
|
T | G | 1 | a0004c0005t0008 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*969T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 969 | chr3 | 136949422 | |||||
| chr3:136949570
|
T | C | 1 | a0001c0001t0003 | 25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1117T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 1117 | chr3 | 136949570 | |||||
| chr3:136949783
|
T | C | 12 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(9): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*1330T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 1330 | chr3 | 136949783 | |||||
| chr3:136949840
|
AT | A | 11 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(8): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*1395delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 1395 | INFO_REALIGN_3_PRIME | chr3 | 136949840 | ||||
| chr3:136950036
|
C | A | 1 | a0001c0001t0010 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1583C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 1583 | chr3 | 136950036 | |||||
| chr3:136950119
|
A | T | 1 | a0004c0005t0008 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1666A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 1666 | chr3 | 136950119 | |||||
| chr3:136950180
|
T | C | 1 | a0001c0001t0011 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1727T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 1727 | chr3 | 136950180 | |||||
| chr3:136950237
|
C | T | 12 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(9): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*1784C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 1784 | chr3 | 136950237 | |||||
| chr3:136950546
|
T | A | 1 | a0004c0005t0008 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 2093 | chr3 | 136950546 | |||||
| chr3:136950602
|
A | G | 1 | a0001c0001t0014 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2149A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 2149 | chr3 | 136950602 | |||||
| chr3:136951025
|
C | T | 1 | a0001c0001t0013 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2572C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 2572 | chr3 | 136951025 | |||||
| chr3:136951069
|
T | C | 1 | a0001c0001t0007 | 2 | HG03139.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2616T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 2616 | chr3 | 136951069 | |||||
| chr3:136951443
|
A | T | 2 | a0001c0001t0005a0001c0001t0009 | 5 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2990A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 2990 | chr3 | 136951443 | |||||
| chr3:136951497
|
A | T | 1 | a0001c0001t0012 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3044A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 3044 | chr3 | 136951497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:136862391
|
C | A | 1 | a0001c0001t0001g0003 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-19+38C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862391 | ||||||
| chr3:136862395
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19+42C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862395 | ||||||
| chr3:136862451
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-19+98C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862451 | ||||||
| chr3:136862644
|
CCGCCCGT others(15): Show |
C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+294_-19+315del others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136862644 | |||||
| chr3:136862682
|
C | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-19+329C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862682 | ||||||
| chr3:136862760
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0016g0004 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+407G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862760 | ||||||
| chr3:136862769
|
G | A | 39 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.-19+416G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862769 | ||||||
| chr3:136862780
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+427C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862780 | ||||||
| chr3:136862808
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19+455C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862808 | ||||||
| chr3:136862853
|
C | G | 2 | a0001c0001t0002g0175a0001c0001t0002g0176 | 2 | HG00280.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-19+500C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862853 | ||||||
| chr3:136862856
|
T | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | NA18939.hp2 NA18955.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+503T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862856 | ||||||
| chr3:136862894
|
GC | G | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+542delC | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862894 | ||||||
| chr3:136863001
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-19+648C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136863001 | ||||||
| chr3:136863013
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+660T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136863013 | ||||||
| chr3:136863016
|
CCTTT | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+667_-19+670del others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136863016 | |||||
| chr3:136863048
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG02129.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-19+695C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136863048 | ||||||
| chr3:136863073
|
G | GTT | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+723_-19+724dup others(2): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136863073 | |||||
| chr3:136863111
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-19+758C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136863111 | ||||||
| chr3:136863195
|
G | T | 25 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(22): Show | 25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-19+842G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136863195 | ||||||
| chr3:136863314
|
G | A | 3 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140 | 3 | HG03491.hp1 HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-19+961G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136863314 | ||||||
| chr3:136863917
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0133 | 2 | HG00099.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.-19+1564C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136863917 | ||||||
| chr3:136864029
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-19+1676A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864029 | ||||||
| chr3:136864030
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-19+1677G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864030 | ||||||
| chr3:136864080
|
G | A | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-19+1727G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864080 | ||||||
| chr3:136864089
|
A | G | 1 | a0001c0001t0013g0131 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-19+1736A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864089 | ||||||
| chr3:136864144
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+1791C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864144 | ||||||
| chr3:136864153
|
G | C | 1 | a0001c0001t0003g0202 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-19+1800G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864153 | ||||||
| chr3:136864240
|
C | A | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-19+1887C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864240 | ||||||
| chr3:136864318
|
G | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+1965G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864318 | ||||||
| chr3:136864362
|
G | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG01256.hp1 HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-19+2009G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864362 | ||||||
| chr3:136864423
|
G | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+2070G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864423 | ||||||
| chr3:136864484
|
T | TCA | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(103): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-19+2142_-19+2143d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136864484 | |||||
| chr3:136864496
|
A | ACAC | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 4 | HG01243.hp2 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+2143_-19+2144i others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864496 | ||||||
| chr3:136864497
|
A | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-19+2144A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864497 | ||||||
| chr3:136864499
|
A | C | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00408.hp1 NA18955.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+2146A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864499 | ||||||
| chr3:136864573
|
A | T | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+2220A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864573 | ||||||
| chr3:136864625
|
A | G | 1 | a0002c0002t0006g0201 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-19+2272A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864625 | ||||||
| chr3:136864668
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-19+2315C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864668 | ||||||
| chr3:136864708
|
A | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(11): Show | 14 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19+2355A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864708 | ||||||
| chr3:136864752
|
T | A | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+2399T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864752 | ||||||
| chr3:136864761
|
C | CT | 6 | a0001c0001t0002g0172a0001c0001t0002g0173a0001c0001t0003g0224others(3): Show | 6 | NA18963.hp2 NA18964.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+2426dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136864761 | |||||
| chr3:136864761
|
CT | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0002g0141others(4): Show | 7 | HG01243.hp2 HG02280.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+2426delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136864761 | |||||
| chr3:136864761
|
CTT | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-19+2425_-19+2426d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136864761 | |||||
| chr3:136864768
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0016g0004 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+2415T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864768 | ||||||
| chr3:136864845
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+2492C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864845 | ||||||
| chr3:136864903
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-19+2550G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864903 | ||||||
| chr3:136864942
|
A | G | 1 | a0001c0001t0003g0223 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-19+2589A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864942 | ||||||
| chr3:136864944
|
A | T | 3 | a0003c0003t0001g0021a0003c0003t0001g0022a0003c0003t0001g0023 | 3 | HG01070.hp2 HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-19+2591A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864944 | ||||||
| chr3:136864981
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-19+2628C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864981 | ||||||
| chr3:136865039
|
A | G | 3 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199 | 3 | HG02280.hp1 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-19+2686A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865039 | ||||||
| chr3:136865114
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-19+2761C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865114 | ||||||
| chr3:136865192
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-19+2839G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865192 | ||||||
| chr3:136865319
|
A | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+2966A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865319 | ||||||
| chr3:136865368
|
C | T | 1 | a0001c0001t0002g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19+3015C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865368 | ||||||
| chr3:136865374
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+3021C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865374 | ||||||
| chr3:136865378
|
G | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-19+3025G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865378 | ||||||
| chr3:136865391
|
C | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02523.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-19+3038C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865391 | ||||||
| chr3:136865482
|
G | T | 1 | a0001c0001t0001g0124 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-19+3129G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865482 | ||||||
| chr3:136865619
|
A | G | 1 | a0001c0001t0014g0020 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-19+3266A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865619 | ||||||
| chr3:136865725
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0016g0004 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+3372T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865725 | ||||||
| chr3:136865778
|
A | G | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0132 | 3 | HG01433.hp1 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-19+3425A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865778 | ||||||
| chr3:136865930
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-19+3577T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865930 | ||||||
| chr3:136865975
|
C | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | NA18939.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-19+3622C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865975 | ||||||
| chr3:136866097
|
C | G | 1 | a0002c0002t0006g0195 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-19+3744C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136866097 | ||||||
| chr3:136866287
|
A | G | 1 | a0001c0001t0002g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19+3934A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136866287 | ||||||
| chr3:136866312
|
C | CT | 28 | a0001c0001t0001g0038a0001c0001t0003g0202a0001c0001t0003g0203others(25): Show | 28 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.-19+3972dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136866312 | |||||
| chr3:136866736
|
TC | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | NA18952.hp1 NA18967.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.-19+4385delC | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136866736 | |||||
| chr3:136866861
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | NA18955.hp1 NA18994.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-19+4508C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136866861 | ||||||
| chr3:136866932
|
AT | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+4589delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136866932 | |||||
| chr3:136866989
|
C | G | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+4636C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136866989 | ||||||
| chr3:136867046
|
GCTTTTCT others(14): Show |
G | 3 | a0001c0001t0001g0032a0001c0001t0001g0084a0001c0001t0001g0130 | 3 | HG03195.hp1 HG03491.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-19+4698_-19+4718d others(23): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867046 | |||||
| chr3:136867046
|
GCTTTTCT others(18): Show |
G | 13 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0026others(10): Show | 13 | HG00609.hp1 HG01891.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+4698_-19+4722d others(27): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867046 | |||||
| chr3:136867046
|
GCTTTTCT others(22): Show |
G | 8 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0048others(5): Show | 8 | HG00140.hp2 HG01070.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+4698_-19+4726d others(31): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867046 | |||||
| chr3:136867046
|
GCTTTTCT others(26): Show |
G | 3 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG01361.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-19+4698_-19+4730d others(35): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867046 | |||||
| chr3:136867046
|
GCTTTTCT others(30): Show |
G | 4 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0029others(1): Show | 4 | HG00544.hp1 HG01256.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+4698_-19+4734d others(39): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867046 | |||||
| chr3:136867046
|
GCTTTTCT others(34): Show |
G | 1 | a0001c0001t0001g0034 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-19+4698_-19+4738d others(43): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867046 | |||||
| chr3:136867049
|
T | TG | 16 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0044others(13): Show | 16 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+4696_-19+4697i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867049 | ||||||
| chr3:136867050
|
T | C | 16 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0044others(13): Show | 16 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+4697T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867050 | ||||||
| chr3:136867050
|
T | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(87): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.-19+4697T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867050 | ||||||
| chr3:136867051
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(87): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.-19+4698T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867051 | ||||||
| chr3:136867052
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(87): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.-19+4699C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867052 | ||||||
| chr3:136867053
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(87): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.-19+4700T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867053 | ||||||
| chr3:136867071
|
T | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0084a0001c0001t0001g0130 | 3 | HG03195.hp1 HG03491.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-19+4718T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867071 | ||||||
| chr3:136867073
|
T | TC | 3 | a0001c0001t0001g0032a0001c0001t0001g0084a0001c0001t0001g0130 | 3 | HG03195.hp1 HG03491.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-19+4720_-19+4721i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867073 | ||||||
| chr3:136867075
|
T | G | 13 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0026others(10): Show | 13 | HG00609.hp1 HG01891.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+4722T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867075 | ||||||
| chr3:136867077
|
T | TC | 13 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0026others(10): Show | 13 | HG00609.hp1 HG01891.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+4724_-19+4725i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867077 | ||||||
| chr3:136867077
|
TTTCTTTC others(57): Show |
T | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+4728_-19+4791d others(66): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867077 | |||||
| chr3:136867079
|
T | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0048others(5): Show | 8 | HG00140.hp2 HG01070.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+4726T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867079 | ||||||
| chr3:136867081
|
T | TC | 8 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0048others(5): Show | 8 | HG00140.hp2 HG01070.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+4728_-19+4729i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867081 | ||||||
| chr3:136867083
|
T | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG01361.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-19+4730T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867083 | ||||||
| chr3:136867085
|
T | TC | 3 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG01361.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-19+4732_-19+4733i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867085 | ||||||
| chr3:136867085
|
TTTCTTTC others(41): Show |
T | 1 | a0002c0002t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+4736_-19+4783d others(50): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867085 | |||||
