Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 590 |
| ensemblid | ENSG00000114200.10 |
| hgncid | 983 |
| symbol | BCHE |
| name | butyrylcholinesterase |
| refseq_nuc | NM_000055.4 |
| refseq_prot | NP_000046.1 |
| ensembl_nuc | ENST00000264381.8 |
| ensembl_prot | ENSP00000264381.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 165772904 |
| end | 165837423 |
| strand | - |
| ver | v1.2 |
| region | chr3:165772904-165837423 |
| region5000 | chr3:165767904-165842423 |
| regionname0 | BCHE_chr3_165772904_165837423 |
| regionname5000 | BCHE_chr3_165767904_165842423 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 602 | 243 | 76 | 47 | 97 | 7 | 15 | 71 | BCHE_chr3_165767904_165842423 | BCHE | MHSKV others(597): Show |
chr3 | 165767904 | 165842423 |
| a0002 | 0/1 | 602 | 52 | 7 | 4 | 31 | 1 | 8 | 25 | BCHE_chr3_165767904_165842423 | BCHE | MHSKV others(597): Show |
chr3 | 165767904 | 165842423 |
| a0003 | 0/0 | 602 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | MHSKV others(597): Show |
chr3 | 165767904 | 165842423 |
| a0004 | 0/0 | 602 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | MHSKV others(597): Show |
chr3 | 165767904 | 165842423 |
| a0005 | 0/0 | 602 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BCHE_chr3_165767904_165842423 | BCHE | MHSKV others(597): Show |
chr3 | 165767904 | 165842423 |
| a0006 | 0/0 | 602 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | MHSKV others(597): Show |
chr3 | 165767904 | 165842423 |
| a0007 | 0/0 | 602 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | MHSKV others(597): Show |
chr3 | 165767904 | 165842423 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1806 | 242 | 76 | 47 | 96 | 7 | 15 | BCHE_chr3_165767904_165842423 | BCHE | ATGCA others(1801): Show |
chr3 | 165767904 | 165842423 | ||
| a0001c0005 | 0/0 | 1806 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | ATGCA others(1801): Show |
chr3 | 165767904 | 165842423 | ||
| a0002c0002 | 0/1 | 1806 | 52 | 7 | 4 | 31 | 1 | 8 | BCHE_chr3_165767904_165842423 | BCHE | ATGCA others(1801): Show |
chr3 | 165767904 | 165842423 | ||
| a0003c0003 | 0/0 | 1806 | 5 | 4 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | ATGCA others(1801): Show |
chr3 | 165767904 | 165842423 | ||
| a0004c0008 | 0/0 | 1806 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | ATGCA others(1801): Show |
chr3 | 165767904 | 165842423 | ||
| a0005c0004 | 0/0 | 1806 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | ATGCA others(1801): Show |
chr3 | 165767904 | 165842423 | ||
| a0006c0007 | 0/0 | 1806 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | ATGCA others(1801): Show |
chr3 | 165767904 | 165842423 | ||
| a0007c0006 | 0/0 | 1806 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | ATGCA others(1801): Show |
chr3 | 165767904 | 165842423 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2406 | 165 | 26 | 39 | 84 | 4 | 12 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2401): Show |
chr3 | 165767904 | 165842423 |
| a0001c0001t0002 | 0/0 | 2406 | 27 | 22 | 3 | 0 | 1 | 1 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2401): Show |
chr3 | 165767904 | 165842423 |
| a0001c0001t0003 | 1/0 | 2405 | 41 | 20 | 4 | 12 | 2 | 2 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2400): Show |
chr3 | 165767904 | 165842423 |
| a0001c0001t0006 | 0/0 | 2406 | 5 | 4 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2401): Show |
chr3 | 165767904 | 165842423 |
| a0001c0001t0007 | 0/0 | 2405 | 3 | 3 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2400): Show |
chr3 | 165767904 | 165842423 |
| a0001c0001t0010 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2401): Show |
chr3 | 165767904 | 165842423 |
| a0001c0005t0001 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2401): Show |
chr3 | 165767904 | 165842423 |
| a0002c0002t0002 | 0/0 | 2406 | 38 | 3 | 1 | 30 | 0 | 4 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2401): Show |
chr3 | 165767904 | 165842423 |
| a0002c0002t0004 | 0/1 | 2406 | 10 | 1 | 3 | 0 | 1 | 4 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2401): Show |
chr3 | 165767904 | 165842423 |
| a0002c0002t0008 | 0/0 | 2406 | 3 | 3 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2401): Show |
chr3 | 165767904 | 165842423 |
| a0002c0002t0009 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2400): Show |
chr3 | 165767904 | 165842423 |
| a0003c0003t0005 | 0/0 | 2406 | 5 | 4 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2401): Show |
chr3 | 165767904 | 165842423 |
| a0004c0008t0003 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2400): Show |
chr3 | 165767904 | 165842423 |
| a0005c0004t0004 | 0/0 | 2406 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2401): Show |
chr3 | 165767904 | 165842423 |
| a0006c0007t0001 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2401): Show |
chr3 | 165767904 | 165842423 |
| a0007c0006t0002 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | AGTGC others(2401): Show |
chr3 | 165767904 | 165842423 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 0 | 5 | 7 | 1 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0004 | 1/0 | 3 | 0 | 0 | 0 | 2 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0001t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0001c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0004g0002 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0004g0003 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0004g0035 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0008g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0008g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0002c0002t0009g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0003c0003t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0003c0003t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0003c0003t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0003c0003t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0004c0008t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0005c0004t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0006c0007t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| a0007c0006t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0240 | EUR | GBR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | CHS | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | CHS | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | CHS | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | CHS | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0079 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01256 | hp1 | a0002 | c0002 | t0004 | g0002 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01258 | hp2 | a0002 | c0002 | t0004 | g0002 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0223 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01496 | hp2 | a0003 | c0003 | t0005 | g0113 | AMR | CLM | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01517 | hp2 | a0002 | c0002 | t0004 | g0003 | EUR | IBS | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01934 | hp2 | a0002 | c0002 | t0004 | g0002 | AMR | PEL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0062 | AMR | PEL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02055 | hp1 | a0002 | c0002 | t0008 | g0121 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02055 | hp2 | a0003 | c0003 | t0005 | g0234 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CDX | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | CDX | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02258 | hp2 | a0002 | c0002 | t0008 | g0122 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02572 | hp1 | a0004 | c0008 | t0003 | g0043 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0054 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0061 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02602 | hp2 | a0002 | c0002 | t0004 | g0002 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02615 | hp2 | a0003 | c0003 | t0005 | g0018 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0065 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02735 | hp1 | a0005 | c0004 | t0004 | g0034 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02738 | hp1 | a0002 | c0002 | t0004 | g0002 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0246 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0221 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0222 | AFR | ESN | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02965 | hp2 | a0002 | c0002 | t0008 | g0120 | AFR | ESN | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | ESN | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0138 | AFR | ESN | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02976 | hp1 | a0003 | c0003 | t0005 | g0018 | AFR | ESN | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | ESN | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | MSL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | MSL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0224 | AFR | MSL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0063 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | MSL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ESN | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03540 | hp2 | a0002 | c0002 | t0004 | g0036 | AFR | GWD | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03654 | hp2 | a0002 | c0002 | t0004 | g0003 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0064 | SAS | BEB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03927 | hp2 | a0002 | c0002 | t0004 | g0003 | SAS | BEB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0091 | SAS | BEB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | YRI | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | YRI | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | YRI | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18957 | hp2 | a0001 | c0005 | t0001 | g0143 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18961 | hp2 | a0002 | c0002 | t0009 | g0102 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18968 | hp2 | a0006 | c0007 | t0001 | g0183 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18982 | hp1 | a0007 | c0006 | t0002 | g0093 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | LWK | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | LWK | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19043 | hp1 | a0003 | c0003 | t0005 | g0112 | AFR | LWK | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0137 | AFR | LWK | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | ASW | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | GIH | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | GIH | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0055 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | ACB | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | MSL | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0164 | AFR | USA | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | USA | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | USA | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | USA | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | LWK | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0136 | AFR | LWK | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0004 | g0035 | REF | REF | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0004 | REF | REF | BCHE_chr3_165767904_165842423 | BCHE | chr3 | 165767904 | 165842423 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:165773492 | C | T | 4 | a0002 a0003 a0005 others(1): Show |
58 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(55): Show |
missense_variant | MODERATE | c.1699G>A | p.Ala567Thr | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 4/4 | 1817/2405 | 1699/1809 | 567/602 | chr3 | 165773492 | |||
