Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MSLCG others(522): Show |
chr17 | 28037677 | 28201381 |
| a0002 | 0/0 | 527 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | MSLCG others(522): Show |
chr17 | 28037677 | 28201381 |
| a0003 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | MSLCG others(522): Show |
chr17 | 28037677 | 28201381 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1581 | 99 | 37 | 16 | 32 | 4 | 8 | NLK_chr17_28037677_28201381 | NLK | ATGTC others(1576): Show |
chr17 | 28037677 | 28201381 | ||
| a0001c0002 | 0/0 | 1581 | 4 | 4 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | ATGTC others(1576): Show |
chr17 | 28037677 | 28201381 | ||
| a0001c0005 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | ATGTC others(1576): Show |
chr17 | 28037677 | 28201381 | ||
| a0001c0006 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | ATGTC others(1576): Show |
chr17 | 28037677 | 28201381 | ||
| a0002c0003 | 0/0 | 1581 | 2 | 0 | 2 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | ATGTC others(1576): Show |
chr17 | 28037677 | 28201381 | ||
| a0003c0004 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | ATGTC others(1576): Show |
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 | CTTTT others(3521): Show |
chr17 | 28037677 | 28201381 |
| a0001c0001t0002 | 0/0 | 3528 | 18 | 7 | 1 | 6 | 1 | 3 | NLK_chr17_28037677_28201381 | NLK | CTTTT others(3523): Show |
chr17 | 28037677 | 28201381 |
| a0001c0001t0003 | 0/1 | 3530 | 8 | 6 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | CTTTT others(3525): Show |
chr17 | 28037677 | 28201381 |
| a0001c0001t0004 | 0/0 | 3536 | 6 | 0 | 0 | 6 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | CTTTT others(3531): Show |
chr17 | 28037677 | 28201381 |
| a0001c0001t0005 | 0/0 | 3524 | 4 | 3 | 0 | 0 | 0 | 1 | NLK_chr17_28037677_28201381 | NLK | CTTTT others(3519): Show |
chr17 | 28037677 | 28201381 |
| a0001c0001t0006 | 0/0 | 3534 | 2 | 2 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | CTTTT others(3529): Show |
chr17 | 28037677 | 28201381 |
| a0001c0001t0007 | 0/0 | 3526 | 1 | 0 | 0 | 1 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | CTTTT others(3521): Show |
chr17 | 28037677 | 28201381 |
| a0001c0002t0003 | 0/0 | 3530 | 4 | 4 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | CTTTT others(3525): Show |
chr17 | 28037677 | 28201381 |
| a0001c0005t0001 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | CTTTT others(3521): Show |
chr17 | 28037677 | 28201381 |
| a0001c0006t0001 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | CTTTT others(3521): Show |
chr17 | 28037677 | 28201381 |
| a0002c0003t0001 | 0/0 | 3526 | 2 | 0 | 2 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | CTTTT others(3521): Show |
chr17 | 28037677 | 28201381 |
| a0003c0004t0001 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | NLK_chr17_28037677_28201381 | NLK | CTTTT others(3521): Show |
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 | a0001 | c0001 | t0003 | g0076 | REF | REF | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0088 | REF | REF | NLK_chr17_28037677_28201381 | NLK | chr17 | 28037677 | 28201381 |
| view | 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 |
| view | 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 |
| view | 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 | a0001c0001t0003 a0001c0002t0003 |
11 | HG00609.hp2 HG02109.hp2 HG02717.hp1 others(8): 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 |
| view | 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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
97 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(94): 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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0002g0081 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0015 a0001c0001t0002g0108 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0077 others(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 | ||||||
| chr17:28051589 | C | G | 2 | a0001c0001t0001g0098 a0003c0004t0001g0018 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0002g0074 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0021 others(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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
98 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(95): 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 | a0001c0001t0001g0019 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0028 a0001c0001t0004g0094 a0001c0001t0006g0006 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0061 a0001c0001t0002g0065 a0001c0001t0004g0094 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0005g0105 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0005g0105 others(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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0003g0016 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0002g0062 a0001c0001t0003g0009 |
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 | a0001c0001t0001g0098 a0001c0002t0003g0008 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0026 a0001c0001t0003g0016 a0001c0001t0005g0105 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
98 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(95): 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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0060 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0046 a0002c0003t0001g0047 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0069 a0001c0002t0003g0008 a0001c0002t0003g0011 others(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 | a0001c0001t0001g0015 a0001c0001t0003g0003 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0029 a0001c0001t0003g0003 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0057 a0001c0001t0002g0090 a0001c0001t0002g0092 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0029 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0089 a0001c0001t0002g0090 a0001c0001t0002g0092 |
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 | 48 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(45): Show |
48 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(45): 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 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0049 others(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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0040 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 |
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 | a0001c0001t0003g0016 a0001c0002t0003g0008 a0001c0002t0003g0011 others(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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0002g0038 a0001c0001t0002g0075 |