| chr3:136867087
|
T | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0029others(1): Show | 4 | HG00544.hp1 HG01256.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+4734T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867087 | ||||||
| chr3:136867088
|
CTTTCTTT others(25): Show |
C | 1 | a0001c0001t0002g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19+4748_-19+4779d others(34): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867088 | |||||
| chr3:136867089
|
T | TC | 4 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0029others(1): Show | 4 | HG00544.hp1 HG01256.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+4736_-19+4737i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867089 | ||||||
| chr3:136867089
|
TTTCTTTC others(37): Show |
T | 1 | a0001c0001t0002g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19+4740_-19+4783d others(46): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867089 | |||||
| chr3:136867089
|
TTTCTTTC others(41): Show |
T | 2 | a0001c0001t0003g0204a0001c0001t0003g0205 | 2 | HG00544.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-19+4740_-19+4787d others(50): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867089 | |||||
| chr3:136867091
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-19+4738T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867091 | ||||||
| chr3:136867092
|
CTTTCTTT others(21): Show |
C | 3 | a0001c0001t0002g0145a0001c0001t0005g0183a0001c0001t0005g0184 | 3 | HG01167.hp1 HG01169.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-19+4752_-19+4779d others(30): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867092 | |||||
| chr3:136867093
|
TTTCTTTC others(33): Show |
T | 1 | a0002c0002t0006g0195 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-19+4744_-19+4783d others(42): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867093 | |||||
| chr3:136867093
|
TTTCTTTC others(37): Show |
T | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(2): Show | 5 | HG02965.hp2 HG04115.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+4744_-19+4787d others(46): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867093 | |||||
| chr3:136867093
|
TTTCTTTC others(49): Show |
T | 2 | a0001c0001t0001g0047a0001c0001t0001g0120 | 2 | NA18994.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-19+4744_-19+4799d others(58): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867093 | |||||
| chr3:136867096
|
CTTTCTTT others(17): Show |
C | 1 | a0001c0001t0002g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19+4756_-19+4779d others(26): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867096 | |||||
| chr3:136867097
|
TTTCTTTC others(29): Show |
T | 7 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0111others(4): Show | 7 | HG00099.hp1 HG01496.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+4748_-19+4783d others(38): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867097 | |||||
| chr3:136867097
|
TTTCTTTC others(33): Show |
T | 11 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0112others(8): Show | 11 | HG00621.hp1 HG01433.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+4748_-19+4787d others(42): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867097 | |||||
| chr3:136867097
|
TTTCTTTC others(37): Show |
T | 2 | a0001c0001t0001g0001a0001c0001t0007g0227 | 3 | HG01074.hp1 HG01346.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+4748_-19+4791d others(46): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867097 | |||||
| chr3:136867100
|
CTTTCTTT others(13): Show |
C | 3 | a0001c0001t0002g0153a0001c0001t0002g0163a0001c0001t0005g0200 | 3 | HG03654.hp1 HG03669.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-19+4760_-19+4779d others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867100 | |||||
| chr3:136867101
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-19+4748T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867101 | ||||||
| chr3:136867101
|
TTTCTTTC others(25): Show |
T | 12 | a0001c0001t0001g0006a0001c0001t0001g0057a0001c0001t0001g0058others(9): Show | 12 | HG00140.hp1 HG01106.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19+4752_-19+4783d others(34): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867101 | |||||
| chr3:136867101
|
TTTCTTTC others(29): Show |
T | 16 | a0001c0001t0001g0117a0001c0001t0001g0229a0001c0001t0002g0138others(13): Show | 16 | HG00408.hp2 HG01070.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+4752_-19+4787d others(38): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867101 | |||||
| chr3:136867101
|
TTTCTTTC others(33): Show |
T | 14 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0042others(11): Show | 14 | HG01243.hp2 HG01257.hp2 HG02976.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19+4752_-19+4791d others(42): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867101 | |||||
| chr3:136867104
|
CTTTCTTT others(9): Show |
C | 8 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0037others(5): Show | 8 | HG02129.hp1 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+4764_-19+4779d others(18): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867104 | |||||
| chr3:136867105
|
TTTCTTTC others(21): Show |
T | 10 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0015others(7): Show | 10 | HG00408.hp1 HG01167.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+4756_-19+4783d others(30): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867105 | |||||
| chr3:136867105
|
TTTCTTTC others(25): Show |
T | 17 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0078others(14): Show | 18 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.-19+4756_-19+4787d others(34): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867105 | |||||
| chr3:136867105
|
TTTCTTTC others(29): Show |
T | 12 | a0001c0001t0001g0041a0001c0001t0001g0080a0001c0001t0001g0081others(9): Show | 12 | HG01099.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-19+4756_-19+4791d others(38): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867105 | |||||
| chr3:136867105
|
TTTCTTTC others(33): Show |
T | 1 | a0001c0001t0002g0162 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-19+4756_-19+4795d others(42): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867105 | |||||
| chr3:136867105
|
TTTCTTTC others(37): Show |
T | 2 | a0001c0001t0001g0008a0001c0001t0001g0121 | 2 | NA18955.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-19+4756_-19+4799d others(46): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867105 | |||||
| chr3:136867108
|
CTTTCTTT others(5): Show |
C | 2 | a0001c0001t0001g0132a0001c0001t0013g0131 | 2 | HG01433.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-19+4767_-19+4778d others(14): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867108 | |||||
| chr3:136867109
|
TTTCTTTC others(17): Show |
T | 10 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(7): Show | 10 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19+4760_-19+4783d others(26): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867109 | |||||
| chr3:136867109
|
TTTCTTTC others(21): Show |
T | 13 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(10): Show | 13 | HG00609.hp2 HG01106.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+4760_-19+4787d others(30): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867109 | |||||
| chr3:136867109
|
TTTCTTTC others(25): Show |
T | 8 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(5): Show | 8 | HG00741.hp1 HG01109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+4760_-19+4791d others(34): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867109 | |||||
| chr3:136867109
|
TTTCTTTC others(29): Show |
T | 2 | a0001c0001t0003g0219a0002c0002t0002g0199 | 2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-19+4760_-19+4795d others(38): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867109 | |||||
| chr3:136867112
|
CTTTCTTT others(10): Show |
C | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-19+4762_-19+4778d others(19): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867112 | |||||
| chr3:136867113
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-19+4760T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867113 | ||||||
| chr3:136867113
|
TTTCTTTG others(13): Show |
T | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(2): Show | 5 | HG02965.hp1 HG03139.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+4764_-19+4783d others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867113 | |||||
| chr3:136867113
|
TTTCTTTG others(17): Show |
T | 6 | a0001c0001t0001g0106a0001c0001t0003g0220a0001c0001t0003g0221others(3): Show | 6 | HG00099.hp2 HG00280.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+4764_-19+4787d others(26): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867113 | |||||
| chr3:136867113
|
TTTCTTTG others(21): Show |
T | 4 | a0001c0001t0001g0024a0001c0001t0002g0167a0001c0001t0002g0191others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+4764_-19+4791d others(30): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867113 | |||||
| chr3:136867115
|
TCTTTGTT others(10): Show |
T | 1 | a0001c0001t0001g0107 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-19+4766_-19+4782d others(19): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867115 | |||||
| chr3:136867115
|
TCTTTGTT others(14): Show |
T | 1 | a0001c0001t0002g0168 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-19+4766_-19+4786d others(23): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867115 | |||||
| chr3:136867117
|
TTTGTTTC others(9): Show |
T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-19+4767_-19+4782d others(18): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867117 | |||||
| chr3:136867117
|
TTTGTTTC others(13): Show |
T | 1 | a0001c0001t0003g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-19+4767_-19+4786d others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867117 | |||||
| chr3:136867117
|
TTTGTTTC others(17): Show |
T | 5 | a0001c0001t0001g0110a0001c0001t0002g0169a0001c0001t0002g0170others(2): Show | 5 | HG00423.hp1 HG00738.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+4767_-19+4790d others(26): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867117 | |||||
| chr3:136867120
|
G | C | 33 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(30): Show | 33 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-19+4767G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867120 | ||||||
| chr3:136867121
|
T | C | 6 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0037others(3): Show | 6 | HG02486.hp1 HG02615.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+4768T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867121 | ||||||
| chr3:136867125
|
T | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0032others(9): Show | 12 | HG01433.hp1 HG02486.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19+4772T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867125 | ||||||
| chr3:136867125
|
TTTCTTTC others(13): Show |
T | 1 | a0001c0001t0002g0171 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-19+4776_-19+4795d others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867125 | |||||
| chr3:136867129
|
T | C | 20 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(17): Show | 20 | HG00609.hp1 HG01433.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19+4776T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867129 | ||||||
| chr3:136867178
|
TTC | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.-19+4827_-19+4828d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867178 | |||||
| chr3:136867181
|
T | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0056others(8): Show | 11 | HG00423.hp1 HG01256.hp1 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+4828T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867181 | ||||||
| chr3:136867183
|
TC | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0056others(2): Show | 5 | HG01256.hp1 HG03710.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+4831delC | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867183 | ||||||
| chr3:136867185
|
TTTC | T | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.-19+4835_-19+4837d others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867185 | |||||
| chr3:136867187
|
T | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0056others(2): Show | 5 | HG01256.hp1 HG03710.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+4834T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867187 | ||||||
| chr3:136867188
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0056others(2): Show | 5 | HG01256.hp1 HG03710.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+4835C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867188 | ||||||
| chr3:136867202
|
CCCTT | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.-19+4868_-19+4871d others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867202 | |||||
| chr3:136867253
|
G | GTC | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.-19+4912_-19+4913d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867253 | |||||
| chr3:136867253
|
G | GTCTC | 2 | a0001c0001t0001g0068a0001c0001t0001g0123 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-19+4910_-19+4913d others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867253 | |||||
| chr3:136867305
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-19+4952C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867305 | ||||||
| chr3:136867312
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-19+4959T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867312 | ||||||
| chr3:136867405
|
A | AT | 13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0024others(10): Show | 13 | HG01257.hp2 HG02055.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+5073dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867405 | |||||
| chr3:136867405
|
A | ATT | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(98): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-19+5072_-19+5073d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867405 | |||||
| chr3:136867405
|
A | ATTT | 25 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0026others(22): Show | 25 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.-19+5071_-19+5073d others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867405 | |||||
| chr3:136867405
|
A | ATTTT | 5 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0036others(2): Show | 5 | HG01261.hp1 HG02738.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+5070_-19+5073d others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867405 | |||||
| chr3:136867664
|
C | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-19+5311C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867664 | ||||||
| chr3:136867776
|
G | A | 68 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-19+5423G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867776 | ||||||
| chr3:136867865
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-19+5512G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867865 | ||||||
| chr3:136867921
|
AT | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+5581delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867921 | |||||
| chr3:136868011
|
G | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+5658G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136868011 | ||||||
| chr3:136868056
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19+5703C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136868056 | ||||||
| chr3:136868213
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-19+5860G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136868213 | ||||||
| chr3:136868275
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-19+5922A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136868275 | ||||||
| chr3:136868350
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-19+5997C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136868350 | ||||||
| chr3:136868481
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-19+6128C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136868481 | ||||||
| chr3:136868592
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-19+6239T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136868592 | ||||||
| chr3:136869082
|
A | T | 13 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(10): Show | 13 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+6729A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136869082 | ||||||
| chr3:136869321
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0002g0186a0001c0001t0002g0196 | 3 | HG01891.hp1 HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-19+6968C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136869321 | ||||||
| chr3:136869664
|
A | G | 3 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199 | 3 | HG02280.hp1 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-19+7311A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136869664 | ||||||
| chr3:136869675
|
C | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0024 | 3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-19+7322C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136869675 | ||||||
| chr3:136870014
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0066 | 2 | HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-19+7661G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870014 | ||||||
| chr3:136870028
|
G | GT | 7 | a0001c0001t0002g0146a0001c0001t0002g0153a0001c0001t0002g0170others(4): Show | 7 | HG00140.hp1 HG01106.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+7697dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870028 | |||||
| chr3:136870028
|
G | GTT | 17 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(14): Show | 17 | HG00639.hp1 HG01169.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.-19+7696_-19+7697d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870028 | |||||
| chr3:136870028
|
G | GTTT | 86 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0012others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.-19+7695_-19+7697d others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870028 | |||||
| chr3:136870028
|
G | GTTTT | 17 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(14): Show | 17 | HG01070.hp2 HG01106.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19+7694_-19+7697d others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870028 | |||||
| chr3:136870028
|
GT | G | 8 | a0001c0001t0002g0142a0001c0001t0002g0147a0001c0001t0002g0175others(5): Show | 8 | HG00099.hp2 HG00280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+7697delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870028 | |||||
| chr3:136870044
|
TTTTTTTA | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0046others(13): Show | 18 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-19+7692_-19+7698d others(9): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870044 | ||||||
| chr3:136870050
|
T | A | 1 | a0002c0002t0002g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19+7697T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870050 | ||||||
| chr3:136870051
|
A | T | 121 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 121 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-19+7698A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870051 | ||||||
| chr3:136870084
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-19+7731T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870084 | ||||||
| chr3:136870341
|
C | CA | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+8001dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870341 | |||||
| chr3:136870360
|
CCTTTT | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(14): Show | 17 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19+8011_-19+8015d others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870360 | |||||
| chr3:136870478
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+8125C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870478 | ||||||
| chr3:136870511
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-19+8158G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870511 | ||||||
| chr3:136870687
|
TA | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(136): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-19+8354delA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870687 | |||||
| chr3:136870687
|
TAA | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0032a0001c0001t0001g0068others(3): Show | 6 | HG01257.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+8353_-19+8354d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870687 | |||||
| chr3:136870687
|
TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+8344_-19+8354d others(13): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870687 | |||||