| chr3:165829857 | C | G | 1 | a0007 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1177G>C | p.Gly393Arg | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/4 | 1295/2405 | 1177/1809 | 393/602 | chr3 | 165829857 | |||
| chr3:165830100 | T | A | 1 | a0006 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.934A>T | p.Thr312Ser | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/4 | 1052/2405 | 934/1809 | 312/602 | chr3 | 165830100 | |||
| chr3:165830154 | T | A | 1 | a0004 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.880A>T | p.Asn294Tyr | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/4 | 998/2405 | 880/1809 | 294/602 | chr3 | 165830154 | |||
| chr3:165830185 | C | G | 1 | a0003 | 5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
missense_variant | MODERATE | c.849G>C | p.Glu283Asp | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/4 | 967/2405 | 849/1809 | 283/602 | chr3 | 165830185 | |||
| chr3:165830525 | A | G | 1 | a0005 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.509T>C | p.Val170Ala | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/4 | 627/2405 | 509/1809 | 170/602 | chr3 | 165830525 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:165830344 | A | G | 1 | a0001c0005 | 1 | NA18957.hp2 | synonymous_variant | LOW | c.690T>C | p.Ala230Ala | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/4 | 808/2405 | 690/1809 | 230/602 | chr3 | 165830344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:165772915 | G | C | 1 | a0001c0001t0007 | 3 | HG02970.hp2 NA19043.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*467C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 4/4 | 467 | chr3 | 165772915 | ||||||
| chr3:165772927 | A | G | 1 | a0001c0001t0010 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*455T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 4/4 | 455 | chr3 | 165772927 | ||||||
| chr3:165773033 | C | T | 1 | a0003c0003t0005 | 5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*349G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 4/4 | 349 | chr3 | 165773033 | ||||||
| chr3:165773088 | G | A | 1 | a0002c0002t0009 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*294C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 4/4 | 294 | chr3 | 165773088 | ||||||
| chr3:165773088 | G | GA | 12 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(9): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*293dupT | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 4/4 | 293 | chr3 | 165773088 | ||||||
| chr3:165773193 | C | T | 4 | a0001c0001t0001 a0001c0001t0006 a0001c0005t0001 others(1): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*189G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 4/4 | 189 | chr3 | 165773193 | ||||||
| chr3:165773202 | C | T | 1 | a0002c0002t0008 | 3 | HG02055.hp1 HG02258.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*180G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 4/4 | 180 | chr3 | 165773202 | ||||||
| chr3:165773243 | A | T | 1 | a0001c0001t0007 | 3 | HG02970.hp2 NA19043.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*139T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 4/4 | 139 | chr3 | 165773243 | ||||||
| chr3:165773369 | G | A | 1 | a0001c0001t0006 | 5 | HG01433.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*13C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 4/4 | 13 | chr3 | 165773369 | ||||||
| chr3:165837337 | C | T | 2 | a0002c0002t0004 a0005c0004t0004 |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-32G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/4 | 6304 | chr3 | 165837337 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:165773611 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0208 |
2 | NA18989.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1685-105C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165773611 | |||||||
| chr3:165773718 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | NA18975.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1685-212T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165773718 | |||||||
| chr3:165773728 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1685-222A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165773728 | |||||||
| chr3:165773741 | ATAT | A | 5 | a0001c0001t0006g0221 a0001c0001t0006g0222 a0001c0001t0006g0223 others(2): Show |
5 | HG01433.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1685-238_1685-236d others(5): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165773741 | |||||||
| chr3:165773796 | AT | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1685-291delA | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165773796 | |||||||
| chr3:165773924 | G | A | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1685-418C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165773924 | |||||||
| chr3:165773977 | G | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1685-471C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165773977 | |||||||
| chr3:165774008 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1685-502T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165774008 | |||||||
| chr3:165774127 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1685-621T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165774127 | |||||||
| chr3:165774240 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | NA18975.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1685-734T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165774240 | |||||||
| chr3:165774346 | T | A | 1 | a0003c0003t0005g0113 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1685-840A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165774346 | |||||||
| chr3:165774394 | C | T | 1 | a0001c0001t0003g0084 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1685-888G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165774394 | |||||||
| chr3:165774410 | C | T | 13 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0213 others(10): Show |
13 | HG00423.hp1 HG00621.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.1685-904G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165774410 | |||||||
| chr3:165774478 | C | T | 1 | a0001c0001t0003g0033 | 2 | HG01255.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1685-972G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165774478 | |||||||
| chr3:165774622 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1685-1116T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165774622 | |||||||
| chr3:165774829 | T | C | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
58 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1685-1323A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165774829 | |||||||
| chr3:165774934 | GAC | G | 35 | a0002c0002t0002g0005 a0002c0002t0002g0017 a0002c0002t0002g0037 others(32): Show |
38 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1685-1430_1685-142 others(6): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165774934 | |||||||
| chr3:165775077 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1685-1571C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165775077 | |||||||
| chr3:165775347 | G | C | 2 | a0002c0002t0002g0054 a0002c0002t0002g0055 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1685-1841C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165775347 | |||||||
| chr3:165775348 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(217): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1685-1842T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165775348 | |||||||
| chr3:165775379 | A | G | 5 | a0001c0001t0006g0221 a0001c0001t0006g0222 a0001c0001t0006g0223 others(2): Show |
5 | HG01433.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1685-1873T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165775379 | |||||||
| chr3:165775632 | T | C | 22 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0019 others(19): Show |
28 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1685-2126A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165775632 | |||||||
| chr3:165775653 | A | T | 1 | a0001c0001t0002g0238 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1685-2147T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165775653 | |||||||
| chr3:165775666 | A | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
102 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1685-2160T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165775666 | |||||||
| chr3:165775706 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1685-2200G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165775706 | |||||||
| chr3:165775877 | G | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0169 |
2 | NA18980.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1685-2371C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165775877 | |||||||
| chr3:165775936 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
102 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1685-2430G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165775936 | |||||||
| chr3:165776031 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1685-2525T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165776031 | |||||||
| chr3:165776594 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1685-3088C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165776594 | |||||||
| chr3:165776608 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1685-3102T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165776608 | |||||||
| chr3:165776682 | A | G | 22 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0019 others(19): Show |
28 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1685-3176T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165776682 | |||||||
| chr3:165776775 | A | G | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
58 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1685-3269T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165776775 | |||||||
| chr3:165776778 | C | T | 1 | a0002c0002t0002g0164 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1685-3272G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165776778 | |||||||
| chr3:165776779 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1685-3273C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165776779 | |||||||
| chr3:165776936 | G | A | 4 | a0003c0003t0005g0018 a0003c0003t0005g0112 a0003c0003t0005g0113 others(1): Show |
5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1685-3430C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165776936 | |||||||
| chr3:165776951 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1685-3445T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165776951 | |||||||
| chr3:165776962 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1685-3456C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165776962 | |||||||
| chr3:165776989 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1685-3483C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165776989 | |||||||
| chr3:165776997 | C | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
111 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1685-3491G>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165776997 | |||||||
| chr3:165777107 | A | G | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1685-3601T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165777107 | |||||||
| chr3:165777333 | C | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1685-3827G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165777333 | |||||||
| chr3:165777354 | AAAT | A | 48 | a0002c0002t0002g0005 a0002c0002t0002g0017 a0002c0002t0002g0037 others(45): Show |
