Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79679 |
| ensemblid | ENSG00000134258.18 |
| hgncid | 28873 |
| symbol | VTCN1 |
| name | V-set domain containing T cell activation inhibitor 1 |
| refseq_nuc | NM_024626.4 |
| refseq_prot | NP_078902.2 |
| ensembl_nuc | ENST00000369458.8 |
| ensembl_prot | ENSP00000358470.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 117143587 |
| end | 117210927 |
| strand | - |
| ver | v1.2 |
| region | chr1:117143587-117210927 |
| region5000 | chr1:117138587-117215927 |
| regionname0 | VTCN1_chr1_117143587_117210927 |
| regionname5000 | VTCN1_chr1_117138587_117215927 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 282 | 242 | 89 | 43 | 60 | 12 | 36 | 40 | VTCN1_chr1_117138587_117215927 | VTCN1 | MASLG others(277): Show |
chr1 | 117138587 | 117215927 |
| a0002 | 0/0 | 282 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | MASLG others(277): Show |
chr1 | 117138587 | 117215927 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 846 | 242 | 89 | 43 | 60 | 12 | 36 | VTCN1_chr1_117138587_117215927 | VTCN1 | ATGGC others(841): Show |
chr1 | 117138587 | 117215927 | ||
| a0002c0002 | 0/0 | 846 | 6 | 5 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | ATGGC others(841): Show |
chr1 | 117138587 | 117215927 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2605 | 105 | 21 | 25 | 30 | 7 | 22 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0002 | 1/0 | 2605 | 40 | 9 | 7 | 16 | 2 | 5 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0003 | 0/0 | 2605 | 33 | 31 | 1 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0004 | 0/1 | 2605 | 20 | 0 | 8 | 2 | 2 | 7 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0005 | 0/0 | 2603 | 12 | 12 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2598): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0006 | 0/0 | 2605 | 11 | 0 | 0 | 9 | 1 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0007 | 0/0 | 2605 | 7 | 7 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0008 | 0/0 | 2605 | 3 | 3 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0009 | 0/0 | 2605 | 3 | 0 | 0 | 3 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0010 | 0/0 | 2603 | 2 | 2 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2598): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0011 | 0/0 | 2605 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0012 | 0/0 | 2605 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0013 | 0/0 | 2605 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0014 | 0/0 | 2605 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0015 | 0/0 | 2603 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2598): Show |
chr1 | 117138587 | 117215927 |
| a0001c0001t0016 | 0/0 | 2605 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0002c0002t0001 | 0/0 | 2605 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0002c0002t0002 | 0/0 | 2605 | 2 | 2 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| a0002c0002t0003 | 0/0 | 2605 | 3 | 2 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | GTGAG others(2600): Show |
chr1 | 117138587 | 117215927 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0007g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0009g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0009g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0009g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0010g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0011g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0012g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0013g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0014g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0015g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0001c0001t0016g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0002c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0002c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0002c0002t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0002c0002t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| a0002c0002t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | GBR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | GBR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0132 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0151 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01361 | hp1 | a0001 | c0001 | t0014 | g0146 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01433 | hp1 | a0002 | c0002 | t0003 | g0211 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | IBS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0227 | EUR | IBS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0106 | EUR | IBS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0057 | EUR | IBS | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01884 | hp2 | a0002 | c0002 | t0003 | g0170 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01891 | hp1 | a0001 | c0001 | t0013 | g0027 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02004 | hp2 | a0001 | c0001 | t0016 | g0237 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0125 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0235 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0233 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0050 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0017 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0200 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0049 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0180 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0120 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0126 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0186 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0208 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0236 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0209 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0061 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0192 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0201 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0135 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0112 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0172 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0130 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | ESN | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0182 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | GWD | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0093 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0118 | SAS | PJL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0039 | SAS | BEB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0228 | SAS | STU | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | STU | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | STU | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | STU | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | YRI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | YRI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CHB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | YRI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | YRI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0225 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18950 | hp1 | a0001 | c0001 | t0009 | g0222 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18950 | hp2 | a0001 | c0001 | t0009 | g0232 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18982 | hp2 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19000 | hp1 | a0001 | c0001 | t0006 | g0224 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | LWK | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | LWK | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19043 | hp1 | a0002 | c0002 | t0003 | g0169 | AFR | LWK | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19063 | hp1 | a0001 | c0001 | t0006 | g0223 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19063 | hp2 | a0001 | c0001 | t0009 | g0226 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19090 | hp2 | a0001 | c0001 | t0006 | g0230 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | YRI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | YRI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0128 | EUR | TSI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | TSI | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | GIH | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0041 | SAS | GIH | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0189 | AFR | ACB | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | MSL | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | USA | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0218 | AFR | USA | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0231 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | USA | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | USA | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | LWK | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0127 | REF | REF | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0030 | REF | REF | VTCN1_chr1_117138587_117215927 | VTCN1 | chr1 | 117138587 | 117215927 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:117170136 | A | G | 1 | a0002 | 6 | HG01433.hp1 HG01884.hp2 HG03225.hp2 others(3): Show |
missense_variant | MODERATE | c.68T>C | p.Ile23Thr | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/6 | 140/2605 | 68/849 | 23/282 | chr1 | 117170136 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:117143870 | C | A | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(12): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1401G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 3788 | chr1 | 117143870 | ||||||
| chr1:117144205 | C | T | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(12): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1066G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 3453 | chr1 | 117144205 | ||||||
| chr1:117144216 | T | C | 1 | a0001c0001t0008 | 3 | HG02055.hp1 HG02486.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1055A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 3442 | chr1 | 117144216 | ||||||
| chr1:117144292 | C | T | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(12): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*979G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 3366 | chr1 | 117144292 | ||||||
| chr1:117144415 | T | C | 2 | a0001c0001t0007 a0001c0001t0013 |
8 | HG01891.hp1 HG02451.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*856A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 3243 | chr1 | 117144415 | ||||||
| chr1:117144503 | A | T | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(12): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*768T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 3155 | chr1 | 117144503 | ||||||
| chr1:117144535 | C | T | 1 | a0001c0001t0012 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*736G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 3123 | chr1 | 117144535 | ||||||
| chr1:117144928 | C | T | 1 | a0001c0001t0011 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*343G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 2730 | chr1 | 117144928 | ||||||
| chr1:117144958 | G | C | 1 | a0001c0001t0014 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*313C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 2700 | chr1 | 117144958 | ||||||
| chr1:117145130 | CTT | C | 3 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0015 |
15 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*139_*140delAA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 6/6 | 2526 | chr1 | 117145130 | ||||||
| chr1:117147630 | T | C | 1 | a0001c0001t0013 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/6 | 28 | chr1 | 117147630 | ||||||
| chr1:117147650 | G | A | 7 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(4): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*8C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/6 | 8 | chr1 | 117147650 | ||||||
| chr1:117210906 | G | A | 2 | a0001c0001t0006 a0001c0001t0009 |
14 | HG01515.hp2 HG02056.hp1 HG02129.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-51C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/6 | 51 | chr1 | 117210906 | ||||||
| chr1:117210911 | C | A | 1 | a0001c0001t0015 | 1 | HG02895.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-56G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/6 | chr1 | 117210911 | |||||||
| chr1:117210921 | G | A | 1 | a0001c0001t0016 | 1 | HG02004.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/6 | 66 | chr1 | 117210921 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:117145328 | T | C | 1 | a0001c0001t0013g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.*46-103A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117145328 | |||||||
| chr1:117145431 | C | G | 6 | a0001c0001t0004g0006 a0001c0001t0004g0037 a0001c0001t0004g0041 others(3): Show |
7 | HG00741.hp1 HG01255.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.*46-206G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117145431 | |||||||
| chr1:117145437 | A | T | 1 | a0001c0001t0002g0167 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.*46-212T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117145437 | |||||||
| chr1:117145530 | G | A | 18 | a0001c0001t0003g0012 a0001c0001t0003g0020 a0001c0001t0003g0035 others(15): Show |
18 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.*46-305C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117145530 | |||||||
| chr1:117145778 | T | C | 32 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(29): Show |
36 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(33): Show |
intron_variant | MODIFIER | c.*46-553A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117145778 | |||||||
| chr1:117145981 | A | G | 1 | a0001c0001t0007g0014 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.*46-756T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117145981 | |||||||
| chr1:117146231 | T | TC | 14 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(11): Show |
15 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.*46-1007dupG | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146231 | |||||||
| chr1:117146233 | A | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(78): Show |
87 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(84): Show |
intron_variant | MODIFIER | c.*46-1008T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146233 | |||||||
| chr1:117146307 | G | A | 12 | a0001c0001t0003g0184 a0001c0001t0003g0185 a0001c0001t0003g0193 others(9): Show |
12 | HG02055.hp1 HG02486.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.*46-1082C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146307 | |||||||
| chr1:117146308 | A | C | 12 | a0001c0001t0003g0184 a0001c0001t0003g0185 a0001c0001t0003g0193 others(9): Show |
12 | HG02055.hp1 HG02486.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.*46-1083T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146308 | |||||||
| chr1:117146315 | C | T | 1 | a0001c0001t0004g0177 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.*46-1090G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146315 | |||||||
| chr1:117146344 | T | G | 14 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(11): Show |
15 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.*46-1119A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146344 | |||||||
| chr1:117146664 | G | C | 1 | a0001c0001t0001g0069 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.*45+949C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146664 | |||||||
| chr1:117146813 | C | A | 1 | a0001c0001t0005g0018 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*45+800G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146813 | |||||||
| chr1:117146853 | A | G | 1 | a0001c0001t0005g0008 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*45+760T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146853 | |||||||
| chr1:117146869 | A | G | 24 | a0001c0001t0003g0012 a0001c0001t0003g0020 a0001c0001t0003g0035 others(21): Show |
24 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.*45+744T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146869 | |||||||
| chr1:117146886 | C | T | 1 | a0001c0001t0004g0004 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.*45+727G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146886 | |||||||
| chr1:117146954 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.*45+659C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117146954 | |||||||
| chr1:117147063 | C | T | 14 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(11): Show |
15 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.*45+550G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147063 | |||||||
| chr1:117147086 | C | G | 14 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(11): Show |
15 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.*45+527G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147086 | |||||||
| chr1:117147089 | T | C | 14 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(11): Show |
15 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.*45+524A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147089 | |||||||
| chr1:117147243 | G | T | 12 | a0001c0001t0003g0184 a0001c0001t0003g0185 a0001c0001t0003g0193 others(9): Show |
12 | HG02055.hp1 HG02486.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.*45+370C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147243 | |||||||
| chr1:117147291 | G | C | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.*45+322C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147291 | |||||||
| chr1:117147300 | C | G | 80 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(77): Show |
86 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(83): Show |
intron_variant | MODIFIER | c.*45+313G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147300 | |||||||
| chr1:117147306 | G | T | 1 | a0001c0001t0012g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*45+307C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147306 | |||||||
| chr1:117147323 | C | T | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.*45+290G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147323 | |||||||
| chr1:117147349 | G | A | 2 | a0001c0001t0003g0136 a0001c0001t0003g0139 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.*45+264C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147349 | |||||||
| chr1:117147402 | T | C | 2 | a0001c0001t0007g0014 a0001c0001t0013g0027 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.*45+211A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147402 | |||||||
| chr1:117147438 | G | A | 1 | a0001c0001t0006g0231 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.*45+175C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147438 | |||||||
| chr1:117147562 | G | C | 4 | a0001c0001t0007g0015 a0001c0001t0007g0126 a0001c0001t0007g0135 others(1): Show |
4 | HG02818.hp1 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.*45+51C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 5/5 | chr1 | 117147562 | |||||||
| chr1:117147927 | C | T | 1 | a0001c0001t0013g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.725-145G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117147927 | |||||||
| chr1:117148006 | C | T | 2 | a0001c0001t0001g0110 a0002c0002t0002g0201 |
2 | HG03225.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.725-224G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148006 | |||||||
| chr1:117148136 | C | T | 71 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(68): Show |
77 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(74): Show |
intron_variant | MODIFIER | c.725-354G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148136 | |||||||
| chr1:117148316 | T | C | 3 | a0002c0002t0003g0169 a0002c0002t0003g0170 a0002c0002t0003g0211 |
3 | HG01433.hp1 HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.725-534A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148316 | |||||||
| chr1:117148578 | T | C | 85 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0002g0003 others(82): Show |
91 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(88): Show |
intron_variant | MODIFIER | c.725-796A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148578 | |||||||
| chr1:117148622 | T | C | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.725-840A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148622 | |||||||
| chr1:117148673 | C | A | 23 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0013 others(20): Show |
25 | HG02083.hp1 HG02523.hp2 HG02818.hp2 others(22): Show |
intron_variant | MODIFIER | c.725-891G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148673 | |||||||
| chr1:117148816 | T | G | 38 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(35): Show |
39 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.725-1034A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148816 | |||||||
| chr1:117148914 | G | A | 10 | a0001c0001t0005g0008 a0001c0001t0005g0009 a0001c0001t0005g0010 others(7): Show |
13 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.725-1132C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148914 | |||||||
| chr1:117148928 | C | T | 5 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0003g0132 others(2): Show |
5 | HG01099.hp1 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.725-1146G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117148928 | |||||||
| chr1:117149083 | G | A | 38 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(35): Show |
39 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.725-1301C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149083 | |||||||
| chr1:117149084 | G | A | 2 | a0001c0001t0004g0006 a0001c0001t0004g0037 |
3 | HG00741.hp1 HG01255.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.725-1302C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149084 | |||||||
| chr1:117149290 | T | TG | 47 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0040 others(44): Show |
51 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.725-1509dupC | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149290 | |||||||
| chr1:117149294 | T | G | 47 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0002g0003 others(44): Show |