| chr3:136870707
|
A | T | 30 | a0001c0001t0002g0143a0001c0001t0002g0144a0001c0001t0002g0147others(27): Show | 30 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19+8354A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870707 | ||||||
| chr3:136870824
|
G | C | 1 | a0001c0001t0010g0113 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-19+8471G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870824 | ||||||
| chr3:136871063
|
T | G | 7 | a0001c0001t0002g0185a0001c0001t0002g0187a0001c0001t0002g0188others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+8710T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871063 | ||||||
| chr3:136871092
|
A | AT | 6 | a0001c0001t0003g0209a0001c0001t0003g0212a0001c0001t0003g0217others(3): Show | 6 | HG01243.hp1 HG02897.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+8748dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136871092 | |||||
| chr3:136871223
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-19+8870C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871223 | ||||||
| chr3:136871282
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-19+8929C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871282 | ||||||
| chr3:136871304
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0016g0004 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+8951G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871304 | ||||||
| chr3:136871354
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0016g0004 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+9001C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871354 | ||||||
| chr3:136871409
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-19+9056A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871409 | ||||||
| chr3:136871460
|
C | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-19+9107C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871460 | ||||||
| chr3:136871569
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+9216C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871569 | ||||||
| chr3:136871628
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-19+9275C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871628 | ||||||
| chr3:136871714
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-19+9361C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871714 | ||||||
| chr3:136871735
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-19+9382G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871735 | ||||||
| chr3:136871751
|
G | A | 4 | a0001c0001t0002g0148a0001c0001t0002g0168a0001c0001t0002g0171others(1): Show | 4 | HG00099.hp2 HG01074.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+9398G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871751 | ||||||
| chr3:136871823
|
C | T | 7 | a0001c0001t0002g0185a0001c0001t0002g0187a0001c0001t0002g0188others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+9470C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871823 | ||||||
| chr3:136871882
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-19+9529T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871882 | ||||||
| chr3:136872018
|
G | T | 6 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162others(3): Show | 6 | HG00423.hp1 NA18963.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+9665G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136872018 | ||||||
| chr3:136872266
|
G | A | 1 | a0001c0001t0002g0186 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-19+9913G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136872266 | ||||||
| chr3:136872306
|
C | A | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+9953C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136872306 | ||||||
| chr3:136872449
|
A | C | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-19+10096A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136872449 | ||||||
| chr3:136872673
|
G | A | 7 | a0002c0002t0002g0180a0002c0002t0002g0197a0002c0002t0002g0198others(4): Show | 7 | HG02280.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+10320G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136872673 | ||||||
| chr3:136872741
|
A | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+10388A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136872741 | ||||||
| chr3:136872780
|
C | T | 1 | a0001c0001t0004g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19+10427C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136872780 | ||||||
| chr3:136873345
|
A | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+10992A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136873345 | ||||||
| chr3:136873375
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+11022G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136873375 | ||||||
| chr3:136873960
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-19+11607T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136873960 | ||||||
| chr3:136873990
|
A | G | 2 | a0001c0001t0014g0020a0001c0001t0015g0019 | 2 | HG01496.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-19+11637A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136873990 | ||||||
| chr3:136874057
|
GTGATAGT others(11): Show |
G | 6 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162others(3): Show | 6 | HG00423.hp1 NA18963.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+11705_-19+1172 others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874057 | ||||||
| chr3:136874074
|
T | C | 1 | a0001c0001t0015g0019 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-19+11721T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874074 | ||||||
| chr3:136874077
|
G | A | 6 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162others(3): Show | 6 | HG00423.hp1 NA18963.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+11724G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874077 | ||||||
| chr3:136874114
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+11761A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874114 | ||||||
| chr3:136874251
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0024 | 3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-19+11898C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874251 | ||||||
| chr3:136874290
|
C | G | 1 | a0001c0001t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-19+11937C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874290 | ||||||
| chr3:136874402
|
AGTCCTGA others(6): Show |
A | 2 | a0001c0001t0001g0046a0001c0001t0001g0053 | 2 | HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-19+12052_-19+1206 others(17): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136874402 | |||||
| chr3:136874422
|
C | A | 8 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0003g0209others(5): Show | 8 | HG01243.hp1 HG02897.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+12069C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874422 | ||||||
| chr3:136874475
|
C | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0196 | 2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-19+12122C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874475 | ||||||
| chr3:136874606
|
A | G | 1 | a0002c0002t0006g0190 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-19+12253A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874606 | ||||||
| chr3:136874809
|
CTT | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-19+12462_-19+1246 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136874809 | |||||
| chr3:136874825
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-19+12472T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874825 | ||||||
| chr3:136874942
|
G | C | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-19+12589G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874942 | ||||||
| chr3:136875505
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+13152A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136875505 | ||||||
| chr3:136875668
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-19+13315C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136875668 | ||||||
| chr3:136875798
|
T | G | 1 | a0001c0001t0001g0133 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-19+13445T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136875798 | ||||||
| chr3:136876087
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | NA18952.hp1 NA18967.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.-19+13734G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876087 | ||||||
| chr3:136876123
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-19+13770A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876123 | ||||||
| chr3:136876126
|
C | G | 1 | a0001c0001t0001g0040 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-19+13773C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876126 | ||||||
| chr3:136876177
|
A | C | 1 | a0001c0001t0002g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19+13824A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876177 | ||||||
| chr3:136876381
|
G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 4 | HG01243.hp2 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+14028G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876381 | ||||||
| chr3:136876513
|
C | G | 1 | a0001c0001t0002g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19+14160C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876513 | ||||||
| chr3:136876540
|
C | T | 1 | a0002c0002t0002g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-19+14187C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876540 | ||||||
| chr3:136876768
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+14415G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876768 | ||||||
| chr3:136876786
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19+14433G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876786 | ||||||
| chr3:136876909
|
T | A | 1 | a0001c0001t0001g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19+14556T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876909 | ||||||
| chr3:136877157
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-19+14804G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136877157 | ||||||
| chr3:136877226
|
T | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0024 | 3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-19+14873T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136877226 | ||||||
| chr3:136877269
|
A | G | 1 | a0001c0001t0003g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-19+14916A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136877269 | ||||||
| chr3:136877280
|
C | A | 1 | a0001c0001t0001g0107 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-19+14927C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136877280 | ||||||
| chr3:136877693
|
A | G | 1 | a0001c0001t0011g0055 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-19+15340A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136877693 | ||||||
| chr3:136877832
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG02129.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-19+15479G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136877832 | ||||||
| chr3:136878129
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0024 | 3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-19+15776C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878129 | ||||||
| chr3:136878131
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0034 | 3 | HG00544.hp1 HG00621.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.-19+15778G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878131 | ||||||
| chr3:136878243
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-19+15890A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878243 | ||||||
| chr3:136878278
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.-19+15925A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878278 | ||||||
| chr3:136878702
|
TA | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+16352delA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136878702 | |||||
| chr3:136878707
|
C | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+16354C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878707 | ||||||
| chr3:136878710
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+16357T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878710 | ||||||
| chr3:136878711
|
T | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+16358T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878711 | ||||||
| chr3:136878712
|
T | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+16359T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878712 | ||||||
| chr3:136878713
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+16360T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878713 | ||||||
| chr3:136878714
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+16361T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878714 | ||||||
| chr3:136878716
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+16363T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878716 | ||||||
| chr3:136878847
|
A | G | 4 | a0002c0002t0002g0180a0002c0002t0006g0190a0002c0002t0006g0195others(1): Show | 4 | HG03139.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+16494A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878847 | ||||||
| chr3:136878848
|
A | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(1): Show | 4 | HG02300.hp2 NA18939.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+16495A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878848 | ||||||
| chr3:136879081
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-19+16728A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136879081 | ||||||
| chr3:136879131
|
C | CA | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-19+16787dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136879131 | |||||
| chr3:136879133
|
A | AC | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+16780_-19+1678 others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136879133 | ||||||
| chr3:136879586
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-19+17233A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136879586 | ||||||
| chr3:136879810
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19+17457G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136879810 | ||||||
| chr3:136879821
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-19+17468A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136879821 | ||||||
| chr3:136879864
|
G | GATAGCAT others(64): Show |
1 | a0001c0001t0001g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19+17513_-19+1758 others(75): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136879864 | |||||
| chr3:136879989
|
T | TAAAAAAA others(3): Show |
123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-19+17640_-19+1764 others(14): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136879989 | |||||
| chr3:136879989
|
T | TAAAAAAA others(4): Show |
11 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0046others(8): Show | 11 | HG01261.hp1 HG01358.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+17639_-19+1764 others(15): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136879989 | |||||
| chr3:136879989
|
T | TAAAAAAA others(5): Show |
1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-19+17638_-19+1764 others(16): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136879989 | |||||
| chr3:136880003
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-19+17650G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880003 | ||||||
| chr3:136880006
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+17653T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880006 | ||||||
| chr3:136880017
|
G | T | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+17664G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880017 | ||||||
| chr3:136880181
|
A | G | 6 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(3): Show | 6 | HG00140.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+17828A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880181 | ||||||
| chr3:136880210
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+17857G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880210 | ||||||
| chr3:136880237
|
A | G | 11 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0205others(8): Show | 11 | HG00544.hp2 HG02135.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+17884A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880237 | ||||||
| chr3:136880321
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0016g0004 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+17968G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880321 | ||||||
| chr3:136880321
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-19+17968G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880321 | ||||||
| chr3:136880370
|
C | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-19+18017C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880370 | ||||||
| chr3:136880972
|
T | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+18619T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880972 | ||||||
| chr3:136881011
|
A | G | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-19+18658A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881011 | ||||||
| chr3:136881206
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+18853C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881206 | ||||||
| chr3:136881241
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+18888A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881241 | ||||||
| chr3:136881373
|
C | G | 1 | a0001c0001t0001g0072 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-19+19020C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881373 | ||||||
| chr3:136881467
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0094 | 3 | HG00609.hp2 NA19065.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-19+19114C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881467 | ||||||
| chr3:136881710
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-19+19357C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881710 | ||||||
| chr3:136881825
|
G | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+19472G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881825 | ||||||
| chr3:136881990
|
G | T | 2 | a0002c0002t0002g0197a0002c0002t0002g0198 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-19+19637G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881990 | ||||||
| chr3:136882103
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+19750A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136882103 | ||||||
| chr3:136882149
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-19+19796T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136882149 | ||||||
| chr3:136882204
|
T | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-19+19851T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136882204 | ||||||
| chr3:136882394
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+20041A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136882394 | ||||||
| chr3:136882547
|
C | CTG | 41 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0028others(38): Show | 41 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.-19+20236_-19+2023 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136882547 | |||||
| chr3:136882547
|
C | CTGTG | 26 | a0001c0001t0001g0030a0001c0001t0001g0050a0001c0001t0001g0068others(23): Show | 26 | HG00140.hp1 HG01070.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.-19+20234_-19+2023 others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136882547 | |||||
| chr3:136882547
|
C | CTGTGTG | 4 | a0001c0001t0003g0206a0001c0001t0003g0223a0001c0001t0007g0227others(1): Show | 4 | HG01433.hp2 HG01517.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+20232_-19+2023 others(10): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136882547 | |||||
| chr3:136882547
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0003g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-19+20228_-19+2023 others(14): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136882547 | |||||
| chr3:136882547
|
CTG | C | 45 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.-19+20236_-19+2023 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136882547 | |||||
| chr3:136882547
|
CTGTG | C | 9 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0063others(6): Show | 9 | HG00621.hp2 HG00741.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19+20234_-19+2023 others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136882547 | |||||
| chr3:136882547
|