58 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1685-3851_1685-384 others(7): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165777354 | |||||||
| chr3:165777562 | T | C | 1 | a0001c0001t0006g0223 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1685-4056A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165777562 | |||||||
| chr3:165777595 | G | A | 3 | a0001c0001t0007g0136 a0001c0001t0007g0137 a0001c0001t0007g0138 |
3 | HG02970.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1685-4089C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165777595 | |||||||
| chr3:165777612 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1685-4106C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165777612 | |||||||
| chr3:165777632 | G | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
102 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1685-4126C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165777632 | |||||||
| chr3:165777732 | C | A | 3 | a0001c0001t0007g0136 a0001c0001t0007g0137 a0001c0001t0007g0138 |
3 | HG02970.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1685-4226G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165777732 | |||||||
| chr3:165778113 | G | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0114 |
3 | HG01346.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1685-4607C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165778113 | |||||||
| chr3:165778136 | A | T | 1 | a0001c0001t0003g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1685-4630T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165778136 | |||||||
| chr3:165778249 | T | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(115): Show |
145 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1685-4743A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165778249 | |||||||
| chr3:165778344 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1685-4838C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165778344 | |||||||
| chr3:165778434 | T | G | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
58 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1685-4928A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165778434 | |||||||
| chr3:165778626 | A | G | 1 | a0002c0002t0002g0101 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1685-5120T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165778626 | |||||||
| chr3:165778632 | C | T | 4 | a0003c0003t0005g0018 a0003c0003t0005g0112 a0003c0003t0005g0113 others(1): Show |
5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1685-5126G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165778632 | |||||||
| chr3:165778834 | A | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1685-5328T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165778834 | |||||||
| chr3:165778910 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1685-5404A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165778910 | |||||||
| chr3:165778915 | AT | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1685-5410delA | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165778915 | |||||||
| chr3:165779043 | C | G | 2 | a0002c0002t0002g0097 a0002c0002t0002g0101 |
2 | NA18956.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1685-5537G>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165779043 | |||||||
| chr3:165779094 | A | G | 1 | a0001c0001t0001g0020 | 2 | NA18985.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1685-5588T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165779094 | |||||||
| chr3:165779138 | C | T | 7 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0129 others(4): Show |
7 | HG00140.hp1 HG00642.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1685-5632G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165779138 | |||||||
| chr3:165779401 | G | C | 22 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0019 others(19): Show |
28 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1685-5895C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165779401 | |||||||
| chr3:165779445 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1685-5939C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165779445 | |||||||
| chr3:165779505 | T | G | 44 | a0002c0002t0002g0005 a0002c0002t0002g0017 a0002c0002t0002g0037 others(41): Show |
48 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1685-5999A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165779505 | |||||||
| chr3:165779523 | G | A | 2 | a0002c0002t0008g0120 a0002c0002t0008g0121 |
2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1685-6017C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165779523 | |||||||
| chr3:165779608 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1685-6102G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165779608 | |||||||
| chr3:165779886 | T | G | 3 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0220 |
3 | HG02015.hp1 NA18989.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1684+6259A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165779886 | |||||||
| chr3:165779981 | T | G | 14 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0235 others(11): Show |
17 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1684+6164A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165779981 | |||||||
| chr3:165780021 | G | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01346.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1684+6124C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780021 | |||||||
| chr3:165780046 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
102 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1684+6099T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780046 | |||||||
| chr3:165780114 | G | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1684+6031C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780114 | |||||||
| chr3:165780120 | C | A | 2 | a0002c0002t0002g0094 a0002c0002t0009g0102 |
2 | NA18961.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1684+6025G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780120 | |||||||
| chr3:165780120 | C | T | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1684+6025G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780120 | |||||||
| chr3:165780310 | G | T | 14 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0235 others(11): Show |
17 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1684+5835C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780310 | |||||||
| chr3:165780405 | C | T | 2 | a0001c0001t0003g0079 a0001c0001t0003g0080 |
2 | HG01069.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1684+5740G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780405 | |||||||
| chr3:165780478 | A | G | 1 | a0001c0001t0003g0091 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1684+5667T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780478 | |||||||
| chr3:165780521 | T | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(217): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1684+5624A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780521 | |||||||
| chr3:165780606 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0114 |
3 | HG01346.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1684+5539C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780606 | |||||||
| chr3:165780649 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1684+5496A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780649 | |||||||
| chr3:165780651 | T | C | 1 | a0003c0003t0005g0113 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1684+5494A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780651 | |||||||
| chr3:165780663 | C | A | 1 | a0002c0002t0002g0057 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1684+5482G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780663 | |||||||
| chr3:165780682 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1684+5463C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780682 | |||||||
| chr3:165780766 | T | A | 2 | a0002c0002t0002g0054 a0002c0002t0002g0055 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1684+5379A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780766 | |||||||
| chr3:165780810 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1684+5335C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165780810 | |||||||
| chr3:165781344 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(4): Show |
9 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1684+4801T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165781344 | |||||||
| chr3:165781347 | GAT | G | 48 | a0002c0002t0002g0005 a0002c0002t0002g0017 a0002c0002t0002g0037 others(45): Show |
58 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1684+4796_1684+479 others(6): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165781347 | |||||||
| chr3:165781423 | T | C | 1 | a0001c0001t0003g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1684+4722A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165781423 | |||||||
| chr3:165781469 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
102 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1684+4676T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165781469 | |||||||
| chr3:165781604 | AG | A | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
58 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1684+4540delC | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165781604 | |||||||
| chr3:165782130 | C | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0176 a0001c0001t0001g0177 |
4 | HG02040.hp2 HG02155.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1684+4015G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165782130 | |||||||
| chr3:165782184 | C | T | 5 | a0001c0001t0003g0052 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1684+3961G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165782184 | |||||||
| chr3:165782253 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(194): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1684+3892C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165782253 | |||||||
| chr3:165782266 | G | A | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
58 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1684+3879C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165782266 | |||||||
| chr3:165782372 | G | T | 15 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0045 others(12): Show |
18 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.1684+3773C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165782372 | |||||||
| chr3:165782447 | G | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(217): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1684+3698C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165782447 | |||||||
| chr3:165782473 | T | A | 1 | a0001c0001t0002g0239 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1684+3672A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165782473 | |||||||
| chr3:165782494 | G | GA | 167 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1684+3650dupT | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165782494 | |||||||
| chr3:165782504 | C | T | 30 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0114 others(27): Show |
36 | HG00140.hp2 HG01106.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1684+3641G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165782504 | |||||||
| chr3:165782621 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
160 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.1684+3524A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165782621 | |||||||
| chr3:165782864 | T | G | 1 | a0001c0001t0001g0114 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1684+3281A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165782864 | |||||||
