Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 3071 |
|---|---|
| ensemblid | ENSG00000123338.13 |
| hgncid | 4862 |
| symbol | NCKAP1L |
| name | NCK associated protein 1 like |
| refseq_nuc | NM_005337.5 |
| refseq_prot | NP_005328.2 |
| ensembl_nuc | ENST00000293373.11 |
| ensembl_prot | ENSP00000293373.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 54497752 |
| end | 54548243 |
| strand | + |
| ver | v1.2 |
| region | chr12:54497752-54548243 |
| region5000 | chr12:54492752-54553243 |
| regionname0 | NCKAP1L_chr12_54497752_54548243 |
| regionname5000 | NCKAP1L_chr12_54492752_54553243 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1127 | 312 | 91 | 61 | 116 | 13 | 29 | 95 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0002 | 0/0 | 1127 | 29 | 6 | 6 | 13 | 0 | 4 | 9 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0003 | 0/0 | 1127 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0004 | 0/0 | 1127 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0005 | 0/0 | 1127 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0006 | 0/0 | 1127 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0007 | 0/0 | 1127 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0008 | 0/0 | 1127 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0009 | 0/0 | 1127 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0010 | 0/0 | 1127 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0011 | 0/0 | 1127 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3384 | 240 | 68 | 44 | 92 | 10 | 25 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0002 | 1/0 | 3384 | 53 | 20 | 12 | 13 | 3 | 4 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0003 | 0/0 | 3384 | 28 | 6 | 5 | 13 | 0 | 4 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0004 | 0/0 | 3384 | 14 | 0 | 4 | 10 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0005 | 0/0 | 3384 | 2 | 0 | 1 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0006 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0007 | 0/0 | 3384 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0008 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0009 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0010 | 0/0 | 3384 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0011 | 0/0 | 3384 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0012 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0013 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0014 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0015 | 0/0 | 3384 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0016 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0017 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| c0018 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 5604 | 77 | 11 | 21 | 18 | 9 | 17 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0002 | 0/0 | 5599 | 40 | 0 | 8 | 27 | 0 | 5 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0003 | 0/0 | 5606 | 28 | 2 | 2 | 21 | 0 | 3 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0004 | 0/0 | 5600 | 25 | 13 | 5 | 1 | 3 | 3 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0005 | 1/0 | 5597 | 25 | 15 | 6 | 2 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0006 | 0/0 | 5602 | 12 | 10 | 0 | 2 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0007 | 0/0 | 5600 | 11 | 1 | 0 | 10 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0008 | 0/0 | 5600 | 9 | 0 | 4 | 5 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0009 | 0/0 | 5600 | 6 | 0 | 1 | 5 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0010 | 0/0 | 5600 | 6 | 0 | 0 | 6 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0011 | 0/0 | 5600 | 6 | 0 | 1 | 5 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0012 | 0/0 | 5598 | 5 | 5 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0013 | 0/0 | 5603 | 5 | 0 | 2 | 3 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0014 | 0/0 | 5602 | 5 | 5 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0015 | 0/0 | 5603 | 4 | 4 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0016 | 0/0 | 5608 | 4 | 2 | 1 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0017 | 0/0 | 5599 | 4 | 2 | 1 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0018 | 0/0 | 5603 | 4 | 0 | 1 | 3 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0019 | 0/0 | 5605 | 3 | 1 | 0 | 2 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0020 | 0/0 | 5604 | 3 | 0 | 0 | 3 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0021 | 0/0 | 5599 | 3 | 2 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0022 | 0/0 | 5595 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0023 | 0/0 | 5607 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0024 | 0/0 | 5601 | 2 | 1 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0025 | 0/0 | 5604 | 2 | 1 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0026 | 0/0 | 5596 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0027 | 0/0 | 5602 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0028 | 0/0 | 5604 | 2 | 0 | 2 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0029 | 0/0 | 5603 | 2 | 0 | 1 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0030 | 0/0 | 5599 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0031 | 0/0 | 5595 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0032 | 0/0 | 5597 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0033 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0034 | 0/0 | 5597 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0035 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0036 | 0/0 | 5604 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0037 | 0/0 | 5604 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0038 | 0/0 | 5606 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0039 | 0/0 | 5600 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0040 | 0/0 | 5597 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0041 | 0/0 | 5601 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0042 | 0/0 | 5602 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0043 | 0/0 | 5606 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0044 | 0/0 | 5607 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0045 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0046 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0047 | 0/0 | 5603 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0048 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0049 | 0/0 | 5609 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0050 | 0/0 | 5603 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0051 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0052 | 0/0 | 5596 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0053 | 0/0 | 5605 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0054 | 0/0 | 5610 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0055 | 0/0 | 5609 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0056 | 0/0 | 5597 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0057 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0058 | 0/0 | 5605 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0059 | 0/0 | 5603 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0060 | 0/0 | 5602 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0061 | 0/0 | 5608 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0062 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0063 | 0/0 | 5608 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0064 | 0/0 | 5610 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0065 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0066 | 0/0 | 5604 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0067 | 0/0 | 5599 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0068 | 0/0 | 5599 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0069 | 0/0 | 5597 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0070 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0071 | 0/0 | 5601 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0072 | 0/0 | 5599 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0073 | 0/0 | 5598 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0074 | 0/0 | 5602 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| t0075 | 0/0 | 5604 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0254 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0266 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3384 | 240 | 68 | 44 | 92 | 10 | 25 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002 | 1/0 | 3384 | 53 | 20 | 12 | 13 | 3 | 4 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0004 | 0/0 | 3384 | 14 | 0 | 4 | 10 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0005 | 0/0 | 3384 | 2 | 0 | 1 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0009 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0012 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0014 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0002c0003 | 0/0 | 3384 | 28 | 6 | 5 | 13 | 0 | 4 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0002c0011 | 0/0 | 3384 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0003c0007 | 0/0 | 3384 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0004c0008 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0005c0016 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0006c0015 | 0/0 | 3384 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0007c0010 | 0/0 | 3384 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0008c0013 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0009c0017 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0010c0018 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0011c0006 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 8987 | 61 | 8 | 16 | 15 | 7 | 14 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0002 | 0/0 | 8982 | 19 | 0 | 5 | 12 | 0 | 2 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0003 | 0/0 | 8989 | 22 | 2 | 2 | 15 | 0 | 3 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0004 | 0/0 | 8983 | 18 | 10 | 4 | 0 | 2 | 2 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0005 | 0/0 | 8980 | 12 | 7 | 5 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0006 | 0/0 | 8985 | 12 | 10 | 0 | 2 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0007 | 0/0 | 8983 | 9 | 0 | 0 | 9 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0008 | 0/0 | 8983 | 6 | 0 | 3 | 3 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0009 | 0/0 | 8983 | 5 | 0 | 0 | 5 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0010 | 0/0 | 8983 | 6 | 0 | 0 | 6 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0011 | 0/0 | 8983 | 4 | 0 | 0 | 4 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0012 | 0/0 | 8981 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0014 | 0/0 | 8985 | 3 | 3 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0015 | 0/0 | 8986 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0016 | 0/0 | 8991 | 4 | 2 | 1 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0017 | 0/0 | 8982 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0018 | 0/0 | 8986 | 4 | 0 | 1 | 3 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0019 | 0/0 | 8988 | 3 | 1 | 0 | 2 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0020 | 0/0 | 8987 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0021 | 0/0 | 8982 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0023 | 0/0 | 8990 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0024 | 0/0 | 8984 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0025 | 0/0 | 8987 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0026 | 0/0 | 8979 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0027 | 0/0 | 8985 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0028 | 0/0 | 8987 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0029 | 0/0 | 8986 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0030 | 0/0 | 8982 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0031 | 0/0 | 8978 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0033 | 0/0 | 8987 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0035 | 0/0 | 8987 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0036 | 0/0 | 8987 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0037 | 0/0 | 8987 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0038 | 0/0 | 8989 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0039 | 0/0 | 8983 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0042 | 0/0 | 8985 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0044 | 0/0 | 8990 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0045 | 0/0 | 8987 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0046 | 0/0 | 8984 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0047 | 0/0 | 8986 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0049 | 0/0 | 8992 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0050 | 0/0 | 8986 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0051 | 0/0 | 8983 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0052 | 0/0 | 8979 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0054 | 0/0 | 8993 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0055 | 0/0 | 8992 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0056 | 0/0 | 8980 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0057 | 0/0 | 8984 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0058 | 0/0 | 8988 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0059 | 0/0 | 8986 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0060 | 0/0 | 8985 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0061 | 0/0 | 8991 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0065 | 0/0 | 8987 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0066 | 0/0 | 8987 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0067 | 0/0 | 8982 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0068 | 0/0 | 8982 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0069 | 0/0 | 8980 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0070 | 0/0 | 8978 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0071 | 0/0 | 8984 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0072 | 0/0 | 8982 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0001t0074 | 0/0 | 8985 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0001 | 0/0 | 8987 | 11 | 1 | 5 | 0 | 2 | 3 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0002 | 0/0 | 8982 | 3 | 0 | 0 | 3 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0003 | 0/0 | 8989 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0004 | 0/0 | 8983 | 4 | 1 | 1 | 1 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0005 | 1/0 | 8980 | 8 | 6 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0007 | 0/0 | 8983 | 2 | 1 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0008 | 0/0 | 8983 | 3 | 0 | 1 | 2 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0009 | 0/0 | 8983 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0011 | 0/0 | 8983 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0012 | 0/0 | 8981 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0014 | 0/0 | 8985 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0015 | 0/0 | 8986 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0017 | 0/0 | 8982 | 3 | 2 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0021 | 0/0 | 8982 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0022 | 0/0 | 8978 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0024 | 0/0 | 8984 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0029 | 0/0 | 8986 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0032 | 0/0 | 8980 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0034 | 0/0 | 8980 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0040 | 0/0 | 8980 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0041 | 0/0 | 8984 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0043 | 0/0 | 8989 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0002t0073 | 0/0 | 8981 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0004t0001 | 0/0 | 8987 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0004t0002 | 0/0 | 8982 | 9 | 0 | 3 | 6 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0004t0003 | 0/0 | 8989 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0004t0005 | 0/0 | 8980 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0004t0011 | 0/0 | 8983 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0005t0063 | 0/0 | 8991 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0005t0064 | 0/0 | 8993 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0009t0004 | 0/0 | 8983 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0012t0015 | 0/0 | 8986 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0001c0014t0032 | 0/0 | 8980 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0002c0003t0001 | 0/0 | 8987 | 3 | 2 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0002c0003t0002 | 0/0 | 8982 | 9 | 0 | 0 | 6 | 0 | 3 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0002c0003t0005 | 0/0 | 8980 | 3 | 1 | 0 | 1 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0002c0003t0012 | 0/0 | 8981 | 3 | 3 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0002c0003t0013 | 0/0 | 8986 | 4 | 0 | 1 | 3 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0002c0003t0020 | 0/0 | 8987 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0002c0003t0028 | 0/0 | 8987 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0002c0003t0048 | 0/0 | 8987 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0002c0003t0053 | 0/0 | 8988 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0002c0003t0062 | 0/0 | 8978 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0002c0011t0013 | 0/0 | 8986 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0003c0007t0025 | 0/0 | 8987 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0004c0008t0004 | 0/0 | 8983 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0005c0016t0003 | 0/0 | 8989 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0006c0015t0004 | 0/0 | 8983 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0007c0010t0075 | 0/0 | 8987 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0008c0013t0003 | 0/0 | 8989 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0009c0017t0014 | 0/0 | 8985 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0010c0018t0003 | 0/0 | 8989 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| a0011c0006t0005 | 0/0 | 8980 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | copy fasta | chr12 | 54492752 | 54553243 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0266 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0007g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0007g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0008g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0008g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0008g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0008g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0008g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0009g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0009g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0009g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0009g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0009g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0010g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0010g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0010g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0010g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0010g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0010g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0011g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0011g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0011g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0011g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0012g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0014g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0014g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0015g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0016g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0016g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0016g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0016g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0017g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0018g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0018g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0018g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0018g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0019g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0019g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0019g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0020g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0021g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0021g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0023g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0023g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0024g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0025g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0026g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0026g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0027g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0027g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0028g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0029g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0030g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0030g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0031g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0031g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0033g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0035g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0036g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0037g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0038g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0039g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0042g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0044g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0045g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0046g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0047g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0049g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0050g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0051g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0052g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0054g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0055g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0056g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0057g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0058g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0059g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0060g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0061g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0065g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0066g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0067g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0068g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0069g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0070g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0071g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0072g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0001t0074g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0004g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0004g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0005g0254 