CTGTGTG | C | 4 | a0001c0001t0001g0024a0001c0001t0002g0187a0001c0001t0002g0193others(1): Show | 4 | HG02055.hp2 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+20232_-19+2023 others(10): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136882547 | |||||
| chr3:136882720
|
T | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+20367T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136882720 | ||||||
| chr3:136882803
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+20450G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136882803 | ||||||
| chr3:136883300
|
G | A | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-19+20947G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136883300 | ||||||
| chr3:136883319
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+20966C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136883319 | ||||||
| chr3:136883606
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-19+21253G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136883606 | ||||||
| chr3:136883997
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-19+21644A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136883997 | ||||||
| chr3:136884601
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-19+22248C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136884601 | ||||||
| chr3:136884718
|
C | CT | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(168): Show | 173 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.-19+22377dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136884718 | |||||
| chr3:136884757
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-19+22404G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136884757 | ||||||
| chr3:136884763
|
C | T | 1 | a0001c0001t0001g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-19+22410C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136884763 | ||||||
| chr3:136884928
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-19+22575T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136884928 | ||||||
| chr3:136884963
|
T | G | 1 | a0001c0001t0001g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-19+22610T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136884963 | ||||||
| chr3:136885198
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-19+22845T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136885198 | ||||||
| chr3:136885461
|
T | G | 13 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(10): Show | 13 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+23108T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136885461 | ||||||
| chr3:136885855
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+23502T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136885855 | ||||||
| chr3:136885963
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-19+23610G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136885963 | ||||||
| chr3:136886128
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-19+23775A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136886128 | ||||||
| chr3:136886305
|
A | G | 2 | a0001c0001t0002g0141a0001c0001t0002g0145 | 2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-19+23952A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136886305 | ||||||
| chr3:136886544
|
T | C | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-19+24191T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136886544 | ||||||
| chr3:136886567
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+24214C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136886567 | ||||||
| chr3:136886787
|
T | G | 1 | a0001c0001t0002g0170 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-19+24434T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136886787 | ||||||
| chr3:136886817
|
CTTT | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(132): Show | 137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-19+24480_-19+2448 others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136886817 | |||||
| chr3:136886955
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+24602T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136886955 | ||||||
| chr3:136887009
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-19+24656A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887009 | ||||||
| chr3:136887319
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0012g0085 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-19+24966C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887319 | ||||||
| chr3:136887429
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-19+25076T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887429 | ||||||
| chr3:136887636
|
C | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+25283C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887636 | ||||||
| chr3:136887724
|
AG | A | 11 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0205others(8): Show | 11 | HG00544.hp2 HG02135.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+25372delG | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887724 | ||||||
| chr3:136887902
|
A | G | 1 | a0001c0001t0002g0164 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-19+25549A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887902 | ||||||
| chr3:136887923
|
TTTTC | T | 35 | a0001c0001t0001g0049a0001c0001t0002g0138a0001c0001t0002g0139others(32): Show | 35 | HG00140.hp1 HG00544.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.-19+25590_-19+2559 others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136887923 | |||||
| chr3:136887975
|
G | A | 3 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140 | 3 | HG03491.hp1 HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-19+25622G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887975 | ||||||
| chr3:136887992
|
T | C | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-19+25639T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887992 | ||||||
| chr3:136888232
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-19+25879C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136888232 | ||||||
| chr3:136888265
|
C | T | 1 | a0001c0001t0003g0224 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-19+25912C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136888265 | ||||||
| chr3:136888356
|
A | G | 14 | a0001c0001t0003g0202a0001c0001t0003g0206a0001c0001t0003g0207others(11): Show | 14 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19+26003A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136888356 | ||||||
| chr3:136888482
|
A | C | 1 | a0003c0003t0001g0023 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-19+26129A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136888482 | ||||||
| chr3:136888505
|
T | C | 1 | a0001c0001t0003g0204 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-19+26152T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136888505 | ||||||
| chr3:136888656
|
C | A | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+26303C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136888656 | ||||||
| chr3:136889044
|
A | AT | 19 | a0001c0001t0002g0143a0001c0001t0002g0152a0001c0001t0002g0153others(16): Show | 19 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19+26721dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | |||||
| chr3:136889044
|
AT | A | 7 | a0001c0001t0002g0168a0001c0001t0003g0203a0001c0001t0003g0205others(4): Show | 7 | HG01106.hp1 HG01256.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+26721delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | |||||
| chr3:136889044
|
ATT | A | 18 | a0001c0001t0003g0204a0001c0001t0003g0206a0001c0001t0003g0207others(15): Show | 18 | HG00544.hp2 HG00738.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-19+26720_-19+2672 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | |||||
| chr3:136889044
|
ATTTTT | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(23): Show | 27 | HG00280.hp2 HG01081.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-19+26717_-19+2672 others(9): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | |||||
| chr3:136889044
|
ATTTTTT | A | 80 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(77): Show | 80 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.-19+26716_-19+2672 others(10): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | |||||
| chr3:136889044
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0003g0202 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-19+26712_-19+2672 others(14): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | |||||
| chr3:136889044
|
ATTTTTTT others(4): Show |
A | 3 | a0001c0001t0002g0160a0001c0001t0007g0227a0001c0001t0007g0228 | 3 | HG03139.hp1 HG03195.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-19+26711_-19+2672 others(15): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | |||||
| chr3:136889044
|
ATTTTTTT others(6): Show |
A | 18 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(15): Show | 18 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-19+26709_-19+2672 others(17): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | |||||
| chr3:136889044
|
ATTTTTTT others(7): Show |
A | 8 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0062others(5): Show | 9 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19+26708_-19+2672 others(18): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | |||||
| chr3:136889140
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+26787T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889140 | ||||||
| chr3:136889289
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-19+26936G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889289 | ||||||
| chr3:136889300
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-19+26947C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889300 | ||||||
| chr3:136889419
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-19+27066C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889419 | ||||||
| chr3:136889526
|
T | C | 18 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(15): Show | 18 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-19+27173T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889526 | ||||||
| chr3:136889540
|
C | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-19+27187C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889540 | ||||||
| chr3:136889603
|
A | G | 50 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.-19+27250A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889603 | ||||||
| chr3:136889635
|
T | G | 12 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(9): Show | 12 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19+27282T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889635 | ||||||
| chr3:136889764
|
C | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+27411C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889764 | ||||||
| chr3:136889807
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+27454G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889807 | ||||||
| chr3:136889836
|
C | T | 17 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(14): Show | 17 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19+27483C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889836 | ||||||
| chr3:136889924
|
C | G | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+27571C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889924 | ||||||
| chr3:136889951
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-19+27598G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889951 | ||||||
| chr3:136889999
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-19+27646C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889999 | ||||||
| chr3:136890036
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+27683C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890036 | ||||||
| chr3:136890057
|
C | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-19+27704C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890057 | ||||||
| chr3:136890130
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+27777C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890130 | ||||||
| chr3:136890175
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-19+27822G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890175 | ||||||
| chr3:136890184
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0095 | 2 | HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-19+27831G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890184 | ||||||
| chr3:136890253
|
C | A | 1 | a0001c0001t0001g0011 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-19+27900C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890253 | ||||||
| chr3:136890353
|
C | T | 4 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0018others(1): Show | 4 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+28000C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890353 | ||||||
| chr3:136890397
|
C | G | 1 | a0001c0001t0001g0031 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-19+28044C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890397 | ||||||
| chr3:136890448
|
A | G | 1 | a0001c0001t0014g0020 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-19+28095A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890448 | ||||||
| chr3:136890676
|
C | G | 1 | a0001c0001t0003g0204 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-19+28323C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890676 | ||||||
| chr3:136890676
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-19+28323C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890676 | ||||||
| chr3:136890778
|
C | T | 1 | a0001c0001t0003g0207 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-19+28425C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890778 | ||||||
| chr3:136890960
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19+28607C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890960 | ||||||
| chr3:136890996
|
T | C | 45 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.-19+28643T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890996 | ||||||
| chr3:136891064
|
A | G | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+28711A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136891064 | ||||||
| chr3:136891087
|
G | A | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+28734G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136891087 | ||||||
| chr3:136891183
|
G | C | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-19+28830G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136891183 | ||||||
| chr3:136891217
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-19+28864C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136891217 | ||||||
| chr3:136891788
|
G | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+29435G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136891788 | ||||||
| chr3:136891791
|
A | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+29438A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136891791 | ||||||
| chr3:136891989
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+29636A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136891989 | ||||||
| chr3:136892033
|
T | G | 1 | a0001c0001t0003g0223 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-19+29680T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892033 | ||||||
| chr3:136892103
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+29750G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892103 | ||||||
| chr3:136892154
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+29801T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892154 | ||||||
| chr3:136892309
|
G | A | 1 | a0001c0001t0002g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19+29956G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892309 | ||||||
| chr3:136892314
|
A | G | 7 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 7 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+29961A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892314 | ||||||
| chr3:136892382
|
C | A | 1 | a0001c0001t0005g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19+30029C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892382 | ||||||
| chr3:136892388
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+30035G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892388 | ||||||
| chr3:136892441
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-19+30088A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892441 | ||||||
| chr3:136892505
|
TTGA | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-19+30158_-19+3016 others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136892505 | |||||
| chr3:136892734
|
T | C | 1 | a0001c0001t0002g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19+30381T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892734 | ||||||
| chr3:136892928
|
C | G | 2 | a0001c0001t0001g0005a0001c0001t0016g0004 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+30575C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892928 | ||||||
| chr3:136893130
|
G | A | 4 | a0001c0001t0002g0148a0001c0001t0002g0168a0001c0001t0002g0171others(1): Show | 4 | HG00099.hp2 HG01074.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+30777G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893130 | ||||||
| chr3:136893147
|
A | AGT | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(87): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-19+30825_-19+3082 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893147 | |||||
| chr3:136893147
|
A | AGTGT | 34 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0043others(31): Show | 34 | HG00423.hp2 HG00621.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-19+30823_-19+3082 others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893147 | |||||
| chr3:136893147
|
A | AGTGTGT | 24 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0049others(21): Show | 24 | HG00544.hp1 HG00544.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+30821_-19+3082 others(10): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893147 | |||||
| chr3:136893147
|
A | AGTGTGTG others(1): Show |
22 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0014others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19+30819_-19+3082 others(12): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893147 | |||||
| chr3:136893147
|
A | AGTGTGTG others(3): Show |
23 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(20): Show | 23 | HG00609.hp1 HG00621.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+30817_-19+3082 others(14): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893147 | |||||
| chr3:136893147
|
A | AGTGTGTG others(5): Show |
3 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0151 | 3 | HG00408.hp2 HG00609.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-19+30815_-19+3082 others(16): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893147 | |||||
| chr3:136893147
|
A | AGTGTGTG others(7): Show |
2 | a0001c0001t0001g0041a0001c0001t0002g0164 | 2 | NA18522.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-19+30813_-19+3082 others(18): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893147 | |||||
| chr3:136893155
|
T | TGC | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+30803_-19+3080 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893155 | |||||
| chr3:136893167
|
T | TGTGTGTG others(29): Show |
3 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199 | 3 | HG02280.hp1 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-19+30826_-19+3082 others(40): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893167 | |||||
| chr3:136893178
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-19+30825G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893178 | ||||||
| chr3:136893178
|
G | GTA | 2 | a0001c0001t0002g0186a0001c0001t0002g0196 | 2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-19+30838_-19+3083 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893178 | |||||
| chr3:136893178
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-19+30826_-19+3082 others(18): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893178 | |||||
| chr3:136893178
|
G | GTGTGTGT others(11): Show |
1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+30826_-19+3082 others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893178 | |||||
| chr3:136893180
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 158 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.-19+30827A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893180 | ||||||
| chr3:136893182
|
A | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(83): Show | 88 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-19+30829A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893182 | ||||||
| chr3:136893184
|
A | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0001g0073others(28): Show | 31 | HG00544.hp2 HG00738.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19+30831A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893184 | ||||||
