Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84329 |
| ensemblid | ENSG00000122986.14 |
| hgncid | 28240 |
| symbol | HVCN1 |
| name | hydrogen voltage gated channel 1 |
| refseq_nuc | NM_032369.4 |
| refseq_prot | NP_115745.2 |
| ensembl_nuc | ENST00000242607.13 |
| ensembl_prot | ENSP00000242607.8 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 110648686 |
| end | 110689115 |
| strand | - |
| ver | v1.2 |
| region | chr12:110648686-110689115 |
| region5000 | chr12:110643686-110694115 |
| regionname0 | HVCN1_chr12_110648686_110689115 |
| regionname5000 | HVCN1_chr12_110643686_110694115 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 273 | 203 | 78 | 46 | 30 | 13 | 36 | 16 | HVCN1_chr12_110643686_110694115 | HVCN1 | MATWD others(268): Show |
chr12 | 110643686 | 110694115 |
| a0002 | 0/0 | 273 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | MATWD others(268): Show |
chr12 | 110643686 | 110694115 |
| a0003 | 0/0 | 273 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | MATWD others(268): Show |
chr12 | 110643686 | 110694115 |
| a0004 | 0/0 | 273 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | MATWD others(268): Show |
chr12 | 110643686 | 110694115 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 819 | 200 | 77 | 46 | 29 | 13 | 35 | HVCN1_chr12_110643686_110694115 | HVCN1 | ATGGC others(814): Show |
chr12 | 110643686 | 110694115 | ||
| a0001c0005 | 0/0 | 819 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | ATGGC others(814): Show |
chr12 | 110643686 | 110694115 | ||
| a0001c0006 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | ATGGC others(814): Show |
chr12 | 110643686 | 110694115 | ||
| a0001c0007 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | ATGGC others(814): Show |
chr12 | 110643686 | 110694115 | ||
| a0002c0002 | 0/0 | 819 | 3 | 0 | 2 | 0 | 1 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | ATGGC others(814): Show |
chr12 | 110643686 | 110694115 | ||
| a0003c0004 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | ATGGC others(814): Show |
chr12 | 110643686 | 110694115 | ||
| a0004c0003 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | ATGGC others(814): Show |
chr12 | 110643686 | 110694115 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1685 | 183 | 68 | 44 | 27 | 12 | 32 | HVCN1_chr12_110643686_110694115 | HVCN1 | AGTCG others(1680): Show |
chr12 | 110643686 | 110694115 |
| a0001c0001t0002 | 0/0 | 1683 | 15 | 8 | 1 | 2 | 1 | 3 | HVCN1_chr12_110643686_110694115 | HVCN1 | AGTCG others(1678): Show |
chr12 | 110643686 | 110694115 |
| a0001c0001t0003 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | AGTCG others(1680): Show |
chr12 | 110643686 | 110694115 |
| a0001c0001t0004 | 0/0 | 1685 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | AGTCG others(1680): Show |
chr12 | 110643686 | 110694115 |
| a0001c0005t0001 | 0/0 | 1685 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | AGTCG others(1680): Show |
chr12 | 110643686 | 110694115 |
| a0001c0006t0001 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | AGTCG others(1680): Show |
chr12 | 110643686 | 110694115 |
| a0001c0007t0001 | 0/0 | 1685 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | AGTCG others(1680): Show |
chr12 | 110643686 | 110694115 |
| a0002c0002t0001 | 0/0 | 1685 | 3 | 0 | 2 | 0 | 1 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | AGTCG others(1680): Show |
chr12 | 110643686 | 110694115 |
| a0003c0004t0005 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | AGTCG others(1680): Show |
chr12 | 110643686 | 110694115 |
| a0004c0003t0001 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | AGTCG others(1680): Show |
chr12 | 110643686 | 110694115 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0002 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0005t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0006t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0001c0007t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0003c0004t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| a0004c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | GBR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | GBR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0075 | EUR | FIN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | FIN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01891 | hp1 | a0003 | c0004 | t0005 | g0195 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0167 | AMR | PEL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02622 | hp1 | a0001 | c0006 | t0001 | g0018 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | MSL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03579 | hp1 | a0004 | c0003 | t0001 | g0115 | AFR | MSL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | BEB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG04204 | hp2 | a0001 | c0005 | t0001 | g0095 | SAS | STU | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | STU | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA18612 | hp2 | a0001 | c0007 | t0001 | g0051 | EAS | CHB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | LWK | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ASW | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ASW | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | TSI | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0174 | EUR | TSI | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | LWK | HVCN1_chr12_110643686_110694115 | HVCN1 | chr12 | 110643686 | 110694115 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110649441 | C | T | 1 | a0003 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.791G>A | p.Arg264Gln | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 8/8 | 930/1685 | 791/822 | 264/273 | chr12 | 110649441 | |||
| chr12:110661197 | C | T | 1 | a0002 | 3 | HG00738.hp2 HG01069.hp1 NA20805.hp2 |
missense_variant | MODERATE | c.273G>A | p.Met91Ile | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/8 | 412/1685 | 273/822 | 91/273 | chr12 | 110661197 | |||
| chr12:110661198 | A | G | 1 | a0002 | 3 | HG00738.hp2 HG01069.hp1 NA20805.hp2 |
missense_variant | MODERATE | c.272T>C | p.Met91Thr | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/8 | 411/1685 | 272/822 | 91/273 | chr12 | 110661198 | |||
| chr12:110661361 | C | T | 1 | a0004 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.109G>A | p.Ala37Thr | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/8 | 248/1685 | 109/822 | 37/273 | chr12 | 110661361 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110650192 | G | A | 1 | a0001c0005 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.732C>T | p.His244His | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 7/8 | 871/1685 | 732/822 | 244/273 | chr12 | 110650192 | |||
| chr12:110651335 | G | A | 1 | a0001c0006 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.525C>T | p.Ala175Ala | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 6/8 | 664/1685 | 525/822 | 175/273 | chr12 | 110651335 | |||
| chr12:110661299 | T | C | 1 | a0002c0002 | 3 | HG00738.hp2 HG01069.hp1 NA20805.hp2 |
synonymous_variant | LOW | c.171A>G | p.Pro57Pro | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/8 | 310/1685 | 171/822 | 57/273 | chr12 | 110661299 | |||
| chr12:110661371 | G | A | 1 | a0001c0007 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.99C>T | p.Asp33Asp | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/8 | 238/1685 | 99/822 | 33/273 | chr12 | 110661371 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110648788 | AAG | A | 1 | a0001c0001t0002 | 15 | HG00323.hp1 HG01175.hp1 HG02055.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*620_*621delCT | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 8/8 | 620 | chr12 | 110648788 | ||||||
| chr12:110648825 | T | C | 1 | a0001c0001t0003 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*585A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 8/8 | 585 | chr12 | 110648825 | ||||||
| chr12:110648960 | G | A | 1 | a0001c0001t0004 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*450C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 8/8 | 450 | chr12 | 110648960 | ||||||
| chr12:110689094 | G | C | 1 | a0003c0004t0005 | 1 | HG01891.hp1 | 5_prime_UTR_variant | MODIFIER | c.-118C>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 1/8 | 5849 | chr12 | 110689094 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110649697 | G | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.757-222C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 7/7 | chr12 | 110649697 | |||||||