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0005g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0007g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0008g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0008g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0008g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0009g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0011g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0012g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0014g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0015g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0015g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0017g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0017g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0017g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0021g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0022g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0022g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0024g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0029g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0032g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0034g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0040g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0041g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0043g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0002t0073g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0004t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0004t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0004t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0004t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0004t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0004t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0004t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0004t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0004t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0004t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0004t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0004t0011g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0005t0063g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0005t0064g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0009t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0012t0015g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0001c0014t0032g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0012g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0013g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0013g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0013g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0013g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0020g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0020g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0028g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0048g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0053g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0003t0062g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0002c0011t0013g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0003c0007t0025g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0004c0008t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0005c0016t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0006c0015t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0007c0010t0075g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0008c0013t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0009c0017t0014g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0010c0018t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| a0011c0006t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | GBR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | GBR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | GBR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00140 | hp2 | a0006 | c0015 | t0004 | g0177 | EUR | GBR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | FIN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0260 | EUR | FIN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0126 | EUR | FIN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | CHS | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00408 | hp2 | a0001 | c0001 | t0006 | g0171 | EAS | CHS | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00423 | hp1 | a0002 | c0003 | t0002 | g0219 | EAS | CHS | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | CHS | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00438 | hp1 | a0001 | c0001 | t0038 | g0031 | EAS | CHS | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00438 | hp2 | a0001 | c0001 | t0006 | g0030 | EAS | CHS | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00558 | hp1 | a0002 | c0003 | t0001 | g0115 | EAS | CHS | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | CHS | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00642 | hp1 | a0001 | c0001 | t0061 | g0024 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0211 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0062 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00738 | hp1 | a0002 | c0003 | t0053 | g0217 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00738 | hp2 | a0002 | c0003 | t0062 | g0251 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0317 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01074 | hp1 | a0003 | c0007 | t0025 | g0332 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01106 | hp2 | a0001 | c0001 | t0045 | g0267 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01109 | hp1 | a0001 | c0002 | t0017 | g0338 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01109 | hp2 | a0001 | c0001 | t0028 | g0168 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0247 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01168 | hp1 | a0001 | c0001 | t0029 | g0271 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0246 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01243 | hp1 | a0001 | c0001 | t0035 | g0113 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01243 | hp2 | a0001 | c0002 | t0005 | g0075 | AMR | PUR | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01346 | hp1 | a0001 | c0005 | t0064 | g0226 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01358 | hp2 | a0001 | c0002 | t0008 | g0311 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01361 | hp1 | a0001 | c0001 | t0016 | g0273 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01361 | hp2 | a0001 | c0002 | t0040 | g0314 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0309 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01433 | hp2 | a0001 | c0002 | t0009 | g0018 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01496 | hp1 | a0002 | c0011 | t0013 | g0307 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0038 | EUR | IBS | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01515 | hp2 | a0001 | c0002 | t0029 | g0296 | EUR | IBS | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0242 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01884 | hp2 | a0002 | c0003 | t0001 | g0175 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01891 | hp1 | a0001 | c0001 | t0070 | g0234 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0278 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01928 | hp1 | a0001 | c0004 | t0002 | g0289 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01928 | hp2 | a0001 | c0001 | t0008 | g0288 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01934 | hp1 | a0001 | c0002 | t0041 | g0305 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01934 | hp2 | a0001 | c0004 | t0011 | g0284 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01943 | hp1 | a0001 | c0001 | t0018 | g0186 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0147 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0286 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01975 | hp2 | a0002 | c0003 | t0028 | g0118 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0225 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01978 | hp2 | a0001 | c0001 | t0054 | g0068 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01981 | hp1 | a0001 | c0004 | t0002 | g0285 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG01981 | hp2 | a0002 | c0003 | t0048 | g0065 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02015 | hp1 | a0001 | c0001 | t0018 | g0220 | EAS | KHV | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02015 | hp2 | a0002 | c0003 | t0002 | g0105 | EAS | KHV | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02040 | hp2 | a0001 | c0004 | t0002 | g0287 | EAS | KHV | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02055 | hp1 | a0001 | c0001 | t0026 | g0090 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02055 | hp2 | a0001 | c0001 | t0019 | g0265 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02071 | hp1 | a0001 | c0004 | t0002 | g0291 | EAS | KHV | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02071 | hp2 | a0001 | c0001 | t0042 | g0253 | EAS | KHV | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02074 | hp1 | a0001 | c0001 | t0019 | g0190 | EAS | KHV | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02074 | hp2 | a0008 | c0013 | t0003 | g0149 | EAS | KHV | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02080 | hp1 | a0001 | c0001 | t0008 | g0112 | EAS | KHV | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02083 | hp1 | a0001 | c0001 | t0007 | g0114 | EAS | KHV | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02145 | hp1 | a0001 | c0001 | t0021 | g0257 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02145 | hp2 | a0001 | c0001 | t0046 | g0272 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02148 | hp1 | a0001 | c0001 | t0072 | g0159 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0143 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02257 | hp1 | a0001 | c0001 | t0027 | g0042 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02257 | hp2 | a0001 | c0001 | t0024 | g0241 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0178 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0069 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02273 | hp2 | a0002 | c0003 | t0013 | g0066 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02280 | hp1 | a0001 | c0001 | t0025 | g0169 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02280 | hp2 | a0001 | c0001 | t0021 | g0058 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0223 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02300 | hp1 | a0001 | c0004 | t0002 | g0290 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02451 | hp1 | a0001 | c0012 | t0015 | g0276 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02572 | hp1 | a0001 | c0002 | t0005 | g0335 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02572 | hp2 | a0001 | c0001 | t0059 | g0164 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02615 | hp1 | a0001 | c0002 | t0022 | g0304 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0154 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0295 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02622 | hp2 | a0001 | c0001 | t0065 | g0128 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02630 | hp1 | a0001 | c0002 | t0005 | g0319 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02630 | hp2 | a0001 | c0001 | t0069 | g0155 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02647 | hp1 | a0001 | c0001 | t0030 | g0028 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0255 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0248 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0043 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02723 | hp1 | a0002 | c0003 | t0005 | g0215 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02723 | hp2 | a0001 | c0002 | t0034 | g0306 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02735 | hp1 | a0001 | c0001 | t0016 | g0011 | SAS | PJL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02735 | hp2 | a0002 | c0003 | t0005 | g0111 | SAS | PJL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0337 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02809 | hp2 | a0001 | c0001 | t0026 | g0082 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02818 | hp1 | a0001 | c0001 | t0014 | g0052 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02818 | hp2 | a0001 | c0001 | t0030 | g0153 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02886 | hp1 | a0001 | c0002 | t0005 | g0318 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02886 | hp2 | a0001 | c0002 | t0017 | g0013 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02895 | hp1 | a0001 | c0002 | t0015 | g0303 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02895 | hp2 | a0002 | c0003 | t0012 | g0060 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02897 | hp1 | a0002 | c0003 | t0012 | g0073 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0050 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02965 | hp1 | a0001 | c0001 | t0051 | g0051 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02970 | hp1 | a0001 | c0002 | t0005 | g0076 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02970 | hp2 | a0001 | c0001 | t0033 | g0054 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02976 | hp2 | a0001 | c0001 | t0031 | g0053 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03017 | hp1 | a0001 | c0001 | t0036 | g0127 | SAS | PJL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03041 | hp1 | a0001 | c0001 | t0015 | g0131 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0047 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | MSL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03098 | hp2 | a0002 | c0003 | t0012 | g0136 | AFR | MSL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0059 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03130 | hp2 | a0001 | c0009 | t0004 | g0322 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0300 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03139 | hp2 | a0001 | c0002 | t0032 | g0021 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0277 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0156 | AFR | MSL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0072 | AFR | MSL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0049 | AFR | MSL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | MSL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03453 | hp1 | a0001 | c0002 | t0015 | g0297 | AFR | MSL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03453 | hp2 | a0001 | c0002 | t0014 | g0336 | AFR | MSL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0089 | AFR | MSL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03492 | hp2 | a0007 | c0010 | t0075 | g0316 | SAS | PJL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03516 | hp1 | a0009 | c0017 | t0014 | g0302 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03516 | hp2 | a0001 | c0001 | t0047 | g0041 | AFR | ESN | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0152 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03540 | hp2 | a0001 | c0002 | t0005 | g0321 | AFR | GWD | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0280 | AFR | MSL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0074 | AFR | MSL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0250 | SAS | PJL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03710 | hp1 | a0001 | c0001 | t0037 | g0213 | SAS | PJL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03710 | hp2 | a0001 | c0002 | t0004 | g0301 | SAS | PJL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | BEB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0218 | SAS | BEB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0184 | SAS | BEB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | BEB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03942 | hp1 | a0001 | c0001 | t0044 | g0166 | SAS | BEB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03942 | hp2 | a0002 | c0003 | t0002 | g0096 | SAS | BEB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG04115 | hp2 | a0002 | c0003 | t0002 | g0243 | SAS | STU | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0141 | SAS | STU | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0315 | SAS | STU | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG04228 | hp1 | a0002 | c0003 | t0002 | g0106 | SAS | STU | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | STU | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18522 | hp1 | a0001 | c0001 | t0060 | g0279 | AFR | YRI | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | YRI | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | CHB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18747 | hp1 | a0002 | c0003 | t0020 | g0087 | EAS | CHB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18747 | hp2 | a0001 | c0001 | t0009 | g0083 | EAS | CHB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18906 | hp1 | a0001 | c0002 | t0012 | g0341 | AFR | YRI | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18944 | hp1 | a0001 | c0002 | t0007 | g0312 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18944 | hp2 | a0001 | c0001 | t0009 | g0245 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18945 | hp2 | a0001 | c0001 | t0010 | g0185 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18948 | hp2 | a0001 | c0001 | t0050 | g0216 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18949 | hp1 | a0001 | c0001 | t0011 | g0036 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18949 | hp2 | a0010 | c0018 | t0003 | g0140 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18952 | hp1 | a0001 | c0005 | t0063 | g0188 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18952 | hp2 | a0001 | c0001 | t0010 | g0199 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18954 | hp2 | a0001 | c0004 | t0002 | g0183 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18957 | hp1 | a0001 | c0001 | t0007 | g0182 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18957 | hp2 | a0002 | c0003 | t0002 | g0067 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18959 | hp1 | a0001 | c0001 | t0007 | g0209 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18960 | hp1 | a0001 | c0004 | t0002 | g0120 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18960 | hp2 | a0001 | c0001 | t0055 | g0084 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18961 | hp1 | a0001 | c0001 | t0071 | g0005 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18961 | hp2 | a0001 | c0002 | t0008 | g0324 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18965 | hp2 | a0001 | c0001 | t0019 | g0228 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18966 | hp1 | a0002 | c0003 | t0002 | g0099 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18968 | hp1 | a0001 | c0001 | t0007 | g0205 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18968 | hp2 | a0001 | c0001 | t0020 | g0023 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18969 | hp1 | a0001 | c0002 | t0004 | g0340 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18973 | hp2 | a0001 | c0002 | t0011 | g0331 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0333 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18974 | hp2 | a0001 | c0001 | t0009 | g0063 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18975 | hp1 | a0001 | c0001 | t0010 | g0033 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18979 | hp1 | a0002 | c0003 | t0002 | g0029 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0323 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18980 | hp2 | a0001 | c0001 | t0008 | g0144 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18981 | hp1 | a0005 | c0016 | t0003 | g0006 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18981 | hp2 | a0001 | c0001 | t0010 | g0196 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18983 | hp1 | a0001 | c0001 | t0018 | g0035 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18985 | hp1 | a0001 | c0001 | t0068 | g0134 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18988 | hp1 | a0001 | c0002 | t0003 | g0327 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18988 | hp2 | a0001 | c0001 | t0009 | g0206 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18990 | hp2 | a0001 | c0001 | t0011 | g0203 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18993 | hp2 | a0001 | c0001 | t0011 | g0179 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18998 | hp1 | a0001 | c0001 | t0007 | g0085 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18999 | hp1 | a0001 | c0001 | t0023 | g0161 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18999 | hp2 | a0001 | c0004 | t0002 | g0103 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19000 | hp2 | a0001 | c0001 | t0011 | g0097 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19001 | hp1 | a0001 | c0001 | t0007 | g0238 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19002 | hp1 | a0001 | c0004 | t0001 | g0233 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19002 | hp2 | a0002 | c0003 | t0020 | g0110 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19003 | hp1 | a0001 | c0001 | t0009 | g0210 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19003 | hp2 | a0001 | c0001 | t0010 | g0200 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19004 | hp1 | a0001 | c0004 | t0005 | g0121 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19004 | hp2 | a0002 | c0003 | t0005 | g0107 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19005 | hp1 | a0002 | c0003 | t0013 | g0061 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19005 | hp2 | a0001 | c0002 | t0021 | g0330 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19007 | hp1 | a0001 | c0001 | t0052 | g0235 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19010 | hp1 | a0001 | c0001 | t0039 | g0162 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19011 | hp1 | a0001 | c0001 | t0018 | g0221 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19011 | hp2 | a0002 | c0003 | t0002 | g0109 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19030 | hp1 | a0001 | c0001 | t0031 | g0055 | AFR | LWK | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19030 | hp2 | a0001 | c0002 | t0017 | g0334 | AFR | LWK | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19043 | hp1 | a0001 | c0002 | t0022 | g0020 | AFR | LWK | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0256 | AFR | LWK | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19056 | hp1 | a0002 | c0003 | t0013 | g0064 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19057 | hp1 | a0001 | c0001 | t0058 | g0192 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19057 | hp2 | a0001 | c0002 | t0008 | g0308 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0339 