Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 51701 |
|---|---|
| ensemblid | ENSG00000087095.13 |
| hgncid | 29858 |
| symbol | NLK |
| name | nemo like kinase |
| refseq_nuc | NM_016231.5 |
| refseq_prot | NP_057315.3 |
| ensembl_nuc | ENST00000407008.8 |
| ensembl_prot | ENSP00000384625.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 28042677 |
| end | 28196381 |
| strand | + |
| ver | v1.2 |
| region | chr17:28042677-28196381 |
| region5000 | chr17:28037677-28201381 |
| regionname0 | NLK_chr17_28042677_28196381 |
| regionname5000 | NLK_chr17_28037677_28201381 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 527 | 105 | 43 | 16 | 32 | 4 | 8 | 18 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0002 | 0/0 | 527 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0003 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1584 | 99 | 37 | 16 | 32 | 4 | 8 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| c0002 | 0/0 | 1584 | 4 | 4 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| c0003 | 0/0 | 1584 | 2 | 0 | 2 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| c0004 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| c0005 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| c0006 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1943 | 65 | 22 | 17 | 18 | 3 | 4 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| t0002 | 0/0 | 1945 | 18 | 7 | 1 | 6 | 1 | 3 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| t0003 | 0/1 | 1947 | 12 | 10 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| t0004 | 0/0 | 1953 | 6 | 0 | 0 | 6 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| t0005 | 0/0 | 1941 | 4 | 3 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| t0006 | 0/0 | 1951 | 2 | 2 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| t0007 | 0/0 | 1943 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1584 | 99 | 37 | 16 | 32 | 4 | 8 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0001c0002 | 0/0 | 1584 | 4 | 4 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0001c0005 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0001c0006 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0002c0003 | 0/0 | 1584 | 2 | 0 | 2 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0003c0004 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3526 | 60 | 19 | 15 | 18 | 3 | 4 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0001c0001t0002 | 0/0 | 3528 | 18 | 7 | 1 | 6 | 1 | 3 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0001c0001t0003 | 0/1 | 3530 | 8 | 6 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0001c0001t0004 | 0/0 | 3536 | 6 | 0 | 0 | 6 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0001c0001t0005 | 0/0 | 3524 | 4 | 3 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0001c0001t0006 | 0/0 | 3534 | 2 | 2 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0001c0001t0007 | 0/0 | 3526 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0001c0002t0003 | 0/0 | 3530 | 4 | 4 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0001c0005t0001 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0001c0006t0001 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0002c0003t0001 | 0/0 | 3526 | 2 | 0 | 2 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| a0003c0004t0001 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | copy fasta | chr17 | 28037677 | 28201381 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0003g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0002t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0002t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0002t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0005t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0001c0006t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0002c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| a0003c0004t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | GBR | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | CHS | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | CHS | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01070 | hp1 | a0002 | c0003 | t0001 | g0043 | AMR | PUR | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0047 | AMR | PUR | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | KHV | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | CDX | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02165 | hp2 | a0001 | c0001 | t0007 | g0058 | EAS | CDX | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | ACB | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02257 | hp2 | a0001 | c0005 | t0001 | g0059 | AFR | ACB | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0107 | AFR | ACB | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02809 | hp1 | a0003 | c0004 | t0001 | g0018 | AFR | GWD | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02970 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | ESN | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | MSL | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | MSL | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | MSL | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | MSL | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0095 | SAS | PJL | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | BEB | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | BEB | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18522 | hp1 | a0001 | c0006 | t0001 | g0087 | AFR | YRI | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | YRI | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0106 | AFR | LWK | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | LWK | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ASW | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ASW | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0090 | EUR | TSI | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | GIH | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | GIH | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | ACB | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | USA | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA20300 | hp2 | a0001 | c0002 | t0003 | g0011 | AFR | USA | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | LWK | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0076 | REF | REF | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0088 | REF | REF | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28043013
|
A | G | 1 | a0002 | 2 | HG01070.hp1 HG01071.hp2 |
missense_variant | MODERATE | c.140A>G | p.His47Arg | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/11 | 337/3526 | 140/1584 | 47/527 | chr17 | 28043013 | ||
| chr17:28191022
|
C | A | 1 | a0003 | 1 | HG02809.hp1 | missense_variant&splice_region_variant | MODERATE | c.1238C>A | p.Ser413Tyr | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 9/11 | 1435/3526 | 1238/1584 | 413/527 | chr17 | 28191022 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28043167
|
A | C | 1 | a0001c0006 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.294A>C | p.Ala98Ala | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/11 | 491/3526 | 294/1584 | 98/527 | chr17 | 28043167 | ||
| chr17:28191081
|
C | A | 1 | a0001c0002 | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.1297C>A | p.Arg433Arg | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 9/11 | 1494/3526 | 1297/1584 | 433/527 | chr17 | 28191081 | ||
| chr17:28192178
|
C | T | 1 | a0001c0005 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1494C>T | p.Ile498Ile | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 10/11 | 1691/3526 | 1494/1584 | 498/527 | chr17 | 28192178 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28194983
|
T | TCA | 1 | a0001c0001t0002 | 18 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*378_*379dupCA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 11/11 | 380 | INFO_REALIGN_3_PRIME | chr17 | 28194983 | ||||
| chr17:28194983
|
T | TCACA | 2 | a0001c0001t0003a0001c0002t0003 | 12 | HG00609.hp2 HG02109.hp2 HG02717.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*376_*379dupCACA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 11/11 | 380 | INFO_REALIGN_3_PRIME | chr17 | 28194983 | ||||
| chr17:28194983
|
T | TCACACAC others(1): Show |
1 | a0001c0001t0006 | 2 | HG02572.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*372_*379dupCACACA others(2): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 11/11 | 380 | INFO_REALIGN_3_PRIME | chr17 | 28194983 | ||||
| chr17:28194983
|
T | TCACACAC others(3): Show |
1 | a0001c0001t0004 | 6 | HG00609.hp1 HG02040.hp1 HG02165.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*370_*379dupCACACA others(4): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 11/11 | 380 | INFO_REALIGN_3_PRIME | chr17 | 28194983 | ||||
| chr17:28194983
|
TCA | T | 1 | a0001c0001t0005 | 4 | HG02257.hp1 HG02451.hp2 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*378_*379delCA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 11/11 | 378 | INFO_REALIGN_3_PRIME | chr17 | 28194983 | ||||
| chr17:28196306
|
G | A | 1 | a0001c0001t0007 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1670G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 11/11 | 1670 | chr17 | 28196306 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28043464
|
C | G | 1 | a0001c0001t0002g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.458+133C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28043464 | ||||||
| chr17:28043474
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.458+143T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28043474 | ||||||
| chr17:28043519
|
G | C | 1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.458+188G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28043519 | ||||||
| chr17:28043581
|
A | G | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.458+250A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28043581 | ||||||
| chr17:28043655
|
T | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(14): Show | 17 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.458+324T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28043655 | ||||||
| chr17:28043715
|
G | A | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.458+384G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28043715 | ||||||
| chr17:28043760
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.458+429A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28043760 | ||||||
| chr17:28043886
|
C | T | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.458+555C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28043886 | ||||||
| chr17:28044303
|
A | G | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG01433.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.458+972A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28044303 | ||||||
| chr17:28044320
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.458+989A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28044320 | ||||||
| chr17:28044522
|
T | C | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.458+1191T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28044522 | ||||||
| chr17:28044535
|
C | A | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.458+1204C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28044535 | ||||||
| chr17:28045042
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+1711G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28045042 | ||||||
| chr17:28045074
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.458+1743A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28045074 | ||||||
| chr17:28045369
|
T | G | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.458+2038T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28045369 | ||||||
| chr17:28045641
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.458+2310A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28045641 | ||||||
| chr17:28046175
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+2844G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28046175 | ||||||
| chr17:28046263
|
T | C | 1 | a0001c0001t0002g0017 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.458+2932T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28046263 | ||||||
| chr17:28046738
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+3407G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28046738 | ||||||
| chr17:28046814
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.458+3483A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28046814 | ||||||
| chr17:28046987
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.458+3656C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28046987 | ||||||
| chr17:28047154
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+3823C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28047154 | ||||||
| chr17:28047310
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.458+3979A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28047310 | ||||||
| chr17:28047550
|
C | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+4219C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28047550 | ||||||
| chr17:28047550
|
C | G | 1 | a0001c0001t0005g0095 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.458+4219C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28047550 | ||||||
| chr17:28047563
|
A | G | 1 | a0001c0001t0004g0094 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.458+4232A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28047563 | ||||||
| chr17:28047608
|
C | G | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.458+4277C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28047608 | ||||||
| chr17:28048193
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.458+4862A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28048193 | ||||||
| chr17:28048355
|
T | C | 1 | a0003c0004t0001g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.458+5024T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28048355 | ||||||
| chr17:28048392
|
G | A | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.458+5061G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28048392 | ||||||
| chr17:28048441
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.458+5110G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28048441 | ||||||
| chr17:28048761
|
A | G | 1 | a0001c0001t0002g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.458+5430A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28048761 | ||||||
| chr17:28049178
|
T | A | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.458+5847T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28049178 | ||||||
| chr17:28049616
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+6285A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28049616 | ||||||
| chr17:28049774
|
A | C | 5 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0002g0081others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.458+6443A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28049774 | ||||||
| chr17:28050942
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+7611T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28050942 | ||||||
| chr17:28050983
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.458+7652G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28050983 | ||||||
| chr17:28051079
|
C | CA | 9 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(6): Show | 9 | HG01243.hp1 HG01433.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.458+7766dupA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28051079 | |||||
| chr17:28051277
|
A | ATTTG | 7 | a0001c0001t0001g0015a0001c0001t0002g0108a0001c0001t0003g0009others(4): Show | 7 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.458+7974_458+7977d others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28051277 | |||||
| chr17:28051363
|
A | AT | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0077others(2): Show | 5 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.458+8047dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28051363 | |||||
| chr17:28051393
|
C | T | 1 | a0001c0001t0003g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.458+8062C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28051393 | ||||||
| chr17:28051589
|
C | G | 2 | a0001c0001t0001g0098a0003c0004t0001g0018 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.458+8258C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28051589 | ||||||
| chr17:28051652
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.458+8321C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28051652 | ||||||
| chr17:28051655
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.458+8330_458+8339d others(12): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28051655 | |||||
| chr17:28052046
|
T | C | 1 | a0001c0001t0003g0086 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.458+8715T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28052046 | ||||||
| chr17:28052104
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+8773G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28052104 | ||||||
| chr17:28052250
|
T | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0021 | 2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.458+8919T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28052250 | ||||||
| chr17:28052383
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.458+9052G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28052383 | ||||||
| chr17:28052741
|
A | G | 1 | a0001c0001t0002g0075 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.458+9410A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28052741 | ||||||
| chr17:28052783
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0074 | 3 | NA18960.hp1 NA18979.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.458+9452A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28052783 | ||||||
| chr17:28052888
|
G | GT | 13 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(10): Show | 13 | HG00438.hp1 HG00438.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.458+9576dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28052888 | |||||
| chr17:28053967
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.458+10636T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28053967 | ||||||
| chr17:28053993
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.458+10662C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28053993 | ||||||
| chr17:28054358
|
T | G | 1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.458+11027T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28054358 | ||||||
| chr17:28054491
|
A | G | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.458+11160A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28054491 | ||||||
| chr17:28054950
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458+11619G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28054950 | ||||||
| chr17:28055095
|
CT | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(10): Show | 13 | HG02572.hp1 HG02647.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.458+11780delT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28055095 | |||||
| chr17:28055218
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.458+11887G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28055218 | ||||||
| chr17:28055241
|
C | T | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.458+11910C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28055241 | ||||||
| chr17:28055346
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.458+12015C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28055346 | ||||||
| chr17:28055522
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.458+12191G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28055522 | ||||||
| chr17:28055654
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.458+12323A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28055654 | ||||||
| chr17:28055870
|
C | A | 1 | a0001c0001t0001g0026 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.458+12539C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28055870 | ||||||
| chr17:28056119
|
T | C | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458+12788T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28056119 | ||||||
| chr17:28056924
|
T | G | 1 | a0001c0001t0001g0027 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.458+13593T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28056924 | ||||||