49 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.725-1512A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149294 | |||||||
| chr1:117149295 | T | G | 1 | a0001c0001t0002g0160 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.725-1513A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149295 | |||||||
| chr1:117149359 | C | T | 38 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(35): Show |
39 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.725-1577G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149359 | |||||||
| chr1:117149425 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.725-1643A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149425 | |||||||
| chr1:117149662 | C | T | 23 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0013 others(20): Show |
25 | HG02083.hp1 HG02523.hp2 HG02818.hp2 others(22): Show |
intron_variant | MODIFIER | c.725-1880G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149662 | |||||||
| chr1:117149801 | C | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0007g0014 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.725-2019G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117149801 | |||||||
| chr1:117150137 | T | C | 12 | a0001c0001t0003g0026 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
15 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.725-2355A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150137 | |||||||
| chr1:117150160 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.725-2378G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150160 | |||||||
| chr1:117150312 | C | T | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.725-2530G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150312 | |||||||
| chr1:117150357 | G | A | 1 | a0002c0002t0002g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.725-2575C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150357 | |||||||
| chr1:117150472 | C | T | 34 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(31): Show |
35 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.724+2619G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150472 | |||||||
| chr1:117150550 | T | C | 2 | a0001c0001t0004g0121 a0001c0001t0004g0177 |
2 | HG02056.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.724+2541A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150550 | |||||||
| chr1:117150597 | TTTAG | T | 15 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(12): Show |
18 | HG00642.hp2 HG01943.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.724+2490_724+2493d others(6): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150597 | |||||||
| chr1:117150679 | T | C | 5 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0087 others(2): Show |
5 | HG01099.hp2 HG02735.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+2412A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150679 | |||||||
| chr1:117150773 | C | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0045 |
2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.724+2318G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150773 | |||||||
| chr1:117150911 | C | T | 13 | a0001c0001t0003g0026 a0001c0001t0005g0008 a0001c0001t0005g0009 others(10): Show |
16 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+2180G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150911 | |||||||
| chr1:117150984 | T | C | 13 | a0001c0001t0003g0026 a0001c0001t0005g0008 a0001c0001t0005g0009 others(10): Show |
16 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+2107A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117150984 | |||||||
| chr1:117151034 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0143 a0001c0001t0001g0161 |
3 | HG01192.hp1 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.724+2057C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151034 | |||||||
| chr1:117151046 | T | G | 1 | a0001c0001t0003g0184 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.724+2045A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151046 | |||||||
| chr1:117151100 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0094 |
2 | HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.724+1991G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151100 | |||||||
| chr1:117151103 | A | C | 1 | a0001c0001t0005g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.724+1988T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151103 | |||||||
| chr1:117151200 | C | CT | 87 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0002g0003 others(84): Show |
93 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(90): Show |
intron_variant | MODIFIER | c.724+1890dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151200 | |||||||
| chr1:117151249 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.724+1842G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151249 | |||||||
| chr1:117151271 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.724+1820A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151271 | |||||||
| chr1:117151281 | T | C | 100 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0002g0003 others(97): Show |
106 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(103): Show |
intron_variant | MODIFIER | c.724+1810A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151281 | |||||||
| chr1:117151354 | C | T | 1 | a0001c0001t0002g0007 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.724+1737G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151354 | |||||||
| chr1:117151408 | G | C | 1 | a0002c0002t0002g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.724+1683C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151408 | |||||||
| chr1:117151418 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.724+1673A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151418 | |||||||
| chr1:117151507 | C | T | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+1584G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151507 | |||||||
| chr1:117151516 | G | A | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+1575C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151516 | |||||||
| chr1:117151523 | C | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG01257.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.724+1568G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151523 | |||||||
| chr1:117151535 | T | TATTGGTC others(17): Show |
19 | a0001c0001t0002g0013 a0001c0001t0002g0022 a0001c0001t0002g0144 others(16): Show |
22 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.724+1532_724+1555d others(26): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151535 | |||||||
| chr1:117151535 | T | TATTGGTC others(17): Show |
1 | a0001c0001t0002g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.724+1555_724+1556i others(26): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151535 | |||||||
| chr1:117151716 | C | T | 4 | a0001c0001t0003g0142 a0001c0001t0007g0015 a0001c0001t0007g0126 others(1): Show |
4 | HG02818.hp1 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.724+1375G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151716 | |||||||
| chr1:117151767 | T | C | 5 | a0001c0001t0001g0044 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG01175.hp1 HG03491.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.724+1324A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151767 | |||||||
| chr1:117151922 | T | C | 1 | a0001c0001t0003g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.724+1169A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117151922 | |||||||
| chr1:117152072 | G | A | 19 | a0001c0001t0003g0012 a0001c0001t0003g0020 a0001c0001t0003g0035 others(16): Show |
19 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.724+1019C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117152072 | |||||||
| chr1:117152200 | T | C | 96 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0002g0003 others(93): Show |
102 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(99): Show |
intron_variant | MODIFIER | c.724+891A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117152200 | |||||||
| chr1:117152201 | G | A | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+890C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117152201 | |||||||
| chr1:117152474 | G | A | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+617C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117152474 | |||||||
| chr1:117152647 | T | A | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+444A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117152647 | |||||||
| chr1:117152688 | GC | G | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.724+402delG | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117152688 | |||||||
| chr1:117153016 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.724+75T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 4/5 | chr1 | 117153016 | |||||||
| chr1:117153415 | G | A | 98 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0002g0003 others(95): Show |
104 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(101): Show |
intron_variant | MODIFIER | c.446-46C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153415 | |||||||
| chr1:117153461 | A | AT | 25 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0207 others(22): Show |
28 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.446-93dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153461 | |||||||
| chr1:117153461 | AT | A | 21 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0108 others(18): Show |
22 | HG00408.hp2 HG01099.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.446-93delA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153461 | |||||||
| chr1:117153526 | A | G | 100 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0002g0003 others(97): Show |
106 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(103): Show |
intron_variant | MODIFIER | c.446-157T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153526 | |||||||
| chr1:117153577 | C | A | 36 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0013 others(33): Show |
41 | HG02083.hp1 HG02109.hp2 HG02257.hp2 others(38): Show |
intron_variant | MODIFIER | c.446-208G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153577 | |||||||
| chr1:117153825 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0114 |
3 | HG02145.hp2 HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.446-456G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153825 | |||||||
| chr1:117153967 | G | T | 1 | a0001c0001t0003g0212 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.446-598C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153967 | |||||||
| chr1:117153968 | C | T | 1 | a0001c0001t0003g0212 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.446-599G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117153968 | |||||||
| chr1:117154302 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.446-933G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154302 | |||||||
| chr1:117154484 | C | A | 1 | a0001c0001t0006g0233 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.446-1115G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154484 | |||||||
| chr1:117154570 | G | T | 3 | a0001c0001t0001g0207 a0001c0001t0010g0208 a0001c0001t0010g0209 |
3 | HG02895.hp1 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.446-1201C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154570 | |||||||
| chr1:117154708 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.446-1339C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154708 | |||||||
| chr1:117154746 | G | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 |
3 | HG00642.hp2 HG01943.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.446-1377C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154746 | |||||||
| chr1:117154783 | C | CA | 4 | a0001c0001t0001g0164 a0001c0001t0002g0003 a0001c0001t0002g0159 others(1): Show |
5 | HG02615.hp1 HG03017.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-1415dupT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154783 | |||||||
| chr1:117154783 | CA | C | 18 | a0001c0001t0001g0019 a0001c0001t0001g0058 a0001c0001t0001g0078 others(15): Show |
18 | HG01243.hp1 HG01515.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.446-1415delT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154783 | |||||||
| chr1:117154800 | A | G | 12 | a0001c0001t0003g0026 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
15 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.446-1431T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154800 | |||||||
| chr1:117154843 | A | G | 23 | a0001c0001t0003g0012 a0001c0001t0003g0020 a0001c0001t0003g0035 others(20): Show |
23 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.446-1474T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117154843 | |||||||
| chr1:117155442 | A | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0197 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.445+1132T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117155442 | |||||||
| chr1:117155838 | C | A | 1 | a0001c0001t0001g0153 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.445+736G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117155838 | |||||||
| chr1:117155910 | A | G | 23 | a0001c0001t0003g0012 a0001c0001t0003g0020 a0001c0001t0003g0035 others(20): Show |
23 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.445+664T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117155910 | |||||||
| chr1:117155945 | T | C | 80 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0002g0003 others(77): Show |
85 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(82): Show |
intron_variant | MODIFIER | c.445+629A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117155945 | |||||||
| chr1:117155992 | G | T | 5 | a0001c0001t0003g0142 a0001c0001t0007g0015 a0001c0001t0007g0126 others(2): Show |
5 | HG02818.hp1 HG03098.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+582C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117155992 | |||||||
| chr1:117156184 | T | C | 2 | a0001c0001t0003g0193 a0001c0001t0003g0195 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.445+390A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117156184 | |||||||
| chr1:117156198 | T | C | 1 | a0001c0001t0004g0118 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.445+376A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 3/5 | chr1 | 117156198 | |||||||
| chr1:117157003 | C | T | 13 | a0001c0001t0003g0026 a0001c0001t0005g0008 a0001c0001t0005g0009 others(10): Show |
16 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.98-82G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157003 | |||||||
| chr1:117157092 | G | GAT | 59 | a0001c0001t0001g0028 a0001c0001t0001g0073 a0001c0001t0001g0083 others(56): Show |
66 | HG00408.hp1 HG00741.hp1 HG01255.hp1 others(63): Show |
intron_variant | MODIFIER | c.98-173_98-172dupAT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATAT | 5 | a0001c0001t0002g0144 a0001c0001t0005g0018 a0001c0001t0007g0135 others(2): Show |
5 | HG01361.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-175_98-172dupAT others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATATAT | 5 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0002g0145 others(2): Show |
5 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-177_98-172dupAT others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATATATA others(1): Show |
4 | a0001c0001t0002g0103 a0001c0001t0007g0172 a0001c0001t0011g0017 others(1): Show |
4 | HG01884.hp2 HG02258.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-179_98-172dupAT others(6): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATATATA others(3): Show |
2 | a0002c0002t0003g0169 a0002c0002t0003g0211 |
2 | HG01433.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.98-181_98-172dupAT others(8): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATATATA others(9): Show |
1 | a0001c0001t0002g0052 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.98-187_98-172dupAT others(14): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATATATA others(11): Show |
2 | a0001c0001t0007g0186 a0001c0001t0007g0200 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.98-189_98-172dupAT others(16): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATATATA others(13): Show |
3 | a0001c0001t0002g0021 a0001c0001t0002g0165 a0001c0001t0003g0148 |
3 | HG02486.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.98-191_98-172dupAT others(18): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATATATA others(15): Show |
11 | a0001c0001t0002g0005 a0001c0001t0002g0076 a0001c0001t0002g0129 others(8): Show |
12 | HG01099.hp1 HG01243.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.98-193_98-172dupAT others(20): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATATATA others(17): Show |
2 | a0001c0001t0003g0012 a0001c0001t0003g0171 |
2 | HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.98-172_98-171insAT others(22): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATATATA others(19): Show |
8 | a0001c0001t0002g0034 a0001c0001t0002g0056 a0001c0001t0002g0057 others(5): Show |
8 | HG01515.hp1 HG01517.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-172_98-171insAT others(24): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATATATA others(21): Show |
4 | a0001c0001t0002g0040 a0001c0001t0003g0035 a0001c0001t0003g0119 others(1): Show |
4 | HG01106.hp2 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-172_98-171insAT others(26): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATATATA others(23): Show |
3 | a0001c0001t0003g0020 a0001c0001t0003g0190 a0001c0001t0003g0212 |
3 | HG02647.hp1 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.98-172_98-171insAT others(28): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATATATA others(25): Show |
2 | a0001c0001t0002g0188 a0001c0001t0003g0181 |
2 | NA18906.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.98-172_98-171insAT others(30): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATATATA others(27): Show |
1 | a0001c0001t0002g0167 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.98-172_98-171insAT others(32): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157092 | G | GATATATA others(29): Show |
1 | a0001c0001t0002g0088 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.98-172_98-171insAT others(34): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157092 | |||||||
| chr1:117157430 | G | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0097 |
3 | HG00280.hp1 HG00323.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.98-509C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157430 | |||||||
| chr1:117157526 | C | A | 4 | a0001c0001t0003g0012 a0001c0001t0003g0171 a0001c0001t0003g0190 others(1): Show |
4 | HG02109.hp1 HG02965.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-605G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157526 | |||||||
| chr1:117157576 | C | T | 1 | a0001c0001t0003g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.98-655G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157576 | |||||||
| chr1:117157595 | C | T | 13 | a0001c0001t0003g0026 a0001c0001t0005g0008 a0001c0001t0005g0009 others(10): Show |
16 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.98-674G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157595 | |||||||
| chr1:117157674 | C | T | 2 | a0001c0001t0002g0167 a0001c0001t0002g0188 |
2 | NA18964.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.98-753G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157674 | |||||||
| chr1:117157899 | G | C | 1 | a0001c0001t0002g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-978C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117157899 | |||||||
| chr1:117158083 | T | C | 19 | a0001c0001t0003g0012 a0001c0001t0003g0020 a0001c0001t0003g0035 others(16): Show |
19 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.98-1162A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158083 | |||||||
| chr1:117158189 | C | T | 1 | a0001c0001t0003g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.98-1268G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158189 | |||||||
| chr1:117158214 | A | C | 30 | a0001c0001t0001g0123 a0001c0001t0002g0003 a0001c0001t0002g0007 others(27): Show |
32 | HG00408.hp1 HG02083.hp1 HG02523.hp2 others(29): Show |
intron_variant | MODIFIER | c.98-1293T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158214 | |||||||
| chr1:117158232 | G | A | 12 | a0001c0001t0003g0026 a0001c0001t0005g0008 a0001c0001t0005g0009 others(9): Show |
15 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.98-1311C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158232 | |||||||
| chr1:117158285 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.98-1364G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158285 | |||||||
| chr1:117158479 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.98-1558C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158479 | |||||||
| chr1:117158546 | A | T | 13 | a0001c0001t0001g0197 a0001c0001t0003g0184 a0001c0001t0003g0185 others(10): Show |
13 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.98-1625T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158546 | |||||||
| chr1:117158720 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.98-1799G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158720 | |||||||
| chr1:117158799 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.98-1878G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158799 | |||||||
| chr1:117158856 | A | G | 2 | a0001c0001t0003g0026 a0001c0001t0011g0017 |
2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.98-1935T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158856 | |||||||
| chr1:117158934 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.98-2013T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158934 | |||||||
| chr1:117158958 | C | G | 1 | a0001c0001t0003g0212 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98-2037G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117158958 | |||||||
| chr1:117159023 | A | T | 84 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0123 others(81): Show |
87 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(84): Show |
intron_variant | MODIFIER | c.98-2102T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117159023 | |||||||