| chr3:136893186
|
A | G | 3 | a0001c0001t0001g0081a0001c0001t0007g0227a0001c0001t0007g0228 | 3 | HG03139.hp1 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-19+30833A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893186 | ||||||
| chr3:136893189
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-19+30836T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893189 | ||||||
| chr3:136893191
|
T | C | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00099.hp1 HG00408.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+30838T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893191 | ||||||
| chr3:136893196
|
A | ACACACAC others(107): Show |
2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+30845_-19+3084 others(118): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893196 | |||||
| chr3:136893196
|
A | ACACACAC others(103): Show |
11 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0044others(8): Show | 11 | HG00621.hp1 HG02135.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+30845_-19+3084 others(114): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893196 | |||||
| chr3:136893196
|
A | ACACACAC others(101): Show |
53 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(50): Show | 53 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.-19+30845_-19+3084 others(112): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893196 | |||||
| chr3:136893196
|
A | ACACACAC others(99): Show |
69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(66): Show | 71 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.-19+30845_-19+3084 others(110): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893196 | |||||
| chr3:136893196
|
A | ACACACAC others(97): Show |
1 | a0003c0003t0001g0021 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-19+30845_-19+3084 others(108): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893196 | |||||
| chr3:136893196
|
A | ACACACAC others(95): Show |
2 | a0001c0001t0001g0013a0001c0001t0001g0032 | 2 | HG02738.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-19+30845_-19+3084 others(106): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893196 | |||||
| chr3:136893196
|
A | ACACACAC others(93): Show |
2 | a0001c0001t0001g0005a0001c0001t0016g0004 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+30845_-19+3084 others(104): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893196 | |||||
| chr3:136893217
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-19+30864G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893217 | ||||||
| chr3:136893307
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+30954T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893307 | ||||||
| chr3:136893354
|
TA | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+31003delA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893354 | |||||
| chr3:136893360
|
G | A | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+31007G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893360 | ||||||
| chr3:136893408
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-19+31055T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893408 | ||||||
| chr3:136893563
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-19+31210G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893563 | ||||||
| chr3:136893919
|
C | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+31566C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893919 | ||||||
| chr3:136893928
|
C | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-19+31575C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893928 | ||||||
| chr3:136894076
|
G | T | 1 | a0001c0001t0001g0125 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-19+31723G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894076 | ||||||
| chr3:136894429
|
C | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-19+32076C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894429 | ||||||
| chr3:136894632
|
T | C | 1 | a0001c0001t0003g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-19+32279T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894632 | ||||||
| chr3:136894642
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-19+32289G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894642 | ||||||
| chr3:136894883
|
T | TG | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+32530_-19+3253 others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894883 | ||||||
| chr3:136894884
|
T | G | 3 | a0001c0001t0002g0153a0001c0001t0007g0227a0001c0001t0007g0228 | 3 | HG03139.hp1 HG03195.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-19+32531T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894884 | ||||||
| chr3:136894944
|
C | T | 7 | a0001c0001t0002g0185a0001c0001t0002g0187a0001c0001t0002g0188others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+32591C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894944 | ||||||
| chr3:136894945
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+32592G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894945 | ||||||
| chr3:136895012
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-19+32659A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136895012 | ||||||
| chr3:136895183
|
T | A | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18-32801T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136895183 | ||||||
| chr3:136895283
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-18-32701A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136895283 | ||||||
| chr3:136895321
|
T | TTA | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-32651_-18-3265 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136895321 | |||||
| chr3:136895397
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-32587C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136895397 | ||||||
| chr3:136895705
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-18-32279C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136895705 | ||||||
| chr3:136895765
|
A | G | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-32219A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136895765 | ||||||
| chr3:136896384
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-31600C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136896384 | ||||||
| chr3:136896426
|
G | A | 69 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.-18-31558G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136896426 | ||||||
| chr3:136896429
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-18-31555A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136896429 | ||||||
| chr3:136896471
|
T | C | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG02129.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-18-31513T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136896471 | ||||||
| chr3:136896602
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-31382A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136896602 | ||||||
| chr3:136896657
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18-31327G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136896657 | ||||||
| chr3:136896797
|
C | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 4 | HG01243.hp2 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-31187C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136896797 | ||||||
| chr3:136897053
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-18-30931A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136897053 | ||||||
| chr3:136897114
|
T | C | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-30870T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136897114 | ||||||
| chr3:136897232
|
G | T | 1 | a0001c0001t0002g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18-30752G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136897232 | ||||||
| chr3:136897738
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-18-30246C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136897738 | ||||||
| chr3:136898120
|
G | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009 | 3 | NA18939.hp2 NA18959.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-18-29864G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136898120 | ||||||
| chr3:136898385
|
C | CA | 20 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(17): Show | 20 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.-18-29580dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136898385 | |||||
| chr3:136898385
|
CA | C | 18 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0046others(15): Show | 20 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18-29580delA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136898385 | |||||
| chr3:136898432
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-29552G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136898432 | ||||||
| chr3:136898461
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | NA18964.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.-18-29523A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136898461 | ||||||
| chr3:136898512
|
A | T | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-29472A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136898512 | ||||||
| chr3:136899023
|
T | G | 1 | a0001c0001t0009g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-18-28961T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899023 | ||||||
| chr3:136899132
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-18-28852G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899132 | ||||||
| chr3:136899156
|
A | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(18): Show | 21 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-28828A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899156 | ||||||
| chr3:136899372
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-28612G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899372 | ||||||
| chr3:136899419
|
C | CT | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.-18-28551dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136899419 | |||||
| chr3:136899433
|
T | A | 1 | a0001c0001t0001g0104 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-18-28551T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899433 | ||||||
| chr3:136899433
|
T | TA | 10 | a0001c0001t0001g0051a0001c0001t0001g0066a0001c0001t0001g0076others(7): Show | 10 | HG00408.hp1 HG00423.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18-28548dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136899433 | |||||
| chr3:136899434
|
A | T | 2 | a0001c0001t0014g0020a0001c0001t0015g0019 | 2 | HG01496.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-18-28550A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899434 | ||||||
| chr3:136899586
|
T | C | 1 | a0001c0001t0001g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-18-28398T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899586 | ||||||
| chr3:136899600
|
C | T | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-28384C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899600 | ||||||
| chr3:136899718
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-18-28266C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899718 | ||||||
| chr3:136899868
|
CT | C | 6 | a0001c0001t0002g0148a0001c0001t0002g0159a0001c0001t0002g0163others(3): Show | 6 | HG00099.hp2 HG01074.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-28106delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136899868 | |||||
| chr3:136899878
|
T | A | 1 | a0001c0001t0002g0179 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-18-28106T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899878 | ||||||
| chr3:136899962
|
A | G | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-28022A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899962 | ||||||
| chr3:136900067
|
G | C | 17 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0046others(14): Show | 19 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-18-27917G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136900067 | ||||||
| chr3:136900724
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-27260A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136900724 | ||||||
| chr3:136901267
|
A | AT | 27 | a0001c0001t0001g0024a0001c0001t0001g0124a0001c0001t0003g0202others(24): Show | 27 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.-18-26704dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136901267 | |||||
| chr3:136901272
|
T | A | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-26712T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136901272 | ||||||
| chr3:136901305
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-18-26679G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136901305 | ||||||
| chr3:136901363
|
C | CT | 5 | a0001c0001t0001g0109a0001c0001t0005g0182a0001c0001t0005g0184others(2): Show | 5 | HG01099.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-26610dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136901363 | |||||
| chr3:136901374
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0016g0004 | 2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-26610T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136901374 | ||||||
| chr3:136901374
|
T | TA | 25 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(22): Show | 25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-26607dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136901374 | |||||
| chr3:136901621
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18-26363A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136901621 | ||||||
| chr3:136901842
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-18-26142C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136901842 | ||||||
| chr3:136901857
|
G | A | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-26127G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136901857 | ||||||
| chr3:136901973
|
T | C | 1 | a0001c0001t0003g0223 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-18-26011T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136901973 | ||||||
| chr3:136902040
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-18-25944C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902040 | ||||||
| chr3:136902113
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-18-25871G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902113 | ||||||
| chr3:136902165
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-25819G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902165 | ||||||
| chr3:136902193
|
T | TTTG | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0024others(3): Show | 6 | HG01358.hp1 HG02572.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-25789_-18-2578 others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136902193 | |||||
| chr3:136902194
|
T | TTTG | 6 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0065others(3): Show | 6 | HG00741.hp2 HG02135.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-25788_-18-2578 others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136902194 | |||||
| chr3:136902197
|
T | G | 35 | a0001c0001t0002g0160a0001c0001t0003g0202a0001c0001t0003g0203others(32): Show | 35 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.-18-25787T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902197 | ||||||
| chr3:136902198
|
T | G | 12 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0024others(9): Show | 12 | HG00741.hp2 HG01358.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18-25786T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902198 | ||||||
| chr3:136902198
|
T | TTTG | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(116): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-18-25784_-18-2578 others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136902198 | |||||
| chr3:136902198
|
T | TTTTG | 6 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(3): Show | 6 | HG00639.hp1 HG02523.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-25783_-18-2578 others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136902198 | |||||
| chr3:136902199
|
T | G | 1 | a0001c0001t0002g0167 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-18-25785T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902199 | ||||||
| chr3:136902203
|
G | T | 2 | a0001c0001t0002g0159a0001c0001t0002g0163 | 2 | HG01261.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-18-25781G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902203 | ||||||
| chr3:136902346
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 174 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.-18-25638T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902346 | ||||||
| chr3:136902483
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-25501T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902483 | ||||||
| chr3:136902496
|
A | G | 17 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0046others(14): Show | 19 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-18-25488A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902496 | ||||||
| chr3:136902596
|
T | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-25388T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902596 | ||||||
| chr3:136902627
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0093 | 2 | HG01167.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-18-25357G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902627 | ||||||
| chr3:136902683
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-18-25301T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902683 | ||||||
| chr3:136902776
|
C | T | 25 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(22): Show | 25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-25208C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902776 | ||||||
| chr3:136902875
|
A | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-25109A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902875 | ||||||
| chr3:136903084
|
C | T | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-24900C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903084 | ||||||
| chr3:136903166
|
C | A | 25 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(22): Show | 25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-24818C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903166 | ||||||
| chr3:136903368
|
G | A | 11 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0205others(8): Show | 11 | HG00544.hp2 HG02135.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-24616G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903368 | ||||||
| chr3:136903400
|
T | A | 4 | a0002c0002t0002g0180a0002c0002t0006g0190a0002c0002t0006g0195others(1): Show | 4 | HG03139.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-24584T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903400 | ||||||
| chr3:136903419
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-18-24565G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903419 | ||||||
| chr3:136903545
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-18-24439T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903545 | ||||||
| chr3:136903624
|
C | T | 7 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0057others(4): Show | 7 | HG01346.hp2 HG01361.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18-24360C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903624 | ||||||
| chr3:136903718
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-18-24266C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903718 | ||||||
| chr3:136903773
|
CAG | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-18-24208_-18-2420 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136903773 | |||||
| chr3:136903835
|
G | C | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-24149G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903835 | ||||||
| chr3:136903842
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-18-24142A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903842 | ||||||
| chr3:136904184
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18-23800G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136904184 | ||||||
| chr3:136904481
|
C | T | 7 | a0001c0001t0002g0185a0001c0001t0002g0187a0001c0001t0002g0188others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18-23503C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136904481 | ||||||
| chr3:136904834
|
A | AT | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(120): Show | 124 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-18-23137dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136904834 | |||||
| chr3:136904834
|
A | ATT | 8 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0057others(5): Show | 8 | HG01346.hp2 HG01361.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-23138_-18-2313 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136904834 | |||||