| chr12:110649774 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.757-299G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 7/7 | chr12 | 110649774 | |||||||
| chr12:110649785 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.757-310C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 7/7 | chr12 | 110649785 | |||||||
| chr12:110649850 | A | G | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.756+318T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 7/7 | chr12 | 110649850 | |||||||
| chr12:110650472 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.644-192T>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 6/7 | chr12 | 110650472 | |||||||
| chr12:110650667 | T | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 |
3 | HG02055.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.644-387A>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 6/7 | chr12 | 110650667 | |||||||
| chr12:110650687 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.644-407T>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 6/7 | chr12 | 110650687 | |||||||
| chr12:110650695 | GT | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(82): Show |
91 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.644-416delA | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 6/7 | chr12 | 110650695 | |||||||
| chr12:110650708 | T | C | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.644-428A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 6/7 | chr12 | 110650708 | |||||||
| chr12:110651183 | C | T | 1 | a0002c0002t0001g0014 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.643+34G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 6/7 | chr12 | 110651183 | |||||||
| chr12:110651501 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.412-53T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110651501 | |||||||
| chr12:110651697 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.412-249G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110651697 | |||||||
| chr12:110651743 | C | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.412-295G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110651743 | |||||||
| chr12:110652316 | A | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0174 a0002c0002t0001g0190 |
3 | HG00738.hp2 HG01069.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.412-868T>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110652316 | |||||||
| chr12:110652380 | A | ACT | 3 | a0002c0002t0001g0014 a0002c0002t0001g0174 a0002c0002t0001g0190 |
3 | HG00738.hp2 HG01069.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.412-934_412-933dup others(2): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110652380 | |||||||
| chr12:110652446 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.412-998T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110652446 | |||||||
| chr12:110652480 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.412-1032G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110652480 | |||||||
| chr12:110652623 | G | A | 1 | a0001c0006t0001g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.412-1175C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110652623 | |||||||
| chr12:110652792 | T | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0174 a0002c0002t0001g0190 |
3 | HG00738.hp2 HG01069.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.412-1344A>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110652792 | |||||||
| chr12:110652793 | T | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0174 a0002c0002t0001g0190 |
3 | HG00738.hp2 HG01069.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.412-1345A>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110652793 | |||||||
| chr12:110652890 | G | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0137 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.412-1442C>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110652890 | |||||||
| chr12:110652904 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.412-1456G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110652904 | |||||||
| chr12:110653110 | C | G | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.412-1662G>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110653110 | |||||||
| chr12:110653186 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0138 |
2 | HG02040.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.412-1738C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110653186 | |||||||
| chr12:110653413 | A | G | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.411+1821T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110653413 | |||||||
| chr12:110653686 | A | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.411+1548T>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110653686 | |||||||
| chr12:110653703 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.411+1531C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110653703 | |||||||
| chr12:110653749 | G | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.411+1485C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110653749 | |||||||
| chr12:110653981 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.411+1253C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110653981 | |||||||
| chr12:110654005 | G | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0152 others(1): Show |
4 | HG01256.hp1 HG03654.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+1229C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110654005 | |||||||
| chr12:110654009 | G | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.411+1225C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110654009 | |||||||
| chr12:110654019 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
6 | HG01167.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.411+1215C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110654019 | |||||||
| chr12:110654329 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.411+905C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110654329 | |||||||
| chr12:110654382 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.411+852C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110654382 | |||||||
| chr12:110654397 | A | G | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.411+837T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110654397 | |||||||
| chr12:110654471 | C | CT | 30 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(27): Show |
34 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.411+762dupA | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110654471 | |||||||
| chr12:110654471 | CT | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0067 a0001c0001t0001g0094 others(8): Show |
11 | HG00738.hp2 HG01069.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.411+762delA | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110654471 | |||||||
| chr12:110654490 | T | C | 1 | a0004c0003t0001g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.411+744A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110654490 | |||||||
| chr12:110654491 | T | C | 2 | a0001c0001t0001g0131 a0004c0003t0001g0115 |
2 | HG01106.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.411+743A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110654491 | |||||||
| chr12:110654727 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.411+507C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110654727 | |||||||
| chr12:110655022 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0101 |
2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.411+212C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110655022 | |||||||
| chr12:110655167 | C | T | 1 | a0004c0003t0001g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.411+67G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 5/7 | chr12 | 110655167 | |||||||
| chr12:110655440 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.307-102C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110655440 | |||||||
| chr12:110655614 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.307-276A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110655614 | |||||||
| chr12:110655679 | C | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.307-341G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110655679 | |||||||