| chr3:165782897 | C | T | 14 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0235 others(11): Show |
17 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1684+3248G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165782897 | |||||||
| chr3:165782911 | A | G | 1 | a0001c0001t0003g0085 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1684+3234T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165782911 | |||||||
| chr3:165783124 | TC | T | 29 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(26): Show |
37 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(34): Show |
intron_variant | MODIFIER | c.1684+3020delG | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165783124 | |||||||
| chr3:165783218 | A | G | 6 | a0001c0001t0003g0072 a0001c0001t0003g0081 a0001c0001t0003g0082 others(3): Show |
6 | HG00423.hp1 NA18950.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1684+2927T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165783218 | |||||||
| chr3:165783290 | TG | T | 4 | a0003c0003t0005g0018 a0003c0003t0005g0112 a0003c0003t0005g0113 others(1): Show |
5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1684+2854delC | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165783290 | |||||||
| chr3:165783373 | T | A | 4 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0117 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1684+2772A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165783373 | |||||||
| chr3:165783382 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
160 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.1684+2763C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165783382 | |||||||
| chr3:165783533 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1684+2612T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165783533 | |||||||
| chr3:165783832 | A | C | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1684+2313T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165783832 | |||||||
| chr3:165783900 | C | A | 1 | a0001c0001t0002g0244 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1684+2245G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165783900 | |||||||
| chr3:165784430 | A | G | 1 | a0002c0002t0002g0095 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1684+1715T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165784430 | |||||||
| chr3:165784488 | C | A | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1684+1657G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165784488 | |||||||
| chr3:165784553 | A | G | 2 | a0002c0002t0002g0054 a0002c0002t0002g0055 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1684+1592T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165784553 | |||||||
| chr3:165784600 | C | A | 1 | a0002c0002t0008g0121 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1684+1545G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165784600 | |||||||
| chr3:165784829 | A | G | 1 | a0001c0001t0003g0033 | 2 | HG01255.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1684+1316T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165784829 | |||||||
| chr3:165784849 | A | C | 1 | a0001c0001t0001g0214 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1684+1296T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165784849 | |||||||
| chr3:165784849 | A | G | 24 | a0002c0002t0002g0005 a0002c0002t0002g0037 a0002c0002t0002g0062 others(21): Show |
26 | HG00621.hp2 HG01978.hp2 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.1684+1296T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165784849 | |||||||
| chr3:165784921 | A | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(156): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1684+1224T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165784921 | |||||||
| chr3:165784924 | G | A | 9 | a0001c0001t0001g0144 a0001c0001t0001g0158 a0001c0001t0001g0185 others(6): Show |
9 | HG00738.hp1 HG01192.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1684+1221C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165784924 | |||||||
| chr3:165784936 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
160 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.1684+1209G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165784936 | |||||||
| chr3:165785122 | G | A | 8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0114 others(5): Show |
8 | HG01346.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1684+1023C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165785122 | |||||||
| chr3:165785127 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0179 a0001c0005t0001g0143 |
4 | NA18956.hp2 NA18957.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.1684+1018G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165785127 | |||||||
| chr3:165785608 | G | A | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1684+537C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165785608 | |||||||
| chr3:165785647 | T | C | 1 | a0001c0001t0002g0032 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1684+498A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165785647 | |||||||
| chr3:165785665 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
160 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.1684+480A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165785665 | |||||||
| chr3:165785839 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1684+306T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165785839 | |||||||
| chr3:165785847 | A | T | 29 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(26): Show |
37 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(34): Show |
intron_variant | MODIFIER | c.1684+298T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165785847 | |||||||
| chr3:165785998 | T | TAAAAATA others(316): Show |
1 | a0003c0003t0005g0018 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1684+146_1684+147i others(325): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165785998 | |||||||
| chr3:165786142 | C | T | 4 | a0001c0001t0003g0007 a0001c0001t0003g0046 a0001c0001t0003g0140 others(1): Show |
6 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1684+3G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 3/3 | chr3 | 165786142 | |||||||
| chr3:165786317 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02129.hp1 | splice_region_variant&intron_variant | LOW | c.1518-6A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165786317 | |||||||
| chr3:165786432 | A | G | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1518-121T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165786432 | |||||||
| chr3:165786468 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1518-157A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165786468 | |||||||
| chr3:165786546 | A | G | 4 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0117 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1518-235T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165786546 | |||||||
| chr3:165786654 | C | G | 3 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0119 |
6 | HG02615.hp1 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1518-343G>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165786654 | |||||||
| chr3:165786875 | C | A | 1 | a0001c0001t0001g0114 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1518-564G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165786875 | |||||||
| chr3:165787058 | G | T | 8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0114 others(5): Show |
8 | HG01346.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1518-747C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165787058 | |||||||
| chr3:165787174 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1518-863C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165787174 | |||||||
| chr3:165787389 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(64): Show |
91 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.1518-1078T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165787389 | |||||||
| chr3:165787486 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
102 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1518-1175T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165787486 | |||||||
| chr3:165787632 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
102 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1518-1321G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165787632 | |||||||
| chr3:165787737 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1518-1426G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165787737 | |||||||
| chr3:165787799 | T | C | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1518-1488A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165787799 | |||||||
| chr3:165787928 | A | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0115 others(4): Show |
10 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1518-1617T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165787928 | |||||||
| chr3:165787971 | T | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(110): Show |
140 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1518-1660A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165787971 | |||||||
| chr3:165788069 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
160 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.1518-1758A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165788069 | |||||||
| chr3:165788098 | G | C | 22 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0019 others(19): Show |
28 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1518-1787C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165788098 | |||||||
| chr3:165788114 | GTTTGT | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(240): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1518-1808_1518-180 others(9): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165788114 | |||||||
| chr3:165788219 | G | T | 1 | a0001c0001t0001g0213 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1518-1908C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165788219 | |||||||
| chr3:165788288 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1518-1977G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165788288 | |||||||
| chr3:165788355 | A | T | 2 | a0001c0001t0006g0221 a0001c0001t0006g0225 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1518-2044T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165788355 | |||||||
| chr3:165788464 | A | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(156): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1518-2153T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165788464 | |||||||
| chr3:165788679 | C | T | 14 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0235 others(11): Show |
17 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1518-2368G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165788679 | |||||||
| chr3:165788731 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0114 |
3 | HG01346.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1518-2420C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165788731 | |||||||
| chr3:165788971 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0114 |
3 | HG01346.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1518-2660G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165788971 | |||||||
| chr3:165789056 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1518-2745T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165789056 | |||||||
| chr3:165789161 | G | A | 1 | a0002c0002t0002g0068 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1518-2850C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165789161 | |||||||