| chr17:28056934
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 99 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.458+13603C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28056934 | ||||||
| chr17:28056947
|
C | CT | 9 | a0001c0001t0001g0019a0001c0001t0001g0063a0001c0001t0001g0064others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.458+13640dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28056947 | |||||
| chr17:28056947
|
C | CTT | 4 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0003g0009others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.458+13639_458+1364 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28056947 | |||||
| chr17:28056947
|
CT | C | 4 | a0001c0001t0001g0028a0001c0001t0004g0094a0001c0001t0006g0006others(1): Show | 4 | HG02572.hp1 HG03579.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+13640delT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28056947 | |||||
| chr17:28057020
|
T | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | NA19062.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.458+13689T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28057020 | ||||||
| chr17:28057291
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.458+13960C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28057291 | ||||||
| chr17:28057512
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.458+14181C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28057512 | ||||||
| chr17:28057907
|
A | T | 1 | a0001c0001t0003g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.458+14576A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28057907 | ||||||
| chr17:28058283
|
G | A | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.458+14952G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28058283 | ||||||
| chr17:28058458
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+15127A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28058458 | ||||||
| chr17:28058660
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.458+15329T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28058660 | ||||||
| chr17:28058807
|
T | C | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.458+15476T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28058807 | ||||||
| chr17:28058838
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458+15507G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28058838 | ||||||
| chr17:28059096
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+15765A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28059096 | ||||||
| chr17:28059145
|
A | T | 1 | a0001c0001t0001g0072 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.458+15814A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28059145 | ||||||
| chr17:28059220
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.458+15889A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28059220 | ||||||
| chr17:28059531
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458+16200G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28059531 | ||||||
| chr17:28059625
|
C | T | 3 | a0001c0001t0001g0061a0001c0001t0002g0065a0001c0001t0004g0094 | 3 | HG02027.hp1 NA18990.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.458+16294C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28059625 | ||||||
| chr17:28059757
|
T | TTG | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0005g0105others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+16427_458+1642 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28059757 | |||||
| chr17:28059808
|
C | T | 1 | a0001c0001t0005g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.458+16477C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28059808 | ||||||
| chr17:28059850
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.458+16519T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28059850 | ||||||
| chr17:28059871
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(12): Show | 15 | HG01243.hp1 HG01884.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.458+16540G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28059871 | ||||||
| chr17:28059927
|
TAATAA | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+16602_458+1660 others(9): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28059927 | |||||
| chr17:28060085
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+16754G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28060085 | ||||||
| chr17:28060183
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.458+16852G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28060183 | ||||||
| chr17:28060451
|
A | G | 1 | a0001c0001t0003g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.458+17120A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28060451 | ||||||
| chr17:28060524
|
C | T | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.458+17193C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28060524 | ||||||
| chr17:28060667
|
G | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+17336G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28060667 | ||||||
| chr17:28060696
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0005g0105others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+17365G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28060696 | ||||||
| chr17:28060824
|
A | C | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.458+17493A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28060824 | ||||||
| chr17:28061283
|
A | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+17952A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28061283 | ||||||
| chr17:28061621
|
A | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+18290A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28061621 | ||||||
| chr17:28061761
|
C | CATATACA others(22): Show |
3 | a0001c0001t0003g0016a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.458+18487_458+1851 others(33): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28061761 | |||||
| chr17:28061817
|
AATATATA others(1): Show |
A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+18500_458+1850 others(12): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28061817 | |||||
| chr17:28061877
|
T | C | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.458+18546T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28061877 | ||||||
| chr17:28061888
|
TATATAC | T | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.458+18567_458+1857 others(10): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28061888 | |||||
| chr17:28061934
|
TA | T | 2 | a0001c0001t0002g0062a0001c0001t0003g0009 | 2 | HG02717.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.458+18604delA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28061934 | ||||||
| chr17:28061935
|
A | T | 4 | a0001c0001t0001g0098a0001c0002t0003g0008a0001c0002t0003g0012others(1): Show | 4 | HG01884.hp1 HG02109.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.458+18604A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28061935 | ||||||
| chr17:28061936
|
T | TA | 12 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0040others(9): Show | 12 | HG00621.hp2 HG01070.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+18605_458+1860 others(5): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28061936 | ||||||
| chr17:28061937
|
T | A | 32 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(29): Show | 32 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.458+18606T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28061937 | ||||||
| chr17:28061938
|
T | A | 4 | a0001c0001t0001g0026a0001c0001t0003g0016a0001c0001t0005g0105others(1): Show | 4 | HG02257.hp1 HG02976.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+18607T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28061938 | ||||||
| chr17:28061939
|
T | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0030others(3): Show | 6 | HG00609.hp1 HG00621.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.458+18608T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28061939 | ||||||
| chr17:28062102
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+18771G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28062102 | ||||||
| chr17:28062114
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 99 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.458+18783C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28062114 | ||||||
| chr17:28062236
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.458+18905C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28062236 | ||||||
| chr17:28062998
|
G | A | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+19667G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28062998 | ||||||
| chr17:28063175
|
G | A | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.458+19844G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28063175 | ||||||
| chr17:28063674
|
A | G | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.458+20343A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28063674 | ||||||
| chr17:28064174
|
C | CT | 72 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.458+20868dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28064174 | |||||
| chr17:28064174
|
C | CTT | 5 | a0001c0001t0001g0024a0001c0001t0001g0060a0001c0001t0001g0096others(2): Show | 5 | HG00621.hp1 HG01975.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.458+20867_458+2086 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28064174 | |||||
| chr17:28064174
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0077 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.458+20856_458+2086 others(17): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28064174 | |||||
| chr17:28064279
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+20948T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28064279 | ||||||
| chr17:28064363
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.458+21032G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28064363 | ||||||
| chr17:28064862
|
T | C | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.458+21531T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28064862 | ||||||
| chr17:28064956
|
C | T | 1 | a0001c0001t0007g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.458+21625C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28064956 | ||||||
| chr17:28065123
|
A | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+21792A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28065123 | ||||||
| chr17:28066032
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458+22701G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28066032 | ||||||
| chr17:28066427
|
T | C | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458+23096T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28066427 | ||||||
| chr17:28066429
|
T | C | 2 | a0001c0001t0001g0046a0002c0003t0001g0047 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.458+23098T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28066429 | ||||||
| chr17:28066703
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+23372A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28066703 | ||||||
| chr17:28066804
|
G | C | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.458+23473G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28066804 | ||||||
| chr17:28067011
|
G | A | 1 | a0001c0006t0001g0087 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.458+23680G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28067011 | ||||||
| chr17:28067196
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.458+23865G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28067196 | ||||||
| chr17:28067328
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+23997C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28067328 | ||||||
| chr17:28067837
|
A | AAT | 5 | a0001c0001t0001g0069a0001c0002t0003g0008a0001c0002t0003g0011others(2): Show | 5 | HG02109.hp2 HG02148.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.458+24525_458+2452 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28067837 | |||||
| chr17:28067837
|
AAT | A | 10 | a0001c0001t0001g0015a0001c0001t0003g0003a0001c0001t0003g0009others(7): Show | 10 | HG02257.hp1 HG02451.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.458+24525_458+2452 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28067837 | |||||
| chr17:28067837
|
AATAT | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+24523_458+2452 others(8): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28067837 | |||||
| chr17:28067973
|
T | C | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.458+24642T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28067973 | ||||||
| chr17:28068084
|
T | G | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.458+24753T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28068084 | ||||||
| chr17:28068140
|
CA | C | 5 | a0001c0001t0001g0029a0001c0001t0003g0003a0001c0001t0003g0009others(2): Show | 5 | HG01257.hp2 HG02717.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.458+24828delA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28068140 | |||||
| chr17:28068170
|
C | T | 1 | a0001c0001t0003g0086 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.458+24839C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28068170 | ||||||
| chr17:28068171
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+24840G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28068171 | ||||||
| chr17:28068842
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.458+25511C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28068842 | ||||||
| chr17:28069085
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+25754C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28069085 | ||||||
| chr17:28069296
|
A | G | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.458+25965A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28069296 | ||||||
| chr17:28069823
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+26492G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28069823 | ||||||
| chr17:28069937
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+26606A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28069937 | ||||||
| chr17:28070263
|
T | A | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.458+26932T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28070263 | ||||||
| chr17:28070354
|
A | AT | 7 | a0001c0001t0001g0057a0001c0001t0002g0090a0001c0001t0002g0092others(4): Show | 7 | HG00642.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.458+27042dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28070354 | |||||
| chr17:28070354
|
AT | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0029others(13): Show | 16 | HG00609.hp2 HG01257.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.458+27042delT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28070354 | |||||
| chr17:28070418
|
G | A | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.458+27087G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28070418 | ||||||
| chr17:28070716
|
A | G | 1 | a0001c0001t0004g0032 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.458+27385A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28070716 | ||||||
| chr17:28070737
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+27406A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28070737 | ||||||
| chr17:28070754
|
A | C | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.458+27423A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28070754 | ||||||
| chr17:28070769
|
A | G | 3 | a0001c0001t0001g0089a0001c0001t0002g0090a0001c0001t0002g0092 | 3 | HG00642.hp2 NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.458+27438A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28070769 | ||||||
| chr17:28071057
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.458+27726T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28071057 | ||||||
| chr17:28071104
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(46): Show | 49 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.458+27773A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28071104 | ||||||
| chr17:28071146
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0049others(2): Show | 5 | HG00438.hp1 HG02040.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.458+27815G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28071146 | ||||||
| chr17:28071353
|
A | G | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+28022A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28071353 | ||||||
| chr17:28071434
|
C | CT | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.458+28121dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28071434 | |||||
| chr17:28071434
|
CT | C | 13 | a0001c0001t0001g0029a0001c0001t0001g0040a0001c0001t0001g0046others(10): Show | 13 | HG01070.hp2 HG01257.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.458+28121delT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28071434 | |||||
| chr17:28071580
|
C | T | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.458+28249C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28071580 | ||||||
| chr17:28072037
|
G | C | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.458+28706G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28072037 | ||||||
| chr17:28072293
|
A | G | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.458+28962A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28072293 | ||||||
| chr17:28072388
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+29057C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28072388 | ||||||
| chr17:28072520
|
G | GTC | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+29192_458+2919 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28072520 | |||||
| chr17:28073106
|
C | T | 1 | a0001c0001t0002g0038 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.458+29775C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28073106 | ||||||
| chr17:28073231
|
C | T | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG01433.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.458+29900C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28073231 | ||||||
| chr17:28073396
|
C | T | 5 | a0001c0001t0003g0016a0001c0002t0003g0008a0001c0002t0003g0011others(2): Show | 5 | HG02109.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+30065C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28073396 | ||||||
| chr17:28073519
|
A | G | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+30188A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28073519 | ||||||
| chr17:28073573
|
A | G | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.458+30242A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28073573 | ||||||
| chr17:28073660
|
T | A | 2 | a0001c0001t0002g0038a0001c0001t0002g0075 | 2 | HG00558.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.458+30329T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28073660 | ||||||
| chr17:28073829
|
A | C | 1 | a0001c0001t0006g0007 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.458+30498A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28073829 | ||||||
| chr17:28073838
|
T | C | 4 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.458+30507T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28073838 | ||||||
| chr17:28073944
|
T | C | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+30613T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28073944 | ||||||
| chr17:28074059
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.458+30728C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28074059 | ||||||
| chr17:28074909
|
C | T | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+31578C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28074909 | ||||||
| chr17:28074924
|
A | G | 1 | a0001c0001t0003g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.458+31593A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28074924 | ||||||
| chr17:28075125
|
G | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | NA18990.hp1 NA19062.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.458+31794G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28075125 | ||||||
| chr17:28075225
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+31894T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28075225 | ||||||