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19064 | hp1 | a0001 | c0001 | t0017 | g0229 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0326 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19066 | hp1 | a0001 | c0001 | t0007 | g0181 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19066 | hp2 | a0001 | c0004 | t0002 | g0093 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19078 | hp2 | a0001 | c0004 | t0001 | g0095 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19079 | hp1 | a0001 | c0001 | t0067 | g0133 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19079 | hp2 | a0001 | c0001 | t0007 | g0139 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19082 | hp1 | a0001 | c0002 | t0073 | g0325 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19082 | hp2 | a0001 | c0004 | t0003 | g0281 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19083 | hp1 | a0001 | c0001 | t0049 | g0195 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19083 | hp2 | a0001 | c0001 | t0074 | g0239 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19084 | hp2 | a0001 | c0001 | t0007 | g0160 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19090 | hp2 | a0001 | c0002 | t0024 | g0328 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19091 | hp1 | a0001 | c0001 | t0010 | g0148 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19091 | hp2 | a0001 | c0001 | t0008 | g0135 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19240 | hp1 | a0001 | c0001 | t0057 | g0293 | AFR | YRI | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0224 | AFR | YRI | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA20129 | hp1 | a0001 | c0002 | t0043 | g0313 | AFR | ASW | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ASW | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | TSI | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | TSI | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0040 | EUR | TSI | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA20805 | hp2 | a0001 | c0001 | t0066 | g0274 | EUR | TSI | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | GIH | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0310 | SAS | GIH | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02109 | hp1 | a0001 | c0014 | t0032 | g0172 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02109 | hp2 | a0011 | c0006 | t0005 | g0174 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02486 | hp1 | a0004 | c0008 | t0004 | g0299 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02486 | hp2 | a0001 | c0001 | t0056 | g0138 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02559 | hp1 | a0001 | c0002 | t0005 | g0320 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0282 | AFR | ACB | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | MSL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | MSL | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | USA | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| HG06807 | hp2 | a0001 | c0001 | t0016 | g0269 | AFR | USA | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18955 | hp1 | a0001 | c0001 | t0023 | g0129 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA18955 | hp2 | a0002 | c0003 | t0013 | g0070 | EAS | JPT | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA20300 | hp1 | a0001 | c0001 | t0016 | g0268 | AFR | USA | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA20300 | hp2 | a0001 | c0002 | t0007 | g0329 | AFR | USA | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| NA21309 | hp2 | a0001 | c0001 | t0027 | g0298 | AFR | LWK | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0266 | REF | REF | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0005 | g0254 | REF | REF | NCKAP1L_chr12_54492752_54553243 | NCKAP1L | chr12 | 54492752 | 54553243 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:54499448
|
G | C | 1 | a0011 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.196G>C | p.Asp66His | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 2/31 | 234/8980 | 196/3384 | 66/1127 | chr12 | 54499448 | ||
| chr12:54500536
|
C | T | 1 | a0010 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.217C>T | p.His73Tyr | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/31 | 255/8980 | 217/3384 | 73/1127 | chr12 | 54500536 | ||
| chr12:54508479
|
C | T | 1 | a0009 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.454C>T | p.Arg152Trp | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 5/31 | 492/8980 | 454/3384 | 152/1127 | chr12 | 54508479 | ||
| chr12:54508480
|
G | A | 1 | a0003 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.455G>A | p.Arg152Gln | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 5/31 | 493/8980 | 455/3384 | 152/1127 | chr12 | 54508480 | ||
| chr12:54517642
|
C | T | 1 | a0002 | 29 | HG00423.hp1 HG00558.hp1 HG00738.hp1 others(26): Show |
missense_variant&splice_region_variant | MODERATE | c.1205C>T | p.Ser402Leu | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 12/31 | 1243/8980 | 1205/3384 | 402/1127 | chr12 | 54517642 | ||
| chr12:54518699
|
G | A | 1 | a0004 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1387G>A | p.Val463Ile | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 14/31 | 1425/8980 | 1387/3384 | 463/1127 | chr12 | 54518699 | ||
| chr12:54519211
|
C | A | 1 | a0008 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.1504C>A | p.Pro502Thr | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/31 | 1542/8980 | 1504/3384 | 502/1127 | chr12 | 54519211 | ||
| chr12:54523419
|
C | T | 1 | a0005 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.1904C>T | p.Thr635Ile | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 19/31 | 1942/8980 | 1904/3384 | 635/1127 | chr12 | 54523419 | ||
| chr12:54526560
|
C | T | 1 | a0006 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.2189C>T | p.Thr730Met | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/31 | 2227/8980 | 2189/3384 | 730/1127 | chr12 | 54526560 | ||
| chr12:54531549
|
C | T | 1 | a0007 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.2663C>T | p.Pro888Leu | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 24/31 | 2701/8980 | 2663/3384 | 888/1127 | chr12 | 54531549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:54512031
|
C | G | 11 | a0001c0001a0001c0004a0001c0005others(8): Show | 291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
synonymous_variant | LOW | c.867C>G | p.Leu289Leu | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/31 | 905/8980 | 867/3384 | 289/1127 | chr12 | 54512031 | ||
| chr12:54512049
|
T | A | 1 | a0001c0012 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.885T>A | p.Arg295Arg | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/31 | 923/8980 | 885/3384 | 295/1127 | chr12 | 54512049 | ||
| chr12:54521148
|
C | T | 1 | a0001c0004 | 14 | HG01928.hp1 HG01934.hp2 HG01981.hp1 others(11): Show |
synonymous_variant | LOW | c.1788C>T | p.His596His | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/31 | 1826/8980 | 1788/3384 | 596/1127 | chr12 | 54521148 | ||
| chr12:54531288
|
C | T | 1 | a0001c0005 | 2 | HG01346.hp1 NA18952.hp1 |
synonymous_variant | LOW | c.2535C>T | p.Gly845Gly | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 23/31 | 2573/8980 | 2535/3384 | 845/1127 | chr12 | 54531288 | ||
| chr12:54531297
|
C | A | 2 | a0001c0009a0001c0014 | 2 | HG02109.hp1 HG03130.hp2 |
synonymous_variant | LOW | c.2544C>A | p.Gly848Gly | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 23/31 | 2582/8980 | 2544/3384 | 848/1127 | chr12 | 54531297 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:54542697
|
T | A | 4 | a0001c0001t0015a0001c0001t0033a0001c0002t0015others(1): Show | 5 | HG02451.hp1 HG02895.hp1 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*12T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 12 | chr12 | 54542697 | |||||
| chr12:54542958
|
A | G | 1 | a0007c0010t0075 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*273A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 273 | chr12 | 54542958 | |||||
| chr12:54543155
|
T | C | 1 | a0001c0002t0034 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*470T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 470 | chr12 | 54543155 | |||||
| chr12:54543286
|
G | C | 1 | a0001c0001t0035 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*601G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 601 | chr12 | 54543286 | |||||
| chr12:54543396
|
C | T | 5 | a0001c0001t0007a0001c0001t0072a0001c0001t0074others(2): Show | 14 | HG02083.hp1 HG02148.hp1 NA18944.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*711C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 711 | chr12 | 54543396 | |||||
| chr12:54543444
|
G | A | 1 | a0001c0002t0022 | 2 | HG02615.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*759G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 759 | chr12 | 54543444 | |||||
| chr12:54543576
|
T | C | 94 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(91): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*891T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 891 | chr12 | 54543576 | |||||
| chr12:54543702
|
C | T | 1 | a0001c0001t0066 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1017C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 1017 | chr12 | 54543702 | |||||
| chr12:54544004
|
T | C | 1 | a0001c0001t0036 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1319T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 1319 | chr12 | 54544004 | |||||
| chr12:54544018
|
T | G | 88 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(85): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*1333T>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 1333 | chr12 | 54544018 | |||||
| chr12:54544257
|
G | A | 93 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(90): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*1572G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 1572 | chr12 | 54544257 | |||||
| chr12:54544296
|
T | C | 1 | a0001c0002t0034 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1611T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 1611 | chr12 | 54544296 | |||||
| chr12:54544434
|
T | C | 1 | a0001c0001t0037 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1749T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 1749 | chr12 | 54544434 | |||||
| chr12:54544542
|
C | A | 2 | a0001c0001t0067a0001c0001t0068 | 2 | NA18985.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1857C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 1857 | chr12 | 54544542 | |||||
| chr12:54544572
|
T | G | 1 | a0002c0003t0062 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1887T>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 1887 | chr12 | 54544572 | |||||
| chr12:54544628
|
G | A | 1 | a0001c0001t0069 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1943G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 1943 | chr12 | 54544628 | |||||
| chr12:54544801
|
G | A | 2 | a0001c0001t0023a0001c0001t0038 | 3 | HG00438.hp1 NA18955.hp1 NA18999.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2116G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 2116 | chr12 | 54544801 | |||||
| chr12:54544802
|
C | G | 1 | a0001c0001t0068 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2117C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 2117 | chr12 | 54544802 | |||||
| chr12:54544985
|
G | A | 1 | a0001c0001t0039 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2300G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 2300 | chr12 | 54544985 | |||||
| chr12:54545017
|
A | T | 1 | a0001c0001t0061 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2332A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 2332 | chr12 | 54545017 | |||||
| chr12:54545149
|
C | T | 2 | a0001c0001t0030a0001c0001t0060 | 3 | HG02647.hp1 HG02818.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2464C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 2464 | chr12 | 54545149 | |||||
| chr12:54545324
|
A | G | 1 | a0002c0003t0062 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2639A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 2639 | chr12 | 54545324 | |||||
| chr12:54545356
|
G | C | 6 | a0001c0001t0008a0001c0001t0042a0001c0002t0008others(3): Show | 13 | HG00642.hp2 HG01358.hp2 HG01361.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2671G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 2671 | chr12 | 54545356 | |||||
| chr12:54545412
|
G | C | 2 | a0001c0005t0063a0001c0005t0064 | 2 | HG01346.hp1 NA18952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2727G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 2727 | chr12 | 54545412 | |||||
| chr12:54545674
|
G | A | 1 | a0001c0001t0044 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2989G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 2989 | chr12 | 54545674 | |||||
| chr12:54545850
|
C | T | 4 | a0001c0001t0014a0001c0001t0059a0001c0002t0014others(1): Show | 6 | HG02572.hp2 HG02615.hp2 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3165C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 3165 | chr12 | 54545850 | |||||
| chr12:54545998
|
C | T | 2 | a0001c0002t0032a0001c0014t0032 | 2 | HG02109.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3313C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 3313 | chr12 | 54545998 | |||||
| chr12:54546251
|
T | C | 1 | a0001c0001t0045 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3566T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 3566 | chr12 | 54546251 | |||||
| chr12:54546361
|
C | CA | 67 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(64): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*3697dupA | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 3698 | INFO_REALIGN_3_PRIME | chr12 | 54546361 | ||||
| chr12:54546361
|
C | CAA | 13 | a0001c0001t0019a0001c0001t0023a0001c0001t0024others(10): Show | 16 | HG01361.hp2 HG01934.hp1 HG01981.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3696_*3697dupAA | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 3698 | INFO_REALIGN_3_PRIME | chr12 | 54546361 | ||||
| chr12:54546615
|
C | T | 2 | a0001c0001t0020a0002c0003t0020 | 3 | NA18747.hp1 NA18968.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3930C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 3930 | chr12 | 54546615 | |||||
| chr12:54546889
|
G | A | 1 | a0001c0001t0050 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4204G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 4204 | chr12 | 54546889 | |||||
| chr12:54547337
|
T | C | 1 | a0001c0001t0051 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4652T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 4652 | chr12 | 54547337 | |||||
| chr12:54547432
|
T | C | 2 | a0001c0001t0025a0003c0007t0025 | 2 | HG01074.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4747T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 4747 | chr12 | 54547432 | |||||
| chr12:54547503
|
C | CGT | 32 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(29): Show | 120 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*4848_*4849dupTG | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 4850 | INFO_REALIGN_3_PRIME | chr12 | 54547503 | ||||
| chr12:54547503
|
C | CGTGT | 12 | a0001c0001t0006a0001c0001t0014a0001c0001t0027others(9): Show | 26 | HG00408.hp2 HG00438.hp2 HG01884.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4846_*4849dupTGTG | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 4850 | INFO_REALIGN_3_PRIME | chr12 | 54547503 | ||||
| chr12:54547503
|
C | CGTGTGT | 29 | a0001c0001t0001a0001c0001t0015a0001c0001t0018others(26): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*4844_*4849dupTGTG others(2): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 4850 | INFO_REALIGN_3_PRIME | chr12 | 54547503 | ||||
| chr12:54547503
|
C | CGTGTGTG others(1): Show |
12 | a0001c0001t0003a0001c0001t0023a0001c0001t0038others(9): Show | 35 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*4842_*4849dupTGTG others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 4850 | INFO_REALIGN_3_PRIME | chr12 | 54547503 | ||||
| chr12:54547503
|
C | CGTGTGTG others(3): Show |
4 | a0001c0001t0016a0001c0001t0049a0001c0001t0061others(1): Show | 7 | HG00642.hp1 HG01361.hp1 HG02735.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4840_*4849dupTGTG others(6): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 4850 | INFO_REALIGN_3_PRIME | chr12 | 54547503 | ||||
| chr12:54547503
|
C | CGTGTGTG others(5): Show |
2 | a0001c0001t0054a0001c0005t0064 | 2 | HG01346.hp1 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4838_*4849dupTGTG others(8): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 4850 | INFO_REALIGN_3_PRIME | chr12 | 54547503 | ||||
| chr12:54547503
|
C | CTGTGTGT others(4): Show |
1 | a0001c0001t0055 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4818_*4819insTGTG others(7): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 4819 | chr12 | 54547503 | |||||
| chr12:54547503
|
CGT | C | 7 | a0001c0001t0026a0001c0001t0031a0001c0001t0052others(4): Show | 10 | HG00738.hp2 HG01361.hp2 HG01891.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4848_*4849delTG | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 4848 | INFO_REALIGN_3_PRIME | chr12 | 54547503 | ||||
| chr12:54547683
|
A | T | 5 | a0001c0001t0028a0001c0001t0029a0001c0001t0037others(2): Show | 5 | HG01109.hp2 HG01168.hp1 HG01515.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4998A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 4998 | chr12 | 54547683 | |||||
| chr12:54548055
|
G | A | 15 | a0001c0001t0004a0001c0001t0012a0001c0001t0021others(12): Show | 40 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*5370G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 5370 | chr12 | 54548055 | |||||
| chr12:54548058
|
AG | A | 5 | a0001c0001t0050a0002c0003t0013a0002c0003t0048others(2): Show | 8 | HG00738.hp1 HG01496.hp1 HG01981.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5375delG | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 5375 | INFO_REALIGN_3_PRIME | chr12 | 54548058 | ||||
| chr12:54548068
|
G | C | 1 | a0001c0001t0010 | 6 | NA18945.hp2 NA18952.hp2 NA18975.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5383G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 5383 | chr12 | 54548068 | |||||
| chr12:54548118
|
C | T | 1 | a0001c0002t0034 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5433C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 31/31 | 5433 | chr12 | 54548118 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:54498104
|
A | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0258others(86): Show | 93 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.102+213A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | chr12 | 54498104 | ||||||
| chr12:54498317
|
A | C | 1 | a0001c0001t0006g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.102+426A>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | chr12 | 54498317 | ||||||
| chr12:54498335
|
G | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(101): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.102+444G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | chr12 | 54498335 | ||||||
| chr12:54498399
|
T | TTG | 24 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0034others(21): Show | 24 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.102+542_102+543dup others(2): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr12 | 54498399 | |||||
| chr12:54498399
|
T | TTGTG | 4 | a0001c0001t0001g0022a0001c0001t0005g0282a0001c0001t0020g0023others(1): Show | 4 | HG02559.hp2 HG02698.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+540_102+543dup others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr12 | 54498399 | |||||
| chr12:54498399
|
T | TTGTGTGT others(3): Show |
5 | a0001c0001t0004g0277a0001c0001t0004g0278a0001c0001t0004g0280others(2): Show | 6 | HG01891.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+534_102+543dup others(10): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr12 | 54498399 | |||||
| chr12:54498399
|
T | TTGTGTGT others(5): Show |
5 | a0001c0001t0001g0275a0001c0001t0016g0273a0001c0001t0046g0272others(2): Show | 5 | HG01361.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+532_102+543dup others(12): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr12 | 54498399 | |||||
| chr12:54498399
|
T | TTGTGTGT others(7): Show |
11 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0263others(8): Show | 14 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.102+530_102+543dup others(14): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr12 | 54498399 | |||||
| chr12:54498399
|
T | TTGTGTGT others(9): Show |
4 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(1): Show | 4 | HG00280.hp1 HG00280.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+528_102+543dup others(16): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr12 | 54498399 | |||||
| chr12:54498399
|
T | TTGTGTGT others(13): Show |
2 | a0001c0001t0006g0256a0001c0001t0021g0257 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.102+524_102+543dup others(20): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr12 | 54498399 | |||||
| chr12:54498399
|
TTGTGTG | T | 42 | a0001c0002t0001g0310a0001c0002t0001g0315a0001c0002t0001g0317others(39): Show | 42 | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.102+538_102+543del others(6): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr12 | 54498399 | |||||
| chr12:54498434
|
T | TGTGTGTG others(8): Show |
1 | a0001c0001t0001g0258 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.102+543_102+544ins others(15): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | chr12 | 54498434 | ||||||
| chr12:54498436
|
T | C | 16 | a0001c0001t0001g0046a0001c0001t0003g0039a0001c0001t0003g0045others(13): Show | 16 | HG01192.hp1 HG02257.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.102+545T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | chr12 | 54498436 | ||||||
| chr12:54498457
|
G | C | 5 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0004g0295others(2): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+566G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | chr12 | 54498457 | ||||||
| chr12:54498913
|
A | ATATT | 10 | a0001c0001t0001g0294a0001c0001t0002g0012a0001c0001t0003g0010others(7): Show | 10 | HG00741.hp1 HG02145.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.103-412_103-409dup others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr12 | 54498913 | |||||
| chr12:54498913
|
A | ATATTTAT others(1): Show |
147 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(144): Show | 152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.103-416_103-409dup others(8): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr12 | 54498913 | |||||
| chr12:54498913
|
A | ATATTTAT others(5): Show |
93 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026others(90): Show | 93 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.103-420_103-409dup others(12): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr12 | 54498913 | |||||
| chr12:54498913
|
A | ATATTTAT others(9): Show |
57 | a0001c0001t0001g0009a0001c0001t0001g0078a0001c0001t0001g0086others(54): Show | 57 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.103-424_103-409dup others(16): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr12 | 54498913 | |||||