| chr3:136904900
|
C | G | 1 | a0001c0001t0014g0020 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-18-23084C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136904900 | ||||||
| chr3:136904949
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18-23035C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136904949 | ||||||
| chr3:136905007
|
C | CT | 26 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0086others(23): Show | 27 | HG00280.hp2 HG00544.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18-22960dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136905007 | |||||
| chr3:136905007
|
C | CTT | 5 | a0001c0001t0001g0087a0001c0001t0003g0203a0001c0001t0003g0211others(2): Show | 5 | HG01109.hp2 NA18959.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-22961_-18-2296 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136905007 | |||||
| chr3:136905007
|
CTTTTTTT others(1): Show |
C | 15 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(12): Show | 16 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.-18-22967_-18-2296 others(12): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136905007 | |||||
| chr3:136905183
|
G | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0024 | 3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-22801G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136905183 | ||||||
| chr3:136905202
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18-22782T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136905202 | ||||||
| chr3:136905224
|
G | A | 2 | a0001c0001t0002g0175a0001c0001t0002g0176 | 2 | HG00280.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-18-22760G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136905224 | ||||||
| chr3:136905280
|
C | T | 2 | a0001c0001t0002g0147a0001c0001t0002g0167 | 2 | HG00639.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-18-22704C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136905280 | ||||||
| chr3:136905641
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0016g0004 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18-22343C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136905641 | ||||||
| chr3:136905952
|
C | T | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-18-22032C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136905952 | ||||||
| chr3:136905984
|
AT | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18-21997delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136905984 | |||||
| chr3:136906161
|
A | G | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-21823A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906161 | ||||||
| chr3:136906312
|
G | C | 18 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(15): Show | 18 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18-21672G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906312 | ||||||
| chr3:136906427
|
G | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(16): Show | 20 | HG00280.hp2 HG00738.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18-21557G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906427 | ||||||
| chr3:136906448
|
G | T | 1 | a0001c0001t0002g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18-21536G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906448 | ||||||
| chr3:136906468
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0016g0004 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18-21516G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906468 | ||||||
| chr3:136906497
|
C | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18-21487C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906497 | ||||||
| chr3:136906594
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(128): Show | 132 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-18-21390G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906594 | ||||||
| chr3:136906652
|
G | A | 3 | a0001c0001t0003g0208a0001c0001t0003g0225a0001c0001t0003g0226 | 3 | NA18987.hp1 NA19012.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-18-21332G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906652 | ||||||
| chr3:136906813
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-18-21171G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906813 | ||||||
| chr3:136906831
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-18-21153G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906831 | ||||||
| chr3:136907060
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18-20924C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136907060 | ||||||
| chr3:136907128
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0024 | 3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-20856C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136907128 | ||||||
| chr3:136907320
|
G | A | 3 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140 | 3 | HG03491.hp1 HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-18-20664G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136907320 | ||||||
| chr3:136907373
|
A | G | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-20611A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136907373 | ||||||
| chr3:136907855
|
G | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18-20129G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136907855 | ||||||
| chr3:136907888
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0016g0004 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18-20096G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136907888 | ||||||
| chr3:136907934
|
C | T | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-20050C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136907934 | ||||||
| chr3:136908624
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-18-19360T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136908624 | ||||||
| chr3:136908916
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-19068G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136908916 | ||||||
| chr3:136910178
|
A | G | 3 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140 | 3 | HG03491.hp1 HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-18-17806A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136910178 | ||||||
| chr3:136910344
|
C | T | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-17640C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136910344 | ||||||
| chr3:136910365
|
C | T | 11 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0205others(8): Show | 11 | HG00544.hp2 HG02135.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-17619C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136910365 | ||||||
| chr3:136910427
|
C | T | 11 | a0001c0001t0002g0144a0001c0001t0002g0149a0001c0001t0002g0150others(8): Show | 11 | HG00408.hp2 HG01070.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-17557C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136910427 | ||||||
| chr3:136910482
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-18-17502T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136910482 | ||||||
| chr3:136910648
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(132): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-18-17336G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136910648 | ||||||
| chr3:136910692
|
A | G | 4 | a0001c0001t0003g0203a0001c0001t0003g0211a0001c0001t0003g0213others(1): Show | 4 | NA18959.hp2 NA18973.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-17292A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136910692 | ||||||
| chr3:136911144
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18-16840A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136911144 | ||||||
| chr3:136911288
|
C | A | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-16696C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136911288 | ||||||
| chr3:136911470
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-18-16514T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136911470 | ||||||
| chr3:136912162
|
C | CT | 71 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0024others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.-18-15804dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136912162 | |||||
| chr3:136912162
|
C | CTT | 18 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(15): Show | 19 | HG00280.hp2 HG00738.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-18-15805_-18-1580 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136912162 | |||||
| chr3:136912162
|
C | CTTT | 9 | a0001c0001t0002g0185a0001c0001t0002g0187a0001c0001t0002g0188others(6): Show | 9 | HG02015.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18-15806_-18-1580 others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136912162 | |||||
| chr3:136912162
|
CT | C | 21 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0029others(18): Show | 21 | HG00544.hp1 HG00621.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-15804delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136912162 | |||||
| chr3:136912162
|
CTTTTTTT others(2): Show |
C | 49 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(46): Show | 49 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.-18-15812_-18-1580 others(13): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136912162 | |||||
| chr3:136912187
|
G | A | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-15797G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912187 | ||||||
| chr3:136912188
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-18-15796A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912188 | ||||||
| chr3:136912230
|
T | C | 1 | a0001c0001t0015g0019 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-18-15754T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912230 | ||||||
| chr3:136912360
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18-15624G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912360 | ||||||
| chr3:136912413
|
C | A | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18-15571C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912413 | ||||||
| chr3:136912433
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18-15551C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912433 | ||||||
| chr3:136912492
|
CTT | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(129): Show | 133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-15479_-18-1547 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136912492 | |||||
| chr3:136912763
|
C | G | 1 | a0001c0001t0001g0128 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-18-15221C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912763 | ||||||
| chr3:136912800
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-18-15184C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912800 | ||||||
| chr3:136912864
|
CTGGTCT | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18-15111_-18-1510 others(10): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136912864 | |||||
| chr3:136913280
|
C | T | 3 | a0003c0003t0001g0021a0003c0003t0001g0022a0003c0003t0001g0023 | 3 | HG01070.hp2 HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-18-14704C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136913280 | ||||||
| chr3:136913298
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-18-14686T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136913298 | ||||||
| chr3:136913413
|
T | C | 2 | a0001c0001t0002g0186a0001c0001t0002g0196 | 2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-18-14571T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136913413 | ||||||
| chr3:136913435
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0016g0004 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18-14549A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136913435 | ||||||
| chr3:136913635
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-18-14349G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136913635 | ||||||
| chr3:136913695
|
A | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-18-14289A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136913695 | ||||||
| chr3:136913911
|
T | TC | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-14073_-18-1407 others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136913911 | ||||||
| chr3:136914094
|
C | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(129): Show | 133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-13890C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136914094 | ||||||
| chr3:136914165
|
T | C | 1 | a0001c0001t0002g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-18-13819T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136914165 | ||||||
| chr3:136914245
|
G | T | 1 | a0001c0001t0001g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18-13739G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136914245 | ||||||
| chr3:136914488
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-18-13496C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136914488 | ||||||
| chr3:136914729
|
A | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18-13255A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136914729 | ||||||
| chr3:136914752
|
C | T | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-13232C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136914752 | ||||||
| chr3:136915151
|
C | T | 1 | a0001c0001t0002g0189 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-18-12833C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136915151 | ||||||
| chr3:136915197
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG02129.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-18-12787C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136915197 | ||||||
| chr3:136915198
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18-12786A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136915198 | ||||||
| chr3:136915604
|
T | A | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18-12380T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136915604 | ||||||
| chr3:136915704
|
T | C | 17 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(14): Show | 18 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18-12280T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136915704 | ||||||
| chr3:136915730
|
G | T | 1 | a0001c0001t0002g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18-12254G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136915730 | ||||||
| chr3:136915959
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-18-12025C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136915959 | ||||||
| chr3:136916179
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18-11805G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136916179 | ||||||
| chr3:136916329
|
A | G | 50 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18-11655A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136916329 | ||||||
| chr3:136916451
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-18-11533T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136916451 | ||||||
| chr3:136916553
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-18-11431A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136916553 | ||||||
| chr3:136916587
|
T | C | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-11397T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136916587 | ||||||
| chr3:136916747
|
C | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(129): Show | 133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-11237C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136916747 | ||||||
| chr3:136916747
|
CAGTT | C | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-18-11236_-18-1123 others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136916747 | ||||||
| chr3:136917232
|
C | CT | 92 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(89): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.-18-10737dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136917232 | |||||
| chr3:136917232
|
C | CTT | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(123): Show | 127 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-18-10738_-18-1073 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136917232 | |||||
| chr3:136917232
|
C | CTTT | 11 | a0001c0001t0001g0033a0001c0001t0001g0056a0001c0001t0001g0063others(8): Show | 11 | HG00609.hp1 HG00609.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18-10739_-18-1073 others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136917232 | |||||
| chr3:136917520
|
C | T | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-10464C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136917520 | ||||||
| chr3:136917741
|
C | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(27): Show | 31 | HG00280.hp2 HG00544.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-18-10243C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136917741 | ||||||
| chr3:136917792
|
C | T | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-10192C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136917792 | ||||||
| chr3:136917843
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(9): Show | 13 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.-18-10141T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136917843 | ||||||
| chr3:136917970
|
G | C | 2 | a0001c0001t0001g0084a0001c0001t0012g0085 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-18-10014G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136917970 | ||||||
| chr3:136918342
|
G | GA | 30 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(27): Show | 31 | HG00280.hp2 HG00544.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-18-9633dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136918342 | |||||
| chr3:136918882
|
A | T | 1 | a0001c0001t0012g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-18-9102A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136918882 | ||||||
| chr3:136919011
|
A | G | 2 | a0001c0001t0002g0175a0001c0001t0002g0176 | 2 | HG00280.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-18-8973A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136919011 | ||||||
| chr3:136919920
|
T | C | 1 | a0001c0001t0005g0184 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-18-8064T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136919920 | ||||||
| chr3:136920133
|
A | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0046others(19): Show | 24 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-18-7851A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920133 | ||||||
| chr3:136920234
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-18-7750T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920234 | ||||||
| chr3:136920257
|
A | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(136): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-18-7727A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920257 | ||||||
| chr3:136920333
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-7651A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920333 | ||||||
| chr3:136920395
|
T | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-18-7589T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920395 | ||||||
| chr3:136920459
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0024 | 3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-7525G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920459 | ||||||
| chr3:136920607
|
C | A | 1 | a0001c0001t0001g0120 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-18-7377C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920607 | ||||||
| chr3:136920652
|
C | G | 1 | a0001c0001t0005g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18-7332C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920652 | ||||||
| chr3:136920673
|
A | G | 25 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(22): Show | 25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-7311A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920673 | ||||||
| chr3:136920962
|
A | G | 1 | a0001c0001t0003g0220 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-18-7022A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920962 | ||||||
| chr3:136921329
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0016g0004 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18-6655C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136921329 | ||||||
| chr3:136921468
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-6516A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136921468 | ||||||
| chr3:136921849
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-18-6135T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136921849 | ||||||
| chr3:136921991
|