| chr17:28075634
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+32303G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28075634 | ||||||
| chr17:28075785
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+32454C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28075785 | ||||||
| chr17:28075860
|
T | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+32529T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28075860 | ||||||
| chr17:28077063
|
CTCTT | C | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+33742_458+3374 others(8): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28077063 | |||||
| chr17:28077073
|
C | CT | 42 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0019others(39): Show | 42 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.458+33767dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28077073 | |||||
| chr17:28077073
|
CT | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0046others(1): Show | 4 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.458+33767delT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28077073 | |||||
| chr17:28077184
|
C | A | 1 | a0001c0001t0003g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.458+33853C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28077184 | ||||||
| chr17:28078614
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.458+35283A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28078614 | ||||||
| chr17:28079472
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.458+36141C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28079472 | ||||||
| chr17:28079851
|
G | T | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458+36520G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28079851 | ||||||
| chr17:28080109
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.458+36778G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28080109 | ||||||
| chr17:28080287
|
A | C | 16 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0028others(13): Show | 16 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.458+36956A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28080287 | ||||||
| chr17:28080746
|
T | G | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+37415T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28080746 | ||||||
| chr17:28080810
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+37479C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28080810 | ||||||
| chr17:28080989
|
A | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0060 | 2 | HG01975.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.458+37658A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28080989 | ||||||
| chr17:28081045
|
A | AC | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.458+37715dupC | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28081045 | |||||
| chr17:28081053
|
C | CT | 5 | a0001c0001t0003g0016a0001c0002t0003g0008a0001c0002t0003g0011others(2): Show | 5 | HG02109.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+37734dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28081053 | |||||
| chr17:28081234
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.458+37903T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28081234 | ||||||
| chr17:28081366
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.458+38035A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28081366 | ||||||
| chr17:28081768
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.458+38437T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28081768 | ||||||
| chr17:28081811
|
C | T | 1 | a0001c0001t0003g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.458+38480C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28081811 | ||||||
| chr17:28081973
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.458+38642A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28081973 | ||||||
| chr17:28082332
|
CATT | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+39006_458+3900 others(7): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28082332 | |||||
| chr17:28082657
|
G | A | 2 | a0001c0001t0005g0105a0001c0001t0005g0106 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.458+39326G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28082657 | ||||||
| chr17:28082844
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.458+39513C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28082844 | ||||||
| chr17:28082895
|
T | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0005g0105others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+39564T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28082895 | ||||||
| chr17:28083038
|
T | G | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-39565T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28083038 | ||||||
| chr17:28083235
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-39368G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28083235 | ||||||
| chr17:28083648
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.459-38955G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28083648 | ||||||
| chr17:28084237
|
A | G | 1 | a0001c0001t0002g0050 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.459-38366A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28084237 | ||||||
| chr17:28084386
|
T | A | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459-38217T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28084386 | ||||||
| chr17:28084580
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.459-38023T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28084580 | ||||||
| chr17:28084724
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-37879C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28084724 | ||||||
| chr17:28084935
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.459-37668G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28084935 | ||||||
| chr17:28085412
|
C | T | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-37191C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28085412 | ||||||
| chr17:28085477
|
C | A | 1 | a0001c0001t0003g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.459-37126C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28085477 | ||||||
| chr17:28085594
|
G | A | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-37009G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28085594 | ||||||
| chr17:28085608
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.459-36995T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28085608 | ||||||
| chr17:28085751
|
AG | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-36851delG | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28085751 | ||||||
| chr17:28085752
|
G | A | 9 | a0001c0001t0001g0015a0001c0001t0003g0003a0001c0001t0003g0010others(6): Show | 9 | HG02257.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.459-36851G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28085752 | ||||||
| chr17:28085798
|
T | C | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 7 | HG00438.hp2 HG01070.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-36805T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28085798 | ||||||
| chr17:28085857
|
A | G | 1 | a0001c0001t0002g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.459-36746A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28085857 | ||||||
| chr17:28085987
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-36616T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28085987 | ||||||
| chr17:28086144
|
A | G | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-36459A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28086144 | ||||||
| chr17:28086260
|
A | G | 1 | a0001c0001t0003g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459-36343A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28086260 | ||||||
| chr17:28086680
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.459-35923A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28086680 | ||||||
| chr17:28086758
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.459-35845A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28086758 | ||||||
| chr17:28087386
|
G | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | NA18990.hp1 NA19062.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.459-35217G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28087386 | ||||||
| chr17:28087775
|
A | AGGTAGAT others(28): Show |
2 | a0001c0001t0005g0105a0001c0001t0005g0106 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.459-34827_459-3479 others(39): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28087775 | |||||
| chr17:28087836
|
A | T | 1 | a0001c0001t0003g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459-34767A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28087836 | ||||||
| chr17:28087874
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0003g0003 | 3 | HG01243.hp1 HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.459-34729G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28087874 | ||||||
| chr17:28087926
|
G | A | 1 | a0001c0001t0002g0075 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.459-34677G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28087926 | ||||||
| chr17:28088505
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.459-34098A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28088505 | ||||||
| chr17:28088855
|
G | A | 1 | a0001c0001t0003g0086 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.459-33748G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28088855 | ||||||
| chr17:28088947
|
A | T | 2 | a0001c0001t0002g0038a0001c0001t0002g0075 | 2 | HG00558.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.459-33656A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28088947 | ||||||
| chr17:28089356
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-33247C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28089356 | ||||||
| chr17:28089357
|
G | A | 4 | a0001c0001t0001g0089a0001c0001t0002g0090a0001c0001t0002g0092others(1): Show | 4 | HG00642.hp2 HG02717.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-33246G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28089357 | ||||||
| chr17:28089593
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-33010A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28089593 | ||||||
| chr17:28089622
|
A | G | 1 | a0001c0001t0003g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.459-32981A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28089622 | ||||||
| chr17:28089709
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-32894C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28089709 | ||||||
| chr17:28089747
|
A | G | 1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.459-32856A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28089747 | ||||||
| chr17:28090906
|
T | C | 3 | a0001c0001t0003g0003a0001c0001t0003g0010a0001c0001t0003g0013 | 3 | HG02717.hp1 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.459-31697T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28090906 | ||||||
| chr17:28091413
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459-31190G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28091413 | ||||||
| chr17:28091414
|
C | A | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459-31189C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28091414 | ||||||
| chr17:28091420
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-31183G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28091420 | ||||||
| chr17:28091475
|
TTA | T | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-31113_459-3111 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28091475 | |||||
| chr17:28091475
|
TTATA | T | 3 | a0001c0001t0003g0003a0001c0001t0003g0010a0001c0001t0003g0013 | 3 | HG02717.hp1 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.459-31115_459-3111 others(8): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28091475 | |||||
| chr17:28091520
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.459-31083T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28091520 | ||||||
| chr17:28091555
|
G | C | 3 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0070 | 3 | HG00438.hp2 HG01975.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.459-31048G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28091555 | ||||||
| chr17:28091901
|
T | A | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-30702T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28091901 | ||||||
| chr17:28092265
|
G | C | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-30338G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28092265 | ||||||
| chr17:28092309
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-30294A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28092309 | ||||||
| chr17:28092712
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.459-29891T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28092712 | ||||||
| chr17:28092747
|
T | TTTTTA | 3 | a0001c0001t0002g0050a0001c0001t0003g0016a0001c0001t0005g0095 | 3 | HG02976.hp1 HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.459-29797_459-2979 others(9): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28092747 | |||||
| chr17:28092747
|
T | TTTTTATT others(3): Show |
3 | a0001c0001t0001g0093a0001c0001t0003g0010a0001c0001t0003g0048 | 3 | HG00609.hp2 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.459-29802_459-2979 others(14): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28092747 | |||||
| chr17:28092747
|
TTTTTA | T | 17 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0061others(14): Show | 17 | HG00140.hp1 HG01433.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.459-29797_459-2979 others(9): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28092747 | |||||
| chr17:28092747
|
TTTTTATT others(3): Show |
T | 4 | a0001c0001t0001g0022a0001c0001t0001g0042a0001c0001t0001g0063others(1): Show | 4 | HG00642.hp1 HG02451.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-29802_459-2979 others(14): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28092747 | |||||
| chr17:28092747
|
TTTTTATT others(8): Show |
T | 7 | a0001c0001t0001g0015a0001c0001t0003g0003a0001c0001t0003g0013others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-29807_459-2979 others(19): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28092747 | |||||
| chr17:28092747
|
TTTTTATT others(13): Show |
T | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.459-29812_459-2979 others(24): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28092747 | |||||
| chr17:28092857
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0046a0001c0001t0001g0079others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-29746G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28092857 | ||||||
| chr17:28093061
|
G | A | 2 | a0001c0001t0001g0046a0002c0003t0001g0047 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.459-29542G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28093061 | ||||||
| chr17:28093636
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.459-28967C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28093636 | ||||||
| chr17:28093686
|
A | G | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-28917A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28093686 | ||||||
| chr17:28093993
|
CA | C | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-28603delA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28093993 | |||||
| chr17:28094194
|
C | T | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-28409C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28094194 | ||||||
| chr17:28094257
|
C | T | 1 | a0001c0001t0002g0017 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.459-28346C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28094257 | ||||||
| chr17:28094280
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.459-28323C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28094280 | ||||||
| chr17:28094326
|
C | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0005g0105others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-28277C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28094326 | ||||||
| chr17:28094474
|
G | A | 1 | a0001c0001t0004g0031 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.459-28129G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28094474 | ||||||
| chr17:28095006
|
A | G | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-27597A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28095006 | ||||||
| chr17:28095154
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.459-27449T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28095154 | ||||||
| chr17:28095356
|
T | A | 1 | a0001c0001t0005g0105 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.459-27247T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28095356 | ||||||
| chr17:28095390
|
C | T | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.459-27213C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28095390 | ||||||
| chr17:28095649
|
C | T | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-26954C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28095649 | ||||||
| chr17:28095770
|
A | C | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459-26833A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28095770 | ||||||
| chr17:28095900
|
G | A | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-26703G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28095900 | ||||||
| chr17:28095910
|
CTTG | C | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.459-26688_459-2668 others(7): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28095910 | |||||
| chr17:28095939
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459-26664T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28095939 | ||||||
| chr17:28096214
|
C | G | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-26389C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28096214 | ||||||
| chr17:28096412
|
A | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-26191A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28096412 | ||||||
| chr17:28096662
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-25941T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28096662 | ||||||
| chr17:28096687
|
C | G | 16 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0028others(13): Show | 16 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.459-25916C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28096687 | ||||||
| chr17:28097288
|
G | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | NA19062.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.459-25315G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28097288 | ||||||
| chr17:28097649
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-24954C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28097649 | ||||||
| chr17:28097794
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.459-24809G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28097794 | ||||||
| chr17:28097991
|
C | G | 1 | a0001c0001t0001g0053 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.459-24612C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28097991 | ||||||
| chr17:28098058
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-24545A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28098058 | ||||||
| chr17:28098545
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.459-24058G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28098545 | ||||||
| chr17:28098660
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-23943T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28098660 | ||||||
| chr17:28098675
|
C | CT | 13 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0028others(10): Show | 13 | HG00438.hp1 HG00609.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.459-23904dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28098675 | |||||
| chr17:28098675
|
CT | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0040others(6): Show | 9 | HG01257.hp1 HG01257.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-23904delT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28098675 | |||||
| chr17:28098837
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(14): Show | 17 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.459-23766G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28098837 | ||||||