| chr12:54498913
|
A | ATATTTAT others(13): Show |
16 | a0001c0001t0001g0056a0001c0001t0001g0283a0001c0001t0004g0057others(13): Show | 16 | HG01934.hp2 HG01975.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.103-428_103-409dup others(20): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr12 | 54498913 | |||||
| chr12:54498913
|
A | ATATTTAT others(17): Show |
2 | a0001c0001t0033g0054a0001c0002t0004g0300 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.103-432_103-409dup others(24): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr12 | 54498913 | |||||
| chr12:54498953
|
T | A | 5 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0004g0295others(2): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-402T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | chr12 | 54498953 | ||||||
| chr12:54499075
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.103-280A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | chr12 | 54499075 | ||||||
| chr12:54499115
|
G | A | 1 | a0001c0002t0017g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.103-240G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | chr12 | 54499115 | ||||||
| chr12:54499184
|
G | A | 2 | a0001c0001t0003g0039a0001c0002t0001g0040 | 2 | HG01192.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.103-171G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | chr12 | 54499184 | ||||||
| chr12:54499194
|
G | A | 16 | a0001c0001t0001g0046a0001c0001t0003g0039a0001c0001t0003g0045others(13): Show | 16 | HG01192.hp1 HG02257.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.103-161G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | chr12 | 54499194 | ||||||
| chr12:54499210
|
C | A | 1 | a0001c0012t0015g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.103-145C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | chr12 | 54499210 | ||||||
| chr12:54499216
|
G | A | 44 | a0001c0002t0001g0310a0001c0002t0001g0315a0001c0002t0001g0317others(41): Show | 44 | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.103-139G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | chr12 | 54499216 | ||||||
| chr12:54499243
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0022others(145): Show | 152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.103-112G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 1/30 | chr12 | 54499243 | ||||||
| chr12:54499779
|
TTGTTTC | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0258others(18): Show | 24 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.213+321_213+326del others(6): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr12 | 54499779 | |||||
| chr12:54500126
|
CT | C | 14 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(11): Show | 16 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.214-392delT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr12 | 54500126 | |||||
| chr12:54500126
|
CTTTT | C | 325 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(322): Show | 330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.214-395_214-392del others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr12 | 54500126 | |||||
| chr12:54500187
|
A | G | 2 | a0001c0001t0004g0277a0001c0001t0004g0278 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.214-346A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 2/30 | chr12 | 54500187 | ||||||
| chr12:54500420
|
G | A | 2 | a0001c0001t0030g0028a0001c0001t0030g0153 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.214-113G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 2/30 | chr12 | 54500420 | ||||||
| chr12:54500650
|
A | G | 3 | a0001c0001t0003g0249a0001c0001t0030g0028a0001c0001t0030g0153 | 3 | HG02647.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.306+25A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54500650 | ||||||
| chr12:54501045
|
A | G | 1 | a0001c0002t0004g0340 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.306+420A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54501045 | ||||||
| chr12:54501137
|
G | A | 1 | a0001c0001t0057g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.306+512G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54501137 | ||||||
| chr12:54501431
|
T | G | 1 | a0002c0003t0062g0251 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.306+806T>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54501431 | ||||||
| chr12:54501489
|
A | T | 3 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0012g0248 | 3 | HG01167.hp1 HG01169.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.306+864A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54501489 | ||||||
| chr12:54501510
|
C | CT | 326 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(323): Show | 331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.306+897dupT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54501510 | |||||
| chr12:54501654
|
G | T | 327 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(324): Show | 332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.306+1029G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54501654 | ||||||
| chr12:54501694
|
T | C | 5 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0004g0295others(2): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+1069T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54501694 | ||||||
| chr12:54501704
|
C | T | 1 | a0001c0002t0002g0339 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.306+1079C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54501704 | ||||||
| chr12:54501722
|
T | C | 10 | a0001c0001t0001g0283a0001c0001t0005g0286a0001c0001t0008g0288others(7): Show | 10 | HG01928.hp1 HG01928.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.306+1097T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54501722 | ||||||
| chr12:54501757
|
C | T | 2 | a0001c0001t0004g0277a0001c0001t0004g0278 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.306+1132C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54501757 | ||||||
| chr12:54501805
|
G | T | 2 | a0001c0001t0004g0277a0001c0001t0004g0278 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.306+1180G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54501805 | ||||||
| chr12:54501902
|
T | C | 131 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0078others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.306+1277T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54501902 | ||||||
| chr12:54501909
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.306+1284G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54501909 | ||||||
| chr12:54502067
|
C | A | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.306+1442C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54502067 | ||||||
| chr12:54502081
|
A | AT | 14 | a0001c0002t0001g0337a0001c0002t0004g0300a0001c0002t0005g0318others(11): Show | 14 | HG01109.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.306+1462dupT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54502081 | |||||
| chr12:54502086
|
T | G | 4 | a0001c0001t0004g0252a0001c0001t0005g0156a0001c0001t0014g0154others(1): Show | 4 | HG02615.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+1461T>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54502086 | ||||||
| chr12:54502254
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.306+1629A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54502254 | ||||||
| chr12:54502273
|
T | A | 332 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(329): Show | 337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.306+1648T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54502273 | ||||||
| chr12:54502351
|
A | G | 1 | a0001c0001t0036g0127 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.306+1726A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54502351 | ||||||
| chr12:54502631
|
C | A | 2 | a0001c0001t0030g0028a0001c0001t0030g0153 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.306+2006C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54502631 | ||||||
| chr12:54502706
|
G | A | 183 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0014others(180): Show | 184 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.306+2081G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54502706 | ||||||
| chr12:54502724
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.306+2099C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54502724 | ||||||
| chr12:54502766
|
C | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(245): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.306+2141C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54502766 | ||||||
| chr12:54502819
|
T | TAC | 35 | a0001c0002t0001g0310a0001c0002t0001g0315a0001c0002t0001g0317others(32): Show | 35 | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.306+2198_306+2199d others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54502819 | |||||
| chr12:54502823
|
C | CA | 136 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0015others(133): Show | 137 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.306+2223dupA | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54502823 | |||||
| chr12:54502823
|
C | CAA | 52 | a0001c0001t0001g0014a0001c0001t0001g0046a0001c0001t0001g0142others(49): Show | 52 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.306+2222_306+2223d others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54502823 | |||||
| chr12:54502823
|
C | CAAA | 84 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0022others(81): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.306+2221_306+2223d others(5): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54502823 | |||||
| chr12:54502823
|
C | CAAAA | 18 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0266others(15): Show | 18 | HG00642.hp1 HG01928.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.306+2220_306+2223d others(6): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54502823 | |||||
| chr12:54502824
|
A | ACAC | 9 | a0001c0002t0003g0323a0001c0002t0005g0318a0001c0002t0005g0335others(6): Show | 9 | HG01515.hp2 HG01934.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.306+2199_306+2200i others(5): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54502824 | ||||||
| chr12:54502825
|
A | C | 35 | a0001c0002t0001g0310a0001c0002t0001g0315a0001c0002t0001g0317others(32): Show | 35 | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.306+2200A>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54502825 | ||||||
| chr12:54503004
|
C | CA | 17 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(14): Show | 17 | HG00544.hp1 HG00733.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.306+2394dupA | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54503004 | |||||
| chr12:54503020
|
G | A | 51 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0056others(48): Show | 51 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.306+2395G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54503020 | ||||||
| chr12:54503024
|
C | A | 52 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026others(49): Show | 52 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.306+2399C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54503024 | ||||||
| chr12:54503267
|
T | C | 5 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0004g0295others(2): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+2642T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54503267 | ||||||
| chr12:54503382
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.306+2757G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54503382 | ||||||
| chr12:54503428
|
A | T | 62 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026others(59): Show | 62 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+2803A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54503428 | ||||||
| chr12:54503633
|
T | A | 1 | a0001c0001t0006g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.306+3008T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54503633 | ||||||
| chr12:54503638
|
C | T | 1 | a0001c0001t0006g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.306+3013C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54503638 | ||||||
| chr12:54503643
|
C | CT | 15 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0004g0130others(12): Show | 16 | HG02055.hp1 HG02145.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.306+3032dupT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54503643 | |||||
| chr12:54503767
|
T | C | 9 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0004g0277others(6): Show | 10 | HG01891.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.306+3142T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54503767 | ||||||
| chr12:54503774
|
G | T | 5 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0004g0295others(2): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+3149G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54503774 | ||||||
| chr12:54503785
|
C | T | 1 | a0001c0001t0004g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.306+3160C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54503785 | ||||||
| chr12:54503786
|
G | A | 332 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(329): Show | 337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.306+3161G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54503786 | ||||||
| chr12:54503795
|
C | T | 45 | a0001c0001t0002g0244a0001c0002t0001g0310a0001c0002t0001g0315others(42): Show | 45 | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.306+3170C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54503795 | ||||||
| chr12:54504225
|
C | G | 2 | a0001c0001t0001g0259a0001c0001t0021g0257 | 2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.306+3600C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54504225 | ||||||
| chr12:54504244
|
T | C | 1 | a0001c0001t0021g0257 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.307-3609T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54504244 | ||||||
| chr12:54504260
|
T | C | 4 | a0001c0001t0004g0277a0001c0001t0004g0278a0001c0001t0005g0282others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-3593T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54504260 | ||||||
| chr12:54504270
|
G | A | 2 | a0001c0001t0030g0028a0001c0001t0030g0153 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.307-3583G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54504270 | ||||||
| chr12:54504382
|
C | T | 1 | a0002c0003t0002g0243 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.307-3471C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54504382 | ||||||
| chr12:54504711
|
A | C | 1 | a0002c0003t0001g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.307-3142A>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54504711 | ||||||
| chr12:54504743
|
C | G | 2 | a0001c0001t0004g0277a0001c0001t0004g0278 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.307-3110C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54504743 | ||||||
| chr12:54504753
|
A | G | 342 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(339): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.307-3100A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54504753 | ||||||
| chr12:54504779
|
G | A | 3 | a0001c0001t0003g0132a0001c0001t0003g0157a0001c0001t0006g0171 | 3 | HG00408.hp2 NA19000.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.307-3074G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54504779 | ||||||
| chr12:54504866
|
T | A | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.307-2987T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54504866 | ||||||
| chr12:54504930
|
G | A | 4 | a0001c0001t0001g0173a0001c0014t0032g0172a0002c0003t0001g0175others(1): Show | 4 | HG01099.hp1 HG01884.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-2923G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54504930 | ||||||
| chr12:54505069
|
A | G | 333 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(330): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.307-2784A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505069 | ||||||
| chr12:54505101
|
T | A | 2 | a0001c0001t0001g0176a0001c0001t0003g0158 | 2 | HG00423.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.307-2752T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505101 | ||||||
| chr12:54505164
|
C | T | 333 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(330): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.307-2689C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505164 | ||||||
| chr12:54505173
|
G | A | 1 | a0001c0002t0014g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.307-2680G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505173 | ||||||
| chr12:54505341
|
C | G | 2 | a0001c0001t0006g0242a0001c0001t0024g0241 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.307-2512C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505341 | ||||||
| chr12:54505343
|
C | T | 1 | a0001c0012t0015g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.307-2510C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505343 | ||||||
| chr12:54505444
|
CT | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(321): Show | 329 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.307-2393delT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54505444 | |||||
| chr12:54505449
|
T | C | 2 | a0001c0001t0001g0259a0001c0001t0021g0257 | 2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.307-2404T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505449 | ||||||
| chr12:54505478
|
A | G | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.307-2375A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505478 | ||||||
| chr12:54505504
|
C | T | 2 | a0001c0001t0007g0238a0001c0001t0074g0239 | 2 | NA19001.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.307-2349C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505504 | ||||||
| chr12:54505508
|
G | T | 2 | a0001c0001t0004g0032a0001c0001t0004g0038 | 2 | HG00639.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.307-2345G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505508 | ||||||
| chr12:54505510
|
T | A | 1 | a0001c0001t0060g0279 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.307-2343T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505510 | ||||||
| chr12:54505634
|
T | C | 1 | a0006c0015t0004g0177 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.307-2219T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505634 | ||||||
| chr12:54505667
|
C | CT | 328 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(325): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.307-2174dupT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54505667 | |||||
| chr12:54505745
|
A | C | 333 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(330): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.307-2108A>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505745 | ||||||
| chr12:54505851
|
G | A | 15 | a0001c0002t0001g0337a0001c0002t0004g0300a0001c0002t0005g0318others(12): Show | 15 | HG01109.hp1 HG02559.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.307-2002G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505851 | ||||||
| chr12:54505878
|
T | A | 1 | a0001c0001t0006g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.307-1975T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505878 | ||||||
| chr12:54505901
|
A | C | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.307-1952A>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505901 | ||||||
| chr12:54505961
|
C | T | 1 | a0001c0001t0005g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.307-1892C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54505961 | ||||||
| chr12:54506197
|
A | G | 3 | a0001c0001t0002g0167a0001c0001t0025g0169a0001c0001t0028g0168 | 3 | HG01109.hp2 HG02280.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.307-1656A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506197 | ||||||
| chr12:54506228
|
T | C | 342 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(339): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.307-1625T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506228 | ||||||
| chr12:54506425
|
CAG | C | 10 | a0001c0001t0001g0283a0001c0001t0005g0286a0001c0001t0008g0288others(7): Show | 10 | HG01928.hp1 HG01928.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.307-1425_307-1424d others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506425 | |||||
| chr12:54506601
|
TA | T | 14 | a0001c0001t0001g0283a0001c0001t0005g0286a0001c0001t0008g0288others(11): Show | 14 | HG01928.hp1 HG01928.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-1251delA | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506601 | ||||||
| chr12:54506602
|
A | T | 315 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(312): Show | 320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.307-1251A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506602 | ||||||
| chr12:54506608
|
A | T | 6 | a0001c0001t0005g0072a0001c0001t0005g0074a0001c0001t0021g0058others(3): Show | 6 | HG02280.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-1245A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506608 | ||||||
| chr12:54506758
|
G | A | 9 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0004g0277others(6): Show | 10 | HG01891.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.307-1095G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506758 | ||||||
| chr12:54506785
|
T | TAA | 6 | a0001c0001t0004g0277a0001c0002t0001g0002a0001c0002t0001g0017others(3): Show | 7 | HG00099.hp2 HG00639.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-1057_307-1056d others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506785 | |||||
| chr12:54506788
|
A | T | 1 | a0001c0001t0038g0031 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.307-1065A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506788 | ||||||
| chr12:54506790
|
A | AATATATA others(9): Show |
1 | a0001c0002t0073g0325 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.307-1062_307-1061i others(18): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506790 | |||||
| chr12:54506790
|
A | T | 1 | a0001c0001t0038g0031 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.307-1063A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506790 | ||||||
| chr12:54506792
|
A | AATATATA others(5): Show |
1 | a0007c0010t0075g0316 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.307-1060_307-1059i others(14): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506792 | |||||
| chr12:54506792
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0026 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.307-1061_307-1060i others(19): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506792 | ||||||
| chr12:54506792
|
A | T | 3 | a0001c0001t0027g0298a0001c0001t0038g0031a0001c0002t0073g0325 | 3 | HG00438.hp1 NA19082.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.307-1061A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506792 | ||||||
| chr12:54506794
|
A | AATATATA others(3): Show |
2 | a0001c0002t0017g0338a0001c0002t0034g0306 | 2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.307-1058_307-1057i others(12): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506794 | |||||