| chr12:110655705 | G | GT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(58): Show |
67 | HG00280.hp1 HG00280.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.307-368dupA | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110655705 | |||||||
| chr12:110655747 | G | A | 1 | a0001c0006t0001g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.307-409C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110655747 | |||||||
| chr12:110656190 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.307-852C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110656190 | |||||||
| chr12:110656416 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0086 |
2 | HG00140.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.307-1078G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110656416 | |||||||
| chr12:110656486 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.307-1148T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110656486 | |||||||
| chr12:110656573 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.307-1235G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110656573 | |||||||
| chr12:110656649 | C | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0020 others(25): Show |
31 | HG00323.hp1 HG01167.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.307-1311G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110656649 | |||||||
| chr12:110657088 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.307-1750T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110657088 | |||||||
| chr12:110657106 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.307-1768C>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110657106 | |||||||
| chr12:110657131 | T | C | 1 | a0001c0001t0002g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.307-1793A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110657131 | |||||||
| chr12:110657262 | G | T | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 |
3 | HG02055.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.307-1924C>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110657262 | |||||||
| chr12:110657508 | G | GA | 30 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0024 others(27): Show |
33 | HG00323.hp1 HG01099.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.307-2171dupT | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110657508 | |||||||
| chr12:110657606 | A | C | 1 | a0001c0001t0001g0027 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.307-2268T>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110657606 | |||||||
| chr12:110658318 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.306+2846A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110658318 | |||||||
| chr12:110658332 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.306+2832A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110658332 | |||||||
| chr12:110658583 | T | G | 5 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0169 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+2581A>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110658583 | |||||||
| chr12:110659001 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.306+2163C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110659001 | |||||||
| chr12:110659115 | C | T | 1 | a0001c0001t0001g0006 | 2 | HG01099.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.306+2049G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110659115 | |||||||
| chr12:110659202 | AT | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(42): Show |
49 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.306+1961delA | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110659202 | |||||||
| chr12:110659317 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.306+1847T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110659317 | |||||||
| chr12:110659557 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.306+1607A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110659557 | |||||||
| chr12:110659707 | C | T | 14 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0071 others(11): Show |
15 | HG00323.hp1 HG01175.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.306+1457G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110659707 | |||||||
| chr12:110659743 | A | T | 1 | a0001c0001t0001g0194 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.306+1421T>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110659743 | |||||||
| chr12:110659763 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0162 a0001c0001t0001g0175 |
3 | HG00741.hp2 HG01074.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.306+1401T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110659763 | |||||||
| chr12:110659778 | C | T | 1 | a0001c0001t0002g0007 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.306+1386G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110659778 | |||||||
| chr12:110659806 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.306+1358C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110659806 | |||||||
| chr12:110660111 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+1053A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110660111 | |||||||
| chr12:110660175 | A | G | 15 | a0001c0001t0001g0177 a0001c0001t0002g0007 a0001c0001t0002g0012 others(12): Show |
16 | HG00323.hp1 HG01175.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.306+989T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110660175 | |||||||
| chr12:110660231 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0152 others(1): Show |
4 | HG01256.hp1 HG03654.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+933G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110660231 | |||||||
| chr12:110660236 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.306+928G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110660236 | |||||||
| chr12:110660454 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.306+710G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110660454 | |||||||
| chr12:110660576 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0101 |
2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.306+588A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110660576 | |||||||
| chr12:110660683 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0174 a0002c0002t0001g0190 |
3 | HG00738.hp2 HG01069.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.306+481T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110660683 | |||||||
| chr12:110660719 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.306+445G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110660719 | |||||||
| chr12:110660773 | A | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.306+391T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110660773 | |||||||
| chr12:110660943 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.306+221G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110660943 | |||||||
| chr12:110661031 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.306+133C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 4/7 | chr12 | 110661031 | |||||||
| chr12:110661575 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.22-127C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110661575 | |||||||
| chr12:110661735 | C | T | 8 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0109 others(5): Show |
9 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.22-287G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110661735 | |||||||
| chr12:110661736 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.22-288C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110661736 | |||||||
| chr12:110661824 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.22-376G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110661824 | |||||||
| chr12:110661914 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.22-466G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110661914 | |||||||
| chr12:110661916 | C | T | 2 | a0001c0001t0002g0073 a0001c0001t0002g0075 |
2 | HG00323.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.22-468G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110661916 | |||||||
| chr12:110662176 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.22-728G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110662176 | |||||||
| chr12:110662188 | C | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0184 a0001c0001t0001g0185 |