| chr1:117159384 | C | G | 13 | a0001c0001t0001g0197 a0001c0001t0003g0184 a0001c0001t0003g0185 others(10): Show |
13 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.98-2463G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117159384 | |||||||
| chr1:117159494 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.98-2573G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117159494 | |||||||
| chr1:117159738 | T | G | 2 | a0001c0001t0002g0168 a0002c0002t0002g0218 |
2 | HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.98-2817A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117159738 | |||||||
| chr1:117159766 | T | A | 86 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0123 others(83): Show |
89 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(86): Show |
intron_variant | MODIFIER | c.98-2845A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117159766 | |||||||
| chr1:117159966 | C | G | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.98-3045G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117159966 | |||||||
| chr1:117160040 | G | A | 7 | a0001c0001t0001g0123 a0001c0001t0002g0074 a0001c0001t0002g0085 others(4): Show |
7 | NA18747.hp2 NA18939.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-3119C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160040 | |||||||
| chr1:117160162 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.98-3241C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160162 | |||||||
| chr1:117160395 | A | C | 1 | a0001c0001t0007g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.98-3474T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160395 | |||||||
| chr1:117160540 | G | A | 8 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0063 others(5): Show |
8 | HG01255.hp2 HG01258.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.98-3619C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160540 | |||||||
| chr1:117160560 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.98-3639C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160560 | |||||||
| chr1:117160622 | T | G | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.98-3701A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160622 | |||||||
| chr1:117160701 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.98-3780A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160701 | |||||||
| chr1:117160954 | G | C | 1 | a0001c0001t0001g0152 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.98-4033C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117160954 | |||||||
| chr1:117161394 | C | T | 52 | a0001c0001t0001g0197 a0001c0001t0002g0005 a0001c0001t0002g0021 others(49): Show |
53 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.98-4473G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117161394 | |||||||
| chr1:117161686 | A | C | 1 | a0001c0001t0003g0205 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.98-4765T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117161686 | |||||||
| chr1:117161734 | C | T | 19 | a0001c0001t0003g0012 a0001c0001t0003g0020 a0001c0001t0003g0035 others(16): Show |
19 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.98-4813G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117161734 | |||||||
| chr1:117161794 | A | G | 2 | a0001c0001t0004g0121 a0001c0001t0004g0177 |
2 | HG02056.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.98-4873T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117161794 | |||||||
| chr1:117161878 | G | A | 48 | a0001c0001t0001g0197 a0001c0001t0002g0005 a0001c0001t0002g0021 others(45): Show |
49 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.98-4957C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117161878 | |||||||
| chr1:117162190 | C | G | 1 | a0001c0001t0004g0041 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.98-5269G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117162190 | |||||||
| chr1:117162341 | C | T | 13 | a0001c0001t0001g0197 a0001c0001t0003g0184 a0001c0001t0003g0185 others(10): Show |
13 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.98-5420G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117162341 | |||||||
| chr1:117162635 | T | G | 13 | a0001c0001t0001g0197 a0001c0001t0003g0184 a0001c0001t0003g0185 others(10): Show |
13 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.98-5714A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117162635 | |||||||
| chr1:117162747 | C | T | 28 | a0001c0001t0001g0197 a0001c0001t0002g0005 a0001c0001t0002g0021 others(25): Show |
29 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.98-5826G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117162747 | |||||||
| chr1:117162798 | G | A | 1 | a0001c0001t0007g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.98-5877C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117162798 | |||||||
| chr1:117163008 | A | G | 30 | a0001c0001t0001g0123 a0001c0001t0002g0003 a0001c0001t0002g0007 others(27): Show |
32 | HG00408.hp1 HG02083.hp1 HG02523.hp2 others(29): Show |
intron_variant | MODIFIER | c.98-6087T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117163008 | |||||||
| chr1:117163101 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.98-6180C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117163101 | |||||||
| chr1:117163306 | T | A | 1 | a0001c0001t0012g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.98-6385A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117163306 | |||||||
| chr1:117163413 | T | A | 77 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0123 others(74): Show |
83 | HG00408.hp1 HG01106.hp2 HG01243.hp2 others(80): Show |
intron_variant | MODIFIER | c.98-6492A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117163413 | |||||||
| chr1:117163872 | G | A | 1 | a0001c0001t0004g0048 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.97+6235C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117163872 | |||||||
| chr1:117164012 | G | T | 1 | a0001c0001t0002g0203 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.97+6095C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164012 | |||||||
| chr1:117164118 | C | T | 3 | a0001c0001t0004g0041 a0001c0001t0004g0093 a0001c0001t0014g0146 |
3 | HG01361.hp1 HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.97+5989G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164118 | |||||||
| chr1:117164342 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.97+5765G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164342 | |||||||
| chr1:117164356 | G | C | 3 | a0001c0001t0003g0193 a0001c0001t0003g0195 a0001c0001t0003g0196 |
3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.97+5751C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164356 | |||||||
| chr1:117164369 | C | T | 3 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0003g0206 |
3 | HG03130.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.97+5738G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164369 | |||||||
| chr1:117164510 | G | A | 1 | a0001c0001t0004g0151 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.97+5597C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164510 | |||||||
| chr1:117164515 | TA | T | 16 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0219 others(13): Show |
19 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.97+5591delT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164515 | |||||||
| chr1:117164537 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.97+5570C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164537 | |||||||
| chr1:117164722 | T | G | 26 | a0001c0001t0001g0123 a0001c0001t0002g0003 a0001c0001t0002g0007 others(23): Show |
28 | HG00408.hp1 HG02083.hp1 HG02523.hp2 others(25): Show |
intron_variant | MODIFIER | c.97+5385A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164722 | |||||||
| chr1:117164728 | A | T | 3 | a0001c0001t0001g0219 a0001c0001t0003g0026 a0001c0001t0011g0017 |
3 | HG02109.hp2 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.97+5379T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164728 | |||||||
| chr1:117164767 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.97+5340G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117164767 | |||||||
| chr1:117165040 | T | C | 4 | a0001c0001t0007g0172 a0002c0002t0001g0112 a0002c0002t0002g0201 others(1): Show |
4 | HG03225.hp2 HG03486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+5067A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165040 | |||||||
| chr1:117165202 | T | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0045 |
2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.97+4905A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165202 | |||||||
| chr1:117165309 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.97+4798A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165309 | |||||||
| chr1:117165454 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 |
3 | HG00642.hp2 HG01943.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.97+4653G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165454 | |||||||
| chr1:117165542 | G | A | 2 | a0001c0001t0002g0038 a0001c0001t0004g0006 |
3 | HG01255.hp1 HG01361.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.97+4565C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165542 | |||||||
| chr1:117165579 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.97+4528G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165579 | |||||||
| chr1:117165611 | A | C | 108 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0028 others(105): Show |
114 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(111): Show |
intron_variant | MODIFIER | c.97+4496T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165611 | |||||||
| chr1:117165712 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0002g0154 a0001c0001t0002g0160 |
3 | NA18747.hp2 NA18969.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.97+4395C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165712 | |||||||
| chr1:117165812 | G | A | 10 | a0001c0001t0005g0008 a0001c0001t0005g0009 a0001c0001t0005g0010 others(7): Show |
13 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+4295C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165812 | |||||||
| chr1:117165855 | T | C | 108 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0028 others(105): Show |
114 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(111): Show |
intron_variant | MODIFIER | c.97+4252A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117165855 | |||||||
| chr1:117166042 | T | C | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.97+4065A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166042 | |||||||
| chr1:117166083 | G | A | 3 | a0001c0001t0003g0133 a0001c0001t0003g0134 a0001c0001t0003g0148 |
3 | HG02486.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.97+4024C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166083 | |||||||
| chr1:117166102 | T | A | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.97+4005A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166102 | |||||||
| chr1:117166133 | T | C | 4 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+3974A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166133 | |||||||
| chr1:117166149 | G | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0213 a0001c0001t0001g0214 others(3): Show |
6 | HG01175.hp1 HG02976.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.97+3958C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166149 | |||||||
| chr1:117166199 | C | T | 25 | a0001c0001t0001g0123 a0001c0001t0001g0210 a0001c0001t0002g0003 others(22): Show |
27 | HG02083.hp1 HG02523.hp2 HG02572.hp1 others(24): Show |
intron_variant | MODIFIER | c.97+3908G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166199 | |||||||
| chr1:117166200 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97+3907C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166200 | |||||||
| chr1:117166247 | A | G | 26 | a0001c0001t0001g0123 a0001c0001t0002g0003 a0001c0001t0002g0007 others(23): Show |
28 | HG00408.hp1 HG02083.hp1 HG02523.hp2 others(25): Show |
intron_variant | MODIFIER | c.97+3860T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166247 | |||||||
| chr1:117166291 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.97+3816T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166291 | |||||||
| chr1:117166375 | T | C | 1 | a0001c0001t0003g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.97+3732A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166375 | |||||||
| chr1:117166466 | C | G | 8 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0003g0132 others(5): Show |
8 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+3641G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166466 | |||||||
| chr1:117166539 | G | C | 2 | a0002c0002t0002g0201 a0002c0002t0002g0218 |
2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.97+3568C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166539 | |||||||
| chr1:117166654 | C | CA | 12 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0002g0221 others(9): Show |
12 | HG00408.hp1 HG01099.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+3452dupT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166654 | |||||||
| chr1:117166816 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.97+3291C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166816 | |||||||
| chr1:117166842 | AG | A | 4 | a0001c0001t0001g0219 a0001c0001t0003g0012 a0001c0001t0003g0026 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+3264delC | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117166842 | |||||||
| chr1:117167071 | C | T | 12 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0003g0193 others(9): Show |
12 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+3036G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167071 | |||||||
| chr1:117167090 | C | CA | 108 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0028 others(105): Show |
114 | HG00408.hp1 HG01099.hp1 HG01106.hp2 others(111): Show |
intron_variant | MODIFIER | c.97+3016dupT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167090 | |||||||
| chr1:117167304 | T | C | 1 | a0001c0001t0007g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.97+2803A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167304 | |||||||
| chr1:117167445 | T | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG01257.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.97+2662A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167445 | |||||||
| chr1:117167466 | C | G | 15 | a0001c0001t0001g0219 a0001c0001t0002g0217 a0001c0001t0003g0012 others(12): Show |
18 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.97+2641G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167466 | |||||||
| chr1:117167470 | T | G | 3 | a0001c0001t0002g0003 a0001c0001t0002g0066 a0001c0001t0002g0159 |
4 | NA18953.hp2 NA18999.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+2637A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167470 | |||||||
| chr1:117167507 | G | A | 4 | a0001c0001t0001g0219 a0001c0001t0003g0012 a0001c0001t0003g0026 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+2600C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167507 | |||||||
| chr1:117167591 | G | A | 1 | a0001c0001t0002g0007 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.97+2516C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167591 | |||||||
| chr1:117167649 | T | C | 2 | a0001c0001t0003g0035 a0001c0001t0003g0036 |
2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.97+2458A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167649 | |||||||
| chr1:117167843 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0045 |
2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.97+2264T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117167843 | |||||||
| chr1:117168012 | A | C | 1 | a0001c0001t0001g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97+2095T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168012 | |||||||
| chr1:117168013 | C | A | 12 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0003g0193 others(9): Show |
12 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+2094G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168013 | |||||||
| chr1:117168061 | T | C | 3 | a0001c0001t0003g0171 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG02109.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97+2046A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168061 | |||||||
| chr1:117168093 | A | C | 6 | a0002c0002t0001g0112 a0002c0002t0002g0201 a0002c0002t0002g0218 others(3): Show |
6 | HG01433.hp1 HG01884.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+2014T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168093 | |||||||
| chr1:117168183 | T | C | 1 | a0001c0001t0016g0237 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.97+1924A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168183 | |||||||
| chr1:117168208 | A | G | 10 | a0001c0001t0005g0008 a0001c0001t0005g0009 a0001c0001t0005g0010 others(7): Show |
13 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+1899T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168208 | |||||||
| chr1:117168349 | T | C | 3 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0006g0231 |
3 | NA18955.hp1 NA18964.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.97+1758A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168349 | |||||||
| chr1:117168433 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0150 a0001c0001t0003g0149 |
3 | HG03195.hp2 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.97+1674A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168433 | |||||||
| chr1:117168539 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+1568T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168539 | |||||||
| chr1:117168725 | A | G | 55 | a0001c0001t0001g0197 a0001c0001t0001g0219 a0001c0001t0002g0217 others(52): Show |
58 | HG01099.hp1 HG01433.hp1 HG01884.hp2 others(55): Show |
intron_variant | MODIFIER | c.97+1382T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168725 | |||||||
| chr1:117168730 | G | A | 5 | a0001c0001t0002g0005 a0001c0001t0002g0040 a0001c0001t0002g0056 others(2): Show |
6 | HG01106.hp2 HG01358.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+1377C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168730 | |||||||
| chr1:117168980 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+1127G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117168980 | |||||||
| chr1:117169073 | C | A | 1 | a0001c0001t0013g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.97+1034G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169073 | |||||||
| chr1:117169183 | T | G | 13 | a0001c0001t0001g0197 a0001c0001t0001g0210 a0001c0001t0003g0185 others(10): Show |
13 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+924A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169183 | |||||||
| chr1:117169289 | G | A | 15 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0034 others(12): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.97+818C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169289 | |||||||
| chr1:117169313 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.97+794T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169313 | |||||||
| chr1:117169415 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.97+692C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169415 | |||||||
| chr1:117169423 | G | A | 24 | a0001c0001t0001g0219 a0001c0001t0003g0012 a0001c0001t0003g0020 others(21): Show |
24 | HG01099.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.97+684C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169423 | |||||||
| chr1:117169436 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.97+671G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169436 | |||||||
| chr1:117169453 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.97+654G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169453 | |||||||
| chr1:117169483 | C | T | 78 | a0001c0001t0001g0123 a0001c0001t0001g0197 a0001c0001t0001g0210 others(75): Show |
83 | HG01099.hp1 HG01433.hp1 HG01884.hp2 others(80): Show |
intron_variant | MODIFIER | c.97+624G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169483 | |||||||
| chr1:117169758 | T | G | 2 | a0002c0002t0002g0201 a0002c0002t0002g0218 |
2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.97+349A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169758 | |||||||
| chr1:117169808 | T | C | 1 | a0002c0002t0002g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97+299A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117169808 | |||||||
| chr1:117170007 | T | A | 72 | a0001c0001t0001g0123 a0001c0001t0001g0197 a0001c0001t0001g0210 others(69): Show |
77 | HG01099.hp1 HG01891.hp1 HG02055.hp1 others(74): Show |
intron_variant | MODIFIER | c.97+100A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 2/5 | chr1 | 117170007 | |||||||
| chr1:117170482 | T | C | 6 | a0002c0002t0001g0112 a0002c0002t0002g0201 a0002c0002t0002g0218 others(3): Show |
6 | HG01433.hp1 HG01884.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-311A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117170482 | |||||||
| chr1:117170512 | G | A | 4 | a0001c0001t0001g0219 a0001c0001t0003g0012 a0001c0001t0003g0026 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-341C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117170512 | |||||||
| chr1:117170736 | A | C | 1 | a0001c0001t0001g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.33-565T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117170736 | |||||||
| chr1:117170886 | C | T | 5 | a0001c0001t0003g0194 a0001c0001t0003g0204 a0001c0001t0008g0125 others(2): Show |
5 | HG02055.hp1 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-715G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117170886 | |||||||
| chr1:117170887 | G | A | 1 | a0001c0001t0003g0036 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.33-716C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117170887 | |||||||
| chr1:117171016 | C | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0124 others(1): Show |
6 | HG00621.hp1 HG02074.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-845G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171016 | |||||||