| chr3:165789162 | T | A | 1 | a0001c0001t0001g0127 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1518-2851A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165789162 | |||||||
| chr3:165789235 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1518-2924G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165789235 | |||||||
| chr3:165789294 | C | CA | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(48): Show |
61 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1518-2984dupT | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165789294 | |||||||
| chr3:165789312 | C | CT | 218 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(215): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1518-3002dupA | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165789312 | |||||||
| chr3:165789375 | T | G | 1 | a0001c0001t0001g0212 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1518-3064A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165789375 | |||||||
| chr3:165789406 | A | G | 5 | a0001c0001t0006g0221 a0001c0001t0006g0222 a0001c0001t0006g0223 others(2): Show |
5 | HG01433.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-3095T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165789406 | |||||||
| chr3:165789633 | T | C | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1518-3322A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165789633 | |||||||
| chr3:165789760 | G | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0047 a0001c0001t0001g0049 |
4 | HG02717.hp1 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1518-3449C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165789760 | |||||||
| chr3:165789785 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1518-3474T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165789785 | |||||||
| chr3:165789963 | A | G | 12 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0114 others(9): Show |
18 | HG01256.hp1 HG01258.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.1518-3652T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165789963 | |||||||
| chr3:165790043 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0163 a0001c0001t0001g0176 others(1): Show |
5 | HG02040.hp2 HG02155.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-3732C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165790043 | |||||||
| chr3:165790191 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1518-3880G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165790191 | |||||||
| chr3:165790314 | T | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
160 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.1518-4003A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165790314 | |||||||
| chr3:165790433 | C | T | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
58 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1518-4122G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165790433 | |||||||
| chr3:165790611 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1518-4300G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165790611 | |||||||
| chr3:165790653 | G | T | 22 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0019 others(19): Show |
28 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1518-4342C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165790653 | |||||||
| chr3:165790654 | A | G | 22 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0019 others(19): Show |
28 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1518-4343T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165790654 | |||||||
| chr3:165790818 | T | C | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
58 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1518-4507A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165790818 | |||||||
| chr3:165790840 | AG | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
102 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1518-4530delC | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165790840 | |||||||
| chr3:165790880 | G | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0152 others(5): Show |
11 | HG01257.hp1 HG01261.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1518-4569C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165790880 | |||||||
| chr3:165791089 | G | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
102 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1518-4778C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791089 | |||||||
| chr3:165791123 | C | T | 8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0114 others(5): Show |
8 | HG01346.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1518-4812G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791123 | |||||||
| chr3:165791148 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1518-4837T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791148 | |||||||
| chr3:165791299 | G | A | 1 | a0002c0002t0008g0120 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1518-4988C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791299 | |||||||
| chr3:165791453 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
160 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.1518-5142C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791453 | |||||||
| chr3:165791464 | A | G | 2 | a0002c0002t0002g0054 a0002c0002t0002g0055 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1518-5153T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791464 | |||||||
| chr3:165791749 | G | A | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
58 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1518-5438C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791749 | |||||||
| chr3:165791841 | G | C | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
58 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1518-5530C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791841 | |||||||
| chr3:165791948 | A | AAAAAT | 24 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0059 others(21): Show |
32 | HG00140.hp1 HG00642.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1518-5642_1518-563 others(9): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791948 | |||||||
| chr3:165791948 | A | AAAAATAA others(3): Show |
16 | a0001c0001t0001g0048 a0001c0001t0001g0159 a0001c0001t0001g0184 others(13): Show |
19 | HG00621.hp1 HG00673.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.1518-5647_1518-563 others(14): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791948 | |||||||
| chr3:165791948 | A | AAAAATAA others(8): Show |
32 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0027 others(29): Show |
38 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1518-5652_1518-563 others(19): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791948 | |||||||
| chr3:165791948 | A | AAAAATAA others(13): Show |
10 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0051 others(7): Show |
12 | HG02109.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1518-5657_1518-563 others(24): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791948 | |||||||
| chr3:165791948 | A | AAAAATAA others(18): Show |
6 | a0001c0001t0001g0050 a0001c0001t0001g0209 a0001c0001t0006g0221 others(3): Show |
6 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1518-5662_1518-563 others(29): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791948 | |||||||
| chr3:165791948 | A | AAAAATAA others(23): Show |
1 | a0001c0001t0006g0223 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1518-5667_1518-563 others(34): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791948 | |||||||
| chr3:165791948 | AAAAATAA others(3): Show |
A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0182 a0002c0002t0002g0111 |
3 | HG00544.hp1 HG01074.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.1518-5647_1518-563 others(14): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791948 | |||||||
| chr3:165791988 | T | TAAAATAA others(8): Show |
7 | a0001c0001t0002g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 others(4): Show |
7 | HG00140.hp2 HG01106.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1518-5678_1518-567 others(19): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791988 | |||||||
| chr3:165791988 | T | TAAAATAA others(13): Show |
6 | a0001c0001t0002g0013 a0001c0001t0002g0238 a0001c0001t0002g0239 others(3): Show |
8 | HG01358.hp2 HG02109.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1518-5678_1518-567 others(24): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791988 | |||||||
| chr3:165791988 | T | TAAAATAA others(33): Show |
1 | a0001c0001t0002g0032 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1518-5678_1518-567 others(44): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165791988 | |||||||
| chr3:165792028 | T | C | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
58 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1518-5717A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165792028 | |||||||
| chr3:165792099 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(212): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1518-5788C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165792099 | |||||||
| chr3:165792099 | G | C | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1518-5788C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165792099 | |||||||
| chr3:165792269 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1518-5958G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165792269 | |||||||
| chr3:165792344 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1518-6033G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165792344 | |||||||
| chr3:165792360 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0114 |
3 | HG01346.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1518-6049C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165792360 | |||||||
| chr3:165792588 | A | G | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1518-6277T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165792588 | |||||||
| chr3:165792677 | G | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0039 others(6): Show |
12 | HG02015.hp2 NA18939.hp1 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.1518-6366C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165792677 | |||||||
| chr3:165792710 | A | T | 4 | a0003c0003t0005g0018 a0003c0003t0005g0112 a0003c0003t0005g0113 others(1): Show |
5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-6399T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165792710 | |||||||
| chr3:165792766 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1518-6455G>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165792766 | |||||||
| chr3:165792834 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1518-6523C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165792834 | |||||||
| chr3:165793030 | A | T | 1 | a0001c0001t0003g0091 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1518-6719T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165793030 | |||||||
| chr3:165793284 | A | T | 1 | a0002c0002t0002g0099 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1518-6973T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165793284 | |||||||
| chr3:165793355 | T | C | 1 | a0002c0002t0002g0099 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1518-7044A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165793355 | |||||||
| chr3:165793650 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0114 |
3 | HG01346.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1518-7339C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165793650 | |||||||
| chr3:165793758 | G | A | 1 | a0004c0008t0003g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1518-7447C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165793758 | |||||||