3 | HG02559.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.22-740G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110662188 | |||||||
| chr12:110662235 | GA | G | 31 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(28): Show |
34 | HG00323.hp1 HG01099.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.22-788delT | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110662235 | |||||||
| chr12:110662574 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0174 a0002c0002t0001g0190 |
3 | HG00738.hp2 HG01069.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.22-1126C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110662574 | |||||||
| chr12:110662677 | C | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0168 |
2 | HG01109.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.22-1229G>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110662677 | |||||||
| chr12:110662680 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.22-1232C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110662680 | |||||||
| chr12:110662822 | T | C | 34 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(31): Show |
37 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.22-1374A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110662822 | |||||||
| chr12:110662872 | T | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(28): Show |
34 | HG00323.hp1 HG01099.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.22-1424A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110662872 | |||||||
| chr12:110663018 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.22-1570C>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110663018 | |||||||
| chr12:110663070 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0184 a0001c0001t0001g0185 |
3 | HG02559.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.22-1622G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110663070 | |||||||
| chr12:110663099 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.22-1651C>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110663099 | |||||||
| chr12:110663171 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.22-1723A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110663171 | |||||||
| chr12:110663187 | A | C | 1 | a0001c0001t0001g0052 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.22-1739T>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110663187 | |||||||
| chr12:110663587 | C | CA | 43 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(40): Show |
45 | HG00621.hp1 HG00738.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.22-2140dupT | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110663587 | |||||||
| chr12:110663587 | C | CAA | 5 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0001g0107 others(2): Show |
5 | HG00738.hp1 HG02738.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.22-2141_22-2140dup others(2): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110663587 | |||||||
| chr12:110663587 | CA | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0083 others(15): Show |
20 | HG01081.hp2 HG01168.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.22-2140delT | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110663587 | |||||||
| chr12:110663913 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0085 others(5): Show |
9 | HG01081.hp2 HG01943.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.22-2465T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110663913 | |||||||
| chr12:110664437 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.22-2989A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110664437 | |||||||
| chr12:110664769 | C | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(28): Show |
34 | HG00323.hp1 HG01099.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.22-3321G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110664769 | |||||||
| chr12:110664822 | T | G | 15 | a0001c0001t0001g0177 a0001c0001t0002g0007 a0001c0001t0002g0012 others(12): Show |
16 | HG00323.hp1 HG01175.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.22-3374A>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110664822 | |||||||
| chr12:110665076 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.22-3628G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110665076 | |||||||
| chr12:110665245 | TAAA | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(28): Show |
34 | HG00323.hp1 HG01099.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.22-3800_22-3798del others(3): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110665245 | |||||||
| chr12:110665556 | C | CA | 8 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0054 others(5): Show |
8 | HG00738.hp2 HG01069.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.22-4109dupT | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110665556 | |||||||
| chr12:110665556 | CA | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(28): Show |
34 | HG00323.hp1 HG01081.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.22-4109delT | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110665556 | |||||||
| chr12:110665864 | T | G | 33 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(30): Show |
36 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.22-4416A>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110665864 | |||||||
| chr12:110665987 | C | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0089 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.22-4539G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110665987 | |||||||
| chr12:110666020 | GA | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0085 others(5): Show |
9 | HG01081.hp2 HG01943.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.22-4573delT | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110666020 | |||||||
| chr12:110666111 | C | T | 1 | a0001c0001t0002g0007 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.22-4663G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110666111 | |||||||
| chr12:110666184 | T | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | HG01261.hp1 HG01515.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.22-4736A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110666184 | |||||||
| chr12:110666190 | G | A | 14 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0071 others(11): Show |
15 | HG00323.hp1 HG01175.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.22-4742C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110666190 | |||||||
| chr12:110666194 | G | A | 4 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
4 | HG02258.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.22-4746C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110666194 | |||||||
| chr12:110666260 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.22-4812T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110666260 | |||||||
| chr12:110666389 | C | G | 31 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(28): Show |
34 | HG00323.hp1 HG01099.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.22-4941G>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110666389 | |||||||
| chr12:110666422 | A | AAAAAG | 11 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0037 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.22-4979_22-4975dup others(5): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110666422 | |||||||
| chr12:110666422 | AAAAAG | A | 4 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0082 others(1): Show |
4 | HG02976.hp1 HG03225.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.22-4979_22-4975del others(5): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110666422 | |||||||
| chr12:110666667 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.22-5219G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110666667 | |||||||
| chr12:110666722 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.22-5274G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110666722 | |||||||
| chr12:110666905 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.22-5457A>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110666905 | |||||||
| chr12:110667050 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0182 |
3 | HG03491.hp1 HG03492.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.22-5602G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110667050 | |||||||