| chr1:117171080 | A | G | 17 | a0001c0001t0005g0008 a0001c0001t0005g0009 a0001c0001t0005g0010 others(14): Show |
20 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.33-909T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171080 | |||||||
| chr1:117171081 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(231): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.33-910G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171081 | |||||||
| chr1:117171152 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.33-981G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171152 | |||||||
| chr1:117171173 | G | A | 18 | a0001c0001t0001g0219 a0001c0001t0003g0012 a0001c0001t0003g0020 others(15): Show |
18 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.33-1002C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171173 | |||||||
| chr1:117171212 | T | C | 1 | a0001c0001t0006g0223 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.33-1041A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171212 | |||||||
| chr1:117171333 | T | C | 45 | a0001c0001t0001g0094 a0001c0001t0001g0123 a0001c0001t0001g0219 others(42): Show |
47 | HG02083.hp1 HG02109.hp2 HG02258.hp1 others(44): Show |
intron_variant | MODIFIER | c.33-1162A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171333 | |||||||
| chr1:117171474 | C | G | 2 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33-1303G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171474 | |||||||
| chr1:117171568 | T | A | 11 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0028 others(8): Show |
11 | HG02055.hp2 HG02280.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-1397A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171568 | |||||||
| chr1:117171598 | C | T | 13 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0040 others(10): Show |
14 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-1427G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171598 | |||||||
| chr1:117171662 | C | T | 8 | a0001c0001t0001g0210 a0001c0001t0002g0022 a0001c0001t0003g0035 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-1491G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171662 | |||||||
| chr1:117171879 | A | G | 1 | a0001c0001t0012g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.33-1708T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171879 | |||||||
| chr1:117171903 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0150 a0001c0001t0003g0149 |
3 | HG03195.hp2 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.33-1732G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171903 | |||||||
| chr1:117171945 | G | A | 19 | a0001c0001t0001g0094 a0001c0001t0002g0003 a0001c0001t0002g0007 others(16): Show |
21 | HG02083.hp1 HG02523.hp2 HG02818.hp1 others(18): Show |
intron_variant | MODIFIER | c.33-1774C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117171945 | |||||||
| chr1:117172127 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(199): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.33-1956A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172127 | |||||||
| chr1:117172331 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.33-2160C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172331 | |||||||
| chr1:117172345 | T | C | 10 | a0001c0001t0005g0008 a0001c0001t0005g0009 a0001c0001t0005g0010 others(7): Show |
13 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.33-2174A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172345 | |||||||
| chr1:117172404 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(134): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.33-2233G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172404 | |||||||
| chr1:117172547 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.33-2376A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172547 | |||||||
| chr1:117172578 | ATTT | A | 32 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0028 others(29): Show |
35 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.33-2410_33-2408del others(3): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172578 | |||||||
| chr1:117172640 | T | C | 1 | a0001c0001t0003g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.33-2469A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172640 | |||||||
| chr1:117172640 | TC | T | 9 | a0001c0001t0001g0210 a0001c0001t0002g0022 a0001c0001t0003g0035 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-2470delG | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172640 | |||||||
| chr1:117172666 | T | C | 13 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0040 others(10): Show |
14 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-2495A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172666 | |||||||
| chr1:117172789 | TAAATGCA others(18): Show |
T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(118): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.33-2643_33-2619del others(25): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172789 | |||||||
| chr1:117172859 | C | T | 38 | a0001c0001t0001g0094 a0001c0001t0001g0123 a0001c0001t0002g0003 others(35): Show |
40 | HG02083.hp1 HG02486.hp1 HG02523.hp2 others(37): Show |
intron_variant | MODIFIER | c.33-2688G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172859 | |||||||
| chr1:117172864 | G | A | 38 | a0001c0001t0001g0094 a0001c0001t0001g0123 a0001c0001t0002g0003 others(35): Show |
40 | HG02083.hp1 HG02486.hp1 HG02523.hp2 others(37): Show |
intron_variant | MODIFIER | c.33-2693C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117172864 | |||||||
| chr1:117173081 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0207 a0001c0001t0002g0031 others(3): Show |
6 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-2910C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173081 | |||||||
| chr1:117173104 | G | C | 2 | a0002c0002t0003g0169 a0002c0002t0003g0211 |
2 | HG01433.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.33-2933C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173104 | |||||||
| chr1:117173154 | G | A | 1 | a0001c0001t0003g0132 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.33-2983C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173154 | |||||||
| chr1:117173159 | C | T | 1 | a0001c0001t0007g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.33-2988G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173159 | |||||||
| chr1:117173195 | C | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0040 others(8): Show |
12 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-3024G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173195 | |||||||
| chr1:117173365 | A | AAC | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(111): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.33-3196_33-3195dup others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | |||||||
| chr1:117173365 | A | AACAC | 48 | a0001c0001t0001g0028 a0001c0001t0001g0044 a0001c0001t0001g0094 others(45): Show |
52 | HG01099.hp1 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.33-3198_33-3195dup others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | |||||||
| chr1:117173365 | A | AACACAC | 21 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0219 others(18): Show |
22 | HG02109.hp2 HG02257.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.33-3200_33-3195dup others(6): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | |||||||
| chr1:117173365 | A | AACACACA others(1): Show |
6 | a0001c0001t0001g0019 a0001c0001t0002g0168 a0001c0001t0003g0012 others(3): Show |
7 | HG02895.hp2 HG02970.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-3202_33-3195dup others(8): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | |||||||
| chr1:117173365 | A | AACACACA others(3): Show |
8 | a0001c0001t0001g0023 a0001c0001t0001g0150 a0001c0001t0001g0220 others(5): Show |
8 | HG01884.hp2 HG01891.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-3204_33-3195dup others(10): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | |||||||
| chr1:117173365 | A | AACACACA others(7): Show |
1 | a0001c0001t0001g0045 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.33-3208_33-3195dup others(14): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | |||||||
| chr1:117173365 | AAC | A | 14 | a0001c0001t0001g0153 a0001c0001t0002g0021 a0001c0001t0002g0217 others(11): Show |
14 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.33-3196_33-3195del others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | |||||||
| chr1:117173365 | AACAC | A | 4 | a0001c0001t0002g0022 a0001c0001t0003g0171 a0001c0001t0003g0190 others(1): Show |
4 | HG02109.hp1 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-3198_33-3195del others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173365 | |||||||
| chr1:117173484 | T | A | 18 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(15): Show |
20 | HG00642.hp2 HG00741.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.33-3313A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173484 | |||||||
| chr1:117173491 | T | G | 2 | a0001c0001t0002g0021 a0001c0001t0003g0148 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.33-3320A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173491 | |||||||
| chr1:117173492 | C | A | 10 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0040 others(7): Show |
11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-3321G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173492 | |||||||
| chr1:117173531 | T | C | 28 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0028 others(25): Show |
30 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.33-3360A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173531 | |||||||
| chr1:117173654 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(127): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.33-3483A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173654 | |||||||
| chr1:117173771 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0003g0184 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.33-3600C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173771 | |||||||
| chr1:117173914 | C | T | 1 | a0001c0001t0004g0037 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.33-3743G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117173914 | |||||||
| chr1:117174057 | TGC | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(123): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.33-3888_33-3887del others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174057 | |||||||
| chr1:117174094 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0131 |
2 | HG01975.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.33-3923T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174094 | |||||||
| chr1:117174111 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.33-3940C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174111 | |||||||
| chr1:117174142 | C | T | 1 | a0001c0001t0007g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.33-3971G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174142 | |||||||
| chr1:117174323 | T | C | 1 | a0001c0001t0003g0139 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.33-4152A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174323 | |||||||
| chr1:117174413 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0072 others(16): Show |
21 | HG00408.hp2 HG00621.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.33-4242G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174413 | |||||||
| chr1:117174577 | G | A | 10 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0040 others(7): Show |
11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-4406C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174577 | |||||||
| chr1:117174638 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33-4467C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174638 | |||||||
| chr1:117174680 | T | C | 10 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0040 others(7): Show |
11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-4509A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174680 | |||||||
| chr1:117174691 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.33-4520G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174691 | |||||||
| chr1:117174867 | G | A | 25 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0150 others(22): Show |
27 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.33-4696C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174867 | |||||||
| chr1:117174947 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.33-4776G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117174947 | |||||||
| chr1:117175086 | A | AGCT | 13 | a0001c0001t0002g0021 a0001c0001t0002g0217 a0001c0001t0003g0133 others(10): Show |
13 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.33-4918_33-4916dup others(3): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175086 | |||||||
| chr1:117175229 | A | G | 1 | a0001c0001t0002g0167 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.33-5058T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175229 | |||||||
| chr1:117175374 | C | T | 1 | a0001c0001t0004g0106 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.33-5203G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175374 | |||||||
| chr1:117175406 | T | C | 10 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0040 others(7): Show |
11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-5235A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175406 | |||||||
| chr1:117175427 | A | G | 9 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0150 others(6): Show |
9 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-5256T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175427 | |||||||
| chr1:117175433 | C | T | 10 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0040 others(7): Show |
11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-5262G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175433 | |||||||
| chr1:117175621 | G | A | 15 | a0001c0001t0002g0022 a0001c0001t0003g0012 a0001c0001t0003g0035 others(12): Show |
17 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.33-5450C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175621 | |||||||
| chr1:117175755 | ATC | A | 13 | a0001c0001t0001g0065 a0001c0001t0001g0091 a0001c0001t0001g0174 others(10): Show |
14 | HG00323.hp1 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.33-5586_33-5585del others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175755 | |||||||
| chr1:117175765 | C | A | 10 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0040 others(7): Show |
11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-5594G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175765 | |||||||
| chr1:117175769 | C | CT | 13 | a0001c0001t0001g0028 a0001c0001t0002g0021 a0001c0001t0002g0217 others(10): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.33-5599dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175769 | |||||||
| chr1:117175771 | C | CT | 10 | a0001c0001t0001g0210 a0001c0001t0001g0219 a0001c0001t0002g0013 others(7): Show |
10 | HG02258.hp1 HG02572.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.33-5601dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175771 | |||||||
| chr1:117175771 | C | T | 14 | a0001c0001t0001g0028 a0001c0001t0002g0021 a0001c0001t0002g0217 others(11): Show |
14 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-5600G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175771 | |||||||
| chr1:117175772 | TC | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(128): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.33-5602delG | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175772 | |||||||
| chr1:117175773 | C | T | 71 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0028 others(68): Show |
76 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(73): Show |
intron_variant | MODIFIER | c.33-5602G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175773 | |||||||
| chr1:117175874 | G | A | 14 | a0001c0001t0001g0028 a0001c0001t0002g0021 a0001c0001t0002g0217 others(11): Show |
14 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-5703C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175874 | |||||||
| chr1:117175928 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.33-5757C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175928 | |||||||
| chr1:117175931 | C | T | 28 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0045 others(25): Show |
30 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.33-5760G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175931 | |||||||
| chr1:117175942 | T | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0002c0002t0003g0170 |
3 | HG01884.hp2 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.33-5771A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117175942 | |||||||
| chr1:117176000 | C | T | 9 | a0001c0001t0003g0012 a0001c0001t0005g0008 a0001c0001t0005g0009 others(6): Show |
11 | HG01891.hp1 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.33-5829G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176000 | |||||||
| chr1:117176114 | A | G | 7 | a0001c0001t0002g0022 a0001c0001t0003g0035 a0001c0001t0003g0036 others(4): Show |
7 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-5943T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176114 | |||||||
| chr1:117176157 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(212): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.33-5986G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176157 | |||||||
| chr1:117176175 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(212): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.33-6004T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176175 | |||||||
| chr1:117176312 | G | T | 1 | a0001c0001t0007g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.33-6141C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176312 | |||||||
| chr1:117176426 | CAAG | C | 27 | a0001c0001t0001g0094 a0001c0001t0001g0123 a0001c0001t0002g0003 others(24): Show |
30 | HG02083.hp1 HG02257.hp2 HG02523.hp2 others(27): Show |
intron_variant | MODIFIER | c.33-6258_33-6256del others(3): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176426 | |||||||
| chr1:117176509 | A | G | 10 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0040 others(7): Show |
11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-6338T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176509 | |||||||
| chr1:117176513 | A | G | 24 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0059 others(21): Show |
24 | HG00323.hp1 HG00408.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.33-6342T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176513 | |||||||
| chr1:117176557 | A | C | 1 | a0001c0001t0001g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.33-6386T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176557 | |||||||
| chr1:117176641 | A | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0117 |
2 | HG01099.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.33-6470T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176641 | |||||||
| chr1:117176680 | T | A | 1 | a0001c0001t0001g0220 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.33-6509A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176680 | |||||||
| chr1:117176822 | A | G | 10 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0040 others(7): Show |
11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-6651T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176822 | |||||||
| chr1:117176853 | C | CT | 4 | a0002c0002t0002g0201 a0002c0002t0002g0218 a0002c0002t0003g0169 others(1): Show |
4 | HG01433.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-6683dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176853 | |||||||
| chr1:117176955 | C | T | 15 | a0001c0001t0001g0028 a0001c0001t0002g0021 a0001c0001t0002g0217 others(12): Show |
15 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.33-6784G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176955 | |||||||
| chr1:117176992 | G | A | 26 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0045 others(23): Show |
28 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.33-6821C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117176992 | |||||||
| chr1:117177040 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(213): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.33-6869A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117177040 | |||||||
| chr1:117177115 | C | G | 1 | a0001c0001t0003g0026 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.33-6944G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117177115 | |||||||
| chr1:117177116 | A | G | 1 | a0001c0001t0003g0026 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.33-6945T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117177116 | |||||||
| chr1:117177677 | C | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0045 others(6): Show |
9 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-7506G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117177677 | |||||||
| chr1:117177697 | G | C | 10 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0040 others(7): Show |
11 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-7526C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117177697 | |||||||
| chr1:117177724 | A | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(202): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.33-7553T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117177724 | |||||||
| chr1:117177921 | C | CT | 27 | a0001c0001t0001g0028 a0001c0001t0001g0100 a0001c0001t0002g0005 others(24): Show |
28 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.33-7751dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117177921 | |||||||
| chr1:117178113 | A | T | 6 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0219 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-7942T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178113 | |||||||
| chr1:117178202 | G | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0002c0002t0003g0170 |
3 | HG01884.hp2 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.33-8031C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178202 | |||||||