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 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0002g0081 others(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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0028 others(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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0057 a0001c0001t0001g0060 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0003g0016 a0001c0002t0003g0008 a0001c0002t0003g0011 others(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 | |||||||
| chr17:28081973 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0005g0105 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0015 a0001c0001t0003g0003 a0001c0001t0003g0010 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0003g0003 |
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 | a0001c0001t0002g0038 a0001c0001t0002g0075 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0089 a0001c0001t0002g0090 a0001c0001t0002g0092 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.459-33010A>G | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 1/10 | chr17 | 28089593 | |||||||
| chr17:28089709 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0070 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0002g0050 a0001c0001t0003g0016 a0001c0001t0005g0095 |
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 | a0001c0001t0001g0093 a0001c0001t0003g0010 a0001c0001t0003g0048 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0015 a0001c0001t0003g0003 a0001c0001t0003g0013 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0046 a0002c0003t0001g0047 |
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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0005g0105 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0028 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0028 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0006g0006 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0080 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0021 |
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 | a0001c0001t0003g0016 a0001c0001t0005g0105 a0001c0001t0005g0106 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | |||||||
| chr17:28107449 | AAAG | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0063 a0001c0001t0002g0092 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0054 a0001c0001t0002g0085 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0002g0081 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0033 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0055 a0002c0003t0001g0043 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0028 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0003g0010 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0045 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0101 a0001c0001t0005g0095 |
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 | a0001c0001t0001g0002 a0001c0001t0002g0108 |
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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0002c0003t0001g0047 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0002g0090 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0089 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0071 others(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 | 2 | a0001c0001t0001g0070 a0001c0001t0004g0031 |
2 | HG00438.hp2 HG02165.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 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0002g0074 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0051 |
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 | a0001c0001t0001g0077 a0001c0001t0001g0098 a0001c0001t0002g0038 others(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 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0052 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0091 a0001c0001t0003g0086 others(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 | a0001c0001t0001g0025 a0001c0001t0003g0016 |
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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0068 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0068 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0073 a0001c0001t0001g0077 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0002g0104 others(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 | a0001c0001t0001g0046 a0001c0005t0001g0059 a0002c0003t0001g0047 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0005g0105 others(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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0028 others(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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | |||||||
| chr17:28115028 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | |||||||
| chr17:28115989 | T | G | 2 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0044 a0001c0001t0001g0057 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0066 a0001c0001t0003g0086 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0077 a0001c0002t0003g0014 a0003c0004t0001g0018 |
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 | a0001c0001t0001g0089 a0001c0001t0002g0090 a0001c0001t0002g0092 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(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 | 6 | a0001c0001t0001g0022 a0001c0001t0001g0051 a0001c0001t0001g0054 others(3): Show |
6 | HG00140.hp2 HG01071.hp1 HG01071.hp2 others(3): 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 | a0001c0001t0003g0010 a0001c0001t0003g0013 a0001c0001t0005g0105 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0009 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0028 others(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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(45): Show |
48 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(45): 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 | 81 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(78): Show |
81 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(78): 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 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0009 |
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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0003g0016 a0001c0002t0003g0008 a0001c0002t0003g0011 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0003g0003 a0001c0002t0003g0008 a0001c0002t0003g0011 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(58): Show |
61 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(58): 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 | a0001c0001t0004g0035 a0001c0001t0004g0037 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0005g0105 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(102): Show |
105 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(102): 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 | a0001c0001t0002g0099 a0001c0006t0001g0087 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0045 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | |||||||