| chr12:54506794
|
A | AATATATA others(5): Show |
1 | a0001c0001t0002g0137 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.307-1058_307-1057i others(14): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506794 | |||||
| chr12:54506794
|
A | AATATATA others(7): Show |
6 | a0001c0001t0003g0125a0001c0002t0002g0339a0001c0002t0022g0304others(3): Show | 6 | HG01074.hp1 HG01361.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-1058_307-1057i others(16): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506794 | |||||
| chr12:54506794
|
A | AATATATA others(9): Show |
1 | a0001c0002t0011g0331 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.307-1058_307-1057i others(18): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506794 | |||||
| chr12:54506794
|
A | AATATATA others(11): Show |
2 | a0001c0001t0004g0295a0001c0002t0014g0336 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.307-1058_307-1057i others(20): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506794 | |||||
| chr12:54506794
|
A | AATATATA others(19): Show |
1 | a0001c0001t0003g0124 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.307-1058_307-1057i others(28): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506794 | |||||
| chr12:54506794
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0044g0166 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.307-1059_307-1058i others(13): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506794 | ||||||
| chr12:54506794
|
A | ATATATAT others(6): Show |
3 | a0001c0001t0001g0025a0001c0001t0003g0237a0001c0001t0061g0024 | 3 | HG00642.hp1 HG03688.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.307-1059_307-1058i others(15): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506794 | ||||||
| chr12:54506794
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0002g0037 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.307-1059_307-1058i others(17): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506794 | ||||||
| chr12:54506794
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0236a0002c0003t0001g0175 | 2 | HG01884.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.307-1059_307-1058i others(19): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506794 | ||||||
| chr12:54506794
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0052g0235 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.307-1059_307-1058i others(21): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506794 | ||||||
| chr12:54506794
|
A | T | 6 | a0001c0001t0001g0026a0001c0001t0027g0298a0001c0001t0038g0031others(3): Show | 6 | HG00438.hp1 HG00741.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-1059A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506794 | ||||||
| chr12:54506796
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0008g0288 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(35): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(28): Show |
1 | a0001c0004t0002g0285 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.307-1056_307-1055i others(37): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(30): Show |
1 | a0001c0004t0011g0284 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(39): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(27): Show |
1 | a0001c0004t0002g0290 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.307-1056_307-1055i others(36): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(32): Show |
1 | a0001c0004t0002g0289 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.307-1056_307-1055i others(41): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0005g0286 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.307-1056_307-1055i others(36): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(15): Show |
1 | a0001c0004t0002g0291 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.307-1056_307-1055i others(24): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(13): Show |
1 | a0001c0004t0002g0287 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(22): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(19): Show |
1 | a0001c0004t0003g0281 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(28): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(3): Show |
1 | a0002c0003t0002g0106 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.307-1056_307-1055i others(12): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(5): Show |
1 | a0002c0003t0002g0099 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.307-1056_307-1055i others(14): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0004g0178 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(16): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(9): Show |
1 | a0002c0003t0002g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(18): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0283 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(30): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(6): Show |
1 | a0002c0003t0005g0107 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(15): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(8): Show |
1 | a0002c0003t0062g0251 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(17): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0011g0179 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(19): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0005g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(23): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0004g0130 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.307-1056_307-1055i others(27): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAT others(4): Show |
4 | a0001c0001t0004g0062a0001c0001t0007g0139a0001c0001t0067g0133others(1): Show | 4 | HG00733.hp2 NA18985.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(13): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAT others(6): Show |
4 | a0001c0001t0001g0004a0001c0001t0001g0294a0001c0001t0010g0185others(1): Show | 5 | HG02976.hp1 HG03486.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(15): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAT others(8): Show |
3 | a0001c0001t0004g0184a0001c0004t0002g0183a0002c0003t0002g0096 | 3 | HG03834.hp1 HG03942.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.307-1056_307-1055i others(17): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAT others(10): Show |
3 | a0001c0001t0007g0181a0001c0001t0007g0182a0001c0002t0005g0319 | 3 | HG02630.hp1 NA18957.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.307-1056_307-1055i others(19): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAT others(12): Show |
2 | a0001c0001t0001g0180a0001c0001t0065g0128 | 2 | HG01256.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.307-1056_307-1055i others(21): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAT others(14): Show |
3 | a0001c0001t0004g0280a0002c0003t0012g0060a0002c0003t0012g0073 | 3 | HG02895.hp2 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.307-1056_307-1055i others(23): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAT others(16): Show |
1 | a0001c0002t0005g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.307-1056_307-1055i others(25): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAAAT others(18): Show |
1 | a0001c0001t0001g0259 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(27): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAATA others(1): Show |
7 | a0001c0001t0003g0141a0001c0001t0003g0146a0001c0001t0004g0077others(4): Show | 7 | HG02809.hp2 HG02970.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(10): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAATA others(3): Show |
4 | a0001c0001t0003g0010a0001c0001t0027g0042a0001c0001t0047g0041others(1): Show | 4 | HG02257.hp1 HG02300.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(12): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAATA others(5): Show |
5 | a0001c0001t0003g0157a0001c0001t0023g0129a0001c0001t0025g0169others(2): Show | 5 | HG02280.hp1 HG03130.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(14): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAATA others(7): Show |
6 | a0001c0001t0006g0047a0001c0001t0007g0160a0001c0001t0028g0168others(3): Show | 6 | HG01109.hp2 HG01496.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(16): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAATA others(9): Show |
2 | a0001c0001t0002g0167a0001c0001t0002g0187 | 2 | HG00544.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.307-1056_307-1055i others(18): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAATA others(11): Show |
5 | a0001c0001t0001g0108a0001c0001t0003g0249a0001c0001t0005g0008others(2): Show | 6 | HG01943.hp1 HG02148.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(20): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAATA others(15): Show |
1 | a0001c0001t0042g0253 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(24): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAAATA others(17): Show |
1 | a0002c0003t0048g0065 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(26): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAATAT others(2): Show |
11 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0078others(8): Show | 11 | HG00423.hp2 HG00733.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(11): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAATAT others(4): Show |
3 | a0001c0001t0004g0252a0001c0001t0024g0241a0001c0001t0030g0153 | 3 | HG02257.hp2 HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.307-1056_307-1055i others(13): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAATAT others(6): Show |
11 | a0001c0001t0001g0142a0001c0001t0001g0198a0001c0001t0003g0197others(8): Show | 11 | HG00558.hp1 HG02083.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(15): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAATAT others(8): Show |
10 | a0001c0001t0001g0056a0001c0001t0008g0112a0001c0001t0010g0196others(7): Show | 10 | HG01243.hp1 HG02080.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(17): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAATAT others(10): Show |
11 | a0001c0001t0001g0009a0001c0001t0001g0194a0001c0001t0002g0189others(8): Show | 11 | HG02074.hp1 HG02083.hp2 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(19): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAATAT others(12): Show |
4 | a0001c0001t0002g0005a0001c0001t0005g0074a0001c0001t0071g0005others(1): Show | 4 | HG01243.hp2 HG03579.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(21): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAAATAT others(14): Show |
1 | a0001c0001t0015g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.307-1056_307-1055i others(23): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAATATA others(3): Show |
12 | a0001c0001t0001g0170a0001c0001t0001g0208a0001c0001t0002g0081others(9): Show | 12 | HG01106.hp1 HG01884.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(12): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAATATA others(5): Show |
6 | a0001c0001t0003g0207a0001c0001t0011g0097a0001c0002t0005g0318others(3): Show | 6 | HG02886.hp1 HG03130.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(14): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAATATA others(7): Show |
5 | a0001c0001t0001g0092a0001c0001t0006g0048a0001c0001t0007g0205others(2): Show | 5 | HG02451.hp2 HG02559.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(16): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAATATA others(9): Show |
3 | a0001c0001t0001g0046a0001c0001t0001g0116a0001c0001t0003g0204 | 3 | HG01081.hp2 HG06807.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.307-1056_307-1055i others(18): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAATATA others(11): Show |
2 | a0001c0001t0001g0100a0001c0001t0011g0203 | 2 | HG02258.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.307-1056_307-1055i others(20): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0151 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.307-1056_307-1055i others(22): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAATATA others(15): Show |
1 | a0001c0001t0003g0202 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.307-1056_307-1055i others(24): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAAT | 8 | a0001c0001t0001g0258a0001c0001t0001g0260a0001c0001t0001g0264others(5): Show | 8 | HG00280.hp2 HG01099.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(5): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAATATAT | 9 | a0001c0001t0001g0016a0001c0001t0001g0263a0001c0001t0004g0071others(6): Show | 9 | HG00323.hp2 HG02055.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(9): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAATATAT others(4): Show |
4 | a0001c0001t0005g0282a0001c0001t0009g0083a0001c0004t0005g0121others(1): Show | 4 | HG02109.hp1 HG02559.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(13): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAATATAT others(6): Show |
12 | a0001c0001t0001g0214a0001c0001t0003g0145a0001c0001t0008g0143others(9): Show | 12 | HG02148.hp2 HG03688.hp2 HG03710.hp1 others(9): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(15): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAATATAT others(8): Show |
10 | a0001c0001t0001g0034a0001c0001t0001g0119a0001c0001t0002g0098others(7): Show | 10 | HG01071.hp2 HG01975.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(17): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAATATAT others(10): Show |
6 | a0001c0001t0001g0117a0001c0001t0008g0211a0001c0001t0009g0210others(3): Show | 6 | HG00642.hp2 HG01978.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-1056_307-1055i others(19): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAATATAT others(12): Show |
2 | a0001c0002t0003g0323a0001c0002t0003g0327 | 2 | NA18980.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.307-1056_307-1055i others(21): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAATATAT others(14): Show |
2 | a0001c0001t0003g0006a0005c0016t0003g0006 | 2 | NA18981.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.307-1056_307-1055i others(23): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AAATATAT others(16): Show |
1 | a0001c0001t0007g0209 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.307-1056_307-1055i others(25): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AATATATA others(3): Show |
4 | a0001c0001t0002g0012a0001c0001t0003g0045a0001c0002t0017g0334others(1): Show | 4 | HG00741.hp1 HG03098.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-1038_307-1029d others(12): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AATATATA others(5): Show |
1 | a0001c0002t0041g0305 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.307-1040_307-1029d others(14): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AATATATA others(7): Show |
2 | a0001c0001t0001g0104a0001c0001t0021g0257 | 2 | HG01257.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.307-1042_307-1029d others(16): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AATATATA others(9): Show |
6 | a0001c0001t0001g0094a0001c0001t0001g0123a0001c0002t0004g0301others(3): Show | 6 | HG01358.hp2 HG02293.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-1044_307-1029d others(18): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AATATATA others(11): Show |
6 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0003g0218others(3): Show | 6 | HG00544.hp1 HG00738.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-1046_307-1029d others(20): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AATATATA others(13): Show |
3 | a0001c0001t0002g0122a0001c0001t0050g0216a0001c0002t0001g0337 | 3 | HG01358.hp1 HG02809.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.307-1048_307-1029d others(22): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | AATATATA others(23): Show |
1 | a0001c0002t0029g0296 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.307-1029_307-1028i others(32): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | 54506796 | |||||
| chr12:54506796
|
A | ATATATAT others(2): Show |
3 | a0001c0002t0021g0330a0001c0004t0001g0233a0009c0017t0014g0302 | 3 | HG03516.hp1 NA19002.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.307-1057_307-1056i others(11): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506796 | ||||||
| chr12:54506796
|
A | ATATATAT others(4): Show |
7 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0001g0231others(4): Show | 7 | HG00639.hp1 HG01099.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-1057_307-1056i others(13): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506796 | ||||||
| chr12:54506796
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0004g0038a0001c0004t0001g0095 | 2 | HG01515.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.307-1057_307-1056i others(15): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506796 | ||||||
| chr12:54506796
|
A | ATATATAT others(8): Show |
5 | a0001c0001t0001g0022a0001c0001t0001g0240a0001c0001t0002g0230others(2): Show | 5 | HG02698.hp1 NA18953.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-1057_307-1056i others(17): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506796 | ||||||
| chr12:54506796
|
A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0227a0001c0001t0005g0225a0001c0001t0014g0224others(1): Show | 4 | HG01346.hp1 HG01978.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-1057_307-1056i others(19): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506796 | ||||||
| chr12:54506796
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0005g0223a0001c0002t0007g0312 | 2 | HG02293.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.307-1057_307-1056i others(21): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506796 | ||||||
| chr12:54506796
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0059g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.307-1057_307-1056i others(23): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506796 | ||||||
| chr12:54506796
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0014g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.307-1057_307-1056i others(25): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506796 | ||||||
| chr12:54506796
|
A | T | 35 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0236others(32): Show | 35 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.307-1057A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506796 | ||||||
| chr12:54506798
|
T | A | 3 | a0001c0001t0004g0277a0001c0001t0004g0278a0001c0002t0032g0021 | 3 | HG01891.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.307-1055T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506798 | ||||||
| chr12:54506808
|
T | A | 1 | a0001c0001t0074g0239 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.307-1045T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506808 | ||||||
| chr12:54506830
|
A | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0258others(18): Show | 24 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.307-1023A>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506830 | ||||||
| chr12:54506892
|
C | G | 44 | a0001c0002t0001g0310a0001c0002t0001g0315a0001c0002t0001g0317others(41): Show | 44 | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.307-961C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54506892 | ||||||
| chr12:54507211
|
G | A | 1 | a0001c0001t0002g0037 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.307-642G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54507211 | ||||||
| chr12:54507534
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.307-319C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54507534 | ||||||
| chr12:54507610
|
G | C | 10 | a0001c0001t0001g0283a0001c0001t0005g0286a0001c0001t0008g0288others(7): Show | 10 | HG01928.hp1 HG01928.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.307-243G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54507610 | ||||||
| chr12:54507762
|
C | A | 4 | a0001c0001t0003g0006a0001c0001t0007g0209a0001c0001t0009g0210others(1): Show | 4 | NA18959.hp1 NA18981.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-91C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | 54507762 | ||||||
| chr12:54508292
|
G | A | 4 | a0001c0001t0009g0063a0002c0003t0013g0061a0002c0003t0013g0064others(1): Show | 4 | NA18955.hp2 NA18974.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-97G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 4/30 | chr12 | 54508292 | ||||||
| chr12:54508312
|
C | T | 1 | a0001c0001t0007g0139 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.364-77C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 4/30 | chr12 | 54508312 | ||||||
| chr12:54508973
|
C | T | 1 | a0001c0001t0024g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.506+442C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 5/30 | chr12 | 54508973 | ||||||
| chr12:54509096
|
G | T | 2 | a0001c0001t0001g0259a0001c0001t0021g0257 | 2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.506+565G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 5/30 | chr12 | 54509096 | ||||||
| chr12:54509188
|
T | C | 26 | a0001c0001t0001g0009a0001c0001t0001g0078a0001c0001t0001g0086others(23): Show | 26 | HG00558.hp2 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.507-481T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 5/30 | chr12 | 54509188 | ||||||
| chr12:54509282
|
T | C | 1 | a0001c0001t0004g0278 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.507-387T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 5/30 | chr12 | 54509282 | ||||||
| chr12:54509309
|
C | T | 1 | a0001c0001t0006g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.507-360C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 5/30 | chr12 | 54509309 | ||||||
| chr12:54509452
|
G | A | 1 | a0001c0002t0034g0306 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.507-217G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 5/30 | chr12 | 54509452 | ||||||
| chr12:54509524
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0014others(180): Show | 184 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.507-145T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 5/30 | chr12 | 54509524 | ||||||
| chr12:54510076
|
A | G | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.735+91A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54510076 | ||||||
| chr12:54510094
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.735+109C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54510094 | ||||||
| chr12:54510108
|
T | C | 1 | a0001c0001t0012g0248 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.735+123T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54510108 | ||||||
| chr12:54510434
|
C | T | 2 | a0001c0001t0004g0277a0001c0001t0004g0278 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.735+449C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54510434 | ||||||
| chr12:54510484
|
G | A | 1 | a0001c0001t0009g0245 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.735+499G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54510484 | ||||||
| chr12:54510571
|
C | T | 9 | a0001c0001t0001g0283a0001c0001t0005g0286a0001c0001t0008g0288others(6): Show | 9 | HG01928.hp2 HG01934.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+586C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54510571 | ||||||