| chr1:117178238 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.33-8067A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178238 | |||||||
| chr1:117178250 | C | CT | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(199): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.33-8080dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178250 | |||||||
| chr1:117178258 | T | TTC | 14 | a0001c0001t0001g0028 a0001c0001t0002g0021 a0001c0001t0002g0217 others(11): Show |
14 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-8088_33-8087ins others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178258 | |||||||
| chr1:117178259 | C | T | 14 | a0001c0001t0001g0028 a0001c0001t0002g0021 a0001c0001t0002g0217 others(11): Show |
14 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-8088G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178259 | |||||||
| chr1:117178300 | A | C | 1 | a0001c0001t0001g0100 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.33-8129T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178300 | |||||||
| chr1:117178352 | G | A | 8 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0063 others(5): Show |
8 | HG01255.hp2 HG01258.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-8181C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178352 | |||||||
| chr1:117178370 | C | A | 1 | a0002c0002t0002g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.33-8199G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178370 | |||||||
| chr1:117178388 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(178): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.33-8217G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178388 | |||||||
| chr1:117178547 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(212): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.33-8376A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178547 | |||||||
| chr1:117178588 | G | GT | 8 | a0001c0001t0001g0042 a0001c0001t0002g0029 a0001c0001t0002g0031 others(5): Show |
8 | HG00642.hp2 HG01175.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-8418dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178588 | |||||||
| chr1:117178588 | G | GTT | 32 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0028 others(29): Show |
32 | HG01884.hp2 HG01975.hp1 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.33-8419_33-8418dup others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178588 | |||||||
| chr1:117178588 | G | GTTT | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(143): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.33-8420_33-8418dup others(3): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178588 | |||||||
| chr1:117178588 | G | GTTTT | 21 | a0001c0001t0001g0032 a0001c0001t0001g0069 a0001c0001t0001g0083 others(18): Show |
21 | HG00408.hp1 HG00642.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-8421_33-8418dup others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178588 | |||||||
| chr1:117178729 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(158): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.33-8558C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178729 | |||||||
| chr1:117178736 | T | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(202): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.33-8565A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178736 | |||||||
| chr1:117178750 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.33-8579G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178750 | |||||||
| chr1:117178751 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(95): Show |
101 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.33-8580C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178751 | |||||||
| chr1:117178816 | C | T | 6 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0219 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-8645G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178816 | |||||||
| chr1:117178923 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(202): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.33-8752A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117178923 | |||||||
| chr1:117179135 | T | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0150 a0001c0001t0001g0220 others(3): Show |
6 | HG03041.hp1 HG03195.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-8964A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179135 | |||||||
| chr1:117179144 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33-8973G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179144 | |||||||
| chr1:117179184 | A | G | 1 | a0001c0001t0005g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.33-9013T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179184 | |||||||
| chr1:117179209 | C | T | 20 | a0001c0001t0001g0023 a0001c0001t0001g0150 a0001c0001t0002g0022 others(17): Show |
22 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.33-9038G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179209 | |||||||
| chr1:117179245 | T | C | 26 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0045 others(23): Show |
28 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.33-9074A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179245 | |||||||
| chr1:117179246 | G | A | 1 | a0002c0002t0002g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.33-9075C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179246 | |||||||
| chr1:117179265 | C | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(117): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.33-9094G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179265 | |||||||
| chr1:117179338 | G | T | 1 | a0001c0001t0002g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.33-9167C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179338 | |||||||
| chr1:117179376 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(216): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.33-9205C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179376 | |||||||
| chr1:117179558 | G | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(216): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.33-9387C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179558 | |||||||
| chr1:117179948 | C | T | 6 | a0001c0001t0005g0008 a0001c0001t0005g0009 a0001c0001t0005g0179 others(3): Show |
8 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-9777G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179948 | |||||||
| chr1:117179960 | G | C | 2 | a0001c0001t0013g0027 a0002c0002t0001g0112 |
2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.33-9789C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117179960 | |||||||
| chr1:117180070 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.33-9899T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180070 | |||||||
| chr1:117180124 | C | G | 1 | a0002c0002t0003g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.33-9953G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180124 | |||||||
| chr1:117180214 | C | CA | 22 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0045 others(19): Show |
24 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.33-10044dupT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180214 | |||||||
| chr1:117180313 | T | C | 22 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0045 others(19): Show |
24 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.33-10142A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180313 | |||||||
| chr1:117180350 | T | G | 22 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0045 others(19): Show |
24 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.33-10179A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180350 | |||||||
| chr1:117180418 | A | G | 2 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33-10247T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180418 | |||||||
| chr1:117180625 | C | G | 23 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0045 others(20): Show |
25 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.33-10454G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180625 | |||||||
| chr1:117180685 | T | A | 12 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0040 others(9): Show |
14 | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.33-10514A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180685 | |||||||
| chr1:117180776 | C | G | 28 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(25): Show |
31 | HG00621.hp2 HG00642.hp2 HG01943.hp2 others(28): Show |
intron_variant | MODIFIER | c.33-10605G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180776 | |||||||
| chr1:117180790 | G | A | 1 | a0001c0001t0004g0151 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.33-10619C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180790 | |||||||
| chr1:117180941 | C | T | 9 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0028 others(6): Show |
9 | HG01433.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-10770G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180941 | |||||||
| chr1:117180967 | G | C | 3 | a0001c0001t0001g0016 a0001c0001t0002g0031 a0001c0001t0003g0184 |
3 | HG03041.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-10796C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117180967 | |||||||
| chr1:117181009 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(173): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.33-10838G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181009 | |||||||
| chr1:117181146 | G | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0024 others(167): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.33-10975C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181146 | |||||||
| chr1:117181156 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG01257.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.33-10985G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181156 | |||||||
| chr1:117181165 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33-10994G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181165 | |||||||
| chr1:117181253 | C | CA | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(98): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.33-11083dupT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181253 | |||||||
| chr1:117181253 | CA | C | 20 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0028 others(17): Show |
22 | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-11083delT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181253 | |||||||
| chr1:117181419 | C | T | 27 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(24): Show |
29 | HG00621.hp2 HG00642.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.33-11248G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181419 | |||||||
| chr1:117181736 | G | T | 4 | a0001c0001t0003g0142 a0001c0001t0003g0171 a0001c0001t0007g0126 others(1): Show |
4 | HG02109.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-11565C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181736 | |||||||
| chr1:117181777 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0150 a0001c0001t0003g0149 others(2): Show |
5 | HG01891.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-11606G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181777 | |||||||
| chr1:117181796 | G | A | 2 | a0001c0001t0003g0190 a0001c0001t0003g0191 |
2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-11625C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181796 | |||||||
| chr1:117181872 | G | A | 2 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33-11701C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117181872 | |||||||
| chr1:117182339 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33-12168T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117182339 | |||||||
| chr1:117182450 | C | T | 9 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0028 others(6): Show |
9 | HG01433.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-12279G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117182450 | |||||||
| chr1:117182549 | A | T | 9 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0028 others(6): Show |
9 | HG01433.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-12378T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117182549 | |||||||
| chr1:117182584 | C | T | 2 | a0001c0001t0005g0009 a0001c0001t0005g0179 |
3 | HG02280.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.33-12413G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117182584 | |||||||
| chr1:117182669 | C | T | 4 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-12498G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117182669 | |||||||
| chr1:117182880 | C | G | 25 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(22): Show |
27 | HG00621.hp2 HG00642.hp2 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.33-12709G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117182880 | |||||||
| chr1:117182949 | C | A | 1 | a0001c0001t0005g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.33-12778G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117182949 | |||||||
| chr1:117183067 | G | T | 11 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0063 others(8): Show |
11 | HG00323.hp1 HG01255.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-12896C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117183067 | |||||||
| chr1:117183720 | C | T | 6 | a0001c0001t0002g0021 a0001c0001t0003g0133 a0001c0001t0003g0134 others(3): Show |
6 | HG02486.hp1 HG02622.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-13549G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117183720 | |||||||
| chr1:117183916 | T | C | 1 | a0001c0001t0002g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.33-13745A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117183916 | |||||||
| chr1:117184163 | C | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0158 |
2 | HG02523.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.33-13992G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117184163 | |||||||
| chr1:117184394 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.33-14223G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117184394 | |||||||
| chr1:117184535 | T | A | 1 | a0001c0001t0001g0082 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.33-14364A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117184535 | |||||||
| chr1:117184580 | C | T | 1 | a0001c0001t0003g0036 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.33-14409G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117184580 | |||||||
| chr1:117184745 | C | T | 28 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(25): Show |
30 | HG00621.hp2 HG00642.hp2 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.33-14574G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117184745 | |||||||
| chr1:117185085 | G | A | 6 | a0001c0001t0002g0021 a0001c0001t0003g0133 a0001c0001t0003g0134 others(3): Show |
6 | HG02486.hp1 HG02622.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-14914C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117185085 | |||||||
| chr1:117185103 | A | C | 5 | a0001c0001t0001g0044 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG01175.hp1 HG03491.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-14932T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117185103 | |||||||
| chr1:117185315 | C | T | 1 | a0002c0002t0002g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.33-15144G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117185315 | |||||||
| chr1:117185579 | A | C | 3 | a0001c0001t0001g0207 a0001c0001t0010g0208 a0001c0001t0010g0209 |
3 | HG02895.hp1 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.33-15408T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117185579 | |||||||
| chr1:117186016 | T | A | 2 | a0001c0001t0001g0150 a0001c0001t0003g0149 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.33-15845A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186016 | |||||||
| chr1:117186030 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0032 others(122): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.33-15859T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186030 | |||||||
| chr1:117186036 | T | C | 1 | a0001c0001t0005g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.33-15865A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186036 | |||||||
| chr1:117186103 | T | C | 1 | a0002c0002t0001g0112 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.33-15932A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186103 | |||||||
| chr1:117186219 | C | T | 2 | a0001c0001t0005g0009 a0001c0001t0005g0179 |
3 | HG02280.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.33-16048G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186219 | |||||||
| chr1:117186283 | C | A | 8 | a0001c0001t0001g0141 a0001c0001t0003g0136 a0001c0001t0003g0137 others(5): Show |
8 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-16112G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186283 | |||||||
| chr1:117186283 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.33-16112G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186283 | |||||||
| chr1:117186619 | A | T | 1 | a0001c0001t0003g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.33-16448T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186619 | |||||||
| chr1:117186734 | C | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG01175.hp1 HG03491.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-16563G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186734 | |||||||
| chr1:117186747 | C | T | 8 | a0001c0001t0002g0168 a0001c0001t0005g0008 a0001c0001t0005g0009 others(5): Show |
10 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-16576G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186747 | |||||||
| chr1:117186799 | G | A | 2 | a0001c0001t0003g0012 a0002c0002t0003g0169 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.33-16628C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186799 | |||||||
| chr1:117186840 | C | A | 1 | a0001c0001t0003g0140 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.33-16669G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186840 | |||||||
| chr1:117186894 | T | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0038 others(8): Show |
13 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.33-16723A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117186894 | |||||||
| chr1:117187061 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0032 others(116): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.33-16890A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187061 | |||||||
| chr1:117187074 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(200): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.33-16903A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187074 | |||||||
| chr1:117187301 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(126): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.33-17130G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187301 | |||||||
| chr1:117187309 | C | CA | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(129): Show |
141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.33-17139dupT | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187309 | |||||||
| chr1:117187309 | C | CAA | 23 | a0001c0001t0001g0016 a0001c0001t0001g0051 a0001c0001t0001g0072 others(20): Show |
23 | HG00408.hp1 HG00741.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.33-17140_33-17139d others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187309 | |||||||
| chr1:117187309 | C | CAAA | 9 | a0001c0001t0002g0021 a0001c0001t0003g0133 a0001c0001t0003g0134 others(6): Show |
9 | HG02486.hp1 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-17141_33-17139d others(5): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187309 | |||||||
| chr1:117187309 | CAA | C | 28 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0042 others(25): Show |
30 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.33-17140_33-17139d others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187309 | |||||||
| chr1:117187353 | T | C | 2 | a0001c0001t0002g0031 a0001c0001t0003g0184 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.33-17182A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187353 | |||||||
| chr1:117187426 | G | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(126): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.33-17255C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187426 | |||||||
| chr1:117187452 | A | G | 33 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0042 others(30): Show |
35 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.33-17281T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187452 | |||||||
| chr1:117187601 | G | C | 33 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0042 others(30): Show |
35 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.33-17430C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187601 | |||||||
| chr1:117187668 | C | T | 1 | a0001c0001t0002g0013 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.33-17497G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187668 | |||||||
| chr1:117187814 | G | A | 3 | a0001c0001t0003g0026 a0001c0001t0003g0035 a0001c0001t0003g0036 |
3 | HG02109.hp2 HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.33-17643C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187814 | |||||||
| chr1:117187918 | T | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 |
3 | HG00642.hp2 HG01943.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.33-17747A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117187918 | |||||||
| chr1:117188001 | G | A | 33 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0207 others(30): Show |
35 | HG00741.hp1 HG01099.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.33-17830C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188001 | |||||||
| chr1:117188058 | T | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(5): Show |
8 | HG01433.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-17887A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188058 | |||||||
| chr1:117188084 | C | T | 33 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0207 others(30): Show |