| chr17:28134836 | T | A | 1 | a0001c0001t0001g0051 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.644+2161T>A | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | chr17 | 28134836 | |||||||
| chr17:28134932 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0052 others(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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0015 a0001c0001t0003g0016 a0001c0001t0006g0006 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0055 a0002c0003t0001g0043 |
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 | a0001c0001t0001g0022 a0001c0001t0005g0105 a0001c0001t0005g0106 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0005g0105 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0045 others(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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0069 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0066 a0001c0001t0003g0086 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0045 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0005g0105 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(92): Show |
95 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(92): 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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0069 |
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 | 44 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(41): Show |
44 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(41): 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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | |||||||
| chr17:28148334 | CTT | C | 2 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.645-12822_645-1282 others(6): Show |
NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 28148334 | ||||||
| chr17:28148361 | TATG | T | 2 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0003g0009 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0005g0105 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 |
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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | |||||||
| chr17:28155350 | A | AT | 2 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | |||||||
| chr17:28157176 | TCACCTAT others(15): Show |
T | 3 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0015 a0001c0001t0002g0056 a0001c0001t0006g0006 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0003g0009 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0041 |
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 | a0001c0001t0003g0010 a0001c0001t0005g0105 a0001c0001t0005g0106 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0005g0105 others(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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0096 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0005g0105 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | 82 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0020 others(79): Show |
82 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(79): 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 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0069 others(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 | a0001c0001t0003g0010 a0001c0001t0003g0013 a0001c0001t0006g0006 others(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 | a0001c0001t0001g0015 a0001c0001t0003g0003 a0001c0001t0005g0105 others(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 | a0001c0001t0001g0055 a0002c0003t0001g0043 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0055 a0002c0003t0001g0043 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0026 a0001c0001t0002g0017 a0001c0001t0002g0038 others(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 | a0001c0001t0001g0072 a0001c0005t0001g0059 |
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 | a0001c0001t0003g0016 a0001c0002t0003g0008 a0001c0002t0003g0011 others(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 | a0001c0001t0002g0056 a0001c0002t0003g0012 |
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 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 |
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 | a0001c0001t0001g0015 a0001c0001t0002g0056 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0002t0003g0008 a0001c0002t0003g0011 a0001c0002t0003g0012 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0002g0050 a0001c0001t0002g0090 a0001c0001t0002g0092 |
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 | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
82 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(79): 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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0061 |
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 | a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | |||||||
| chr17:28179852 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0028 others(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 | a0001c0001t0003g0013 a0001c0001t0005g0105 a0001c0001t0005g0106 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0002g0050 a0001c0001t0002g0090 a0001c0001t0002g0092 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 |
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 | a0001c0001t0001g0066 a0001c0001t0001g0098 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 |
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 | a0001c0001t0001g0015 a0001c0001t0003g0003 a0001c0001t0003g0009 others(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 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0002t0003g0011 a0001c0002t0003g0012 a0001c0002t0003g0014 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0071 a0001c0001t0002g0056 a0001c0001t0003g0010 others(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 | 45 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(42): Show |
45 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(42): 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 | a0001c0001t0003g0010 a0001c0001t0003g0013 |
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 | 44 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0021 others(41): Show |
44 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(41): 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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(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 | a0001c0001t0001g0015 a0001c0001t0006g0006 a0001c0001t0006g0007 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0005g0105 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1530-439T>C | NLK | ENSG00000087095.13 | transcript | ENST00000407008.8 | protein_coding | 10/10 | chr17 | 28194143 |