| chr17:28098843
|
C | T | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-23760C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28098843 | ||||||
| chr17:28098909
|
C | G | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459-23694C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28098909 | ||||||
| chr17:28098972
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.459-23631G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28098972 | ||||||
| chr17:28099568
|
C | CTTTTTT | 8 | a0001c0001t0003g0003a0001c0001t0003g0010a0001c0001t0006g0006others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.459-23019_459-2301 others(10): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28099568 | |||||
| chr17:28099568
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0005g0105 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.459-23024_459-2301 others(15): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28099568 | |||||
| chr17:28100085
|
A | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0080a0001c0001t0001g0083others(3): Show | 6 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-22518A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28100085 | ||||||
| chr17:28100603
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-22000A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28100603 | ||||||
| chr17:28100868
|
G | A | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-21735G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28100868 | ||||||
| chr17:28100931
|
T | C | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459-21672T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28100931 | ||||||
| chr17:28101140
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.459-21463A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28101140 | ||||||
| chr17:28101526
|
T | G | 1 | a0001c0001t0001g0049 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.459-21077T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28101526 | ||||||
| chr17:28101954
|
C | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-20649C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28101954 | ||||||
| chr17:28102439
|
A | G | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459-20164A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28102439 | ||||||
| chr17:28102494
|
C | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0021 | 2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.459-20109C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28102494 | ||||||
| chr17:28102542
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.459-20061G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28102542 | ||||||
| chr17:28102648
|
C | CA | 4 | a0001c0001t0003g0016a0001c0001t0005g0105a0001c0001t0005g0106others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-19938dupA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28102648 | |||||
| chr17:28102962
|
C | T | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-19641C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28102962 | ||||||
| chr17:28102993
|
A | G | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(14): Show | 17 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.459-19610A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28102993 | ||||||
| chr17:28103367
|
T | G | 1 | a0001c0001t0001g0053 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.459-19236T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28103367 | ||||||
| chr17:28103517
|
A | G | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-19086A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28103517 | ||||||
| chr17:28103790
|
G | A | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-18813G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28103790 | ||||||
| chr17:28104209
|
T | C | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.459-18394T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28104209 | ||||||
| chr17:28104281
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.459-18322G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28104281 | ||||||
| chr17:28104358
|
GA | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-18243delA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28104358 | |||||
| chr17:28104366
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-18237C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28104366 | ||||||
| chr17:28104435
|
T | C | 1 | a0001c0001t0005g0106 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.459-18168T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28104435 | ||||||
| chr17:28104448
|
G | A | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-18155G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28104448 | ||||||
| chr17:28104554
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.459-18049G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28104554 | ||||||
| chr17:28104633
|
C | T | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-17970C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28104633 | ||||||
| chr17:28104911
|
T | TCCATTTT others(343): Show |
1 | a0001c0001t0001g0026 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.459-17674_459-1767 others(354): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28104911 | |||||
| chr17:28105188
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.459-17415G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28105188 | ||||||
| chr17:28105403
|
A | G | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-17200A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28105403 | ||||||
| chr17:28105573
|
C | T | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.459-17030C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28105573 | ||||||
| chr17:28105606
|
T | G | 1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.459-16997T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28105606 | ||||||
| chr17:28105837
|
G | C | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-16766G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28105837 | ||||||
| chr17:28106624
|
A | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-15979A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28106624 | ||||||
| chr17:28106813
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.459-15790A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28106813 | ||||||
| chr17:28106993
|
C | CA | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-15610_459-1560 others(5): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28106993 | ||||||
| chr17:28107088
|
T | C | 1 | a0001c0006t0001g0087 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.459-15515T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28107088 | ||||||
| chr17:28107367
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459-15236G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28107367 | ||||||
| chr17:28107415
|
C | T | 1 | a0001c0001t0003g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.459-15188C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28107415 | ||||||
| chr17:28107449
|
AAAG | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-15151_459-1514 others(7): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28107449 | |||||
| chr17:28107504
|
GT | G | 2 | a0001c0001t0001g0063a0001c0001t0002g0092 | 2 | HG00642.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.459-15096delT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28107504 | |||||
| chr17:28107620
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.459-14983A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28107620 | ||||||
| chr17:28107677
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-14926G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28107677 | ||||||
| chr17:28108175
|
G | T | 1 | a0001c0001t0002g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.459-14428G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28108175 | ||||||
| chr17:28108372
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-14231G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28108372 | ||||||
| chr17:28108530
|
TTTAAG | T | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-14068_459-1406 others(9): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28108530 | |||||
| chr17:28108554
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.459-14049G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28108554 | ||||||
| chr17:28108748
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-13855C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28108748 | ||||||
| chr17:28108890
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.459-13713C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28108890 | ||||||
| chr17:28108955
|
T | G | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-13648T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28108955 | ||||||
| chr17:28108986
|
G | C | 2 | a0001c0001t0001g0054a0001c0001t0002g0085 | 2 | HG01071.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.459-13617G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28108986 | ||||||
| chr17:28109095
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-13508T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28109095 | ||||||
| chr17:28109096
|
G | T | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459-13507G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28109096 | ||||||
| chr17:28109158
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.459-13445G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28109158 | ||||||
| chr17:28109177
|
G | GA | 6 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0002g0081others(3): Show | 6 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-13412dupA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28109177 | |||||
| chr17:28109385
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-13218G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28109385 | ||||||
| chr17:28109423
|
A | C | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.459-13180A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28109423 | ||||||
| chr17:28109659
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-12944A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28109659 | ||||||
| chr17:28109827
|
C | T | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-12776C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28109827 | ||||||
| chr17:28109972
|
G | C | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.459-12631G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28109972 | ||||||
| chr17:28110181
|
T | G | 3 | a0001c0001t0003g0003a0001c0001t0003g0010a0001c0001t0003g0013 | 3 | HG02717.hp1 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.459-12422T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28110181 | ||||||
| chr17:28110217
|
T | TTA | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0033 | 3 | HG01243.hp1 HG01884.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.459-12374_459-1237 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28110217 | |||||
| chr17:28110488
|
GT | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.459-12103delT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28110488 | |||||
| chr17:28110495
|
T | C | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-12108T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28110495 | ||||||
| chr17:28110500
|
T | A | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.459-12103T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28110500 | ||||||
| chr17:28110628
|
A | T | 1 | a0001c0001t0002g0017 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.459-11975A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28110628 | ||||||
| chr17:28110810
|
TAAAC | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-11790_459-1178 others(8): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28110810 | |||||
| chr17:28110853
|
G | T | 2 | a0001c0001t0001g0055a0002c0003t0001g0043 | 2 | HG01070.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.459-11750G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28110853 | ||||||
| chr17:28110862
|
T | TG | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-11740dupG | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28110862 | |||||
| chr17:28110875
|
C | T | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.459-11728C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28110875 | ||||||
| chr17:28111011
|
A | T | 1 | a0001c0001t0002g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.459-11592A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111011 | ||||||
| chr17:28111026
|
A | C | 1 | a0001c0001t0002g0056 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.459-11577A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111026 | ||||||
| chr17:28111046
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.459-11557G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111046 | ||||||
| chr17:28111086
|
C | T | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-11517C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111086 | ||||||
| chr17:28111118
|
C | T | 1 | a0001c0001t0003g0086 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.459-11485C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111118 | ||||||
| chr17:28111201
|
G | A | 32 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0028others(29): Show | 32 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.459-11402G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111201 | ||||||
| chr17:28111248
|
G | A | 1 | a0001c0001t0005g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.459-11355G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111248 | ||||||
| chr17:28111353
|
A | AT | 4 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0003g0010others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-11235dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111353 | |||||
| chr17:28111354
|
T | A | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0002g0045others(2): Show | 5 | HG00642.hp1 HG03834.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.459-11249T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111354 | ||||||
| chr17:28111550
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-11053C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111550 | ||||||
| chr17:28111592
|
A | C | 1 | a0001c0001t0001g0077 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.459-11011A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111592 | ||||||
| chr17:28111861
|
C | CGT | 3 | a0001c0001t0001g0024a0001c0001t0001g0101a0001c0001t0005g0095 | 3 | HG02647.hp2 HG03710.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.459-10708_459-1070 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111861 | |||||
| chr17:28111861
|
CGTGT | C | 2 | a0001c0001t0001g0002a0001c0001t0002g0108 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.459-10710_459-1070 others(8): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111861 | |||||
| chr17:28111862
|
G | A | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-10741G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111862 | ||||||
| chr17:28111867
|
TGTGTGTG others(22): Show |
T | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459-10706_459-1067 others(33): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111867 | |||||
| chr17:28111885
|
TGTGTGTG others(4): Show |
T | 1 | a0001c0001t0003g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459-10706_459-1069 others(15): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111885 | |||||
| chr17:28111886
|
GTGTGTGT others(15): Show |
G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-10716_459-1069 others(26): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111886 | ||||||
| chr17:28111890
|
GTGTGTGG others(5): Show |
G | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-10712_459-1070 others(16): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111890 | ||||||
| chr17:28111893
|
TGTG | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0046a0002c0003t0001g0047 | 3 | HG01070.hp2 HG01071.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.459-10706_459-1070 others(7): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111893 | |||||
| chr17:28111895
|
T | G | 1 | a0001c0001t0001g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.459-10708T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111895 | ||||||
| chr17:28111895
|
TG | T | 6 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0002g0090others(3): Show | 6 | HG00621.hp1 HG02040.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-10706delG | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111895 | |||||
| chr17:28111896
|
G | GGT | 7 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0061others(4): Show | 7 | HG03834.hp1 HG03834.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-10658_459-1065 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111896 | |||||
| chr17:28111896
|
G | GGTGT | 7 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0030others(4): Show | 7 | HG00438.hp1 HG00642.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-10660_459-1065 others(8): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111896 | |||||
| chr17:28111896
|
G | GGTGTGT | 4 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0096others(1): Show | 4 | HG00642.hp1 HG02622.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-10662_459-1065 others(10): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111896 | |||||
| chr17:28111896
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0033 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.459-10666_459-1065 others(14): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111896 | |||||
| chr17:28111896
|
G | GT | 6 | a0001c0001t0001g0053a0001c0001t0001g0067a0001c0001t0001g0071others(3): Show | 6 | HG01243.hp2 HG02809.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.459-10707_459-1070 others(5): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111896 | ||||||
| chr17:28111896
|
G | GTGGT | 3 | a0001c0001t0001g0070a0001c0001t0003g0076a0001c0001t0004g0031 | 3 | HG00438.hp2 HG02165.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.459-10707_459-1070 others(8): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111896 | ||||||
| chr17:28111896
|
G | GTGGTGT | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0002g0074others(1): Show | 4 | HG00558.hp1 NA18980.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-10707_459-1070 others(10): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111896 | ||||||
| chr17:28111896
|
G | GTGGTGTG others(1): Show |
3 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0051 | 3 | HG00140.hp2 HG02027.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.459-10707_459-1070 others(12): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111896 | ||||||
| chr17:28111896
|
G | GTGT | 4 | a0001c0001t0001g0077a0001c0001t0001g0098a0001c0001t0002g0038others(1): Show | 4 | HG00609.hp2 HG01884.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-10707_459-1070 others(7): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111896 | ||||||
| chr17:28111896
|
G | GTGTGGTG others(3): Show |
2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.459-10707_459-1070 others(14): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111896 | ||||||
| chr17:28111896
|
G | GTGTGGTG others(5): Show |
1 | a0001c0001t0002g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.459-10707_459-1070 others(16): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111896 | ||||||
| chr17:28111896
|
G | GTGTGT | 6 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0055others(3): Show | 6 | HG01433.hp2 HG01496.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-10707_459-1070 others(9): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111896 | ||||||
| chr17:28111896
|
G | GTGTGTGT others(12): Show |
1 | a0001c0001t0001g0020 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.459-10707_459-1070 others(23): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111896 | ||||||
| chr17:28111896
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.459-10707G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111896 | ||||||
| chr17:28111896
|
GGT | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0091a0001c0001t0003g0086others(2): Show | 5 | HG01975.hp1 HG01975.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-10658_459-1065 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111896 | |||||