| chr3:165793875 | G | A | 4 | a0003c0003t0005g0018 a0003c0003t0005g0112 a0003c0003t0005g0113 others(1): Show |
5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-7564C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165793875 | |||||||
| chr3:165793901 | G | A | 29 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(26): Show |
37 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(34): Show |
intron_variant | MODIFIER | c.1518-7590C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165793901 | |||||||
| chr3:165793923 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1518-7612A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165793923 | |||||||
| chr3:165793955 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0114 |
3 | HG01346.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1518-7644C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165793955 | |||||||
| chr3:165794050 | TA | T | 5 | a0001c0001t0001g0191 a0001c0001t0003g0007 a0001c0001t0003g0046 others(2): Show |
7 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1518-7740delT | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165794050 | |||||||
| chr3:165794170 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1518-7859A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165794170 | |||||||
| chr3:165794185 | G | C | 1 | a0001c0001t0003g0053 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1518-7874C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165794185 | |||||||
| chr3:165794185 | G | T | 1 | a0002c0002t0002g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1518-7874C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165794185 | |||||||
| chr3:165794245 | A | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0203 a0001c0001t0001g0206 others(2): Show |
6 | NA18952.hp1 NA18966.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.1518-7934T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165794245 | |||||||
| chr3:165794310 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1518-7999T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165794310 | |||||||
| chr3:165794599 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1518-8288T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165794599 | |||||||
| chr3:165794631 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1518-8320G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165794631 | |||||||
| chr3:165794724 | G | A | 1 | a0001c0001t0003g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1518-8413C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165794724 | |||||||
| chr3:165794749 | CAT | C | 2 | a0001c0001t0001g0131 a0001c0001t0003g0033 |
3 | HG01255.hp1 HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1518-8440_1518-843 others(6): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165794749 | |||||||
| chr3:165794768 | G | A | 22 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0019 others(19): Show |
28 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1518-8457C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165794768 | |||||||
| chr3:165794820 | T | C | 1 | a0006c0007t0001g0183 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1518-8509A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165794820 | |||||||
| chr3:165794895 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1518-8584T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165794895 | |||||||
| chr3:165794982 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1518-8671T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165794982 | |||||||
| chr3:165795219 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1518-8908C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165795219 | |||||||
| chr3:165795387 | ATAACTGT others(640): Show |
A | 1 | a0001c0001t0001g0172 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1518-9723_1518-907 others(4): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165795387 | |||||||
| chr3:165795527 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1518-9216G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165795527 | |||||||
| chr3:165795786 | G | C | 22 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0019 others(19): Show |
28 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1518-9475C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165795786 | |||||||
| chr3:165795843 | C | T | 1 | a0001c0001t0003g0079 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1518-9532G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165795843 | |||||||
| chr3:165795898 | T | C | 8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0114 others(5): Show |
8 | HG01346.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1518-9587A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165795898 | |||||||
| chr3:165796089 | C | T | 3 | a0002c0002t0008g0120 a0002c0002t0008g0121 a0002c0002t0008g0122 |
3 | HG02055.hp1 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1518-9778G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165796089 | |||||||
| chr3:165796115 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01346.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1518-9804G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165796115 | |||||||
| chr3:165797096 | C | A | 1 | a0001c0001t0001g0229 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1518-10785G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797096 | |||||||
| chr3:165797124 | C | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(8): Show |
19 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.1518-10813G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797124 | |||||||
| chr3:165797137 | C | A | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(8): Show |
19 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.1518-10826G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797137 | |||||||
| chr3:165797189 | G | C | 56 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(53): Show |
69 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1518-10878C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797189 | |||||||
| chr3:165797190 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1518-10879A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797190 | |||||||
| chr3:165797193 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1518-10882A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797193 | |||||||
| chr3:165797195 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1518-10884G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797195 | |||||||
| chr3:165797199 | C | CCCTCCCC others(112): Show |
1 | a0001c0001t0001g0193 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1518-10889_1518-10 others(125): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797199 | |||||||
| chr3:165797199 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1518-10888G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797199 | |||||||
| chr3:165797218 | T | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0193 |
2 | HG01074.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1518-10907A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797218 | |||||||
| chr3:165797218 | T | TTCCCTCC others(172): Show |
1 | a0001c0001t0001g0204 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1518-10908_1518-10 others(185): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797218 | |||||||
| chr3:165797218 | T | TTCCCTCC others(171): Show |
1 | a0001c0001t0001g0203 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1518-10908_1518-10 others(184): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797218 | |||||||
| chr3:165797218 | T | TTCCCTCC others(140): Show |
1 | a0001c0001t0001g0216 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1518-10908_1518-10 others(153): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797218 | |||||||
| chr3:165797218 | T | TTCCCTCC others(159): Show |
4 | a0003c0003t0005g0018 a0003c0003t0005g0112 a0003c0003t0005g0113 others(1): Show |
5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-10908_1518-10 others(172): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797218 | |||||||
| chr3:165797218 | T | TTCCTTCC others(236): Show |
3 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 |
9 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1518-10908_1518-10 others(249): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797218 | |||||||
| chr3:165797227 | T | TC | 64 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
77 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1518-10917dupG | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797227 | |||||||
| chr3:165797229 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(156): Show |
200 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(197): Show |
intron_variant | MODIFIER | c.1518-10918A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797229 | |||||||
| chr3:165797231 | T | C | 64 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
77 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1518-10920A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797231 | |||||||
| chr3:165797233 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(139): Show |
176 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.1518-10922A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797233 | |||||||
| chr3:165797234 | T | TTCCTTCC others(66): Show |
6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(3): Show |
8 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1518-10924_1518-10 others(79): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797234 | |||||||
| chr3:165797235 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
168 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.1518-10924G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797235 | |||||||
| chr3:165797238 | TC | T | 59 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(56): Show |
72 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1518-10928delG | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797238 | |||||||
| chr3:165797239 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
168 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.1518-10928G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797239 | |||||||
| chr3:165797240 | C | CTTCCTT | 5 | a0001c0001t0006g0221 a0001c0001t0006g0222 a0001c0001t0006g0223 others(2): Show |
5 | HG01433.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-10930_1518-10 others(12): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797240 | |||||||
| chr3:165797241 | CT | C | 12 | a0001c0001t0001g0182 a0001c0001t0001g0193 a0001c0001t0001g0203 others(9): Show |
19 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1518-10931delA | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797241 | |||||||
| chr3:165797242 | T | TCCCCCCT others(258): Show |
3 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 |
3 | HG02451.hp1 HG02717.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1518-10932_1518-10 others(271): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797242 | |||||||
| chr3:165797242 | T | TCCCCCCT others(273): Show |
1 | a0005c0004t0004g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1518-10932_1518-10 others(286): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797242 | |||||||
| chr3:165797242 | T | TCCCCCCT others(257): Show |
1 | a0001c0001t0002g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1518-10932_1518-10 others(270): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797242 | |||||||
| chr3:165797244 | C | CCTT | 4 | a0001c0001t0001g0024 a0001c0001t0001g0180 a0002c0002t0002g0057 others(1): Show |