| chr12:110667055 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.22-5607C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110667055 | |||||||
| chr12:110667259 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.22-5811G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110667259 | |||||||
| chr12:110667367 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0100 |
2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.22-5919G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110667367 | |||||||
| chr12:110667424 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.22-5976C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110667424 | |||||||
| chr12:110667679 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.22-6231C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110667679 | |||||||
| chr12:110667720 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.22-6272T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110667720 | |||||||
| chr12:110668277 | A | G | 34 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(31): Show |
37 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.22-6829T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110668277 | |||||||
| chr12:110668380 | T | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(30): Show |
36 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.22-6932A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110668380 | |||||||
| chr12:110668395 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.22-6947G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110668395 | |||||||
| chr12:110668412 | T | C | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.22-6964A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110668412 | |||||||
| chr12:110668975 | G | GA | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.22-7528dupT | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110668975 | |||||||
| chr12:110668981 | G | T | 1 | a0001c0001t0001g0048 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.22-7533C>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110668981 | |||||||
| chr12:110669044 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.22-7596G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110669044 | |||||||
| chr12:110669155 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.22-7707G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110669155 | |||||||
| chr12:110669390 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.22-7942G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110669390 | |||||||
| chr12:110669628 | T | C | 3 | a0001c0001t0001g0191 a0002c0002t0001g0014 a0002c0002t0001g0190 |
3 | HG00738.hp2 HG01069.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.22-8180A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110669628 | |||||||
| chr12:110669665 | A | G | 34 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(31): Show |
37 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.22-8217T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110669665 | |||||||
| chr12:110670009 | G | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.22-8561C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110670009 | |||||||
| chr12:110670378 | G | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.22-8930C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110670378 | |||||||
| chr12:110670598 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.22-9150C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110670598 | |||||||
| chr12:110670671 | A | G | 3 | a0001c0001t0001g0191 a0002c0002t0001g0014 a0002c0002t0001g0190 |
3 | HG00738.hp2 HG01069.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.22-9223T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110670671 | |||||||
| chr12:110670919 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.22-9471G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110670919 | |||||||
| chr12:110671013 | A | G | 32 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(29): Show |
35 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.22-9565T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110671013 | |||||||
| chr12:110671051 | G | C | 2 | a0001c0001t0002g0072 a0001c0001t0002g0077 |
2 | HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.22-9603C>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110671051 | |||||||
| chr12:110671184 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.22-9736C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110671184 | |||||||
| chr12:110671667 | C | T | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.22-10219G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110671667 | |||||||
| chr12:110672173 | G | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0147 a0001c0001t0001g0164 |
3 | HG02965.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.22-10725C>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110672173 | |||||||
| chr12:110672222 | G | T | 1 | a0001c0001t0001g0044 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.22-10774C>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110672222 | |||||||
| chr12:110672378 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.21+10847C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110672378 | |||||||
| chr12:110672433 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.21+10792C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110672433 | |||||||
| chr12:110672463 | A | T | 1 | a0001c0001t0001g0151 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.21+10762T>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110672463 | |||||||
| chr12:110672751 | T | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02559.hp1 HG02615.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.21+10474A>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110672751 | |||||||
| chr12:110672958 | T | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0041 others(16): Show |
22 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.21+10267A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110672958 | |||||||
| chr12:110672972 | G | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.21+10253C>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110672972 | |||||||
| chr12:110672975 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.21+10250T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110672975 | |||||||
| chr12:110673100 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.21+10125C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110673100 | |||||||
| chr12:110673461 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.21+9764C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110673461 | |||||||
| chr12:110673678 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.21+9547G>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110673678 | |||||||
| chr12:110673761 | G | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.21+9464C>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110673761 | |||||||
| chr12:110674124 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.21+9101G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110674124 | |||||||
| chr12:110674292 | A | AC | 6 | a0001c0001t0002g0007 a0001c0001t0002g0071 a0001c0001t0002g0074 others(3): Show |
7 | HG02055.hp1 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.21+8932_21+8933ins others(1): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110674292 | |||||||
| chr12:110674293 | A | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(30): Show |
36 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.21+8932T>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110674293 | |||||||
| chr12:110674298 | C | T | 1 | a0002c0002t0001g0014 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.21+8927G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110674298 | |||||||
| chr12:110674514 | T | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(59): Show |
66 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.21+8711A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110674514 | |||||||
| chr12:110674569 | G | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.21+8656C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110674569 | |||||||
| chr12:110674665 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.21+8560C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110674665 | |||||||
| chr12:110674695 | C | T | 3 | a0001c0001t0001g0191 a0002c0002t0001g0014 a0002c0002t0001g0190 |