| chr17:28111896
|
GGTGT | G | 2 | a0001c0001t0001g0025a0001c0001t0003g0016 | 2 | HG00140.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.459-10660_459-1065 others(8): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111896 | |||||
| chr17:28111896
|
GGTGTGT | G | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-10662_459-1065 others(10): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111896 | |||||
| chr17:28111896
|
GGTGTGTG others(7): Show |
G | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-10670_459-1065 others(18): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111896 | |||||
| chr17:28111897
|
G | T | 7 | a0001c0001t0001g0023a0001c0001t0001g0068a0001c0001t0001g0103others(4): Show | 7 | HG00609.hp1 HG01070.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-10706G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111897 | ||||||
| chr17:28111898
|
T | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0068a0001c0001t0001g0103others(4): Show | 7 | HG00609.hp1 HG01070.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-10705T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111898 | ||||||
| chr17:28111898
|
T | TG | 6 | a0001c0001t0001g0052a0001c0001t0001g0073a0001c0001t0001g0077others(3): Show | 6 | HG00609.hp2 HG01243.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.459-10704dupG | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28111898 | |||||
| chr17:28111899
|
GT | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0002g0104others(1): Show | 4 | HG00621.hp1 HG02040.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-10703delT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111899 | ||||||
| chr17:28111903
|
GT | G | 3 | a0001c0001t0001g0046a0001c0005t0001g0059a0002c0003t0001g0047 | 3 | HG01070.hp2 HG01071.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.459-10699delT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111903 | ||||||
| chr17:28111917
|
G | C | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-10686G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111917 | ||||||
| chr17:28111947
|
A | G | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.459-10656A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28111947 | ||||||
| chr17:28112236
|
G | C | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-10367G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28112236 | ||||||
| chr17:28112417
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.459-10186G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28112417 | ||||||
| chr17:28112527
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459-10076C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28112527 | ||||||
| chr17:28112542
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-10061C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28112542 | ||||||
| chr17:28112720
|
A | G | 7 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-9883A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28112720 | ||||||
| chr17:28112755
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-9848C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28112755 | ||||||
| chr17:28112879
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0005g0105others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-9724G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28112879 | ||||||
| chr17:28113151
|
ATTAT | A | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-9448_459-9445d others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28113151 | |||||
| chr17:28113561
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459-9042G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28113561 | ||||||
| chr17:28113585
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-9018G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28113585 | ||||||
| chr17:28113688
|
G | A | 1 | a0001c0001t0004g0094 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.459-8915G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28113688 | ||||||
| chr17:28113816
|
C | T | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-8787C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28113816 | ||||||
| chr17:28114140
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0067others(1): Show | 4 | HG02647.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-8463C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28114140 | ||||||
| chr17:28114145
|
T | G | 1 | a0001c0005t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.459-8458T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28114145 | ||||||
| chr17:28114259
|
C | A | 32 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0028others(29): Show | 32 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.459-8344C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28114259 | ||||||
| chr17:28114401
|
T | G | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459-8202T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28114401 | ||||||
| chr17:28114461
|
G | A | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.459-8142G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28114461 | ||||||
| chr17:28114475
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-8128A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28114475 | ||||||
| chr17:28114648
|
C | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-7955C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28114648 | ||||||
| chr17:28114689
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.459-7914T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28114689 | ||||||
| chr17:28115028
|
G | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.459-7575G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28115028 | ||||||
| chr17:28115106
|
G | A | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.459-7497G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28115106 | ||||||
| chr17:28115202
|
C | CTTCCTAT others(14): Show |
1 | a0001c0001t0003g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.459-7401_459-7400i others(23): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28115202 | ||||||
| chr17:28115203
|
A | T | 1 | a0001c0001t0003g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.459-7400A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28115203 | ||||||
| chr17:28115229
|
C | T | 1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.459-7374C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28115229 | ||||||
| chr17:28115279
|
G | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-7324G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28115279 | ||||||
| chr17:28115382
|
A | G | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459-7221A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28115382 | ||||||
| chr17:28115669
|
C | A | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.459-6934C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28115669 | ||||||
| chr17:28115762
|
T | C | 1 | a0001c0001t0005g0105 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.459-6841T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28115762 | ||||||
| chr17:28115914
|
T | G | 1 | a0001c0001t0003g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.459-6689T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28115914 | ||||||
| chr17:28115989
|
T | G | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.459-6614T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28115989 | ||||||
| chr17:28116123
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.459-6480A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28116123 | ||||||
| chr17:28116154
|
A | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-6449A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28116154 | ||||||
| chr17:28116239
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.459-6364G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28116239 | ||||||
| chr17:28116364
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.459-6239C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28116364 | ||||||
| chr17:28116767
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-5836C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28116767 | ||||||
| chr17:28116777
|
A | G | 1 | a0001c0001t0003g0086 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.459-5826A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28116777 | ||||||
| chr17:28116800
|
T | C | 1 | a0001c0001t0003g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.459-5803T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28116800 | ||||||
| chr17:28116844
|
G | A | 5 | a0001c0001t0001g0044a0001c0001t0001g0057a0001c0001t0001g0060others(2): Show | 5 | HG00621.hp2 HG01975.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.459-5759G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28116844 | ||||||
| chr17:28117062
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0003g0086 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.459-5541A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28117062 | ||||||
| chr17:28117188
|
G | T | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459-5415G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28117188 | ||||||
| chr17:28117549
|
C | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-5054C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28117549 | ||||||
| chr17:28117764
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459-4839G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28117764 | ||||||
| chr17:28118258
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-4345A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28118258 | ||||||
| chr17:28118549
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-4054A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28118549 | ||||||
| chr17:28118688
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.459-3915T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28118688 | ||||||
| chr17:28118896
|
C | T | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459-3707C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28118896 | ||||||
| chr17:28119163
|
C | A | 1 | a0001c0001t0001g0040 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.459-3440C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28119163 | ||||||
| chr17:28119189
|
T | G | 1 | a0003c0004t0001g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.459-3414T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28119189 | ||||||
| chr17:28119573
|
A | T | 1 | a0001c0001t0003g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.459-3030A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28119573 | ||||||
| chr17:28119665
|
G | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-2938G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28119665 | ||||||
| chr17:28119683
|
G | T | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-2920G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28119683 | ||||||
| chr17:28120070
|
G | T | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.459-2533G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28120070 | ||||||
| chr17:28120235
|
G | GGT | 3 | a0001c0001t0001g0077a0001c0002t0003g0014a0003c0004t0001g0018 | 3 | HG02109.hp2 HG02809.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.459-2331_459-2330d others(4): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28120235 | |||||
| chr17:28120235
|
G | GGTGT | 3 | a0001c0001t0001g0089a0001c0001t0002g0090a0001c0001t0002g0092 | 3 | HG00642.hp2 NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.459-2333_459-2330d others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28120235 | |||||
| chr17:28120235
|
G | T | 1 | a0001c0001t0002g0050 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.459-2368G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28120235 | ||||||
| chr17:28120235
|
GGT | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0020others(29): Show | 32 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.459-2331_459-2330d others(4): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28120235 | |||||
| chr17:28120235
|
GGTGT | G | 7 | a0001c0001t0001g0022a0001c0001t0001g0051a0001c0001t0001g0054others(4): Show | 7 | HG00140.hp2 HG01071.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-2333_459-2330d others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28120235 | |||||
| chr17:28120235
|
GGTGTGTG others(3): Show |
G | 5 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0005g0105others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.459-2339_459-2330d others(12): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28120235 | |||||
| chr17:28120235
|
GGTGTGTG others(5): Show |
G | 2 | a0001c0001t0003g0003a0001c0001t0003g0009 | 2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.459-2341_459-2330d others(14): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28120235 | |||||
| chr17:28120235
|
GGTGTGTG others(9): Show |
G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-2345_459-2330d others(18): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28120235 | |||||
| chr17:28120256
|
G | GTA | 33 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0028others(30): Show | 33 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.459-2346_459-2345i others(4): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28120256 | |||||
| chr17:28120274
|
A | G | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-2329A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28120274 | ||||||
| chr17:28120319
|
A | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.459-2284A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28120319 | ||||||
| chr17:28120379
|
T | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-2224T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28120379 | ||||||
| chr17:28121049
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.459-1554G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28121049 | ||||||
| chr17:28121213
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.459-1390A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28121213 | ||||||
| chr17:28121391
|
GA | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(46): Show | 49 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.459-1199delA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28121391 | |||||
| chr17:28121495
|
C | CT | 82 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(79): Show | 82 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.459-1083dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28121495 | |||||
| chr17:28121495
|
C | CTT | 14 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0028others(11): Show | 14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.459-1084_459-1083d others(4): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 28121495 | |||||
| chr17:28122048
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-555C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28122048 | ||||||
| chr17:28122065
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459-538G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28122065 | ||||||
| chr17:28122245
|
A | G | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-358A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28122245 | ||||||
| chr17:28122741
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.588+9A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28122741 | ||||||
| chr17:28122790
|
T | C | 2 | a0001c0001t0003g0003a0001c0001t0003g0009 | 2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.588+58T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28122790 | ||||||
| chr17:28122904
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.588+172C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28122904 | ||||||
| chr17:28122908
|
T | C | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.588+176T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28122908 | ||||||
| chr17:28123505
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.588+773C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28123505 | ||||||
| chr17:28123554
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.588+822A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28123554 | ||||||
| chr17:28123631
|
G | T | 5 | a0001c0001t0003g0016a0001c0002t0003g0008a0001c0002t0003g0011others(2): Show | 5 | HG02109.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+899G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28123631 | ||||||
| chr17:28124520
|
A | C | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.588+1788A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28124520 | ||||||
| chr17:28124658
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.588+1926T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28124658 | ||||||
| chr17:28124815
|
C | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.588+2083C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28124815 | ||||||
| chr17:28124937
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.588+2205T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28124937 | ||||||
| chr17:28125053
|
A | G | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.588+2321A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28125053 | ||||||
| chr17:28125424
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.588+2692A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28125424 | ||||||
| chr17:28126049
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.588+3317T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28126049 | ||||||
| chr17:28126352
|
A | T | 5 | a0001c0001t0003g0003a0001c0002t0003g0008a0001c0002t0003g0011others(2): Show | 5 | HG02109.hp2 HG02717.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.588+3620A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28126352 | ||||||
| chr17:28126365
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.588+3633A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28126365 | ||||||
| chr17:28126448
|
A | G | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.588+3716A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28126448 | ||||||
| chr17:28126906
|
T | C | 1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.588+4174T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28126906 | ||||||
| chr17:28126972
|
A | G | 1 | a0001c0001t0003g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.588+4240A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28126972 | ||||||
| chr17:28127381
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.588+4649G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28127381 | ||||||
| chr17:28127388
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.588+4656A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28127388 | ||||||
| chr17:28127720
|
T | C | 1 | a0001c0001t0002g0062 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.589-4900T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28127720 | ||||||
| chr17:28127798
|
G | A | 2 | a0001c0001t0004g0035a0001c0001t0004g0037 | 2 | NA18951.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.589-4822G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28127798 | ||||||
| chr17:28128013
|
C | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0005g0105others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-4607C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28128013 | ||||||
| chr17:28128013
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.589-4607C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28128013 | ||||||
| chr17:28128234
|
T | C | 1 | a0001c0001t0006g0007 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.589-4386T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28128234 | ||||||
| chr17:28128628
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.589-3992T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28128628 | ||||||
| chr17:28128689
|
C | A | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.589-3931C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28128689 | ||||||
| chr17:28128709
|
G | A | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589-3911G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28128709 | ||||||
| chr17:28128798