5 | HG01261.hp1 HG01496.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-10936_1518-10 others(9): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797244 | |||||||
| chr3:165797246 | T | C | 5 | a0001c0001t0006g0221 a0001c0001t0006g0222 a0001c0001t0006g0223 others(2): Show |
5 | HG01433.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-10935A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797246 | |||||||
| chr3:165797246 | T | TTCTTCCC others(246): Show |
1 | a0001c0001t0003g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1518-10936_1518-10 others(259): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797246 | |||||||
| chr3:165797247 | TC | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(184): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1518-10937delG | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797247 | |||||||
| chr3:165797250 | T | C | 10 | a0001c0001t0001g0024 a0001c0001t0001g0180 a0001c0001t0003g0087 others(7): Show |
11 | HG01261.hp1 HG01433.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1518-10939A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797250 | |||||||
| chr3:165797250 | T | TCCC | 16 | a0001c0001t0001g0182 a0001c0001t0001g0193 a0001c0001t0001g0203 others(13): Show |
23 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1518-10940_1518-10 others(9): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797250 | |||||||
| chr3:165797250 | T | TTCTTCCC others(96): Show |
1 | a0001c0001t0007g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1518-10940_1518-10 others(109): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797250 | |||||||
| chr3:165797250 | T | TTCTTCCC others(169): Show |
1 | a0001c0001t0007g0137 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1518-10940_1518-10 others(182): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797250 | |||||||
| chr3:165797254 | C | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(3): Show |
8 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1518-10943G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797254 | |||||||
| chr3:165797254 | CT | C | 5 | a0001c0001t0006g0221 a0001c0001t0006g0222 a0001c0001t0006g0223 others(2): Show |
5 | HG01433.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-10944delA | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797254 | |||||||
| chr3:165797255 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1518-10944A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797255 | |||||||
| chr3:165797255 | T | TCCC | 4 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0117 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1518-10945_1518-10 others(9): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797255 | |||||||
| chr3:165797255 | T | TCCCTCCC others(312): Show |
2 | a0002c0002t0002g0054 a0002c0002t0002g0055 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1518-10945_1518-10 others(325): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797255 | |||||||
| chr3:165797255 | T | TCCCTCCC others(246): Show |
1 | a0001c0001t0003g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1518-10945_1518-10 others(259): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797255 | |||||||
| chr3:165797255 | T | TCCCTCCC others(192): Show |
6 | a0001c0001t0002g0236 a0001c0001t0002g0240 a0001c0001t0002g0241 others(3): Show |
6 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1518-10945_1518-10 others(205): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797255 | |||||||
| chr3:165797255 | T | TCCCTCCC others(177): Show |
2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01346.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1518-10945_1518-10 others(190): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797255 | |||||||
| chr3:165797255 | T | TCCCTCCC others(177): Show |
12 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0045 others(9): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1518-10945_1518-10 others(190): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797255 | |||||||
| chr3:165797255 | T | TCCCTCCC others(251): Show |
1 | a0001c0001t0003g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1518-10945_1518-10 others(264): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797255 | |||||||
| chr3:165797255 | T | TCCCTCCC others(250): Show |
2 | a0001c0001t0003g0052 a0001c0001t0003g0074 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1518-10945_1518-10 others(263): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797255 | |||||||
| chr3:165797255 | T | TCCCTCCC others(358): Show |
3 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0119 |
6 | HG02615.hp1 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1518-10945_1518-10 others(371): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797255 | |||||||
| chr3:165797255 | T | TCCCTCCC others(133): Show |
1 | a0001c0001t0001g0114 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1518-10945_1518-10 others(146): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797255 | |||||||
| chr3:165797257 | CT | C | 9 | a0001c0001t0001g0182 a0001c0001t0001g0193 a0002c0002t0004g0002 others(6): Show |
16 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1518-10947delA | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797257 | |||||||
| chr3:165797258 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(205): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1518-10947A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797258 | |||||||
| chr3:165797258 | T | TTCGTTCT others(321): Show |
6 | a0001c0001t0003g0004 a0001c0001t0003g0053 a0001c0001t0003g0073 others(3): Show |
7 | HG01243.hp1 HG01261.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1518-10948_1518-10 others(334): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797258 | |||||||
| chr3:165797258 | T | TTCGTTCT others(321): Show |
14 | a0001c0001t0003g0014 a0001c0001t0003g0072 a0001c0001t0003g0077 others(11): Show |
14 | HG00423.hp1 HG01069.hp1 HG03486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1518-10948_1518-10 others(334): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797258 | |||||||
| chr3:165797258 | T | TTCGTTCT others(395): Show |
1 | a0001c0001t0003g0014 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1518-10948_1518-10 others(408): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797258 | |||||||
| chr3:165797259 | T | C | 16 | a0001c0001t0001g0024 a0001c0001t0001g0180 a0001c0001t0001g0182 others(13): Show |
24 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1518-10948A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797259 | |||||||
| chr3:165797259 | T | TCCC | 87 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(84): Show |
110 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1518-10951_1518-10 others(9): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797259 | |||||||
| chr3:165797259 | T | TCCCCCCC others(170): Show |
1 | a0002c0002t0002g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1518-10949_1518-10 others(183): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797259 | |||||||
| chr3:165797259 | T | TCCCCCCC others(174): Show |
1 | a0001c0001t0001g0212 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1518-10949_1518-10 others(187): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797259 | |||||||
| chr3:165797259 | T | TCCCCCCT others(174): Show |
1 | a0001c0001t0001g0198 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1518-10949_1518-10 others(187): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797259 | |||||||
| chr3:165797259 | T | TCCCCCCT others(169): Show |
28 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0128 others(25): Show |
33 | HG00609.hp2 HG00621.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1518-10949_1518-10 others(182): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797259 | |||||||
| chr3:165797259 | T | TCCCCCCT others(333): Show |
1 | a0002c0002t0002g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1518-10949_1518-10 others(346): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797259 | |||||||
| chr3:165797259 | T | TCCCCCCT others(173): Show |
38 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(35): Show |
48 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1518-10949_1518-10 others(186): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797259 | |||||||
| chr3:165797259 | T | TCCCCCCT others(188): Show |
1 | a0001c0001t0001g0134 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1518-10949_1518-10 others(201): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797259 | |||||||
| chr3:165797259 | T | TCCCCCCT others(374): Show |
2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | NA18975.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1518-10949_1518-10 others(387): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797259 | |||||||
| chr3:165797259 | T | TCGTTCTT others(213): Show |
1 | a0001c0001t0001g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1518-10949_1518-10 others(226): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797259 | |||||||
| chr3:165797260 | C | CCT | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(2): Show |
7 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1518-10950_1518-10 others(8): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797260 | |||||||
| chr3:165797260 | C | CGTTCTTC others(267): Show |
1 | a0001c0001t0003g0033 | 2 | HG01255.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1518-10950_1518-10 others(280): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797260 | |||||||
| chr3:165797263 | T | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(5): Show |
11 | HG01255.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1518-10952A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797263 | |||||||
| chr3:165797264 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(175): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1518-10953A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797264 | |||||||
| chr3:165797267 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(4): Show |
10 | HG01255.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1518-10956A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797267 | |||||||
| chr3:165797268 | T | TCCTTCTT others(162): Show |
3 | a0001c0001t0006g0222 a0001c0001t0006g0223 a0001c0001t0006g0224 |
3 | HG01433.hp2 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1518-10958_1518-10 others(175): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797268 | |||||||
| chr3:165797268 | T | TCCTTCTT others(166): Show |
2 | a0001c0001t0006g0221 a0001c0001t0006g0225 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1518-10958_1518-10 others(179): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797268 | |||||||
| chr3:165797278 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(94): Show |
124 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.1518-10967G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797278 | |||||||
| chr3:165797280 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(94): Show |
124 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.1518-10969A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797280 | |||||||
| chr3:165797284 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0170 |
3 | HG03704.hp2 NA18975.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1518-10973G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797284 | |||||||
| chr3:165797302 | TC | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(3): Show |
8 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1518-10992delG | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797302 | |||||||
| chr3:165797303 | C | CCCCCCTC others(65): Show |