35 | HG00741.hp1 HG01099.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.33-17913G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188084 | |||||||
| chr1:117188157 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.33-17986T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188157 | |||||||
| chr1:117188221 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.33-18050C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188221 | |||||||
| chr1:117188441 | G | A | 33 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0042 others(30): Show |
35 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.33-18270C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188441 | |||||||
| chr1:117188515 | G | A | 1 | a0001c0001t0005g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.33-18344C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188515 | |||||||
| chr1:117188598 | A | G | 1 | a0002c0002t0003g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.33-18427T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188598 | |||||||
| chr1:117188617 | A | C | 2 | a0001c0001t0001g0150 a0001c0001t0003g0149 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.33-18446T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188617 | |||||||
| chr1:117188879 | C | G | 1 | a0002c0002t0002g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.33-18708G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188879 | |||||||
| chr1:117188935 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.33-18764T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117188935 | |||||||
| chr1:117189019 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.33-18848C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189019 | |||||||
| chr1:117189350 | G | A | 114 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0019 others(111): Show |
120 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(117): Show |
intron_variant | MODIFIER | c.33-19179C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189350 | |||||||
| chr1:117189351 | T | A | 2 | a0001c0001t0003g0035 a0001c0001t0003g0036 |
2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.33-19180A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189351 | |||||||
| chr1:117189509 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.33-19338G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189509 | |||||||
| chr1:117189549 | G | A | 28 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0207 others(25): Show |
30 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.33-19378C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189549 | |||||||
| chr1:117189671 | A | G | 1 | a0001c0001t0003g0136 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.33-19500T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189671 | |||||||
| chr1:117189790 | T | A | 4 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-19619A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189790 | |||||||
| chr1:117189811 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(200): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.33-19640G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189811 | |||||||
| chr1:117189894 | C | A | 35 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0042 others(32): Show |
37 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.33-19723G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189894 | |||||||
| chr1:117189910 | C | CAAG | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.33-19742_33-19740d others(5): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117189910 | |||||||
| chr1:117190236 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.33-20065G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190236 | |||||||
| chr1:117190252 | A | G | 4 | a0001c0001t0003g0185 a0001c0001t0008g0125 a0001c0001t0008g0189 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-20081T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190252 | |||||||
| chr1:117190278 | T | G | 12 | a0001c0001t0002g0031 a0001c0001t0002g0168 a0001c0001t0003g0020 others(9): Show |
14 | HG02280.hp2 HG02647.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.33-20107A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190278 | |||||||
| chr1:117190544 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.32+20280T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190544 | |||||||
| chr1:117190594 | C | A | 5 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0219 others(2): Show |
5 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+20230G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190594 | |||||||
| chr1:117190664 | C | G | 2 | a0001c0001t0005g0008 a0001c0001t0015g0236 |
3 | HG02895.hp2 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.32+20160G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190664 | |||||||
| chr1:117190853 | T | C | 14 | a0001c0001t0002g0031 a0001c0001t0002g0168 a0001c0001t0003g0020 others(11): Show |
16 | HG02257.hp1 HG02280.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+19971A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190853 | |||||||
| chr1:117190879 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32+19945C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117190879 | |||||||
| chr1:117191068 | C | T | 2 | a0001c0001t0002g0031 a0001c0001t0003g0184 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.32+19756G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191068 | |||||||
| chr1:117191144 | G | A | 2 | a0001c0001t0004g0121 a0001c0001t0004g0177 |
2 | HG02056.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.32+19680C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191144 | |||||||
| chr1:117191406 | C | A | 1 | a0001c0001t0002g0040 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.32+19418G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191406 | |||||||
| chr1:117191638 | C | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | NA18939.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.32+19186G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191638 | |||||||
| chr1:117191639 | G | A | 5 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0219 others(2): Show |
5 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+19185C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191639 | |||||||
| chr1:117191675 | G | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0034 a0001c0001t0002g0038 others(8): Show |
13 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.32+19149C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191675 | |||||||
| chr1:117191868 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.32+18956C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191868 | |||||||
| chr1:117191879 | C | T | 1 | a0001c0001t0004g0177 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.32+18945G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191879 | |||||||
| chr1:117191929 | T | A | 2 | a0001c0001t0003g0035 a0001c0001t0003g0036 |
2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.32+18895A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191929 | |||||||
| chr1:117191971 | G | A | 2 | a0001c0001t0003g0035 a0001c0001t0003g0036 |
2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.32+18853C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191971 | |||||||
| chr1:117191978 | T | C | 1 | a0001c0001t0004g0151 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.32+18846A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191978 | |||||||
| chr1:117191991 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(209): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.32+18833A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117191991 | |||||||
| chr1:117192008 | G | GAT | 10 | a0001c0001t0001g0067 a0001c0001t0001g0090 a0001c0001t0001g0104 others(7): Show |
10 | HG00140.hp1 HG00741.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.32+18814_32+18815d others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192008 | |||||||
| chr1:117192008 | G | GATAT | 39 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0042 others(36): Show |
42 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.32+18812_32+18815d others(6): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192008 | |||||||
| chr1:117192008 | G | GATATAT | 6 | a0001c0001t0001g0046 a0001c0001t0002g0007 a0001c0001t0002g0031 others(3): Show |
7 | HG01943.hp2 HG03041.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+18810_32+18815d others(8): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192008 | |||||||
| chr1:117192008 | G | GATATATA others(3): Show |
1 | a0001c0001t0002g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.32+18815_32+18816i others(12): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192008 | |||||||
| chr1:117192008 | G | GATATATA others(5): Show |
1 | a0001c0001t0002g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.32+18815_32+18816i others(14): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192008 | |||||||
| chr1:117192010 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.32+18814A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192010 | |||||||
| chr1:117192016 | G | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(198): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.32+18808C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192016 | |||||||
| chr1:117192028 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32+18796A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192028 | |||||||
| chr1:117192057 | A | G | 9 | a0001c0001t0002g0021 a0001c0001t0003g0133 a0001c0001t0003g0134 others(6): Show |
9 | HG02145.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+18767T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192057 | |||||||
| chr1:117192069 | G | A | 1 | a0002c0002t0002g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.32+18755C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192069 | |||||||
| chr1:117192659 | G | A | 1 | a0001c0001t0004g0093 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.32+18165C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192659 | |||||||
| chr1:117192925 | G | T | 12 | a0001c0001t0002g0031 a0001c0001t0002g0168 a0001c0001t0003g0020 others(9): Show |
14 | HG02280.hp2 HG02647.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.32+17899C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117192925 | |||||||
| chr1:117193124 | T | C | 1 | a0001c0001t0002g0221 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.32+17700A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193124 | |||||||
| chr1:117193244 | T | C | 35 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0042 others(32): Show |
37 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.32+17580A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193244 | |||||||
| chr1:117193257 | C | A | 1 | a0001c0001t0007g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.32+17567G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193257 | |||||||
| chr1:117193261 | A | T | 20 | a0001c0001t0001g0122 a0001c0001t0001g0141 a0001c0001t0002g0052 others(17): Show |
20 | HG00741.hp2 HG01243.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.32+17563T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193261 | |||||||
| chr1:117193349 | T | C | 30 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0042 others(27): Show |
32 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.32+17475A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193349 | |||||||
| chr1:117193415 | G | A | 1 | a0001c0001t0016g0237 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.32+17409C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193415 | |||||||
| chr1:117193577 | A | AC | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(200): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.32+17246dupG | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193577 | |||||||
| chr1:117193632 | A | G | 9 | a0001c0001t0002g0021 a0001c0001t0003g0133 a0001c0001t0003g0134 others(6): Show |
9 | HG02145.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+17192T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193632 | |||||||
| chr1:117193673 | T | G | 14 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0005 others(11): Show |
16 | HG00741.hp1 HG01099.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.32+17151A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193673 | |||||||
| chr1:117193895 | T | C | 9 | a0001c0001t0002g0074 a0001c0001t0002g0085 a0001c0001t0002g0103 others(6): Show |
9 | HG01515.hp2 HG02056.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+16929A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193895 | |||||||
| chr1:117193928 | A | G | 9 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(6): Show |
9 | HG01433.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+16896T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193928 | |||||||
| chr1:117193963 | A | G | 2 | a0001c0001t0003g0035 a0001c0001t0003g0036 |
2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.32+16861T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117193963 | |||||||
| chr1:117194073 | G | A | 1 | a0001c0001t0004g0151 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.32+16751C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117194073 | |||||||
| chr1:117194114 | A | G | 5 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0219 others(2): Show |
5 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+16710T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117194114 | |||||||
| chr1:117194192 | T | C | 1 | a0001c0001t0005g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.32+16632A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117194192 | |||||||
| chr1:117194770 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0011g0017 |
2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.32+16054T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117194770 | |||||||
| chr1:117194864 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(201): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.32+15960T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117194864 | |||||||
| chr1:117195072 | C | CCTGA | 81 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0028 others(78): Show |
85 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.32+15751_32+15752i others(6): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195072 | |||||||
| chr1:117195114 | C | T | 81 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0028 others(78): Show |
85 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.32+15710G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195114 | |||||||
| chr1:117195170 | G | A | 1 | a0001c0001t0012g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.32+15654C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195170 | |||||||
| chr1:117195262 | A | AAAT | 25 | a0001c0001t0001g0069 a0001c0001t0001g0094 a0001c0001t0001g0153 others(22): Show |
25 | HG00642.hp1 HG02056.hp2 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.32+15559_32+15561d others(5): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195262 | |||||||
| chr1:117195262 | A | AAATAAT | 31 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0042 others(28): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.32+15556_32+15561d others(8): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195262 | |||||||
| chr1:117195262 | A | AAATAATA others(2): Show |
9 | a0001c0001t0001g0158 a0001c0001t0001g0161 a0001c0001t0001g0173 others(6): Show |
10 | HG00621.hp2 HG01192.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.32+15553_32+15561d others(11): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195262 | |||||||
| chr1:117195262 | AAAT | A | 14 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0051 others(11): Show |
14 | HG01099.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.32+15559_32+15561d others(5): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195262 | |||||||
| chr1:117195262 | AAATAAT | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0032 others(103): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.32+15556_32+15561d others(8): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195262 | |||||||
| chr1:117195262 | AAATAATA others(2): Show |
A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0198 others(4): Show |
7 | HG01433.hp1 HG01891.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+15553_32+15561d others(11): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195262 | |||||||
| chr1:117195312 | A | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0002c0002t0003g0170 |
3 | HG01884.hp2 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.32+15512T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195312 | |||||||
| chr1:117195357 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.32+15467G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195357 | |||||||
| chr1:117195417 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+15407C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195417 | |||||||
| chr1:117195533 | C | T | 3 | a0001c0001t0005g0049 a0001c0001t0007g0172 a0002c0002t0003g0169 |
3 | HG02622.hp1 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.32+15291G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195533 | |||||||
| chr1:117195570 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0011g0017 |
2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.32+15254A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195570 | |||||||
| chr1:117195670 | T | A | 1 | a0001c0001t0003g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.32+15154A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195670 | |||||||
| chr1:117195680 | G | A | 2 | a0001c0001t0004g0121 a0001c0001t0004g0177 |
2 | HG02056.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.32+15144C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195680 | |||||||
| chr1:117195890 | C | T | 1 | a0001c0001t0004g0130 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.32+14934G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195890 | |||||||
| chr1:117195954 | C | T | 4 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+14870G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117195954 | |||||||
| chr1:117196015 | A | G | 112 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0019 others(109): Show |
118 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.32+14809T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196015 | |||||||
| chr1:117196091 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0003g0149 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.32+14733C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196091 | |||||||
| chr1:117196118 | C | T | 13 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0005 others(10): Show |
15 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.32+14706G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196118 | |||||||
| chr1:117196193 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0044 others(84): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.32+14631T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196193 | |||||||
| chr1:117196389 | CAT | C | 12 | a0001c0001t0003g0026 a0001c0001t0003g0132 a0001c0001t0003g0204 others(9): Show |
12 | HG01099.hp1 HG02056.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.32+14433_32+14434d others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196389 | |||||||
| chr1:117196401 | T | G | 6 | a0001c0001t0001g0087 a0001c0001t0001g0152 a0001c0001t0001g0161 others(3): Show |
7 | HG01192.hp1 HG02257.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+14423A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196401 | |||||||
| chr1:117196401 | T | TAG | 5 | a0001c0001t0002g0021 a0001c0001t0003g0133 a0001c0001t0003g0134 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+14422_32+14423i others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196401 | |||||||
| chr1:117196403 | T | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(72): Show |
82 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.32+14421A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196403 | |||||||
| chr1:117196403 | T | TAG | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0002g0203 |
3 | HG02083.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.32+14419_32+14420d others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196403 | |||||||
| chr1:117196403 | TAG | T | 30 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0075 others(27): Show |
30 | HG00642.hp1 HG01884.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.32+14419_32+14420d others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196403 | |||||||
| chr1:117196405 | G | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(64): Show |
70 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.32+14419C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196405 | |||||||
| chr1:117196407 | G | T | 27 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0063 others(24): Show |
28 | HG00642.hp1 HG01258.hp1 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.32+14417C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196407 | |||||||
| chr1:117196409 | G | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0063 others(3): Show |
6 | HG01258.hp1 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+14415C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196409 | |||||||
| chr1:117196425 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0007g0014 |
2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+14399G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196425 | |||||||
| chr1:117196480 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.32+14344C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196480 | |||||||
| chr1:117196482 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0011g0017 |
2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.32+14342A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196482 | |||||||
| chr1:117196580 | A | T | 1 | a0001c0001t0001g0032 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.32+14244T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196580 | |||||||
| chr1:117196631 | T | C | 1 | a0001c0001t0003g0134 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.32+14193A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196631 | |||||||