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.589-3822C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28128798 | ||||||
| chr17:28129628
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.589-2992C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28129628 | ||||||
| chr17:28129731
|
T | C | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589-2889T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28129731 | ||||||
| chr17:28129874
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.589-2746C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28129874 | ||||||
| chr17:28129969
|
A | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.589-2651A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28129969 | ||||||
| chr17:28129980
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.589-2640C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28129980 | ||||||
| chr17:28130257
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(103): Show | 106 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.589-2363G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28130257 | ||||||
| chr17:28130266
|
C | T | 2 | a0001c0001t0002g0099a0001c0006t0001g0087 | 2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.589-2354C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28130266 | ||||||
| chr17:28130577
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.589-2043T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28130577 | ||||||
| chr17:28130588
|
T | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.589-2032T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28130588 | ||||||
| chr17:28130785
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.589-1835G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28130785 | ||||||
| chr17:28131073
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.589-1547G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28131073 | ||||||
| chr17:28131135
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.589-1485A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28131135 | ||||||
| chr17:28131586
|
T | TA | 16 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0033others(13): Show | 16 | HG00621.hp2 HG00642.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.589-1006dupA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 28131586 | |||||
| chr17:28131586
|
TA | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(9): Show | 12 | HG01070.hp2 HG01433.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.589-1006delA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 28131586 | |||||
| chr17:28131586
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0002g0074 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.589-1016_589-1006d others(13): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 28131586 | |||||
| chr17:28131586
|
TAAAAAAA others(5): Show |
T | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0002g0045 | 3 | HG00642.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.589-1017_589-1006d others(14): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 28131586 | |||||
| chr17:28131986
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.589-634C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28131986 | ||||||
| chr17:28132370
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.589-250G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 2/10 | chr17 | 28132370 | ||||||
| chr17:28132976
|
G | A | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.644+301G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28132976 | ||||||
| chr17:28133500
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0021 | 2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.644+825G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28133500 | ||||||
| chr17:28133656
|
A | G | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.644+981A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28133656 | ||||||
| chr17:28133934
|
G | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0003g0009others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.644+1259G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28133934 | ||||||
| chr17:28133950
|
C | A | 1 | a0001c0001t0001g0029 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.644+1275C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28133950 | ||||||
| chr17:28133978
|
T | C | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG01433.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.644+1303T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28133978 | ||||||
| chr17:28134363
|
T | C | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.644+1688T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28134363 | ||||||
| chr17:28134640
|
T | C | 3 | a0001c0001t0003g0003a0001c0001t0003g0010a0001c0001t0003g0013 | 3 | HG02717.hp1 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.644+1965T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28134640 | ||||||
| chr17:28134810
|
C | T | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+2135C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28134810 | ||||||
| chr17:28134835
|
T | TA | 2 | a0001c0001t0001g0051a0001c0001t0003g0076 | 2 | HG00140.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.644+2160_644+2161i others(3): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28134835 | ||||||
| chr17:28134836
|
T | A | 2 | a0001c0001t0001g0051a0001c0001t0003g0076 | 2 | HG00140.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.644+2161T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28134836 | ||||||
| chr17:28134932
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.644+2257G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28134932 | ||||||
| chr17:28135112
|
T | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.644+2437T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28135112 | ||||||
| chr17:28135467
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.644+2792T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28135467 | ||||||
| chr17:28135516
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.644+2841A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28135516 | ||||||
| chr17:28135599
|
C | T | 1 | a0003c0004t0001g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.644+2924C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28135599 | ||||||
| chr17:28135726
|
A | G | 1 | a0001c0001t0007g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.644+3051A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28135726 | ||||||
| chr17:28135798
|
C | T | 1 | a0001c0001t0005g0095 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.644+3123C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28135798 | ||||||
| chr17:28135863
|
A | G | 11 | a0001c0001t0001g0029a0001c0001t0001g0046a0001c0001t0001g0052others(8): Show | 11 | HG00609.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.644+3188A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28135863 | ||||||
| chr17:28136409
|
A | G | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.644+3734A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28136409 | ||||||
| chr17:28136539
|
C | T | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+3864C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28136539 | ||||||
| chr17:28136848
|
C | T | 1 | a0003c0004t0001g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.644+4173C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28136848 | ||||||
| chr17:28136871
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.644+4196C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28136871 | ||||||
| chr17:28136950
|
C | CA | 11 | a0001c0001t0001g0022a0001c0001t0001g0063a0001c0001t0001g0064others(8): Show | 11 | HG00642.hp1 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.644+4295dupA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 28136950 | |||||
| chr17:28136950
|
CA | C | 4 | a0001c0001t0001g0015a0001c0001t0003g0016a0001c0001t0006g0006others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+4295delA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 28136950 | |||||
| chr17:28137508
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.644+4833C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28137508 | ||||||
| chr17:28137859
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.644+5184A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28137859 | ||||||
| chr17:28137906
|
C | CT | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.644+5232dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 28137906 | |||||
| chr17:28137959
|
C | T | 2 | a0001c0001t0001g0055a0002c0003t0001g0043 | 2 | HG01070.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.644+5284C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28137959 | ||||||
| chr17:28138362
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0005g0105a0001c0001t0005g0106others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+5687G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28138362 | ||||||
| chr17:28138406
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.644+5731G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28138406 | ||||||
| chr17:28138643
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.644+5968A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28138643 | ||||||
| chr17:28138908
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0005g0105others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.644+6233A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28138908 | ||||||
| chr17:28139132
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.644+6457A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28139132 | ||||||
| chr17:28139290
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.644+6615C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28139290 | ||||||
| chr17:28139622
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.644+6947C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28139622 | ||||||
| chr17:28139698
|
G | A | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.644+7023G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28139698 | ||||||
| chr17:28139799
|
G | A | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.644+7124G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28139799 | ||||||
| chr17:28139897
|
C | T | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.644+7222C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28139897 | ||||||
| chr17:28140016
|
T | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.644+7341T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28140016 | ||||||
| chr17:28140887
|
C | T | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.644+8212C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28140887 | ||||||
| chr17:28140914
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.644+8239G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28140914 | ||||||
| chr17:28140947
|
T | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.644+8272T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28140947 | ||||||
| chr17:28141306
|
C | G | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.644+8631C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28141306 | ||||||
| chr17:28141946
|
C | T | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0002g0045others(1): Show | 4 | HG00642.hp1 HG03834.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+9271C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28141946 | ||||||
| chr17:28142218
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.644+9543A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28142218 | ||||||
| chr17:28142227
|
A | AT | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+9561dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 28142227 | |||||
| chr17:28142347
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0069 | 3 | HG01496.hp1 HG02148.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.644+9672G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28142347 | ||||||
| chr17:28142510
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.644+9835C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28142510 | ||||||
| chr17:28142528
|
A | T | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.644+9853A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28142528 | ||||||
| chr17:28142652
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.644+9977A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28142652 | ||||||
| chr17:28142717
|
T | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.644+10042T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28142717 | ||||||
| chr17:28142778
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.644+10103A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28142778 | ||||||
| chr17:28143187
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.644+10512G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28143187 | ||||||
| chr17:28143267
|
C | T | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.644+10592C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28143267 | ||||||
| chr17:28143356
|
TTAAAAAA | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.644+10682_644+1068 others(11): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28143356 | ||||||
| chr17:28143478
|
AG | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.644+10804delG | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28143478 | ||||||
| chr17:28143829
|
T | C | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.644+11154T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28143829 | ||||||
| chr17:28143901
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.644+11226C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28143901 | ||||||
| chr17:28144012
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.644+11337A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28144012 | ||||||
| chr17:28144190
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0003g0086 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.644+11515A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28144190 | ||||||
| chr17:28144247
|
T | C | 1 | a0001c0001t0003g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.644+11572T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28144247 | ||||||
| chr17:28144396
|
C | CA | 47 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0019others(44): Show | 47 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.644+11740dupA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 28144396 | |||||
| chr17:28144431
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.644+11756A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28144431 | ||||||
| chr17:28145017
|
T | G | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.644+12342T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28145017 | ||||||
| chr17:28145384
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.644+12709T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28145384 | ||||||
| chr17:28145406
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.644+12731T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28145406 | ||||||
| chr17:28145481
|
T | C | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+12806T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28145481 | ||||||
| chr17:28145508
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.644+12833G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28145508 | ||||||
| chr17:28145597
|
C | G | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0002g0045others(1): Show | 4 | HG00642.hp1 HG03834.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+12922C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28145597 | ||||||
| chr17:28145851
|
G | C | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.644+13176G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28145851 | ||||||
| chr17:28146028
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0005g0105others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.644+13353T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28146028 | ||||||
| chr17:28146101
|
T | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.644+13426T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28146101 | ||||||
| chr17:28146240
|
A | G | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.644+13565A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28146240 | ||||||
| chr17:28146382
|
T | TTGA | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.644+13729_644+1373 others(7): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 28146382 | |||||
| chr17:28146392
|
TGATGATG others(8): Show |
T | 1 | a0001c0001t0001g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.644+13732_644+1374 others(19): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 28146392 | |||||
| chr17:28146407
|
C | T | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.644+13732C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28146407 | ||||||
| chr17:28146437
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.644+13762C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28146437 | ||||||
| chr17:28146582
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0069 | 3 | HG01496.hp1 HG02148.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.644+13907A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28146582 | ||||||
| chr17:28146597
|
C | G | 1 | a0001c0001t0003g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.644+13922C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28146597 | ||||||
| chr17:28146674
|
C | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.644+13999C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28146674 | ||||||
| chr17:28146857
|
T | G | 1 | a0001c0001t0002g0104 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.644+14182T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28146857 | ||||||
| chr17:28147181
|
A | G | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.645-13979A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28147181 | ||||||
| chr17:28147872
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.645-13288A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28147872 | ||||||
| chr17:28147987
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.645-13173A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28147987 | ||||||
| chr17:28148024
|
C | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(14): Show | 17 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.645-13136C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28148024 | ||||||
| chr17:28148361
|
TATG | T | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.645-12797_645-1279 others(7): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 28148361 | |||||
| chr17:28148434
|
A | G | 1 | a0001c0001t0006g0007 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.645-12726A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28148434 | ||||||
| chr17:28148475
|
T | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0003g0009 | 3 | HG01243.hp1 HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.645-12685T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28148475 | ||||||
| chr17:28148771
|
A | AT | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0005g0105others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.645-12385dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 28148771 | |||||
| chr17:28149091
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.645-12069C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28149091 | ||||||
| chr17:28149124
|
A | G | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.645-12036A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28149124 | ||||||
| chr17:28149424
|
C | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(14): Show | 17 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.645-11736C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28149424 | ||||||
| chr17:28149816
|
G | A | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.645-11344G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28149816 | ||||||
| chr17:28150078
|
A | G | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.645-11082A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28150078 | ||||||
| chr17:28150102
|
T | C | 2 | a0001c0001t0005g0105a0001c0001t0005g0106 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.645-11058T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28150102 | ||||||