| chr12:54510648
|
T | C | 2 | a0001c0001t0004g0277a0001c0001t0004g0278 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.735+663T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54510648 | ||||||
| chr12:54510661
|
C | T | 9 | a0001c0001t0001g0283a0001c0001t0005g0286a0001c0001t0008g0288others(6): Show | 9 | HG01928.hp2 HG01934.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+676C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54510661 | ||||||
| chr12:54510676
|
A | AT | 70 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026others(67): Show | 70 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.735+708dupT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr12 | 54510676 | |||||
| chr12:54510676
|
AT | A | 6 | a0001c0001t0001g0180a0001c0001t0027g0298a0002c0003t0005g0215others(3): Show | 6 | HG01256.hp2 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+708delT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr12 | 54510676 | |||||
| chr12:54510680
|
T | A | 9 | a0001c0001t0001g0283a0001c0001t0005g0286a0001c0001t0008g0288others(6): Show | 9 | HG01928.hp2 HG01934.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+695T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54510680 | ||||||
| chr12:54510984
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0004g0178a0001c0001t0006g0242others(1): Show | 5 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.736-819T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54510984 | ||||||
| chr12:54510994
|
T | C | 7 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0017others(4): Show | 9 | HG00099.hp2 HG00639.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.736-809T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54510994 | ||||||
| chr12:54511007
|
C | T | 1 | a0001c0001t0005g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.736-796C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54511007 | ||||||
| chr12:54511105
|
G | C | 1 | a0001c0001t0021g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.736-698G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54511105 | ||||||
| chr12:54511237
|
G | A | 45 | a0001c0002t0001g0310a0001c0002t0001g0315a0001c0002t0001g0317others(42): Show | 45 | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.736-566G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54511237 | ||||||
| chr12:54511272
|
G | A | 1 | a0002c0003t0048g0065 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.736-531G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54511272 | ||||||
| chr12:54511524
|
C | T | 1 | a0002c0003t0002g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.736-279C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54511524 | ||||||
| chr12:54511660
|
G | T | 1 | a0001c0001t0005g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.736-143G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 7/30 | chr12 | 54511660 | ||||||
| chr12:54512586
|
C | T | 1 | a0001c0001t0009g0083 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.941+481C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54512586 | ||||||
| chr12:54512764
|
ATG | A | 154 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0014others(151): Show | 157 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.941+685_941+686del others(2): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr12 | 54512764 | |||||
| chr12:54512764
|
ATGTG | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0022others(82): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.941+683_941+686del others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr12 | 54512764 | |||||
| chr12:54512764
|
ATGTGTG | A | 59 | a0001c0001t0001g0283a0001c0001t0005g0286a0001c0001t0008g0288others(56): Show | 59 | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.941+681_941+686del others(6): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr12 | 54512764 | |||||
| chr12:54512793
|
T | A | 1 | a0001c0001t0005g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.941+688T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54512793 | ||||||
| chr12:54512794
|
G | T | 1 | a0001c0001t0005g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.941+689G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54512794 | ||||||
| chr12:54512798
|
G | A | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.941+693G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54512798 | ||||||
| chr12:54512799
|
A | T | 1 | a0001c0001t0005g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.941+694A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54512799 | ||||||
| chr12:54512800
|
G | T | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.941+695G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54512800 | ||||||
| chr12:54512802
|
A | T | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.941+697A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54512802 | ||||||
| chr12:54512803
|
A | T | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.941+698A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54512803 | ||||||
| chr12:54512804
|
T | G | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.941+699T>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54512804 | ||||||
| chr12:54512804
|
T | TTG | 5 | a0001c0001t0006g0044a0001c0001t0009g0063a0002c0003t0013g0061others(2): Show | 5 | HG03471.hp2 NA18955.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.941+716_941+717dup others(2): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr12 | 54512804 | |||||
| chr12:54512827
|
T | C | 2 | a0001c0001t0005g0282a0001c0001t0027g0298 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.941+722T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54512827 | ||||||
| chr12:54512964
|
G | A | 3 | a0001c0001t0002g0167a0001c0001t0005g0069a0001c0001t0028g0168 | 3 | HG01109.hp2 HG02273.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.941+859G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54512964 | ||||||
| chr12:54512972
|
A | G | 1 | a0001c0004t0002g0287 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.941+867A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54512972 | ||||||
| chr12:54513057
|
A | T | 1 | a0001c0002t0017g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.941+952A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54513057 | ||||||
| chr12:54513206
|
A | G | 1 | a0001c0001t0004g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.941+1101A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54513206 | ||||||
| chr12:54513293
|
C | T | 11 | a0001c0001t0001g0259a0001c0001t0001g0283a0001c0001t0005g0286others(8): Show | 11 | HG01928.hp2 HG01934.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.941+1188C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54513293 | ||||||
| chr12:54513317
|
C | G | 1 | a0001c0002t0008g0308 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.941+1212C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54513317 | ||||||
| chr12:54513407
|
A | G | 1 | a0001c0001t0003g0249 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.941+1302A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54513407 | ||||||
| chr12:54513555
|
G | A | 2 | a0001c0001t0001g0263a0001c0001t0019g0265 | 2 | HG00323.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.941+1450G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54513555 | ||||||
| chr12:54513670
|
T | C | 67 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026others(64): Show | 68 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.941+1565T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54513670 | ||||||
| chr12:54513968
|
A | ATG | 8 | a0001c0001t0001g0283a0001c0001t0002g0189a0001c0001t0023g0129others(5): Show | 8 | HG02040.hp2 HG02071.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.941+1895_941+1896d others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr12 | 54513968 | |||||
| chr12:54513968
|
A | ATGTG | 143 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 143 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.941+1893_941+1896d others(6): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr12 | 54513968 | |||||
| chr12:54513968
|
A | ATGTGTG | 35 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0086others(32): Show | 36 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.941+1891_941+1896d others(8): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr12 | 54513968 | |||||
| chr12:54513968
|
A | ATGTGTGT others(1): Show |
7 | a0001c0001t0004g0038a0001c0001t0010g0033a0001c0001t0010g0185others(4): Show | 7 | HG01515.hp1 HG04115.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.941+1889_941+1896d others(10): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr12 | 54513968 | |||||
| chr12:54513968
|
ATG | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0022others(121): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.941+1895_941+1896d others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr12 | 54513968 | |||||
| chr12:54513968
|
ATGTG | A | 7 | a0001c0001t0005g0008a0001c0001t0006g0256a0001c0001t0016g0268others(4): Show | 8 | HG01361.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.941+1893_941+1896d others(6): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr12 | 54513968 | |||||
| chr12:54513968
|
ATGTGTGT others(5): Show |
A | 1 | a0001c0001t0037g0213 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.941+1885_941+1896d others(14): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr12 | 54513968 | |||||
| chr12:54514100
|
A | G | 9 | a0001c0001t0001g0094a0001c0001t0001g0101a0001c0001t0001g0104others(6): Show | 9 | HG00558.hp1 HG01071.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.941+1995A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514100 | ||||||
| chr12:54514103
|
A | G | 2 | a0002c0003t0005g0215a0002c0003t0012g0136 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.941+1998A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514103 | ||||||
| chr12:54514148
|
T | G | 5 | a0001c0001t0007g0181a0001c0001t0007g0182a0001c0001t0007g0238others(2): Show | 5 | NA18954.hp2 NA18957.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.941+2043T>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514148 | ||||||
| chr12:54514177
|
C | T | 1 | a0001c0001t0004g0280 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.942-2062C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514177 | ||||||
| chr12:54514197
|
G | A | 325 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(322): Show | 330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.942-2042G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514197 | ||||||
| chr12:54514197
|
G | T | 1 | a0001c0002t0017g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.942-2042G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514197 | ||||||
| chr12:54514287
|
G | A | 10 | a0001c0001t0001g0283a0001c0001t0005g0286a0001c0001t0008g0288others(7): Show | 10 | HG01928.hp2 HG01934.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.942-1952G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514287 | ||||||
| chr12:54514326
|
C | CT | 141 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(138): Show | 142 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.942-1902dupT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr12 | 54514326 | |||||
| chr12:54514393
|
T | C | 1 | a0001c0001t0004g0278 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.942-1846T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514393 | ||||||
| chr12:54514412
|
G | C | 95 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026others(92): Show | 96 | HG00099.hp1 HG00423.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.942-1827G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514412 | ||||||
| chr12:54514473
|
A | G | 1 | a0001c0002t0001g0019 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.942-1766A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514473 | ||||||
| chr12:54514479
|
C | G | 29 | a0001c0001t0001g0056a0001c0001t0001g0094a0001c0001t0001g0101others(26): Show | 29 | HG00423.hp1 HG00558.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.942-1760C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514479 | ||||||
| chr12:54514624
|
T | C | 6 | a0001c0001t0005g0008a0001c0001t0005g0282a0001c0001t0012g0248others(3): Show | 7 | HG02559.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.942-1615T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514624 | ||||||
| chr12:54514762
|
A | G | 1 | a0001c0001t0007g0085 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.942-1477A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514762 | ||||||
| chr12:54514788
|
A | G | 22 | a0001c0001t0008g0288a0001c0001t0010g0033a0001c0001t0010g0148others(19): Show | 22 | HG01928.hp1 HG01928.hp2 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.942-1451A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514788 | ||||||
| chr12:54514891
|
G | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(209): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.942-1348G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54514891 | ||||||
| chr12:54515127
|
G | A | 1 | a0001c0001t0003g0125 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.942-1112G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54515127 | ||||||
| chr12:54515128
|
G | C | 22 | a0001c0001t0001g0046a0001c0001t0001g0294a0001c0001t0004g0077others(19): Show | 23 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.942-1111G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54515128 | ||||||
| chr12:54515321
|
TGTG | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0258a0001c0001t0001g0260 | 3 | HG00280.hp2 HG01081.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.942-913_942-911del others(3): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr12 | 54515321 | |||||
| chr12:54515360
|
G | A | 264 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(261): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.942-879G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54515360 | ||||||
| chr12:54515394
|
T | C | 13 | a0001c0001t0001g0046a0001c0001t0001g0294a0001c0001t0006g0043others(10): Show | 13 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.942-845T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54515394 | ||||||
| chr12:54515505
|
A | G | 13 | a0001c0001t0001g0046a0001c0001t0001g0294a0001c0001t0006g0043others(10): Show | 13 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.942-734A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54515505 | ||||||
| chr12:54515640
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(193): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.942-599G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54515640 | ||||||
| chr12:54515688
|
C | A | 52 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0086others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.942-551C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54515688 | ||||||
| chr12:54515953
|
C | T | 1 | a0002c0003t0002g0219 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.942-286C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54515953 | ||||||
| chr12:54516014
|
A | AT | 16 | a0001c0001t0001g0094a0001c0001t0001g0101a0001c0001t0001g0104others(13): Show | 16 | HG01071.hp2 HG01243.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.942-221dupT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr12 | 54516014 | |||||
| chr12:54516019
|
C | G | 1 | a0001c0002t0014g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.942-220C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54516019 | ||||||
| chr12:54516041
|
T | C | 1 | a0001c0002t0029g0296 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.942-198T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54516041 | ||||||
| chr12:54516052
|
G | T | 4 | a0001c0001t0004g0295a0001c0001t0006g0152a0001c0001t0070g0234others(1): Show | 4 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.942-187G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54516052 | ||||||
| chr12:54516082
|
G | A | 16 | a0001c0001t0001g0094a0001c0001t0001g0101a0001c0001t0001g0104others(13): Show | 16 | HG01071.hp2 HG01243.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.942-157G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54516082 | ||||||
| chr12:54516197
|
G | A | 4 | a0001c0001t0001g0173a0001c0002t0004g0300a0001c0012t0015g0276others(1): Show | 4 | HG01099.hp1 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.942-42G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54516197 | ||||||
| chr12:54516197
|
G | C | 1 | a0001c0002t0002g0333 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.942-42G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 9/30 | chr12 | 54516197 | ||||||
| chr12:54516344
|
C | T | 1 | a0001c0001t0003g0132 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.998+49C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 10/30 | chr12 | 54516344 | ||||||
| chr12:54516377
|
A | T | 4 | a0001c0001t0001g0173a0001c0002t0004g0300a0001c0012t0015g0276others(1): Show | 4 | HG01099.hp1 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.998+82A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 10/30 | chr12 | 54516377 | ||||||
| chr12:54516450
|
C | CT | 37 | a0001c0001t0001g0046a0001c0001t0001g0094a0001c0001t0001g0101others(34): Show | 38 | HG01071.hp2 HG01243.hp1 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.998+169dupT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 10/30 | INFO_REALIGN_3_PRIME | chr12 | 54516450 | |||||
| chr12:54516450
|
C | G | 65 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0086others(62): Show | 65 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.998+155C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 10/30 | chr12 | 54516450 | ||||||
| chr12:54516450
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.998+155C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 10/30 | chr12 | 54516450 | ||||||
| chr12:54516494
|
T | G | 16 | a0001c0001t0001g0094a0001c0001t0001g0101a0001c0001t0001g0104others(13): Show | 16 | HG01071.hp2 HG01243.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.998+199T>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 10/30 | chr12 | 54516494 | ||||||
| chr12:54516708
|
C | A | 88 | a0001c0001t0001g0046a0001c0001t0001g0094a0001c0001t0001g0101others(85): Show | 89 | HG00423.hp1 HG00558.hp1 HG00738.hp1 others(86): Show |
intron_variant | MODIFIER | c.999-188C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 10/30 | chr12 | 54516708 | ||||||
| chr12:54516828
|
C | T | 2 | a0001c0001t0007g0182a0001c0002t0003g0327 | 2 | NA18957.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.999-68C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 10/30 | chr12 | 54516828 | ||||||
| chr12:54516999
|
G | A | 4 | a0001c0001t0004g0295a0001c0001t0006g0152a0001c0001t0070g0234others(1): Show | 4 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1095+7G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 11/30 | chr12 | 54516999 | ||||||
| chr12:54517053
|
G | A | 318 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(315): Show | 323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.1095+61G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 11/30 | chr12 | 54517053 | ||||||
| chr12:54517122
|
T | G | 20 | a0001c0001t0010g0033a0001c0001t0010g0148a0001c0001t0010g0185others(17): Show | 20 | HG01928.hp1 HG01934.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.1095+130T>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 11/30 | chr12 | 54517122 | ||||||
| chr12:54517659
|
G | T | 4 | a0001c0002t0005g0318a0001c0002t0005g0320a0001c0002t0005g0321others(1): Show | 4 | HG02559.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1205+17G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 12/30 | chr12 | 54517659 | ||||||
| chr12:54517736
|
A | T | 5 | a0001c0001t0001g0292a0001c0001t0005g0282a0001c0001t0012g0248others(2): Show | 5 | HG02559.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1206-70A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 12/30 | chr12 | 54517736 | ||||||
| chr12:54517784
|
G | C | 1 | a0001c0002t0034g0306 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1206-22G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 12/30 | chr12 | 54517784 | ||||||
| chr12:54517984
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(186): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1338+46C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 13/30 | chr12 | 54517984 | ||||||
| chr12:54517996
|
C | T | 1 | a0001c0001t0060g0279 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1338+58C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 13/30 | chr12 | 54517996 | ||||||
| chr12:54518080
|
T | C | 24 | a0001c0001t0005g0282a0001c0001t0010g0033a0001c0001t0010g0148others(21): Show | 24 | HG01928.hp1 HG01934.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.1338+142T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 13/30 | chr12 | 54518080 | ||||||
| chr12:54518090
|
A | C | 24 | a0001c0001t0005g0282a0001c0001t0010g0033a0001c0001t0010g0148others(21): Show | 24 | HG01928.hp1 HG01934.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.1338+152A>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 13/30 | chr12 | 54518090 | ||||||
| chr12:54518199
|
G | A | 125 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0025others(122): Show | 126 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1338+261G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 13/30 | chr12 | 54518199 | ||||||
| chr12:54518294
|
A | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0214others(1): Show | 4 | HG02258.hp1 HG03688.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1338+356A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 13/30 | chr12 | 54518294 | ||||||
| chr12:54518320
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1339-331C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 13/30 | chr12 | 54518320 | ||||||
| chr12:54518341
|
C | CA | 25 | a0001c0001t0001g0232a0001c0001t0005g0282a0001c0001t0010g0033others(22): Show | 25 | HG01167.hp2 HG01928.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.1339-299dupA | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr12 | 54518341 | |||||
| chr12:54518392
|
A | G | 1 | a0001c0001t0050g0216 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1339-259A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 13/30 | chr12 | 54518392 | ||||||
| chr12:54518496
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1339-155C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 13/30 | chr12 | 54518496 | ||||||
| chr12:54518841
|
A | G | 1 | a0001c0001t0004g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1421-73A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 14/30 | chr12 | 54518841 | ||||||
| chr12:54519352
|
T | G | 17 | a0001c0001t0001g0094a0001c0001t0001g0101a0001c0001t0001g0104others(14): Show | 17 | HG01071.hp2 HG01243.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1625+20T>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | chr12 | 54519352 | ||||||
| chr12:54519429
|