| chr1:117196824 | A | C | 2 | a0001c0001t0003g0035 a0001c0001t0003g0036 |
2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.32+14000T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196824 | |||||||
| chr1:117196919 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.32+13905C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117196919 | |||||||
| chr1:117197176 | G | A | 111 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0028 others(108): Show |
115 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.32+13648C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197176 | |||||||
| chr1:117197190 | G | A | 1 | a0001c0001t0002g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.32+13634C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197190 | |||||||
| chr1:117197210 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+13614C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197210 | |||||||
| chr1:117197224 | C | T | 111 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0028 others(108): Show |
115 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.32+13600G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197224 | |||||||
| chr1:117197291 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0011g0017 |
2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.32+13533C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197291 | |||||||
| chr1:117197311 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.32+13513G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197311 | |||||||
| chr1:117197315 | T | A | 1 | a0001c0001t0013g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+13509A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197315 | |||||||
| chr1:117197598 | G | A | 49 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0028 others(46): Show |
51 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.32+13226C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197598 | |||||||
| chr1:117197734 | C | T | 1 | a0001c0001t0004g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.32+13090G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197734 | |||||||
| chr1:117197735 | A | G | 75 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0028 others(72): Show |
79 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.32+13089T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197735 | |||||||
| chr1:117197820 | T | C | 1 | a0001c0001t0007g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.32+13004A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117197820 | |||||||
| chr1:117198061 | C | A | 1 | a0001c0001t0004g0006 | 2 | HG01255.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.32+12763G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198061 | |||||||
| chr1:117198181 | G | T | 1 | a0001c0001t0003g0026 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32+12643C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198181 | |||||||
| chr1:117198418 | C | A | 30 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(27): Show |
33 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.32+12406G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198418 | |||||||
| chr1:117198500 | G | A | 1 | a0001c0001t0003g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.32+12324C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198500 | |||||||
| chr1:117198508 | C | T | 8 | a0001c0001t0002g0168 a0001c0001t0005g0008 a0001c0001t0005g0009 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.32+12316G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198508 | |||||||
| chr1:117198517 | C | G | 1 | a0001c0001t0001g0155 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.32+12307G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198517 | |||||||
| chr1:117198633 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(192): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.32+12191G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198633 | |||||||
| chr1:117198841 | C | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(192): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.32+11983G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198841 | |||||||
| chr1:117198913 | G | A | 19 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0002g0013 others(16): Show |
19 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.32+11911C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117198913 | |||||||
| chr1:117199098 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.32+11726C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199098 | |||||||
| chr1:117199177 | T | A | 1 | a0001c0001t0003g0132 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.32+11647A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199177 | |||||||
| chr1:117199225 | C | CTTCT | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(192): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.32+11598_32+11599i others(6): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199225 | |||||||
| chr1:117199314 | A | G | 7 | a0001c0001t0002g0168 a0001c0001t0005g0008 a0001c0001t0005g0009 others(4): Show |
9 | HG02280.hp2 HG02647.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+11510T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199314 | |||||||
| chr1:117199421 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.32+11403C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199421 | |||||||
| chr1:117199446 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(151): Show |
162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.32+11378G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199446 | |||||||
| chr1:117199605 | C | T | 16 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0153 others(13): Show |
16 | HG00642.hp1 HG01433.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+11219G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199605 | |||||||
| chr1:117199611 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+11213G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199611 | |||||||
| chr1:117199633 | A | AT | 12 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0028 others(9): Show |
12 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.32+11190dupA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199633 | |||||||
| chr1:117199633 | AT | A | 8 | a0001c0001t0001g0046 a0001c0001t0001g0091 a0001c0001t0001g0092 others(5): Show |
8 | HG00323.hp1 HG01943.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+11190delA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199633 | |||||||
| chr1:117199776 | C | T | 11 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(8): Show |
12 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+11048G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199776 | |||||||
| chr1:117199895 | A | C | 1 | a0001c0001t0007g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.32+10929T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117199895 | |||||||
| chr1:117200130 | A | T | 1 | a0001c0001t0002g0007 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.32+10694T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200130 | |||||||
| chr1:117200240 | T | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | NA18939.hp1 NA18999.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.32+10584A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200240 | |||||||
| chr1:117200449 | A | T | 1 | a0002c0002t0002g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.32+10375T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200449 | |||||||
| chr1:117200494 | C | T | 1 | a0001c0001t0003g0132 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.32+10330G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200494 | |||||||
| chr1:117200569 | C | G | 2 | a0001c0001t0011g0017 a0002c0002t0002g0201 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.32+10255G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200569 | |||||||
| chr1:117200581 | T | A | 2 | a0001c0001t0011g0017 a0002c0002t0002g0201 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.32+10243A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200581 | |||||||
| chr1:117200586 | C | T | 1 | a0001c0001t0003g0026 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32+10238G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200586 | |||||||
| chr1:117200704 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0219 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.32+10120G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200704 | |||||||
| chr1:117200824 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.32+10000G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200824 | |||||||
| chr1:117200858 | C | A | 1 | a0001c0001t0012g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.32+9966G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200858 | |||||||
| chr1:117200979 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.32+9845C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117200979 | |||||||
| chr1:117201086 | T | G | 2 | a0001c0001t0011g0017 a0002c0002t0002g0201 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.32+9738A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201086 | |||||||
| chr1:117201346 | G | A | 3 | a0001c0001t0003g0171 a0002c0002t0003g0169 a0002c0002t0003g0170 |
3 | HG01884.hp2 HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.32+9478C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201346 | |||||||
| chr1:117201360 | T | C | 3 | a0001c0001t0001g0150 a0001c0001t0003g0148 a0001c0001t0003g0149 |
3 | HG02486.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.32+9464A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201360 | |||||||
| chr1:117201531 | T | C | 1 | a0001c0001t0002g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.32+9293A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201531 | |||||||
| chr1:117201534 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.32+9290C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201534 | |||||||
| chr1:117201641 | A | T | 4 | a0001c0001t0003g0026 a0001c0001t0003g0171 a0002c0002t0003g0169 others(1): Show |
4 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+9183T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201641 | |||||||
| chr1:117201642 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG02451.hp1 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+9182G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201642 | |||||||
| chr1:117201682 | A | G | 8 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0026 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+9142T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201682 | |||||||
| chr1:117201791 | C | G | 1 | a0001c0001t0004g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.32+9033G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201791 | |||||||
| chr1:117201823 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.32+9001A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201823 | |||||||
| chr1:117201855 | T | C | 1 | a0001c0001t0003g0026 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32+8969A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117201855 | |||||||
| chr1:117202027 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.32+8797G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117202027 | |||||||
| chr1:117202188 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.32+8636T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117202188 | |||||||
| chr1:117202316 | C | T | 7 | a0001c0001t0002g0168 a0001c0001t0003g0181 a0001c0001t0005g0008 others(4): Show |
9 | HG02280.hp2 HG02647.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+8508G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117202316 | |||||||
| chr1:117202330 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.32+8494G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117202330 | |||||||
| chr1:117202396 | G | C | 1 | a0002c0002t0002g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.32+8428C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117202396 | |||||||
| chr1:117202538 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+8286T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117202538 | |||||||
| chr1:117202861 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 |
3 | HG02647.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.32+7963C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117202861 | |||||||
| chr1:117203088 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.32+7736G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203088 | |||||||
| chr1:117203203 | T | A | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG00642.hp1 HG01943.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+7621A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203203 | |||||||
| chr1:117203325 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(231): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.32+7499A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203325 | |||||||
| chr1:117203390 | C | T | 2 | a0001c0001t0002g0056 a0001c0001t0002g0057 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.32+7434G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203390 | |||||||
| chr1:117203428 | T | C | 3 | a0001c0001t0003g0171 a0002c0002t0003g0169 a0002c0002t0003g0170 |
3 | HG01884.hp2 HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.32+7396A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203428 | |||||||
| chr1:117203460 | AAG | A | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+7362_32+7363del others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203460 | |||||||
| chr1:117203534 | G | C | 18 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0042 others(15): Show |
19 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.32+7290C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203534 | |||||||
| chr1:117203583 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.32+7241G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203583 | |||||||
| chr1:117203589 | C | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0051 others(111): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.32+7235G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203589 | |||||||
| chr1:117203660 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.32+7164G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203660 | |||||||
| chr1:117203781 | A | C | 1 | a0001c0001t0001g0111 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.32+7043T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203781 | |||||||
| chr1:117203783 | C | A | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+7041G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203783 | |||||||
| chr1:117203951 | C | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0019 others(155): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.32+6873G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117203951 | |||||||
| chr1:117204017 | G | A | 67 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0033 others(64): Show |
69 | HG00642.hp2 HG00741.hp1 HG01099.hp1 others(66): Show |
intron_variant | MODIFIER | c.32+6807C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204017 | |||||||
| chr1:117204019 | A | G | 2 | a0001c0001t0005g0049 a0001c0001t0012g0050 |
2 | HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.32+6805T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204019 | |||||||
| chr1:117204046 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+6778C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204046 | |||||||
| chr1:117204048 | T | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
7 | HG00280.hp2 HG01106.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+6776A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204048 | |||||||
| chr1:117204049 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(231): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.32+6775C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204049 | |||||||
| chr1:117204169 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+6655G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204169 | |||||||
| chr1:117204472 | T | A | 22 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0042 others(19): Show |
23 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.32+6352A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204472 | |||||||
| chr1:117204489 | T | C | 8 | a0001c0001t0002g0013 a0001c0001t0002g0217 a0001c0001t0003g0012 others(5): Show |
8 | HG02055.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+6335A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204489 | |||||||
| chr1:117204531 | T | C | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+6293A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204531 | |||||||
| chr1:117204594 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG02451.hp1 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+6230G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204594 | |||||||
| chr1:117204598 | G | T | 7 | a0001c0001t0002g0168 a0001c0001t0003g0181 a0001c0001t0005g0008 others(4): Show |
9 | HG02280.hp2 HG02647.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+6226C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204598 | |||||||
| chr1:117204642 | G | A | 3 | a0001c0001t0003g0171 a0002c0002t0003g0169 a0002c0002t0003g0170 |
3 | HG01884.hp2 HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.32+6182C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204642 | |||||||
| chr1:117204662 | G | T | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+6162C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204662 | |||||||
| chr1:117204726 | T | C | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+6098A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204726 | |||||||
| chr1:117204814 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
7 | HG00280.hp2 HG01106.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+6010G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204814 | |||||||
| chr1:117204840 | TGGGCAAC others(5): Show |
T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(179): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.32+5972_32+5983del others(12): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204840 | |||||||
| chr1:117204971 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.32+5853G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117204971 | |||||||
| chr1:117205009 | T | TACGCATA others(29): Show |
4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5814_32+5815ins others(36): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205009 | |||||||
| chr1:117205021 | TAC | T | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5801_32+5802del others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205021 | |||||||
| chr1:117205025 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(179): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.32+5799G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205025 | |||||||
| chr1:117205028 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5796T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205028 | |||||||
| chr1:117205063 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5761T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205063 | |||||||
| chr1:117205078 | CATGTATA others(7): Show |
C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(179): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.32+5732_32+5745del others(14): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205078 | |||||||
| chr1:117205081 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5743C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205081 | |||||||
| chr1:117205087 | GTATGTAT others(3): Show |
G | 3 | a0001c0001t0003g0171 a0002c0002t0003g0169 a0002c0002t0003g0170 |
3 | HG01884.hp2 HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.32+5727_32+5736del others(10): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205087 | |||||||
| chr1:117205127 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(205): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.32+5697T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205127 | |||||||
| chr1:117205136 | A | G | 2 | a0001c0001t0001g0220 a0002c0002t0002g0218 |
2 | HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.32+5688T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205136 | |||||||
| chr1:117205142 | T | TTATA | 4 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+5681_32+5682ins others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205142 | |||||||
| chr1:117205144 | T | A | 13 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0094 others(10): Show |
13 | HG01261.hp1 HG02004.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.32+5680A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205144 | |||||||
| chr1:117205144 | T | TTA | 36 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0123 others(33): Show |
40 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.32+5678_32+5679dup others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205144 | |||||||
| chr1:117205144 | T | TTATA | 55 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0042 others(52): Show |
56 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.32+5676_32+5679dup others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205144 | |||||||
| chr1:117205149 | TATATATA others(18): Show |
T | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5650_32+5674del others(25): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205149 | |||||||
| chr1:117205155 | T | G | 1 | a0001c0001t0004g0093 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.32+5669A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205155 | |||||||
| chr1:117205155 | T | TAG | 10 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(7): Show |
11 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+5668_32+5669ins others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205155 | |||||||
| chr1:117205157 | T | G | 16 | a0001c0001t0001g0078 a0001c0001t0001g0174 a0001c0001t0002g0203 others(13): Show |
17 | HG01261.hp1 HG02083.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.32+5667A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205157 | |||||||