| chr17:28150599
|
G | C | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.645-10561G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28150599 | ||||||
| chr17:28150603
|
TTGTTAC | T | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.645-10555_645-1055 others(10): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 28150603 | |||||
| chr17:28150610
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.645-10550T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28150610 | ||||||
| chr17:28150612
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.645-10548C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28150612 | ||||||
| chr17:28150614
|
C | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.645-10546C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28150614 | ||||||
| chr17:28150651
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.645-10509C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28150651 | ||||||
| chr17:28151130
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(9): Show | 12 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.645-10030C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28151130 | ||||||
| chr17:28151387
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.645-9773T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28151387 | ||||||
| chr17:28152190
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.645-8970A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28152190 | ||||||
| chr17:28152328
|
G | A | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.645-8832G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28152328 | ||||||
| chr17:28152651
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.645-8509C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28152651 | ||||||
| chr17:28152803
|
T | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(31): Show | 34 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.645-8357T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28152803 | ||||||
| chr17:28153044
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.645-8116C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28153044 | ||||||
| chr17:28153274
|
C | CA | 5 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107others(2): Show | 5 | HG02257.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.645-7871dupA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 28153274 | |||||
| chr17:28153616
|
C | A | 1 | a0001c0001t0003g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.645-7544C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28153616 | ||||||
| chr17:28153733
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.645-7427C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28153733 | ||||||
| chr17:28153966
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.645-7194T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28153966 | ||||||
| chr17:28154888
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.645-6272C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28154888 | ||||||
| chr17:28155211
|
A | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.645-5949A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28155211 | ||||||
| chr17:28155350
|
A | AT | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.645-5810_645-5809i others(3): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28155350 | ||||||
| chr17:28155416
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.645-5744G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28155416 | ||||||
| chr17:28155416
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.645-5744G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28155416 | ||||||
| chr17:28155463
|
A | G | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.645-5697A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28155463 | ||||||
| chr17:28155554
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.645-5606G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28155554 | ||||||
| chr17:28155699
|
A | G | 1 | a0001c0001t0002g0062 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.645-5461A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28155699 | ||||||
| chr17:28155754
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.645-5406G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28155754 | ||||||
| chr17:28155779
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.645-5381G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28155779 | ||||||
| chr17:28156086
|
T | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.645-5074T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28156086 | ||||||
| chr17:28156136
|
AATATGCA others(5): Show |
A | 1 | a0001c0001t0003g0086 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.645-5019_645-5008d others(14): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 28156136 | |||||
| chr17:28156151
|
A | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.645-5009A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28156151 | ||||||
| chr17:28156340
|
A | G | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.645-4820A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28156340 | ||||||
| chr17:28156567
|
T | TGGGAGG | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0067others(1): Show | 4 | HG02647.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.645-4582_645-4577d others(8): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 28156567 | |||||
| chr17:28156867
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.645-4293G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28156867 | ||||||
| chr17:28157148
|
C | T | 1 | a0001c0001t0003g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.645-4012C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28157148 | ||||||
| chr17:28157176
|
TCACCTAT others(15): Show |
T | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.645-3983_645-3962d others(24): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28157176 | ||||||
| chr17:28157198
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.645-3962A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28157198 | ||||||
| chr17:28157199
|
T | A | 4 | a0001c0001t0001g0015a0001c0001t0002g0056a0001c0001t0006g0006others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.645-3961T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28157199 | ||||||
| chr17:28157319
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.645-3841T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28157319 | ||||||
| chr17:28157849
|
C | G | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(14): Show | 17 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.645-3311C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28157849 | ||||||
| chr17:28157876
|
A | AG | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.645-3284_645-3283i others(3): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28157876 | ||||||
| chr17:28158043
|
C | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 53 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.645-3117C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28158043 | ||||||
| chr17:28158287
|
A | C | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.645-2873A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28158287 | ||||||
| chr17:28158355
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0003g0009 | 3 | HG01243.hp1 HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.645-2805C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28158355 | ||||||
| chr17:28158694
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.645-2466A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28158694 | ||||||
| chr17:28158938
|
C | G | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.645-2222C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28158938 | ||||||
| chr17:28158979
|
C | T | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.645-2181C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28158979 | ||||||
| chr17:28159646
|
T | G | 3 | a0001c0001t0003g0003a0001c0001t0003g0010a0001c0001t0003g0013 | 3 | HG02717.hp1 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.645-1514T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28159646 | ||||||
| chr17:28160097
|
T | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.645-1063T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28160097 | ||||||
| chr17:28160140
|
A | G | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.645-1020A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28160140 | ||||||
| chr17:28160270
|
A | G | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG01433.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.645-890A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28160270 | ||||||
| chr17:28160302
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.645-858G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28160302 | ||||||
| chr17:28160559
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.645-601A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28160559 | ||||||
| chr17:28160744
|
G | A | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.645-416G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28160744 | ||||||
| chr17:28161280
|
A | G | 1 | a0001c0001t0007g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.751+14A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 4/10 | chr17 | 28161280 | ||||||
| chr17:28162015
|
A | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0041 | 2 | NA19062.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.751+749A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 4/10 | chr17 | 28162015 | ||||||
| chr17:28162024
|
A | AT | 4 | a0001c0001t0003g0010a0001c0001t0005g0105a0001c0001t0005g0106others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.751+767dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 28162024 | |||||
| chr17:28162079
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.751+813G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 4/10 | chr17 | 28162079 | ||||||
| chr17:28162245
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.751+979G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 4/10 | chr17 | 28162245 | ||||||
| chr17:28162324
|
A | G | 1 | a0001c0001t0002g0074 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.751+1058A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 4/10 | chr17 | 28162324 | ||||||
| chr17:28162567
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.752-976G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 4/10 | chr17 | 28162567 | ||||||
| chr17:28162923
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.752-607_752-595del others(13): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 28162923 | |||||
| chr17:28162927
|
A | AAAAG | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0005g0105others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.752-612_752-609dup others(4): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 28162927 | |||||
| chr17:28163132
|
T | G | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.752-411T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 4/10 | chr17 | 28163132 | ||||||
| chr17:28163431
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.752-112T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 4/10 | chr17 | 28163431 | ||||||
| chr17:28163800
|
T | G | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+172T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28163800 | ||||||
| chr17:28164369
|
C | CAA | 4 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0096others(1): Show | 4 | HG01975.hp2 HG02148.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+759_837+760dup others(2): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 28164369 | |||||
| chr17:28164394
|
A | C | 1 | a0001c0001t0001g0060 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.837+766A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28164394 | ||||||
| chr17:28164479
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.837+851G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28164479 | ||||||
| chr17:28164636
|
G | A | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.837+1008G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28164636 | ||||||
| chr17:28164665
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.837+1037G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28164665 | ||||||
| chr17:28164885
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.837+1257A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28164885 | ||||||
| chr17:28164935
|
C | T | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.837+1307C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28164935 | ||||||
| chr17:28165184
|
A | T | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.837+1556A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28165184 | ||||||
| chr17:28165239
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.837+1611C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28165239 | ||||||
| chr17:28165244
|
G | C | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+1616G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28165244 | ||||||
| chr17:28165362
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0005g0105others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.837+1734G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28165362 | ||||||
| chr17:28165848
|
TCTTTC | T | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.837+2225_837+2229d others(7): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 28165848 | |||||
| chr17:28166219
|
T | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.838-2229T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28166219 | ||||||
| chr17:28166221
|
T | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.838-2227T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28166221 | ||||||
| chr17:28167112
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.838-1336C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28167112 | ||||||
| chr17:28167313
|
T | G | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.838-1135T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28167313 | ||||||
| chr17:28167516
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.838-932A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | chr17 | 28167516 | ||||||
| chr17:28168171
|
CA | C | 83 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(80): Show | 83 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.838-262delA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 28168171 | |||||
| chr17:28168171
|
CAA | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0025others(6): Show | 9 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(6): Show |
intron_variant | MODIFIER | c.838-263_838-262del others(2): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 28168171 | |||||
| chr17:28168335
|
CA | C | 9 | a0001c0001t0001g0080a0001c0001t0002g0081a0001c0001t0002g0082others(6): Show | 9 | HG02257.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.838-97delA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 28168335 | |||||
| chr17:28168989
|
G | A | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047+332G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28168989 | ||||||
| chr17:28169122
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1047+465G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28169122 | ||||||
| chr17:28169167
|
T | A | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1047+510T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28169167 | ||||||
| chr17:28169237
|
A | C | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1047+580A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28169237 | ||||||
| chr17:28169545
|
A | G | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1047+888A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28169545 | ||||||
| chr17:28169688
|
C | CTCTG | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1047+1033_1047+103 others(8): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 28169688 | |||||
| chr17:28169711
|
G | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1047+1054G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28169711 | ||||||
| chr17:28169714
|
T | G | 1 | a0001c0001t0001g0061 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1047+1057T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28169714 | ||||||
| chr17:28169721
|
C | CT | 10 | a0001c0001t0001g0020a0001c0001t0001g0033a0001c0001t0001g0069others(7): Show | 10 | HG00609.hp2 HG01433.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.1047+1082dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 28169721 | |||||
| chr17:28169721
|
C | CTTTTTTT others(1): Show |
4 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0006g0006others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047+1075_1047+108 others(12): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 28169721 | |||||
| chr17:28169721
|
C | CTTTTTTT others(2): Show |
5 | a0001c0001t0001g0015a0001c0001t0003g0003a0001c0001t0005g0105others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047+1074_1047+108 others(13): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 28169721 | |||||
| chr17:28169901
|
C | G | 2 | a0001c0001t0001g0055a0002c0003t0001g0043 | 2 | HG01070.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1047+1244C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28169901 | ||||||
| chr17:28170083
|
A | T | 1 | a0001c0001t0001g0053 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1047+1426A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28170083 | ||||||
| chr17:28170338
|
CTGACTAC others(152): Show |
C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1047+1683_1047+184 others(4): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 28170338 | |||||
| chr17:28170948
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1048-1569C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28170948 | ||||||
| chr17:28171022
|
T | C | 34 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0030others(31): Show | 34 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1048-1495T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28171022 | ||||||
| chr17:28171311
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1048-1206A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28171311 | ||||||
| chr17:28171565
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1048-952C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28171565 | ||||||
| chr17:28171586
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1048-931C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28171586 | ||||||
| chr17:28171767
|
A | C | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1048-750A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28171767 | ||||||
| chr17:28171882
|
T | A | 1 | a0001c0001t0003g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1048-635T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28171882 | ||||||
| chr17:28171882
|
T | G | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1048-635T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28171882 | ||||||
| chr17:28171981
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1048-536A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28171981 | ||||||
| chr17:28172116
|
C | CAGGAATT others(20): Show |
15 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0025others(12): Show | 15 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1048-279_1048-253d others(29): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 28172116 | |||||
| chr17:28172116
|
C | CAGGAATT others(47): Show |
3 | a0001c0001t0001g0029a0001c0001t0001g0055a0002c0003t0001g0043 | 3 | HG01070.hp1 HG01257.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1048-306_1048-253d others(56): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 28172116 | |||||
| chr17:28172116
|
C | CAGGAATT others(101): Show |
1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1048-360_1048-253d others(110): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 28172116 | |||||
| chr17:28172116
|
C | CAGGAATT others(263): Show |
1 | a0001c0001t0006g0007 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1048-253_1048-252i others(272): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 28172116 | |||||