A | AT | 183 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0025others(180): Show | 184 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1625+118dupT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | INFO_REALIGN_3_PRIME | chr12 | 54519429 | |||||
| chr12:54519429
|
A | ATT | 65 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(62): Show | 69 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1625+117_1625+118d others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | INFO_REALIGN_3_PRIME | chr12 | 54519429 | |||||
| chr12:54519429
|
A | ATTTTT | 18 | a0001c0001t0010g0033a0001c0001t0010g0148a0001c0001t0010g0185others(15): Show | 18 | HG01928.hp1 HG01934.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.1625+114_1625+118d others(7): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | INFO_REALIGN_3_PRIME | chr12 | 54519429 | |||||
| chr12:54519429
|
AT | A | 14 | a0001c0001t0001g0046a0001c0001t0001g0294a0001c0001t0006g0043others(11): Show | 14 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1625+118delT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | INFO_REALIGN_3_PRIME | chr12 | 54519429 | |||||
| chr12:54519498
|
G | C | 1 | a0001c0001t0054g0068 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1625+166G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | chr12 | 54519498 | ||||||
| chr12:54519549
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1625+217G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | chr12 | 54519549 | ||||||
| chr12:54519613
|
C | T | 2 | a0001c0001t0006g0050a0011c0006t0005g0174 | 2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1625+281C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | chr12 | 54519613 | ||||||
| chr12:54519663
|
A | G | 5 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0214others(2): Show | 5 | HG00642.hp1 HG02258.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1625+331A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | chr12 | 54519663 | ||||||
| chr12:54519765
|
T | C | 341 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(338): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1625+433T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | chr12 | 54519765 | ||||||
| chr12:54519779
|
G | A | 1 | a0002c0003t0002g0099 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1625+447G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | chr12 | 54519779 | ||||||
| chr12:54519821
|
G | A | 4 | a0001c0001t0005g0282a0001c0001t0012g0248a0001c0001t0015g0131others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1625+489G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | chr12 | 54519821 | ||||||
| chr12:54519875
|
A | AT | 10 | a0001c0001t0001g0056a0001c0001t0001g0283a0001c0001t0001g0292others(7): Show | 10 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1625+561dupT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | INFO_REALIGN_3_PRIME | chr12 | 54519875 | |||||
| chr12:54520182
|
G | C | 9 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0266others(6): Show | 9 | HG00280.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1626-512G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | chr12 | 54520182 | ||||||
| chr12:54520199
|
A | G | 1 | a0001c0001t0006g0049 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1626-495A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | chr12 | 54520199 | ||||||
| chr12:54520250
|
A | G | 3 | a0001c0001t0002g0244a0001c0001t0018g0035a0001c0001t0018g0221 | 3 | NA18983.hp1 NA19010.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1626-444A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | chr12 | 54520250 | ||||||
| chr12:54520469
|
A | G | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1626-225A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | chr12 | 54520469 | ||||||
| chr12:54520500
|
C | T | 1 | a0001c0001t0018g0186 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1626-194C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | chr12 | 54520500 | ||||||
| chr12:54520533
|
A | G | 24 | a0001c0001t0005g0282a0001c0001t0010g0033a0001c0001t0010g0148others(21): Show | 24 | HG01928.hp1 HG01934.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.1626-161A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 16/30 | chr12 | 54520533 | ||||||
| chr12:54520867
|
A | G | 20 | a0001c0001t0010g0033a0001c0001t0010g0148a0001c0001t0010g0185others(17): Show | 20 | HG01928.hp1 HG01934.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.1758+41A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 17/30 | chr12 | 54520867 | ||||||
| chr12:54521520
|
G | T | 1 | a0001c0001t0003g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1878+282G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | chr12 | 54521520 | ||||||
| chr12:54521747
|
G | A | 2 | a0002c0003t0002g0099a0002c0003t0005g0107 | 2 | NA18966.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1878+509G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | chr12 | 54521747 | ||||||
| chr12:54521886
|
A | ATG | 159 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0056others(156): Show | 159 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1878+676_1878+677d others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr12 | 54521886 | |||||
| chr12:54521886
|
A | ATGTG | 21 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0034others(18): Show | 21 | HG00558.hp1 HG00741.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.1878+674_1878+677d others(6): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr12 | 54521886 | |||||
| chr12:54521886
|
A | ATGTGTG | 3 | a0001c0001t0058g0192a0001c0002t0008g0308a0010c0018t0003g0140 | 3 | NA18949.hp2 NA19057.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1878+672_1878+677d others(8): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr12 | 54521886 | |||||
| chr12:54521886
|
A | ATGTGTGT others(3): Show |
1 | a0002c0003t0002g0106 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1878+668_1878+677d others(12): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr12 | 54521886 | |||||
| chr12:54521886
|
ATG | A | 19 | a0001c0001t0003g0006a0001c0001t0012g0248a0001c0001t0015g0131others(16): Show | 19 | HG01928.hp1 HG01934.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1878+676_1878+677d others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr12 | 54521886 | |||||
| chr12:54521886
|
ATGTG | A | 3 | a0001c0001t0001g0292a0001c0001t0003g0045a0001c0001t0003g0249 | 3 | HG02922.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1878+674_1878+677d others(6): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr12 | 54521886 | |||||
| chr12:54521916
|
A | G | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1878+678A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | chr12 | 54521916 | ||||||
| chr12:54522074
|
A | G | 1 | a0001c0002t0005g0319 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1878+836A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | chr12 | 54522074 | ||||||
| chr12:54522182
|
G | T | 1 | a0001c0002t0014g0336 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1878+944G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | chr12 | 54522182 | ||||||
| chr12:54522419
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1879-975C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | chr12 | 54522419 | ||||||
| chr12:54522583
|
A | G | 1 | a0001c0002t0029g0296 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1879-811A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | chr12 | 54522583 | ||||||
| chr12:54522744
|
C | T | 2 | a0001c0001t0004g0246a0001c0001t0004g0247 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1879-650C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | chr12 | 54522744 | ||||||
| chr12:54522796
|
G | A | 1 | a0001c0002t0073g0325 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1879-598G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | chr12 | 54522796 | ||||||
| chr12:54522874
|
A | G | 1 | a0001c0001t0001g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1879-520A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | chr12 | 54522874 | ||||||
| chr12:54522875
|
C | T | 4 | a0001c0001t0001g0292a0001c0001t0012g0248a0001c0001t0015g0131others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1879-519C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | chr12 | 54522875 | ||||||
| chr12:54522906
|
C | T | 3 | a0001c0001t0012g0248a0001c0001t0015g0131a0001c0001t0065g0128 | 3 | HG02622.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1879-488C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | chr12 | 54522906 | ||||||
| chr12:54523100
|
C | T | 1 | a0001c0002t0005g0335 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1879-294C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 18/30 | chr12 | 54523100 | ||||||
| chr12:54524023
|
T | C | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2156+67T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54524023 | ||||||
| chr12:54524217
|
C | T | 1 | a0001c0001t0004g0126 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2156+261C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54524217 | ||||||
| chr12:54524229
|
A | C | 1 | a0001c0001t0069g0155 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2156+273A>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54524229 | ||||||
| chr12:54524317
|
A | G | 1 | a0001c0001t0004g0280 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2156+361A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54524317 | ||||||
| chr12:54524455
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(257): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2156+499T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54524455 | ||||||
| chr12:54525263
|
C | T | 20 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0266others(17): Show | 20 | HG00280.hp1 HG01071.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2157-1265C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54525263 | ||||||
| chr12:54525283
|
G | A | 2 | a0002c0003t0012g0060a0002c0003t0012g0073 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2157-1245G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54525283 | ||||||
| chr12:54525554
|
T | C | 1 | a0002c0003t0002g0106 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2157-974T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54525554 | ||||||
| chr12:54525640
|
GC | G | 3 | a0001c0001t0006g0152a0001c0009t0004g0322a0001c0014t0032g0172 | 3 | HG02109.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2157-885delC | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr12 | 54525640 | |||||
| chr12:54525641
|
C | A | 1 | a0001c0001t0001g0283 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2157-887C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54525641 | ||||||
| chr12:54525655
|
C | T | 1 | a0001c0002t0034g0306 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2157-873C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54525655 | ||||||
| chr12:54525672
|
C | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(23): Show | 29 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.2157-856C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54525672 | ||||||
| chr12:54525831
|
T | C | 1 | a0001c0001t0056g0138 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2157-697T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54525831 | ||||||
| chr12:54525868
|
A | G | 4 | a0001c0001t0015g0131a0001c0001t0065g0128a0001c0005t0063g0188others(1): Show | 4 | HG01346.hp1 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2157-660A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54525868 | ||||||
| chr12:54525966
|
C | A | 80 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0078others(77): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.2157-562C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54525966 | ||||||
| chr12:54526039
|
A | G | 5 | a0001c0001t0004g0130a0001c0001t0004g0178a0001c0001t0006g0242others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2157-489A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54526039 | ||||||
| chr12:54526245
|
C | G | 1 | a0010c0018t0003g0140 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2157-283C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 20/30 | chr12 | 54526245 | ||||||
| chr12:54526752
|
T | C | 2 | a0001c0001t0006g0030a0001c0001t0006g0171 | 2 | HG00408.hp2 HG00438.hp2 |
splice_region_variant&intron_variant | LOW | c.2375+6T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/30 | chr12 | 54526752 | ||||||
| chr12:54526782
|
T | C | 79 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0078others(76): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.2375+36T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/30 | chr12 | 54526782 | ||||||
| chr12:54526807
|
G | A | 71 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0078others(68): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.2375+61G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/30 | chr12 | 54526807 | ||||||
| chr12:54526825
|
G | A | 1 | a0001c0002t0009g0018 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2375+79G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/30 | chr12 | 54526825 | ||||||
| chr12:54526860
|
T | C | 1 | a0001c0002t0005g0319 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2375+114T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/30 | chr12 | 54526860 | ||||||
| chr12:54526879
|
G | C | 79 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0078others(76): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.2375+133G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/30 | chr12 | 54526879 | ||||||
| chr12:54526989
|
C | A | 2 | a0001c0005t0063g0188a0001c0005t0064g0226 | 2 | HG01346.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.2375+243C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/30 | chr12 | 54526989 | ||||||
| chr12:54526995
|
T | C | 86 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0078others(83): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.2375+249T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/30 | chr12 | 54526995 | ||||||
| chr12:54527188
|
A | G | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2375+442A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/30 | chr12 | 54527188 | ||||||
| chr12:54527288
|
C | G | 1 | a0001c0002t0022g0020 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2375+542C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/30 | chr12 | 54527288 | ||||||
| chr12:54527352
|
C | T | 2 | a0001c0009t0004g0322a0001c0014t0032g0172 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2375+606C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/30 | chr12 | 54527352 | ||||||
| chr12:54527387
|
G | A | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2375+641G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/30 | chr12 | 54527387 | ||||||
| chr12:54527628
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0180 | 2 | HG01256.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2376-619G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/30 | chr12 | 54527628 | ||||||
| chr12:54527668
|
C | T | 3 | a0001c0001t0014g0224a0001c0012t0015g0276a0009c0017t0014g0302 | 3 | HG02451.hp1 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2376-579C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 21/30 | chr12 | 54527668 | ||||||
| chr12:54528446
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2506+69C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54528446 | ||||||
| chr12:54528535
|
G | C | 1 | a0001c0004t0002g0289 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2506+158G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54528535 | ||||||
| chr12:54528556
|
A | G | 170 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0078others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.2506+179A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54528556 | ||||||
| chr12:54528611
|
A | ATCT | 5 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026others(2): Show | 5 | HG02698.hp1 HG02723.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.2506+254_2506+256d others(5): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr12 | 54528611 | |||||
| chr12:54528702
|
C | T | 56 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0091others(53): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.2506+325C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54528702 | ||||||
| chr12:54528713
|
C | T | 1 | a0001c0002t0034g0306 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2506+336C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54528713 | ||||||
| chr12:54528797
|
TTA | T | 58 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0091others(55): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.2506+434_2506+435d others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr12 | 54528797 | |||||
| chr12:54529118
|
G | A | 3 | a0001c0001t0030g0028a0001c0001t0033g0054a0001c0002t0022g0304 | 3 | HG02615.hp1 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2506+741G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54529118 | ||||||
| chr12:54529250
|
C | T | 58 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0091others(55): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.2506+873C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54529250 | ||||||
| chr12:54529254
|
G | C | 2 | a0001c0001t0067g0133a0001c0001t0068g0134 | 2 | NA18985.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2506+877G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54529254 | ||||||
| chr12:54529298
|
A | G | 83 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0078others(80): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.2506+921A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54529298 | ||||||
| chr12:54529310
|
T | A | 15 | a0001c0001t0001g0046a0001c0001t0001g0294a0001c0001t0006g0043others(12): Show | 15 | HG02109.hp2 HG02451.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.2506+933T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54529310 | ||||||
| chr12:54529316
|
G | C | 1 | a0001c0002t0034g0306 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2506+939G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54529316 | ||||||
| chr12:54529327
|
G | A | 13 | a0001c0001t0007g0085a0001c0001t0007g0114a0001c0001t0007g0139others(10): Show | 13 | HG02083.hp1 HG02148.hp1 NA18944.hp1 others(10): Show |
intron_variant | MODIFIER | c.2506+950G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54529327 | ||||||
| chr12:54529498
|
G | A | 2 | a0001c0001t0015g0131a0001c0001t0065g0128 | 2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2506+1121G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54529498 | ||||||
| chr12:54529540
|
C | A | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2506+1163C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54529540 | ||||||
| chr12:54529904
|
T | C | 1 | a0001c0001t0002g0230 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2507-1356T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54529904 | ||||||
| chr12:54529908
|
T | A | 1 | a0001c0005t0064g0226 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2507-1352T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54529908 | ||||||
| chr12:54529979
|
A | G | 1 | a0001c0001t0001g0266 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2507-1281A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54529979 | ||||||
| chr12:54529986
|
C | T | 1 | a0001c0001t0057g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2507-1274C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54529986 | ||||||
| chr12:54530168
|
G | A | 1 | a0002c0003t0002g0029 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2507-1092G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54530168 | ||||||
| chr12:54530362
|
C | T | 18 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0266others(15): Show | 18 | HG00280.hp1 HG01071.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2507-898C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54530362 | ||||||
| chr12:54530396
|
G | A | 17 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0266others(14): Show | 17 | HG00280.hp1 HG01071.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.2507-864G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54530396 | ||||||
| chr12:54530606
|
A | G | 4 | a0001c0001t0031g0053a0001c0001t0031g0055a0001c0002t0005g0076others(1): Show | 4 | HG02970.hp1 HG02976.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2507-654A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54530606 | ||||||
| chr12:54530720
|
C | T | 65 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0091others(62): Show | 68 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.2507-540C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54530720 | ||||||
| chr12:54530734
|
A | G | 1 | a0001c0002t0034g0306 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2507-526A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54530734 | ||||||
| chr12:54530767
|
C | T | 2 | a0001c0001t0002g0122a0002c0003t0005g0111 | 2 | HG01358.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.2507-493C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54530767 | ||||||
| chr12:54530786
|
T | A | 2 | a0001c0001t0033g0054a0001c0001t0056g0138 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2507-474T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54530786 | ||||||
| chr12:54530923
|
C | T | 3 | a0001c0001t0001g0292a0001c0001t0004g0184a0002c0003t0012g0136 | 3 | HG03098.hp2 HG03834.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2507-337C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54530923 | ||||||
| chr12:54530924
|
G | A | 1 | a0001c0001t0057g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2507-336G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54530924 | ||||||
| chr12:54530988
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0091a0001c0001t0001g0094others(40): Show | 46 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.2507-272G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54530988 | ||||||
| chr12:54531087
|
A | T | 2 | a0001c0001t0033g0054a0001c0001t0056g0138 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2507-173A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 22/30 | chr12 | 54531087 | ||||||
| chr12:54531632
|
T | A | 1 | a0001c0001t0004g0250 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2698+48T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 24/30 | chr12 | 54531632 | ||||||
| chr12:54531890
|
T | G | 16 | a0001c0001t0001g0078a0001c0001t0001g0261a0001c0001t0001g0262others(13): Show | 16 | HG00280.hp1 HG00733.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.2781+65T>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 25/30 | chr12 | 54531890 | ||||||
| chr12:54531938
|
G | A | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2781+113G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 25/30 | chr12 | 54531938 | ||||||
| chr12:54531945
|
G | A | 1 | a0001c0001t0044g0166 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2781+120G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 25/30 | chr12 | 54531945 | ||||||
| chr12:54531966
|