| chr1:117205157 | T | TAG | 13 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0001g0150 others(10): Show |
13 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.32+5665_32+5666dup others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205157 | |||||||
| chr1:117205157 | T | TAGAG | 14 | a0001c0001t0001g0055 a0001c0001t0001g0073 a0001c0001t0001g0079 others(11): Show |
14 | HG00140.hp2 HG01192.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.32+5663_32+5666dup others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205157 | |||||||
| chr1:117205157 | T | TATAG | 48 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0051 others(45): Show |
51 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.32+5666_32+5667ins others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205157 | |||||||
| chr1:117205157 | T | TATATAG | 3 | a0001c0001t0005g0049 a0001c0001t0006g0227 a0001c0001t0012g0050 |
3 | HG01515.hp2 HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.32+5666_32+5667ins others(6): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205157 | |||||||
| chr1:117205159 | G | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0023 others(90): Show |
97 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.32+5665C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205159 | |||||||
| chr1:117205161 | G | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0023 others(30): Show |
34 | HG00621.hp1 HG00741.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.32+5663C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205161 | |||||||
| chr1:117205163 | G | T | 7 | a0001c0001t0001g0045 a0001c0001t0001g0210 a0001c0001t0002g0038 others(4): Show |
7 | HG01255.hp1 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+5661C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205163 | |||||||
| chr1:117205176 | A | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0147 a0001c0001t0002g0052 others(4): Show |
7 | HG02004.hp1 HG02056.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+5648T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205176 | |||||||
| chr1:117205181 | G | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | NA18939.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.32+5643C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205181 | |||||||
| chr1:117205190 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(157): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.32+5634G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205190 | |||||||
| chr1:117205218 | C | G | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5606G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205218 | |||||||
| chr1:117205244 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5580G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205244 | |||||||
| chr1:117205251 | G | C | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+5573C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205251 | |||||||
| chr1:117205360 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(183): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.32+5464T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205360 | |||||||
| chr1:117205405 | C | T | 22 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0042 others(19): Show |
23 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.32+5419G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205405 | |||||||
| chr1:117205467 | T | C | 3 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 |
3 | HG02630.hp2 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.32+5357A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205467 | |||||||
| chr1:117205550 | A | G | 1 | a0001c0001t0009g0222 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.32+5274T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205550 | |||||||
| chr1:117205884 | A | T | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+4940T>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205884 | |||||||
| chr1:117205886 | C | T | 1 | a0001c0001t0013g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+4938G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205886 | |||||||
| chr1:117205949 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(179): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.32+4875G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117205949 | |||||||
| chr1:117206148 | AT | A | 22 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0024 others(19): Show |
24 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.32+4675delA | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206148 | |||||||
| chr1:117206148 | ATT | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(163): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.32+4674_32+4675del others(2): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206148 | |||||||
| chr1:117206148 | ATTT | A | 16 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0155 others(13): Show |
17 | HG00408.hp2 HG00621.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.32+4673_32+4675del others(3): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206148 | |||||||
| chr1:117206176 | C | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG02451.hp1 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+4648G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206176 | |||||||
| chr1:117206203 | A | C | 1 | a0001c0001t0014g0146 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.32+4621T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206203 | |||||||
| chr1:117206308 | T | A | 2 | a0001c0001t0003g0212 a0002c0002t0003g0211 |
2 | HG01433.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.32+4516A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206308 | |||||||
| chr1:117206408 | A | G | 1 | a0001c0001t0014g0146 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.32+4416T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206408 | |||||||
| chr1:117206497 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0007g0014 a0001c0001t0007g0015 |
3 | HG02723.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+4327A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206497 | |||||||
| chr1:117206576 | C | T | 3 | a0001c0001t0007g0126 a0001c0001t0007g0135 a0001c0001t0008g0125 |
3 | HG02055.hp1 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.32+4248G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206576 | |||||||
| chr1:117206585 | C | G | 3 | a0001c0001t0001g0220 a0001c0001t0003g0026 a0002c0002t0002g0218 |
3 | HG02109.hp2 HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.32+4239G>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206585 | |||||||
| chr1:117206608 | G | A | 1 | a0001c0001t0007g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.32+4216C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206608 | |||||||
| chr1:117206645 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 |
3 | HG02647.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.32+4179G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206645 | |||||||
| chr1:117206669 | T | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(200): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.32+4155A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206669 | |||||||
| chr1:117206670 | C | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(200): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.32+4154G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206670 | |||||||
| chr1:117206671 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(200): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.32+4153A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206671 | |||||||
| chr1:117206672 | G | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(200): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.32+4152C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206672 | |||||||
| chr1:117206673 | TTGA | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(200): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.32+4148_32+4150del others(3): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206673 | |||||||
| chr1:117206677 | T | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(200): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.32+4147A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206677 | |||||||
| chr1:117206845 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(205): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.32+3979T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206845 | |||||||
| chr1:117206959 | T | C | 1 | a0001c0001t0015g0236 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.32+3865A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117206959 | |||||||
| chr1:117207069 | G | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0117 |
3 | HG01257.hp2 HG03704.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.32+3755C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207069 | |||||||
| chr1:117207135 | T | C | 1 | a0001c0001t0006g0235 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.32+3689A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207135 | |||||||
| chr1:117207147 | G | A | 3 | a0001c0001t0001g0207 a0001c0001t0010g0208 a0001c0001t0010g0209 |
3 | HG02895.hp1 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.32+3677C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207147 | |||||||
| chr1:117207149 | A | G | 3 | a0001c0001t0001g0220 a0001c0001t0003g0026 a0002c0002t0002g0218 |
3 | HG02109.hp2 HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.32+3675T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207149 | |||||||
| chr1:117207187 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(183): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.32+3637G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207187 | |||||||
| chr1:117207224 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(179): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.32+3600T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207224 | |||||||
| chr1:117207323 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+3501C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207323 | |||||||
| chr1:117207334 | T | C | 1 | a0001c0001t0007g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.32+3490A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207334 | |||||||
| chr1:117207393 | A | G | 4 | a0001c0001t0001g0016 a0001c0001t0007g0014 a0001c0001t0007g0015 others(1): Show |
4 | HG02723.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+3431T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207393 | |||||||
| chr1:117207532 | C | T | 1 | a0001c0001t0015g0236 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.32+3292G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207532 | |||||||
| chr1:117207565 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0123 others(5): Show |
10 | HG00621.hp1 HG00741.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.32+3259G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207565 | |||||||
| chr1:117207773 | T | C | 6 | a0001c0001t0001g0143 a0001c0001t0001g0150 a0001c0001t0002g0144 others(3): Show |
6 | HG02486.hp1 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+3051A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207773 | |||||||
| chr1:117207989 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(230): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.32+2835G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207989 | |||||||
| chr1:117207990 | G | T | 1 | a0001c0001t0004g0120 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.32+2834C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117207990 | |||||||
| chr1:117208064 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0123 others(39): Show |
46 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.32+2760G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208064 | |||||||
| chr1:117208097 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0019 others(116): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.32+2727T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208097 | |||||||
| chr1:117208170 | C | T | 2 | a0001c0001t0003g0119 a0001c0001t0004g0118 |
2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.32+2654G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208170 | |||||||
| chr1:117208177 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(181): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.32+2647A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208177 | |||||||
| chr1:117208195 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.32+2629C>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208195 | |||||||
| chr1:117208245 | A | G | 7 | a0001c0001t0002g0168 a0001c0001t0003g0181 a0001c0001t0005g0008 others(4): Show |
9 | HG02280.hp2 HG02647.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+2579T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208245 | |||||||
| chr1:117208249 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.32+2575T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208249 | |||||||
| chr1:117208326 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.32+2498T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208326 | |||||||
| chr1:117208342 | A | G | 1 | a0001c0001t0002g0007 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.32+2482T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208342 | |||||||
| chr1:117208383 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+2441T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208383 | |||||||
| chr1:117208409 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+2415G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208409 | |||||||
| chr1:117208442 | A | C | 2 | a0001c0001t0005g0049 a0001c0001t0012g0050 |
2 | HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.32+2382T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208442 | |||||||
| chr1:117208743 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0123 others(39): Show |
46 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.32+2081G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208743 | |||||||
| chr1:117208824 | A | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG02258.hp1 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+2000T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208824 | |||||||
| chr1:117208894 | A | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(181): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.32+1930T>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117208894 | |||||||
| chr1:117209089 | G | A | 2 | a0001c0001t0002g0165 a0001c0001t0003g0166 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.32+1735C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209089 | |||||||
| chr1:117209103 | C | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0051 others(93): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.32+1721G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209103 | |||||||
| chr1:117209114 | G | A | 17 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0042 others(14): Show |
18 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.32+1710C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209114 | |||||||
| chr1:117209129 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.32+1695C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209129 | |||||||
| chr1:117209145 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(231): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.32+1679G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209145 | |||||||
| chr1:117209241 | T | G | 1 | a0001c0001t0002g0167 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.32+1583A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209241 | |||||||
| chr1:117209278 | C | T | 2 | a0001c0001t0005g0049 a0001c0001t0012g0050 |
2 | HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.32+1546G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209278 | |||||||
| chr1:117209380 | T | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(230): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.32+1444A>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209380 | |||||||
| chr1:117209389 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+1435T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209389 | |||||||
| chr1:117209430 | G | T | 26 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(23): Show |
26 | HG00642.hp1 HG01891.hp2 HG01943.hp1 others(23): Show |
intron_variant | MODIFIER | c.32+1394C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209430 | |||||||
| chr1:117209483 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(184): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.32+1341A>G | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209483 | |||||||
| chr1:117209488 | C | A | 1 | a0001c0001t0014g0146 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.32+1336G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209488 | |||||||
| chr1:117209604 | A | G | 1 | a0001c0001t0011g0017 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.32+1220T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209604 | |||||||
| chr1:117209723 | C | T | 2 | a0001c0001t0004g0047 a0001c0001t0004g0048 |
2 | HG01928.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.32+1101G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209723 | |||||||
| chr1:117209849 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.32+975G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209849 | |||||||
| chr1:117209859 | G | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(226): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.32+965C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209859 | |||||||
| chr1:117209876 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(153): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.32+948C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209876 | |||||||
| chr1:117209975 | G | T | 1 | a0001c0001t0013g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+849C>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117209975 | |||||||
| chr1:117210091 | T | A | 1 | a0001c0001t0002g0221 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.32+733A>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210091 | |||||||
| chr1:117210137 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0003g0148 a0001c0001t0003g0149 |
3 | HG02486.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.32+687C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210137 | |||||||
| chr1:117210212 | T | TCAG | 20 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0155 others(17): Show |
21 | HG00408.hp2 HG01175.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.32+609_32+611dupCT others(1): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | |||||||
| chr1:117210212 | T | TCAGCAG | 9 | a0001c0001t0001g0016 a0001c0001t0001g0173 a0001c0001t0002g0168 others(6): Show |
9 | HG00621.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+606_32+611dupCT others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | |||||||
| chr1:117210212 | T | TCAGCAGC others(2): Show |
18 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(15): Show |
21 | HG00642.hp1 HG01943.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+603_32+611dupCT others(7): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | |||||||
| chr1:117210212 | T | TCAGCAGC others(5): Show |
21 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(18): Show |
21 | HG01891.hp2 HG02083.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+600_32+611dupCT others(10): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | |||||||
| chr1:117210212 | T | TCAGCAGC others(8): Show |
3 | a0001c0001t0001g0210 a0001c0001t0001g0219 a0002c0002t0002g0218 |
3 | HG02572.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.32+597_32+611dupCT others(13): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | |||||||
| chr1:117210212 | T | TCAGCAGC others(11): Show |
1 | a0001c0001t0001g0220 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.32+594_32+611dupCT others(16): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | |||||||
| chr1:117210212 | TCAGCAG | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG02109.hp2 HG02451.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+606_32+611delCT others(4): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | |||||||
| chr1:117210212 | TCAGCAGC others(2): Show |
T | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0005g0018 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+603_32+611delCT others(7): Show |
VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210212 | |||||||
| chr1:117210315 | G | A | 2 | a0001c0001t0003g0212 a0002c0002t0003g0211 |
2 | HG01433.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.32+509C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210315 | |||||||
| chr1:117210354 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0007g0014 a0001c0001t0007g0015 |
3 | HG02723.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+470T>C | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210354 | |||||||
| chr1:117210435 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0003g0012 |
2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.32+389G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210435 | |||||||
| chr1:117210468 | C | A | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG01175.hp1 HG03491.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+356G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210468 | |||||||
| chr1:117210493 | C | A | 1 | a0001c0001t0002g0217 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.32+331G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210493 | |||||||
| chr1:117210540 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.32+284G>A | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210540 | |||||||
| chr1:117210546 | C | A | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0002c0002t0002g0218 |
3 | HG03139.hp2 HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.32+278G>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210546 | |||||||
| chr1:117210573 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.32+251C>T | VTCN1 | ENSG00000134258.18 | transcript | ENST00000369458.8 | protein_coding | 1/5 | chr1 | 117210573 |