G | T | 1 | a0001c0001t0002g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18-5993G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136921991 | ||||||
| chr3:136922003
|
T | A | 1 | a0001c0001t0001g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-18-5981T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136922003 | ||||||
| chr3:136922234
|
C | T | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-5750C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136922234 | ||||||
| chr3:136922358
|
G | C | 1 | a0001c0001t0002g0154 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-18-5626G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136922358 | ||||||
| chr3:136922388
|
G | A | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-5596G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136922388 | ||||||
| chr3:136922604
|
A | C | 1 | a0001c0001t0001g0061 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-18-5380A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136922604 | ||||||
| chr3:136922808
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-18-5176G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136922808 | ||||||
| chr3:136923071
|
A | G | 1 | a0001c0001t0003g0205 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-18-4913A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136923071 | ||||||
| chr3:136923105
|
A | ATG | 19 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0046others(16): Show | 21 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18-4864_-18-4863d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923105 | |||||
| chr3:136923228
|
T | A | 1 | a0002c0002t0002g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-18-4756T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136923228 | ||||||
| chr3:136923269
|
G | C | 1 | a0001c0001t0001g0044 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-18-4715G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136923269 | ||||||
| chr3:136923316
|
G | GA | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-18-4667dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923316 | |||||
| chr3:136923330
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0012g0085 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-18-4654C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136923330 | ||||||
| chr3:136923555
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-18-4429G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136923555 | ||||||
| chr3:136923559
|
C | CAAAT | 13 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0080others(10): Show | 13 | HG00140.hp2 HG01099.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18-4392_-18-4389d others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923559 | |||||
| chr3:136923559
|
C | CAAATAAA others(1): Show |
22 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0002g0138others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.-18-4396_-18-4389d others(10): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923559 | |||||
| chr3:136923559
|
C | CAAATAAA others(5): Show |
51 | a0001c0001t0002g0139a0001c0001t0002g0141a0001c0001t0002g0143others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-18-4400_-18-4389d others(14): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923559 | |||||
| chr3:136923559
|
C | CAAATAAA others(9): Show |
17 | a0001c0001t0002g0178a0001c0001t0002g0186a0001c0001t0002g0187others(14): Show | 17 | HG01167.hp1 HG01169.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.-18-4404_-18-4389d others(18): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923559 | |||||
| chr3:136923559
|
C | CAAATAAA others(13): Show |
1 | a0001c0001t0005g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18-4408_-18-4389d others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923559 | |||||
| chr3:136923559
|
C | CAAATAAA others(17): Show |
1 | a0001c0001t0002g0185 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-18-4412_-18-4389d others(26): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923559 | |||||
| chr3:136923571
|
TA | T | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0132 | 3 | HG01433.hp1 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-18-4410delA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923571 | |||||
| chr3:136923881
|
ACT | A | 2 | a0001c0001t0002g0138a0001c0001t0002g0140 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-18-4100_-18-4099d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923881 | |||||
| chr3:136923981
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-4003C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136923981 | ||||||
| chr3:136924160
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0068 | 2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-18-3824A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136924160 | ||||||
| chr3:136924203
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-18-3781A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136924203 | ||||||
| chr3:136924239
|
G | A | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-3745G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136924239 | ||||||
| chr3:136924434
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18-3550A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136924434 | ||||||
| chr3:136924729
|
T | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-18-3255T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136924729 | ||||||
| chr3:136924791
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18-3193C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136924791 | ||||||
| chr3:136924892
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-18-3092A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136924892 | ||||||
| chr3:136925017
|
C | T | 1 | a0001c0001t0002g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-18-2967C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136925017 | ||||||
| chr3:136925335
|
T | A | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-2649T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136925335 | ||||||
| chr3:136925436
|
A | G | 25 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(22): Show | 25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-2548A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136925436 | ||||||
| chr3:136925535
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-18-2449C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136925535 | ||||||
| chr3:136925558
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-18-2426C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136925558 | ||||||
| chr3:136925693
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-18-2291A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136925693 | ||||||
| chr3:136926045
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-1939G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926045 | ||||||
| chr3:136926240
|
C | G | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-18-1744C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926240 | ||||||
| chr3:136926369
|
G | T | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-18-1615G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926369 | ||||||
| chr3:136926401
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-18-1583A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926401 | ||||||
| chr3:136926462
|
A | G | 1 | a0001c0001t0002g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18-1522A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926462 | ||||||
| chr3:136926571
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-1413G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926571 | ||||||
| chr3:136926575
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-1409A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926575 | ||||||
| chr3:136926967
|
G | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-1017G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926967 | ||||||
| chr3:136926985
|
T | G | 9 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0111others(6): Show | 9 | HG00621.hp1 HG02135.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18-999T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926985 | ||||||
| chr3:136927117
|
G | A | 1 | a0001c0001t0009g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-18-867G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927117 | ||||||
| chr3:136927226
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-758C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927226 | ||||||
| chr3:136927320
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0024 | 3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-664C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927320 | ||||||
| chr3:136927358
|
C | T | 1 | a0001c0001t0010g0113 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-18-626C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927358 | ||||||
| chr3:136927434
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-18-550C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927434 | ||||||
| chr3:136927545
|
C | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-439C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927545 | ||||||
| chr3:136927797
|
G | A | 1 | a0001c0001t0002g0159 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-18-187G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927797 | ||||||
| chr3:136927894
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-18-90T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927894 | ||||||
| chr3:136927963
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-18-21A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927963 | ||||||
| chr3:136928316
|
T | C | 1 | a0001c0001t0014g0020 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.226+89T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928316 | ||||||
| chr3:136928404
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+177A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928404 | ||||||
| chr3:136928639
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.226+412G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928639 | ||||||
| chr3:136928787
|
G | GGCCCTAA others(1): Show |
6 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(3): Show | 6 | HG00140.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+561_226+562ins others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136928787 | |||||
| chr3:136928789
|
A | G | 6 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(3): Show | 6 | HG00140.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+562A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928789 | ||||||
| chr3:136928790
|
G | A | 6 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(3): Show | 6 | HG00140.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+563G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928790 | ||||||
| chr3:136928795
|
C | A | 6 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(3): Show | 6 | HG00140.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+568C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928795 | ||||||
| chr3:136928796
|
T | G | 6 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(3): Show | 6 | HG00140.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+569T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928796 | ||||||
| chr3:136928807
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.226+580C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928807 | ||||||
| chr3:136928858
|
C | CT | 6 | a0001c0001t0002g0141a0001c0001t0002g0188a0001c0001t0002g0189others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+634dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136928858 | |||||
| chr3:136928861
|
T | TA | 11 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0054others(8): Show | 11 | HG00423.hp1 HG01358.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.226+658dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136928861 | |||||
| chr3:136928861
|
TA | T | 15 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0026others(12): Show | 15 | HG00140.hp2 HG01074.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.226+658delA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136928861 | |||||
| chr3:136928943
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.226+716G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928943 | ||||||
| chr3:136928965
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+738C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928965 | ||||||
| chr3:136929062
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+835T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136929062 | ||||||
| chr3:136929063
|
G | A | 1 | a0001c0001t0003g0202 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.226+836G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136929063 | ||||||
| chr3:136929765
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+1538T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136929765 | ||||||
| chr3:136929801
|
T | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.226+1574T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136929801 | ||||||
| chr3:136929851
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+1624G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136929851 | ||||||
| chr3:136930015
|
C | G | 1 | a0001c0001t0001g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.226+1788C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136930015 | ||||||
| chr3:136930216
|
T | TGAAAGTT others(6103): Show |
1 | a0001c0001t0002g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.226+2004_226+2005i others(6112): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136930216 | |||||
| chr3:136930231
|
A | G | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.226+2004A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136930231 | ||||||
| chr3:136930621
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.226+2394C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136930621 | ||||||
| chr3:136930768
|
C | T | 11 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0205others(8): Show | 11 | HG00544.hp2 HG02135.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.226+2541C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136930768 | ||||||
| chr3:136930812
|
A | G | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.226+2585A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136930812 | ||||||
| chr3:136930980
|
CT | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.226+2765delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136930980 | |||||
| chr3:136931004
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.226+2777G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136931004 | ||||||
| chr3:136931017
|
T | A | 1 | a0001c0001t0001g0013 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.226+2790T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136931017 | ||||||
| chr3:136931022
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.226+2795G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136931022 | ||||||
| chr3:136931394
|
A | G | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.226+3167A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136931394 | ||||||
| chr3:136931568
|
AT | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+3346delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136931568 | |||||
| chr3:136931858
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.226+3631G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136931858 | ||||||
| chr3:136931929
|
G | C | 1 | a0001c0001t0001g0054 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.226+3702G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136931929 | ||||||
| chr3:136932085
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.226+3858T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932085 | ||||||
| chr3:136932118
|
C | CA | 13 | a0001c0001t0001g0026a0001c0001t0001g0128a0001c0001t0003g0203others(10): Show | 13 | HG00544.hp2 HG02135.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.226+3910dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136932118 | |||||
| chr3:136932118
|
CA | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0024others(8): Show | 11 | HG00408.hp2 HG01256.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.226+3910delA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136932118 | |||||
| chr3:136932133
|
A | AG | 13 | a0001c0001t0003g0202a0001c0001t0003g0206a0001c0001t0003g0207others(10): Show | 13 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.226+3906_226+3907i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932133 | ||||||
| chr3:136932133
|
A | G | 1 | a0001c0001t0003g0220 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.226+3906A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932133 | ||||||
| chr3:136932311
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.226+4084A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932311 | ||||||
| chr3:136932597
|
C | G | 6 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162others(3): Show | 6 | HG00423.hp1 NA18963.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+4370C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932597 | ||||||
| chr3:136932675
|
G | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+4448G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932675 | ||||||
| chr3:136932757
|
T | G | 1 | a0001c0001t0014g0020 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.226+4530T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932757 | ||||||
| chr3:136932780
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.226+4553C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932780 | ||||||
| chr3:136932827
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.226+4600A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932827 | ||||||
| chr3:136933122
|
A | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.226+4895A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136933122 | ||||||
| chr3:136933292
|
A | G | 25 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(22): Show | 25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.226+5065A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136933292 | ||||||
| chr3:136933355
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0012g0085 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.226+5128C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136933355 | ||||||
| chr3:136933710
|
CT | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.226+5494delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136933710 | |||||
| chr3:136934039
|
T | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+5812T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136934039 | ||||||
| chr3:136934615
|
A | G | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.226+6388A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136934615 | ||||||
| chr3:136934829
|
A | T | 1 | a0001c0001t0001g0012 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.226+6602A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136934829 | ||||||
| chr3:136934841
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.226+6614G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136934841 | ||||||
| chr3:136935086
|
C | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+6859C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136935086 | ||||||
| chr3:136935225
|
A | G | 1 | a0001c0001t0005g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.226+6998A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136935225 | ||||||
| chr3:136935842
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+7615C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136935842 | ||||||
| chr3:136936004
|
A | C | 1 | a0001c0001t0001g0009 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.226+7777A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936004 | ||||||
| chr3:136936038
|
CT | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(106): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.226+7829delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136936038 | |||||
| chr3:136936038
|
CTT | C | 25 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0028others(22): Show | 25 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.226+7828_226+7829d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136936038 | |||||
| chr3:136936102
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0070 | 3 | HG02523.hp2 NA18971.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.226+7875G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936102 | ||||||
| chr3:136936110
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+7883A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936110 | ||||||
| chr3:136936304