3 | HG00738.hp2 HG01069.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.21+8530G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110674695 | |||||||
| chr12:110674751 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.21+8474C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110674751 | |||||||
| chr12:110674806 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0060 others(5): Show |
10 | HG01167.hp1 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.21+8419C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110674806 | |||||||
| chr12:110674910 | G | GT | 2 | a0001c0001t0001g0013 a0001c0001t0001g0089 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.21+8314dupA | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110674910 | |||||||
| chr12:110675078 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.21+8147C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110675078 | |||||||
| chr12:110675098 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.21+8127G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110675098 | |||||||
| chr12:110675187 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.21+8038C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110675187 | |||||||
| chr12:110675214 | T | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0085 others(5): Show |
9 | HG01081.hp2 HG01943.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.21+8011A>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110675214 | |||||||
| chr12:110675262 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.21+7963G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110675262 | |||||||
| chr12:110676037 | C | A | 1 | a0004c0003t0001g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.21+7188G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110676037 | |||||||
| chr12:110676264 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.21+6961G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110676264 | |||||||
| chr12:110676374 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.21+6851G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110676374 | |||||||
| chr12:110676984 | C | A | 1 | a0001c0001t0001g0099 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.21+6241G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110676984 | |||||||
| chr12:110677016 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.21+6209G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110677016 | |||||||
| chr12:110677033 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.21+6192C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110677033 | |||||||
| chr12:110677114 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.21+6111G>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110677114 | |||||||
| chr12:110677137 | T | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(30): Show |
36 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.21+6088A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110677137 | |||||||
| chr12:110677244 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.21+5981G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110677244 | |||||||
| chr12:110677247 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.21+5978G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110677247 | |||||||
| chr12:110677308 | G | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(59): Show |
66 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.21+5917C>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110677308 | |||||||
| chr12:110677336 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.21+5889G>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110677336 | |||||||
| chr12:110677379 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0175 |
2 | HG00741.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.21+5846C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110677379 | |||||||
| chr12:110677849 | G | T | 1 | a0001c0005t0001g0095 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.21+5376C>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110677849 | |||||||
| chr12:110677924 | G | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.21+5301C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110677924 | |||||||
| chr12:110678050 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.21+5175C>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678050 | |||||||
| chr12:110678057 | C | T | 4 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
4 | HG02258.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.21+5168G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678057 | |||||||
| chr12:110678439 | C | CT | 16 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0039 others(13): Show |
16 | HG00642.hp1 HG00735.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.21+4785dupA | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678439 | |||||||
| chr12:110678439 | CT | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.21+4785delA | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678439 | |||||||
| chr12:110678439 | CTT | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0024 others(18): Show |
22 | HG00323.hp1 HG01081.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.21+4784_21+4785del others(2): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678439 | |||||||
| chr12:110678439 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.21+4775_21+4785del others(11): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678439 | |||||||
| chr12:110678439 | CTTTTTTT others(5): Show |
C | 16 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0092 others(13): Show |
16 | HG01884.hp1 HG01884.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.21+4774_21+4785del others(12): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678439 | |||||||
| chr12:110678439 | CTTTTTTT others(9): Show |
C | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.21+4770_21+4785del others(16): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678439 | |||||||
| chr12:110678439 | CTTTTTTT others(10): Show |
C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0004g0167 |
3 | HG01433.hp1 HG01952.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.21+4769_21+4785del others(17): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678439 | |||||||
| chr12:110678560 | C | T | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.21+4665G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678560 | |||||||
| chr12:110678624 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.21+4601C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678624 | |||||||
| chr12:110678832 | G | C | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.21+4393C>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678832 | |||||||
| chr12:110678846 | C | T | 14 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0071 others(11): Show |
15 | HG00323.hp1 HG01175.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.21+4379G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678846 | |||||||
| chr12:110678850 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(86): Show |
96 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.21+4375A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678850 | |||||||
| chr12:110678932 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.21+4293C>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110678932 | |||||||
| chr12:110679030 | C | T | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.21+4195G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110679030 | |||||||
| chr12:110679191 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.21+4034G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110679191 | |||||||
| chr12:110679193 | A | G | 1 | a0004c0003t0001g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.21+4032T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110679193 | |||||||
| chr12:110679213 | G | A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(30): Show |
36 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.21+4012C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110679213 | |||||||
| chr12:110679478 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.21+3747G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110679478 | |||||||
| chr12:110679480 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