| chr17:28172116
|
CAGGAATT others(47): Show |
C | 1 | a0001c0001t0001g0051 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1048-306_1048-253d others(56): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 28172116 | |||||
| chr17:28172179
|
ATTTAAAT others(111): Show |
A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1048-306_1048-189d others(2): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 28172179 | |||||
| chr17:28172233
|
A | ATTTAAAT others(25): Show |
14 | a0001c0001t0001g0026a0001c0001t0002g0017a0001c0001t0002g0038others(11): Show | 14 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1048-218_1048-187d others(34): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 28172233 | |||||
| chr17:28172233
|
ATTTAAAT others(25): Show |
A | 2 | a0001c0001t0001g0072a0001c0005t0001g0059 | 2 | HG02257.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1048-218_1048-187d others(34): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 28172233 | |||||
| chr17:28172260
|
ATTTAT | A | 4 | a0001c0001t0003g0016a0001c0002t0003g0008a0001c0002t0003g0011others(1): Show | 4 | HG02109.hp2 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048-252_1048-248d others(7): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 28172260 | |||||
| chr17:28172264
|
A | AAATTCCT others(15): Show |
2 | a0001c0001t0002g0056a0001c0002t0003g0012 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1048-253_1048-252i others(24): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28172264 | ||||||
| chr17:28172264
|
A | AAATTCCT others(42): Show |
3 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0013 | 3 | HG02717.hp2 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1048-253_1048-252i others(51): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28172264 | ||||||
| chr17:28172264
|
A | AAATTCCT others(96): Show |
1 | a0001c0001t0001g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1048-253_1048-252i others(105): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28172264 | ||||||
| chr17:28172264
|
A | AAATTCCT others(177): Show |
2 | a0001c0001t0005g0105a0001c0001t0005g0106 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1048-253_1048-252i others(186): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28172264 | ||||||
| chr17:28172264
|
A | AAATTCCT others(204): Show |
1 | a0001c0001t0005g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1048-253_1048-252i others(213): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28172264 | ||||||
| chr17:28172264
|
A | AAATTCCT others(231): Show |
1 | a0001c0001t0006g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1048-253_1048-252i others(240): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28172264 | ||||||
| chr17:28172265
|
T | A | 10 | a0001c0001t0001g0015a0001c0001t0002g0056a0001c0001t0003g0009others(7): Show | 10 | HG02257.hp1 HG02451.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1048-252T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 6/10 | chr17 | 28172265 | ||||||
| chr17:28172726
|
AT | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(14): Show | 17 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1149+119delT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 28172726 | |||||
| chr17:28172779
|
A | G | 4 | a0001c0002t0003g0008a0001c0002t0003g0011a0001c0002t0003g0012others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1149+161A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28172779 | ||||||
| chr17:28173769
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1149+1151T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28173769 | ||||||
| chr17:28174134
|
G | A | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1149+1516G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28174134 | ||||||
| chr17:28174433
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1149+1815C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28174433 | ||||||
| chr17:28174865
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1149+2247G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28174865 | ||||||
| chr17:28174902
|
G | A | 1 | a0001c0006t0001g0087 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1149+2284G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28174902 | ||||||
| chr17:28174985
|
A | AT | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1149+2385dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 28174985 | |||||
| chr17:28175288
|
A | T | 1 | a0001c0001t0002g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1149+2670A>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28175288 | ||||||
| chr17:28175429
|
C | T | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1149+2811C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28175429 | ||||||
| chr17:28175445
|
C | G | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1149+2827C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28175445 | ||||||
| chr17:28175446
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1149+2828G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28175446 | ||||||
| chr17:28175536
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1149+2918C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28175536 | ||||||
| chr17:28175941
|
A | G | 3 | a0001c0001t0002g0050a0001c0001t0002g0090a0001c0001t0002g0092 | 3 | HG00642.hp2 NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1149+3323A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28175941 | ||||||
| chr17:28175980
|
T | G | 1 | a0001c0001t0001g0057 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1149+3362T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28175980 | ||||||
| chr17:28176869
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(80): Show | 83 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1149+4251C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28176869 | ||||||
| chr17:28176908
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1149+4290G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28176908 | ||||||
| chr17:28176930
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1149+4312C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28176930 | ||||||
| chr17:28177149
|
G | A | 1 | a0001c0001t0003g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1149+4531G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28177149 | ||||||
| chr17:28177225
|
T | A | 1 | a0001c0001t0001g0053 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1149+4607T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28177225 | ||||||
| chr17:28177513
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0061 | 2 | NA18990.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1149+4895G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28177513 | ||||||
| chr17:28177799
|
C | T | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1149+5181C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28177799 | ||||||
| chr17:28178049
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1149+5431G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28178049 | ||||||
| chr17:28178130
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1149+5512T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28178130 | ||||||
| chr17:28178620
|
C | G | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1149+6002C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28178620 | ||||||
| chr17:28178688
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1149+6070C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28178688 | ||||||
| chr17:28178898
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1149+6280C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28178898 | ||||||
| chr17:28179602
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1150-5577C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28179602 | ||||||
| chr17:28179689
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1150-5490G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28179689 | ||||||
| chr17:28179831
|
C | A | 1 | a0001c0001t0003g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1150-5348C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28179831 | ||||||
| chr17:28179852
|
C | T | 1 | a0001c0001t0003g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1150-5327C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28179852 | ||||||
| chr17:28179872
|
G | GT | 32 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0028others(29): Show | 32 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1150-5282dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 28179872 | |||||
| chr17:28179872
|
GTT | G | 4 | a0001c0001t0003g0013a0001c0001t0005g0105a0001c0001t0005g0106others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-5283_1150-528 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 28179872 | |||||
| chr17:28179881
|
T | G | 7 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(4): Show | 7 | HG01070.hp1 HG01257.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150-5298T>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28179881 | ||||||
| chr17:28179960
|
T | C | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150-5219T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28179960 | ||||||
| chr17:28180750
|
C | G | 1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1150-4429C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28180750 | ||||||
| chr17:28181193
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1150-3986G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28181193 | ||||||
| chr17:28181261
|
G | A | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1150-3918G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28181261 | ||||||
| chr17:28181302
|
G | A | 1 | a0001c0001t0003g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1150-3877G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28181302 | ||||||
| chr17:28181550
|
T | C | 1 | a0001c0001t0002g0017 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1150-3629T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28181550 | ||||||
| chr17:28181711
|
T | C | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1150-3468T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28181711 | ||||||
| chr17:28181975
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1150-3204G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28181975 | ||||||
| chr17:28182645
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1150-2534G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28182645 | ||||||
| chr17:28182788
|
A | G | 3 | a0001c0001t0002g0050a0001c0001t0002g0090a0001c0001t0002g0092 | 3 | HG00642.hp2 NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1150-2391A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28182788 | ||||||
| chr17:28182906
|
T | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1150-2273T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28182906 | ||||||
| chr17:28183136
|
G | A | 1 | a0001c0001t0005g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1150-2043G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28183136 | ||||||
| chr17:28183191
|
A | C | 4 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007others(1): Show | 4 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150-1988A>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28183191 | ||||||
| chr17:28183370
|
C | G | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1150-1809C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28183370 | ||||||
| chr17:28183714
|
G | T | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1150-1465G>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28183714 | ||||||
| chr17:28183717
|
G | A | 1 | a0001c0001t0003g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1150-1462G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28183717 | ||||||
| chr17:28184145
|
A | G | 2 | a0001c0001t0005g0105a0001c0001t0005g0106 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1150-1034A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28184145 | ||||||
| chr17:28184477
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | NA18990.hp1 NA19062.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1150-702T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28184477 | ||||||
| chr17:28184519
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0098 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1150-660C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28184519 | ||||||
| chr17:28184674
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1150-505G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28184674 | ||||||
| chr17:28184686
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1150-493G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28184686 | ||||||
| chr17:28184714
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1150-465G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28184714 | ||||||
| chr17:28184880
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1150-299G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28184880 | ||||||
| chr17:28184997
|
C | T | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1150-182C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 7/10 | chr17 | 28184997 | ||||||
| chr17:28185565
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | NA18990.hp1 NA19062.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1236+300T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28185565 | ||||||
| chr17:28185650
|
G | C | 1 | a0001c0001t0002g0050 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1236+385G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28185650 | ||||||
| chr17:28186622
|
C | CT | 16 | a0001c0001t0001g0015a0001c0001t0003g0003a0001c0001t0003g0009others(13): Show | 16 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1236+1358dupT | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 28186622 | |||||
| chr17:28186742
|
C | A | 1 | a0003c0004t0001g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1236+1477C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28186742 | ||||||
| chr17:28187288
|
T | TGTTTG | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG02257.hp1 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1236+2046_1236+205 others(9): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 28187288 | |||||
| chr17:28188027
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1236+2762G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28188027 | ||||||
| chr17:28188067
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1236+2802G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28188067 | ||||||
| chr17:28188503
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1237-2518G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28188503 | ||||||
| chr17:28188548
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1237-2473G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28188548 | ||||||
| chr17:28188980
|
G | GAC | 4 | a0001c0001t0001g0026a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG00642.hp1 HG03834.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237-2010_1237-200 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 28188980 | |||||
| chr17:28188980
|
G | GACACAC | 3 | a0001c0002t0003g0011a0001c0002t0003g0012a0001c0002t0003g0014 | 3 | HG02109.hp2 HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1237-2014_1237-200 others(10): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 28188980 | |||||
| chr17:28188980
|
G | GACACACA others(3): Show |
1 | a0001c0002t0003g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1237-2018_1237-200 others(14): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 28188980 | |||||
| chr17:28188980
|
GAC | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0022others(34): Show | 37 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1237-2010_1237-200 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 28188980 | |||||
| chr17:28188980
|
GACACAC | G | 4 | a0001c0001t0001g0071a0001c0001t0002g0056a0001c0001t0003g0010others(1): Show | 4 | HG02976.hp2 HG03486.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-2014_1237-200 others(10): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 28188980 | |||||
| chr17:28189047
|
A | G | 1 | a0001c0001t0002g0090 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1237-1974A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28189047 | ||||||
| chr17:28189182
|
G | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(43): Show | 46 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1237-1839G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28189182 | ||||||
| chr17:28189471
|
G | A | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1237-1550G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28189471 | ||||||
| chr17:28189871
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1237-1150G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28189871 | ||||||
| chr17:28189899
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1237-1122C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28189899 | ||||||
| chr17:28190116
|
T | A | 1 | a0001c0001t0001g0069 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1237-905T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28190116 | ||||||
| chr17:28190423
|
C | T | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1237-598C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28190423 | ||||||
| chr17:28190480
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1237-541C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28190480 | ||||||
| chr17:28190684
|
C | T | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1237-337C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28190684 | ||||||
| chr17:28190901
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1237-120G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 8/10 | chr17 | 28190901 | ||||||
| chr17:28191375
|
C | G | 1 | a0001c0001t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1435+156C>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 9/10 | chr17 | 28191375 | ||||||
| chr17:28191526
|
A | G | 1 | a0001c0001t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1435+307A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 9/10 | chr17 | 28191526 | ||||||
| chr17:28191695
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0021others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1436-425C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 9/10 | chr17 | 28191695 | ||||||
| chr17:28191726
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1436-394A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 9/10 | chr17 | 28191726 | ||||||
| chr17:28191739
|
A | G | 1 | a0001c0001t0003g0086 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1436-381A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 9/10 | chr17 | 28191739 | ||||||
| chr17:28191905
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1436-215G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 9/10 | chr17 | 28191905 | ||||||
| chr17:28192396
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1529+183C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 10/10 | chr17 | 28192396 | ||||||
| chr17:28192460
|
G | C | 1 | a0001c0001t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1529+247G>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 10/10 | chr17 | 28192460 | ||||||
| chr17:28192609
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1529+396G>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 10/10 | chr17 | 28192609 | ||||||
| chr17:28192668
|
C | CA | 8 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1529+466dupA | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr17 | 28192668 | |||||
| chr17:28193508
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02572.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1530-1074C>T | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 10/10 | chr17 | 28193508 | ||||||
| chr17:28194142
|
C | A | 5 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0005g0105others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1530-440C>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 10/10 | chr17 | 28194142 | ||||||
| chr17:28194143
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1530-439T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 10/10 | chr17 | 28194143 |