A | C | 340 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(337): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.2781+141A>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 25/30 | chr12 | 54531966 | ||||||
| chr12:54532065
|
T | C | 1 | a0001c0001t0057g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2782-105T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 25/30 | chr12 | 54532065 | ||||||
| chr12:54532087
|
CT | C | 18 | a0001c0001t0001g0078a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 18 | HG00280.hp1 HG00733.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2782-68delT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr12 | 54532087 | |||||
| chr12:54532087
|
CTT | C | 67 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0091others(64): Show | 70 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.2782-69_2782-68del others(2): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr12 | 54532087 | |||||
| chr12:54532363
|
C | T | 2 | a0001c0001t0003g0141a0001c0002t0001g0310 | 2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2862+113C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54532363 | ||||||
| chr12:54532423
|
G | A | 1 | a0001c0002t0034g0306 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2862+173G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54532423 | ||||||
| chr12:54532468
|
A | G | 1 | a0001c0001t0027g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2862+218A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54532468 | ||||||
| chr12:54532545
|
G | A | 64 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0091others(61): Show | 67 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.2862+295G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54532545 | ||||||
| chr12:54532584
|
G | A | 1 | a0004c0008t0004g0299 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2862+334G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54532584 | ||||||
| chr12:54532646
|
C | A | 2 | a0001c0009t0004g0322a0001c0014t0032g0172 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2862+396C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54532646 | ||||||
| chr12:54532816
|
C | A | 4 | a0001c0001t0027g0298a0001c0001t0033g0054a0001c0001t0056g0138others(1): Show | 4 | HG02486.hp2 HG02970.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2862+566C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54532816 | ||||||
| chr12:54533033
|
T | G | 74 | a0001c0001t0001g0102a0001c0001t0001g0194a0001c0001t0002g0005others(71): Show | 74 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.2862+783T>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54533033 | ||||||
| chr12:54533098
|
G | A | 4 | a0001c0001t0027g0298a0001c0001t0033g0054a0001c0001t0056g0138others(1): Show | 4 | HG02486.hp2 HG02970.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2862+848G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54533098 | ||||||
| chr12:54533249
|
T | C | 2 | a0001c0001t0033g0054a0001c0001t0056g0138 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2862+999T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54533249 | ||||||
| chr12:54533250
|
G | C | 3 | a0001c0001t0001g0151a0001c0002t0001g0310a0001c0002t0001g0317 | 3 | HG00099.hp1 HG00741.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2862+1000G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54533250 | ||||||
| chr12:54533450
|
G | A | 1 | a0001c0004t0002g0287 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2862+1200G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54533450 | ||||||
| chr12:54533460
|
A | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0263others(4): Show | 10 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2862+1210A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54533460 | ||||||
| chr12:54533464
|
G | C | 20 | a0001c0001t0001g0046a0001c0001t0001g0294a0001c0001t0006g0043others(17): Show | 20 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.2862+1214G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54533464 | ||||||
| chr12:54533476
|
A | C | 2 | a0001c0001t0059g0164a0001c0002t0014g0336 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2862+1226A>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54533476 | ||||||
| chr12:54533492
|
A | T | 2 | a0001c0001t0025g0169a0003c0007t0025g0332 | 2 | HG01074.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2862+1242A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54533492 | ||||||
| chr12:54533577
|
CT | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0091a0001c0001t0001g0151others(14): Show | 20 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.2862+1338delT | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr12 | 54533577 | |||||
| chr12:54533838
|
G | A | 1 | a0001c0001t0030g0153 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2863-1266G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54533838 | ||||||
| chr12:54533944
|
T | C | 22 | a0001c0001t0001g0046a0001c0001t0001g0294a0001c0001t0006g0043others(19): Show | 22 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.2863-1160T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54533944 | ||||||
| chr12:54534043
|
G | T | 2 | a0001c0001t0003g0006a0005c0016t0003g0006 | 2 | NA18981.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2863-1061G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54534043 | ||||||
| chr12:54534262
|
G | A | 169 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0025others(166): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2863-842G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54534262 | ||||||
| chr12:54534527
|
C | T | 2 | a0001c0001t0033g0054a0001c0001t0056g0138 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2863-577C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54534527 | ||||||
| chr12:54534563
|
A | G | 1 | a0001c0002t0008g0308 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2863-541A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54534563 | ||||||
| chr12:54534586
|
G | A | 8 | a0001c0001t0001g0176a0001c0001t0003g0132a0001c0001t0003g0157others(5): Show | 8 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(5): Show |
intron_variant | MODIFIER | c.2863-518G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54534586 | ||||||
| chr12:54534658
|
G | C | 1 | a0001c0001t0004g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2863-446G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54534658 | ||||||
| chr12:54534785
|
G | A | 1 | a0001c0001t0004g0278 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2863-319G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54534785 | ||||||
| chr12:54534813
|
T | A | 11 | a0001c0001t0001g0292a0001c0001t0004g0077a0001c0001t0004g0280others(8): Show | 11 | HG00738.hp2 HG01346.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2863-291T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54534813 | ||||||
| chr12:54534850
|
C | T | 38 | a0001c0001t0001g0046a0001c0001t0001g0078a0001c0001t0001g0261others(35): Show | 38 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.2863-254C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54534850 | ||||||
| chr12:54534997
|
T | TA | 19 | a0001c0001t0001g0078a0001c0001t0001g0259a0001c0001t0001g0261others(16): Show | 19 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2863-97dupA | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr12 | 54534997 | |||||
| chr12:54535041
|
T | A | 1 | a0001c0001t0004g0038 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2863-63T>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 26/30 | chr12 | 54535041 | ||||||
| chr12:54535280
|
G | A | 1 | a0001c0001t0004g0250 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2956+83G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 27/30 | chr12 | 54535280 | ||||||
| chr12:54535307
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2956+110G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 27/30 | chr12 | 54535307 | ||||||
| chr12:54535389
|
A | C | 1 | a0001c0001t0021g0257 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2956+192A>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 27/30 | chr12 | 54535389 | ||||||
| chr12:54535431
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2956+234C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 27/30 | chr12 | 54535431 | ||||||
| chr12:54535451
|
A | C | 1 | a0001c0001t0007g0238 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2956+254A>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 27/30 | chr12 | 54535451 | ||||||
| chr12:54535488
|
C | G | 75 | a0001c0001t0001g0046a0001c0001t0001g0078a0001c0001t0001g0259others(72): Show | 75 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.2956+291C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 27/30 | chr12 | 54535488 | ||||||
| chr12:54535539
|
G | T | 1 | a0001c0001t0061g0024 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2956+342G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 27/30 | chr12 | 54535539 | ||||||
| chr12:54535561
|
G | A | 1 | a0001c0001t0030g0028 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2956+364G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 27/30 | chr12 | 54535561 | ||||||
| chr12:54535571
|
G | A | 1 | a0001c0001t0004g0250 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2956+374G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 27/30 | chr12 | 54535571 | ||||||
| chr12:54535580
|
C | T | 75 | a0001c0001t0001g0046a0001c0001t0001g0078a0001c0001t0001g0259others(72): Show | 75 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.2956+383C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 27/30 | chr12 | 54535580 | ||||||
| chr12:54535782
|
C | G | 1 | a0001c0001t0006g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2957-347C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 27/30 | chr12 | 54535782 | ||||||
| chr12:54536054
|
AG | A | 19 | a0001c0001t0001g0078a0001c0001t0001g0259a0001c0001t0001g0261others(16): Show | 19 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2957-73delG | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 27/30 | INFO_REALIGN_3_PRIME | chr12 | 54536054 | |||||
| chr12:54536370
|
C | T | 1 | a0001c0001t0016g0269 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3073+125C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 28/30 | chr12 | 54536370 | ||||||
| chr12:54536716
|
G | GAA | 13 | a0001c0001t0001g0292a0001c0001t0004g0280a0001c0001t0005g0089others(10): Show | 13 | HG00738.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3074-216_3074-215d others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 28/30 | INFO_REALIGN_3_PRIME | chr12 | 54536716 | |||||
| chr12:54536716
|
GA | G | 137 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0015others(134): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.3074-215delA | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 28/30 | INFO_REALIGN_3_PRIME | chr12 | 54536716 | |||||
| chr12:54536716
|
GAA | G | 114 | a0001c0001t0001g0078a0001c0001t0001g0102a0001c0001t0001g0259others(111): Show | 114 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.3074-216_3074-215d others(4): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 28/30 | INFO_REALIGN_3_PRIME | chr12 | 54536716 | |||||
| chr12:54536747
|
A | G | 99 | a0001c0001t0001g0102a0001c0001t0001g0194a0001c0001t0001g0259others(96): Show | 99 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.3074-197A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 28/30 | chr12 | 54536747 | ||||||
| chr12:54537130
|
A | G | 92 | a0001c0001t0001g0102a0001c0001t0001g0194a0001c0001t0001g0259others(89): Show | 92 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.3183+77A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54537130 | ||||||
| chr12:54537142
|
G | A | 4 | a0001c0001t0070g0234a0001c0002t0005g0318a0001c0002t0005g0320others(1): Show | 4 | HG01891.hp1 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3183+89G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54537142 | ||||||
| chr12:54537433
|
C | A | 12 | a0001c0001t0001g0292a0001c0001t0004g0280a0001c0001t0005g0089others(9): Show | 12 | HG00738.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.3183+380C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54537433 | ||||||
| chr12:54537521
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01074.hp2 HG01081.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.3183+468G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54537521 | ||||||
| chr12:54537691
|
G | T | 7 | a0001c0001t0006g0256a0001c0001t0059g0164a0001c0001t0070g0234others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3183+638G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54537691 | ||||||
| chr12:54537709
|
T | G | 3 | a0001c0001t0004g0077a0001c0001t0030g0028a0001c0001t0056g0138 | 3 | HG02486.hp2 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3183+656T>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54537709 | ||||||
| chr12:54537771
|
A | G | 117 | a0001c0001t0001g0078a0001c0001t0001g0102a0001c0001t0001g0194others(114): Show | 117 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.3183+718A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54537771 | ||||||
| chr12:54537829
|
G | A | 131 | a0001c0001t0001g0078a0001c0001t0001g0102a0001c0001t0001g0194others(128): Show | 131 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.3183+776G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54537829 | ||||||
| chr12:54537860
|
A | T | 93 | a0001c0001t0001g0102a0001c0001t0001g0194a0001c0001t0001g0259others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.3183+807A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54537860 | ||||||
| chr12:54537922
|
A | G | 115 | a0001c0001t0001g0078a0001c0001t0001g0102a0001c0001t0001g0194others(112): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.3183+869A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54537922 | ||||||
| chr12:54538033
|
C | T | 7 | a0001c0001t0006g0256a0001c0001t0059g0164a0001c0001t0070g0234others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3184-851C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54538033 | ||||||
| chr12:54538093
|
G | A | 7 | a0001c0001t0006g0256a0001c0001t0059g0164a0001c0001t0070g0234others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3184-791G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54538093 | ||||||
| chr12:54538244
|
C | A | 4 | a0001c0004t0002g0285a0001c0004t0002g0289a0001c0004t0002g0290others(1): Show | 4 | HG01928.hp1 HG01934.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.3184-640C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54538244 | ||||||
| chr12:54538283
|
G | A | 1 | a0001c0001t0021g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3184-601G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54538283 | ||||||
| chr12:54538622
|
C | T | 22 | a0001c0001t0001g0078a0001c0001t0001g0261a0001c0001t0001g0262others(19): Show | 22 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.3184-262C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 29/30 | chr12 | 54538622 | ||||||
| chr12:54538992
|
T | C | 1 | a0001c0002t0034g0306 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3273+19T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54538992 | ||||||
| chr12:54539004
|
T | C | 300 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(297): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.3273+31T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539004 | ||||||
| chr12:54539068
|
A | T | 1 | a0002c0003t0012g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3273+95A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539068 | ||||||
| chr12:54539273
|
G | C | 149 | a0001c0001t0001g0034a0001c0001t0001g0078a0001c0001t0001g0102others(146): Show | 150 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.3273+300G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539273 | ||||||
| chr12:54539359
|
A | T | 14 | a0001c0001t0004g0278a0001c0001t0006g0256a0001c0001t0015g0131others(11): Show | 14 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.3273+386A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539359 | ||||||
| chr12:54539416
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3273+443G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539416 | ||||||
| chr12:54539458
|
C | A | 1 | a0001c0001t0001g0264 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3273+485C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539458 | ||||||
| chr12:54539480
|
G | T | 1 | a0001c0001t0056g0138 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3273+507G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539480 | ||||||
| chr12:54539525
|
T | C | 2 | a0001c0001t0004g0032a0001c0001t0004g0038 | 2 | HG00639.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.3273+552T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539525 | ||||||
| chr12:54539656
|
T | C | 10 | a0001c0001t0001g0176a0001c0001t0003g0132a0001c0001t0003g0157others(7): Show | 10 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(7): Show |
intron_variant | MODIFIER | c.3273+683T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539656 | ||||||
| chr12:54539666
|
C | G | 1 | a0001c0001t0009g0063 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3273+693C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539666 | ||||||
| chr12:54539681
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3273+708C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539681 | ||||||
| chr12:54539780
|
C | T | 2 | a0001c0002t0005g0076a0001c0002t0022g0020 | 2 | HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3273+807C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539780 | ||||||
| chr12:54539848
|
G | A | 1 | a0001c0002t0004g0340 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3273+875G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539848 | ||||||
| chr12:54539881
|
C | T | 1 | a0001c0002t0001g0040 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3273+908C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539881 | ||||||
| chr12:54539887
|
G | A | 3 | a0001c0001t0001g0261a0001c0001t0001g0266a0001c0002t0001g0040 | 3 | HG01071.hp1 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3273+914G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539887 | ||||||
| chr12:54539923
|
C | T | 3 | a0001c0002t0017g0013a0001c0002t0017g0334a0001c0002t0017g0338 | 3 | HG01109.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3273+950C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539923 | ||||||
| chr12:54539924
|
G | A | 1 | a0002c0003t0001g0175 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3273+951G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539924 | ||||||
| chr12:54539928
|
G | T | 6 | a0001c0001t0001g0259a0001c0001t0003g0045a0001c0001t0003g0249others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3273+955G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54539928 | ||||||
| chr12:54540108
|
C | G | 1 | a0002c0003t0001g0175 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3273+1135C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54540108 | ||||||
| chr12:54540207
|
G | A | 8 | a0001c0001t0001g0102a0001c0001t0001g0123a0001c0001t0001g0283others(5): Show | 8 | HG00544.hp1 HG02074.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.3273+1234G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54540207 | ||||||
| chr12:54540594
|
A | G | 1 | a0001c0002t0015g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3273+1621A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54540594 | ||||||
| chr12:54540618
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3273+1645A>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54540618 | ||||||
| chr12:54540748
|
C | T | 2 | a0001c0001t0003g0006a0005c0016t0003g0006 | 2 | NA18981.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.3273+1775C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54540748 | ||||||
| chr12:54540964
|
G | T | 2 | a0001c0001t0031g0053a0001c0001t0031g0055 | 2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3274-1611G>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54540964 | ||||||
| chr12:54541103
|
G | A | 2 | a0001c0001t0004g0032a0001c0001t0004g0038 | 2 | HG00639.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.3274-1472G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54541103 | ||||||
| chr12:54541113
|
C | A | 10 | a0001c0001t0001g0046a0001c0001t0006g0043a0001c0001t0006g0044others(7): Show | 10 | HG02451.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3274-1462C>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54541113 | ||||||
| chr12:54541148
|
A | G | 40 | a0001c0001t0003g0218a0001c0001t0004g0032a0001c0001t0004g0038others(37): Show | 40 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.3274-1427A>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54541148 | ||||||
| chr12:54541487
|
CTTGAAAG others(4): Show |
C | 3 | a0001c0001t0031g0053a0001c0001t0031g0055a0002c0003t0062g0251 | 3 | HG00738.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3274-1087_3274-107 others(15): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54541487 | ||||||
| chr12:54541891
|
G | A | 3 | a0001c0001t0031g0053a0001c0001t0031g0055a0002c0003t0062g0251 | 3 | HG00738.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3274-684G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54541891 | ||||||
| chr12:54541953
|
C | G | 1 | a0008c0013t0003g0149 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3274-622C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54541953 | ||||||
| chr12:54542004
|
G | C | 2 | a0001c0001t0004g0062a0001c0001t0004g0126 | 2 | HG00323.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.3274-571G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54542004 | ||||||
| chr12:54542025
|
G | A | 1 | a0001c0001t0004g0250 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3274-550G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54542025 | ||||||
| chr12:54542151
|
G | A | 1 | a0001c0002t0073g0325 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.3274-424G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54542151 | ||||||
| chr12:54542165
|
C | G | 1 | a0001c0001t0002g0167 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3274-410C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54542165 | ||||||
| chr12:54542232
|
C | T | 2 | a0001c0001t0030g0028a0001c0001t0030g0153 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3274-343C>T | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54542232 | ||||||
| chr12:54542259
|
C | G | 1 | a0001c0002t0005g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3274-316C>G | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54542259 | ||||||
| chr12:54542440
|
G | A | 1 | a0001c0001t0054g0068 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3274-135G>A | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54542440 | ||||||
| chr12:54542445
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3274-130T>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54542445 | ||||||
| chr12:54542516
|
G | C | 1 | a0001c0001t0001g0262 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3274-59G>C | NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 30/30 | chr12 | 54542516 |