11 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.21+3745C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110679480 | |||||||
| chr12:110679576 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.21+3649C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110679576 | |||||||
| chr12:110679667 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.21+3558G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110679667 | |||||||
| chr12:110679721 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.21+3504G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110679721 | |||||||
| chr12:110679779 | G | T | 1 | a0001c0001t0001g0024 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.21+3446C>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110679779 | |||||||
| chr12:110679796 | T | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(32): Show |
37 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.21+3429A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110679796 | |||||||
| chr12:110679854 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.21+3371G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110679854 | |||||||
| chr12:110679859 | C | CA | 9 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0023 others(6): Show |
9 | HG00741.hp2 HG01099.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.21+3365dupT | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110679859 | |||||||
| chr12:110680126 | A | C | 30 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(27): Show |
33 | HG00323.hp1 HG01099.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.21+3099T>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110680126 | |||||||
| chr12:110680259 | G | A | 1 | a0004c0003t0001g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.21+2966C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110680259 | |||||||
| chr12:110680645 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.21+2580C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110680645 | |||||||
| chr12:110680704 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.21+2521C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110680704 | |||||||
| chr12:110680798 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.21+2427G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110680798 | |||||||
| chr12:110680831 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.21+2394C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110680831 | |||||||
| chr12:110681152 | G | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.21+2073C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110681152 | |||||||
| chr12:110681178 | TACTTTTT others(3): Show |
T | 1 | a0001c0001t0002g0073 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.21+2037_21+2046del others(10): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110681178 | |||||||
| chr12:110681673 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.21+1552G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110681673 | |||||||
| chr12:110681681 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.21+1544G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110681681 | |||||||
| chr12:110681826 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(23): Show |
29 | HG00323.hp1 HG01167.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.21+1399G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110681826 | |||||||
| chr12:110682267 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.21+958G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110682267 | |||||||
| chr12:110682287 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.21+938G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110682287 | |||||||
| chr12:110682710 | GCA | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG00642.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.21+513_21+514delTG | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110682710 | |||||||
| chr12:110682942 | A | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(34): Show |
40 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.21+283T>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110682942 | |||||||
| chr12:110682964 | C | CA | 27 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0020 others(24): Show |
29 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.21+260dupT | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110682964 | |||||||
| chr12:110682988 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.21+237G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110682988 | |||||||
| chr12:110683161 | A | G | 4 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0180 others(1): Show |
4 | HG01884.hp2 HG02965.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.21+64T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 3/7 | chr12 | 110683161 | |||||||
| chr12:110683314 | G | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(33): Show |
39 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-19-50C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110683314 | |||||||
| chr12:110683353 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-19-89A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110683353 | |||||||
| chr12:110683497 | G | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0019 others(34): Show |
40 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.-19-233C>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110683497 | |||||||
| chr12:110683536 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0002g0078 a0001c0001t0002g0079 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-272G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110683536 | |||||||
| chr12:110683598 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-19-334G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110683598 | |||||||
| chr12:110683650 | T | A | 14 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0071 others(11): Show |
15 | HG00323.hp1 HG01175.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-386A>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110683650 | |||||||
| chr12:110683739 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-19-475G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110683739 | |||||||
| chr12:110683860 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-19-596C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110683860 | |||||||
| chr12:110683909 | T | TA | 13 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0060 others(10): Show |
13 | HG01884.hp1 HG02071.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-646dupT | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110683909 | |||||||
| chr12:110683912 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0002g0072 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-19-663_-19-649del others(15): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110683912 | |||||||
| chr12:110683913 | AAAAAAAA others(7): Show |
A | 13 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0071 others(10): Show |
14 | HG00323.hp1 HG01175.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19-663_-19-650del others(14): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110683913 | |||||||
| chr12:110683925 | A | AAG | 11 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(8): Show |
13 | HG01167.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-662_-19-661ins others(2): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110683925 | |||||||
| chr12:110683927 | G | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(8): Show |
13 | HG01167.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-663C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110683927 | |||||||
| chr12:110683927 | G | GA | 20 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0058 others(17): Show |
21 | HG00738.hp2 HG01069.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-19-664dupT | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110683927 | |||||||
| chr12:110684071 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-19-807A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110684071 | |||||||
| chr12:110684096 | T | G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(9): Show |
14 | HG01167.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19-832A>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110684096 | |||||||