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG02129.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.226+8077G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936304 | ||||||
| chr3:136936443
|
C | T | 5 | a0001c0001t0005g0182a0001c0001t0005g0183a0001c0001t0005g0184others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+8216C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936443 | ||||||
| chr3:136936471
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.226+8244T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936471 | ||||||
| chr3:136936570
|
A | G | 1 | a0001c0001t0003g0207 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.226+8343A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936570 | ||||||
| chr3:136936774
|
C | T | 4 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0018others(1): Show | 4 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+8547C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936774 | ||||||
| chr3:136936830
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+8603T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936830 | ||||||
| chr3:136936899
|
A | G | 3 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140 | 3 | HG03491.hp1 HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.226+8672A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936899 | ||||||
| chr3:136937088
|
G | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0069 | 3 | HG03239.hp1 HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.227-8495G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937088 | ||||||
| chr3:136937092
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.227-8491T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937092 | ||||||
| chr3:136937122
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0002g0152 | 2 | HG02135.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.227-8461C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937122 | ||||||
| chr3:136937187
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.227-8396A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937187 | ||||||
| chr3:136937300
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | NA18964.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.227-8283C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937300 | ||||||
| chr3:136937571
|
C | T | 5 | a0001c0001t0005g0182a0001c0001t0005g0183a0001c0001t0005g0184others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.227-8012C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937571 | ||||||
| chr3:136937751
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0046others(12): Show | 17 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.227-7832C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937751 | ||||||
| chr3:136937894
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.227-7689C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937894 | ||||||
| chr3:136937952
|
AG | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.227-7629delG | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136937952 | |||||
| chr3:136938110
|
T | A | 1 | a0001c0001t0002g0143 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.227-7473T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136938110 | ||||||
| chr3:136938428
|
TCTGATGT others(3): Show |
T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.227-7153_227-7144d others(12): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136938428 | |||||
| chr3:136938439
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.227-7144C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136938439 | ||||||
| chr3:136938517
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(1): Show | 4 | HG00099.hp1 HG01256.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-7066T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136938517 | ||||||
| chr3:136938521
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.227-7062A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136938521 | ||||||
| chr3:136938578
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.227-7005A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136938578 | ||||||
| chr3:136938765
|
A | C | 1 | a0001c0001t0001g0075 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.227-6818A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136938765 | ||||||
| chr3:136939701
|
C | T | 1 | a0001c0001t0003g0207 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.227-5882C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136939701 | ||||||
| chr3:136939839
|
C | CT | 52 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(49): Show | 52 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.227-5721dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136939839 | |||||
| chr3:136939839
|
C | CTT | 7 | a0001c0001t0002g0148a0001c0001t0002g0163a0001c0001t0002g0168others(4): Show | 7 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.227-5722_227-5721d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136939839 | |||||
| chr3:136939846
|
T | G | 3 | a0001c0001t0001g0065a0001c0001t0001g0099a0001c0001t0001g0103 | 3 | HG02451.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.227-5737T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136939846 | ||||||
| chr3:136939858
|
TTTTTA | T | 5 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0112others(2): Show | 5 | HG02615.hp1 HG02897.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.227-5724_227-5720d others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136939858 | ||||||
| chr3:136939859
|
TTTTA | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.227-5723_227-5720d others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136939859 | ||||||
| chr3:136939860
|
TTTA | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0038others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.227-5722_227-5720d others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136939860 | ||||||
| chr3:136939863
|
A | T | 90 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.227-5720A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136939863 | ||||||
| chr3:136939925
|
A | G | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.227-5658A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136939925 | ||||||
| chr3:136940074
|
G | C | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-5509G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940074 | ||||||
| chr3:136940126
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | NA18939.hp2 NA18955.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-5457G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940126 | ||||||
| chr3:136940270
|
T | G | 1 | a0001c0001t0001g0054 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.227-5313T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940270 | ||||||
| chr3:136940320
|
A | G | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-5263A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940320 | ||||||
| chr3:136940499
|
C | G | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.227-5084C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940499 | ||||||
| chr3:136940810
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.227-4773G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940810 | ||||||
| chr3:136940882
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.227-4701C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940882 | ||||||
| chr3:136940937
|
G | T | 38 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0143others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.227-4646G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940937 | ||||||
| chr3:136940999
|
A | G | 14 | a0001c0001t0003g0202a0001c0001t0003g0206a0001c0001t0003g0207others(11): Show | 14 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.227-4584A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940999 | ||||||
| chr3:136941116
|
CT | C | 59 | a0001c0001t0001g0046a0001c0001t0001g0066a0001c0001t0002g0138others(56): Show | 59 | HG00140.hp1 HG00544.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.227-4449delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136941116 | |||||
| chr3:136941116
|
CTT | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.227-4450_227-4449d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136941116 | |||||
| chr3:136941318
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.227-4265C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136941318 | ||||||
| chr3:136941381
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.227-4202T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136941381 | ||||||
| chr3:136941623
|
C | A | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-3960C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136941623 | ||||||
| chr3:136941713
|
C | CA | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.227-3861dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136941713 | |||||
| chr3:136941943
|
A | G | 1 | a0001c0001t0009g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.227-3640A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136941943 | ||||||
| chr3:136942088
|
G | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.227-3495G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136942088 | ||||||
| chr3:136942237
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.227-3346G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136942237 | ||||||
| chr3:136942505
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.227-3078A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136942505 | ||||||
| chr3:136942741
|
T | A | 1 | a0001c0001t0002g0164 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.227-2842T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136942741 | ||||||
| chr3:136942901
|
A | C | 1 | a0001c0001t0002g0143 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.227-2682A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136942901 | ||||||
| chr3:136942955
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.227-2628C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136942955 | ||||||
| chr3:136943220
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.227-2363G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136943220 | ||||||
| chr3:136943298
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.227-2285T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136943298 | ||||||
| chr3:136943492
|
G | GAACCTTC others(8): Show |
1 | a0004c0005t0008g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.227-2088_227-2074d others(17): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136943492 | |||||
| chr3:136943687
|
C | T | 25 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(22): Show | 25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.227-1896C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136943687 | ||||||
| chr3:136943761
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.227-1822G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136943761 | ||||||
| chr3:136943766
|
C | A | 1 | a0004c0005t0008g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.227-1817C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136943766 | ||||||
| chr3:136943767
|
A | C | 1 | a0004c0005t0008g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.227-1816A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136943767 | ||||||
| chr3:136944015
|
A | T | 1 | a0004c0005t0008g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.227-1568A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944015 | ||||||
| chr3:136944110
|
AC | A | 34 | a0001c0001t0001g0046a0001c0001t0002g0144a0001c0001t0002g0147others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.227-1471delC | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136944110 | |||||
| chr3:136944111
|
C | CT | 6 | a0001c0001t0002g0170a0001c0001t0002g0193a0001c0001t0002g0230others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944111
|
C | CTTTTTT | 5 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0063others(2): Show | 6 | HG01074.hp1 HG01346.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944111
|
C | CTTTTTTT | 12 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(9): Show | 13 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(9): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944111
|
C | CTTTTTTT others(1): Show |
7 | a0001c0001t0001g0039a0001c0001t0001g0065a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp2 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(10): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944111
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0068others(3): Show | 6 | HG01109.hp1 HG01891.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(11): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944111
|
C | CTTTTTTT others(3): Show |
10 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0082others(7): Show | 10 | HG00609.hp2 HG00738.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(12): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944111
|
C | CTTTTTTT others(4): Show |
11 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0031others(8): Show | 11 | HG00544.hp1 HG01261.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(13): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944111
|
C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(5): Show | 8 | HG00621.hp2 HG01167.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(14): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944111
|
CCT | C | 17 | a0001c0001t0001g0093a0001c0001t0003g0203a0001c0001t0003g0206others(14): Show | 17 | HG00738.hp2 HG01106.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.227-1471_227-1470d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944111
|
CCTT | C | 6 | a0001c0001t0003g0209a0001c0001t0003g0212a0001c0001t0003g0217others(3): Show | 6 | HG01243.hp1 HG02897.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-1471_227-1469d others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944111
|
CCTTT | C | 8 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0066others(5): Show | 8 | HG00408.hp1 HG00741.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.227-1471_227-1468d others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944111
|
CCTTTT | C | 59 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 59 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.227-1471_227-1467d others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944111
|
CCTTTTT | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0071a0001c0001t0001g0089 | 3 | HG01169.hp1 NA19060.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.227-1471_227-1466d others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944111
|
CCTTTTTT others(7): Show |
C | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-1471_227-1458d others(16): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944111
|
CCTTTTTT others(8): Show |
C | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.227-1471_227-1457d others(17): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | ||||||
| chr3:136944112
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 100 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.227-1471C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944112 | ||||||
| chr3:136944199
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.227-1384A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944199 | ||||||
| chr3:136944428
|
A | G | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-1155A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944428 | ||||||
| chr3:136944448
|
G | A | 1 | a0001c0001t0015g0019 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.227-1135G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944448 | ||||||
| chr3:136944457
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0068 | 2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.227-1126A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944457 | ||||||
| chr3:136944561
|
A | T | 1 | a0004c0005t0008g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.227-1022A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944561 | ||||||
| chr3:136944642
|
A | T | 1 | a0004c0005t0008g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.227-941A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944642 | ||||||
| chr3:136944793
|
C | T | 17 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0028others(14): Show | 17 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.227-790C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944793 | ||||||
| chr3:136945054
|
G | T | 1 | a0001c0001t0002g0179 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.227-529G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136945054 | ||||||
| chr3:136945055
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.227-528C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136945055 | ||||||
| chr3:136945216
|
G | A | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.227-367G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136945216 | ||||||
| chr3:136945285
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.227-298A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136945285 | ||||||
| chr3:136945313
|
T | G | 1 | a0001c0001t0001g0073 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.227-270T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136945313 | ||||||
| chr3:136945561
|
T | C | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-22T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136945561 | ||||||
| chr3:136946349
|
A | G | 1 | a0001c0001t0009g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.939+54A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136946349 | ||||||
| chr3:136946436
|
A | G | 2 | a0001c0001t0003g0204a0001c0001t0003g0224 | 2 | HG00544.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.939+141A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136946436 | ||||||
| chr3:136946666
|
TTGGATGC others(9): Show |
T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.939+372_939+387del others(16): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136946666 | ||||||
| chr3:136946684
|
A | G | 1 | a0004c0005t0008g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.939+389A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136946684 | ||||||
| chr3:136946711
|
T | C | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.939+416T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136946711 | ||||||
| chr3:136946799
|
A | T | 1 | a0001c0001t0002g0186 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.939+504A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136946799 | ||||||
| chr3:136946981
|
C | CT | 19 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0028others(16): Show | 19 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.939+689dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 136946981 | |||||
| chr3:136947055
|
G | A | 1 | a0001c0001t0014g0020 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.939+760G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947055 | ||||||
| chr3:136947153
|
G | C | 1 | a0001c0001t0001g0044 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.939+858G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947153 | ||||||
| chr3:136947204
|
T | G | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.939+909T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947204 | ||||||
| chr3:136947467
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0132 | 3 | HG01433.hp1 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.940-792G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947467 | ||||||
| chr3:136947525
|
T | G | 1 | a0004c0005t0008g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.940-734T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947525 | ||||||
| chr3:136947527
|
G | T | 1 | a0004c0005t0008g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.940-732G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947527 | ||||||
| chr3:136947528
|
C | G | 1 | a0004c0005t0008g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.940-731C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947528 | ||||||
| chr3:136947612
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.940-647C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947612 | ||||||
| chr3:136947757
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.940-502A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947757 | ||||||
| chr3:136948042
|
G | A | 2 | a0001c0001t0003g0204a0001c0001t0003g0224 | 2 | HG00544.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.940-217G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136948042 | ||||||
| chr3:136948194
|
A | C | 1 | a0002c0002t0002g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.940-65A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136948194 |