| chr12:110684301 | CT | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.-19-1038delA | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110684301 | |||||||
| chr12:110684549 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(9): Show |
14 | HG01167.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19-1285G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110684549 | |||||||
| chr12:110684569 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-19-1305G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110684569 | |||||||
| chr12:110684611 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-19-1347G>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110684611 | |||||||
| chr12:110684661 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG02071.hp2 HG04115.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-1397G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110684661 | |||||||
| chr12:110684733 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19-1469G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110684733 | |||||||
| chr12:110684883 | T | C | 2 | a0002c0002t0001g0014 a0002c0002t0001g0190 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.-19-1619A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110684883 | |||||||
| chr12:110685150 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0026 |
3 | HG01891.hp2 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-19-1886A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110685150 | |||||||
| chr12:110685680 | T | G | 15 | a0001c0001t0001g0088 a0001c0001t0002g0007 a0001c0001t0002g0012 others(12): Show |
16 | HG00323.hp1 HG00735.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-2416A>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110685680 | |||||||
| chr12:110685873 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19-2609C>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110685873 | |||||||
| chr12:110686029 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-20+2596G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110686029 | |||||||
| chr12:110686158 | C | G | 1 | a0001c0001t0001g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-20+2467G>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110686158 | |||||||
| chr12:110686160 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-20+2465T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110686160 | |||||||
| chr12:110686344 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(9): Show |
14 | HG01167.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-20+2281G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110686344 | |||||||
| chr12:110686389 | C | CA | 4 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0180 others(1): Show |
4 | HG01884.hp2 HG02965.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+2235dupT | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110686389 | |||||||
| chr12:110686402 | G | T | 1 | a0001c0001t0001g0027 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-20+2223C>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110686402 | |||||||
| chr12:110686858 | A | T | 1 | a0001c0001t0001g0083 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-20+1767T>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110686858 | |||||||
| chr12:110687004 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-20+1621C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687004 | |||||||
| chr12:110687094 | A | G | 13 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
15 | HG01167.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-20+1531T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687094 | |||||||
| chr12:110687257 | A | AC | 27 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(24): Show |
28 | HG00280.hp2 HG00621.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.-20+1367dupG | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687257 | |||||||
| chr12:110687257 | A | ACC | 11 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(8): Show |
11 | HG02055.hp2 HG02071.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20+1366_-20+1367d others(4): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687257 | |||||||
| chr12:110687257 | AC | A | 12 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0061 others(9): Show |
14 | HG00738.hp2 HG01069.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+1367delG | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687257 | |||||||
| chr12:110687257 | ACC | A | 18 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(15): Show |
19 | HG00323.hp1 HG01175.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-20+1366_-20+1367d others(4): Show |
HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687257 | |||||||
| chr12:110687264 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-20+1361G>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687264 | |||||||
| chr12:110687264 | C | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0085 others(5): Show |
9 | HG01081.hp2 HG01943.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+1361G>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687264 | |||||||
| chr12:110687265 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-20+1360G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687265 | |||||||
| chr12:110687267 | C | G | 1 | a0001c0001t0001g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-20+1358G>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687267 | |||||||
| chr12:110687437 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 |
3 | HG02055.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-20+1188C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687437 | |||||||
| chr12:110687600 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-20+1025C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687600 | |||||||
| chr12:110687652 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-20+973C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687652 | |||||||
| chr12:110687746 | G | T | 13 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0092 others(10): Show |
13 | HG01884.hp1 HG02071.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20+879C>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687746 | |||||||
| chr12:110687960 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+665A>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687960 | |||||||
| chr12:110687969 | C | G | 14 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0071 others(11): Show |
15 | HG00323.hp1 HG01175.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+656G>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110687969 | |||||||
| chr12:110688291 | G | C | 21 | a0001c0001t0001g0066 a0001c0001t0001g0081 a0001c0001t0001g0082 others(18): Show |
22 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.-20+334C>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110688291 | |||||||
| chr12:110688447 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-20+178C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 2/7 | chr12 | 110688447 | |||||||
| chr12:110688794 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-103-86T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 1/7 | chr12 | 110688794 | |||||||
| chr12:110688804 | C | T | 25 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0066 others(22): Show |
26 | HG00323.hp1 HG00738.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.-103-96G>A | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 1/7 | chr12 | 110688804 | |||||||
| chr12:110688831 | A | G | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0066 others(26): Show |
31 | HG00323.hp1 HG00735.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-103-123T>C | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 1/7 | chr12 | 110688831 | |||||||
| chr12:110688977 | CG | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(132): Show |
142 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(139): Show |
intron_variant | MODIFIER | c.-104+102delC | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 1/7 | chr12 | 110688977 | |||||||
| chr12:110689017 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-104+63C>T | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 1/7 | chr12 | 110689017 | |||||||
| chr12:110689040 | G | C | 1 | a0001c0001t0001g0194 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-104+40C>G | HVCN1 | ENSG00000122986.14 | transcript | ENST00000242607.13 | protein_coding | 1/7 | chr12 | 110689040 |