1 | a0001c0001t0001g0051 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1518-10993_1518-10 others(78): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797303 | |||||||
| chr3:165797306 | C | CCCT | 87 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(84): Show |
111 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1518-10996_1518-10 others(9): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797306 | |||||||
| chr3:165797306 | CCCCTT | C | 22 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0128 others(19): Show |
25 | HG00609.hp2 HG00621.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1518-11000_1518-10 others(11): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797306 | |||||||
| chr3:165797307 | C | CCTCCCTT others(4): Show |
1 | a0001c0001t0003g0033 | 2 | HG01255.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1518-10997_1518-10 others(17): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797307 | |||||||
| chr3:165797307 | CCCTT | C | 21 | a0001c0001t0003g0007 a0001c0001t0003g0040 a0001c0001t0003g0041 others(18): Show |
24 | HG01433.hp2 HG02055.hp2 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.1518-11000_1518-10 others(10): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797307 | |||||||
| chr3:165797310 | T | TCCCTTCC others(135): Show |
1 | a0002c0002t0002g0111 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1518-11000_1518-10 others(148): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797310 | |||||||
| chr3:165797310 | T | TCCCTTCC others(135): Show |
1 | a0001c0001t0001g0232 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1518-11000_1518-10 others(148): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797310 | |||||||
| chr3:165797311 | T | C | 2 | a0001c0001t0001g0232 a0002c0002t0002g0111 |
2 | HG00544.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1518-11000A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797311 | |||||||
| chr3:165797311 | T | TCCTTCCT others(159): Show |
1 | a0002c0002t0002g0068 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1518-11001_1518-11 others(172): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797311 | |||||||
| chr3:165797311 | T | TCCTTCCT others(158): Show |
16 | a0002c0002t0002g0037 a0002c0002t0002g0057 a0002c0002t0002g0062 others(13): Show |
16 | HG01978.hp2 HG02056.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.1518-11001_1518-11 others(171): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797311 | |||||||
| chr3:165797311 | T | TCCTTCCT others(85): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0182 |
2 | HG01074.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1518-11001_1518-11 others(98): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797311 | |||||||
| chr3:165797311 | T | TCCTTCCT others(132): Show |
1 | a0001c0001t0001g0024 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1518-11001_1518-11 others(145): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797311 | |||||||
| chr3:165797311 | T | TCCTTCCT others(132): Show |
3 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0180 |
3 | HG01175.hp2 HG02056.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1518-11001_1518-11 others(145): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797311 | |||||||
| chr3:165797311 | T | TCCTTCCT others(185): Show |
4 | a0001c0001t0001g0038 a0001c0001t0001g0168 a0001c0001t0001g0188 others(1): Show |
4 | HG01192.hp1 HG01256.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1518-11001_1518-11 others(198): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797311 | |||||||
| chr3:165797311 | T | TCCTTCCT others(127): Show |
1 | a0001c0001t0001g0031 | 2 | NA18973.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1518-11001_1518-11 others(140): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797311 | |||||||
| chr3:165797311 | T | TCCTTCCT others(131): Show |
56 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
77 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1518-11001_1518-11 others(144): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797311 | |||||||
| chr3:165797315 | T | TCCTTCTT others(127): Show |
5 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | HG00642.hp2 HG01106.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1518-11005_1518-11 others(140): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797315 | |||||||
| chr3:165797331 | C | CCCTCCCT others(37): Show |
1 | a0001c0001t0001g0114 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1518-11064_1518-11 others(50): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797331 | |||||||
| chr3:165797340 | C | T | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1518-11029G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797340 | |||||||
| chr3:165797592 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1518-11281A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797592 | |||||||
| chr3:165797743 | T | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | NA18971.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1518-11432A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797743 | |||||||
| chr3:165797835 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1518-11524T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797835 | |||||||
| chr3:165797933 | G | T | 9 | a0001c0001t0001g0114 a0001c0001t0002g0006 a0001c0001t0002g0019 others(6): Show |
12 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1518-11622C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797933 | |||||||
| chr3:165797972 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(195): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1518-11661C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165797972 | |||||||
| chr3:165798061 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0119 |
3 | HG02615.hp1 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1518-11750G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165798061 | |||||||
| chr3:165798762 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(126): Show |
159 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.1518-12451T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165798762 | |||||||
| chr3:165798826 | CA | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(195): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1518-12516delT | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165798826 | |||||||
| chr3:165798885 | A | C | 1 | a0001c0001t0003g0033 | 2 | HG01255.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1518-12574T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165798885 | |||||||
| chr3:165799267 | T | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1518-12956A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165799267 | |||||||
| chr3:165799403 | C | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0230 a0001c0001t0001g0231 |
5 | HG01167.hp2 HG01169.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-13092G>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165799403 | |||||||
| chr3:165799425 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1518-13114C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165799425 | |||||||
| chr3:165799802 | C | A | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1518-13491G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165799802 | |||||||
| chr3:165799944 | A | G | 5 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(2): Show |
5 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-13633T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165799944 | |||||||
| chr3:165800021 | C | CTTTAT | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1518-13715_1518-13 others(11): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165800021 | |||||||
| chr3:165800028 | A | G | 4 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0117 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1518-13717T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165800028 | |||||||
| chr3:165800115 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1518-13804T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165800115 | |||||||
| chr3:165800138 | A | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0006c0007t0001g0183 |
3 | HG00673.hp1 HG02056.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1518-13827T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165800138 | |||||||
| chr3:165800472 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1518-14161G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165800472 | |||||||
| chr3:165800524 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1518-14213A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165800524 | |||||||
| chr3:165800591 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1518-14280G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165800591 | |||||||
| chr3:165800638 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1518-14327A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165800638 | |||||||
| chr3:165800651 | A | G | 1 | a0002c0002t0002g0065 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1518-14340T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165800651 | |||||||
| chr3:165800908 | A | C | 1 | a0001c0001t0007g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1518-14597T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165800908 | |||||||
| chr3:165801506 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
171 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.1518-15195A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165801506 | |||||||
| chr3:165801539 | A | G | 1 | a0002c0002t0002g0064 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1518-15228T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165801539 | |||||||
| chr3:165801575 | G | A | 1 | a0002c0002t0002g0069 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1518-15264C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165801575 | |||||||
| chr3:165802106 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1518-15795C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165802106 | |||||||
| chr3:165802194 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1518-15883A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165802194 | |||||||
| chr3:165802458 | G | A | 1 | a0001c0001t0006g0223 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1518-16147C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165802458 | |||||||
| chr3:165802570 | C | G | 5 | a0001c0001t0003g0052 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-16259G>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165802570 | |||||||
| chr3:165802628 | G | GT | 18 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(15): Show |
26 | HG01175.hp2 HG01256.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1518-16318dupA | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165802628 | |||||||
| chr3:165802628 | GT | G | 7 | a0001c0001t0001g0231 a0001c0001t0002g0115 a0001c0001t0002g0116 others(4): Show |
7 | HG00621.hp2 HG01169.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.1518-16318delA | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165802628 | |||||||
| chr3:165802630 | T | G | 1 | a0002c0002t0002g0099 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1518-16319A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165802630 | |||||||
| chr3:165802647 | T | C | 1 | a0002c0002t0002g0100 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1518-16336A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165802647 | |||||||
| chr3:165802746 | T | G | 1 | a0001c0001t0002g0117 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1518-16435A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165802746 | |||||||
| chr3:165802998 | C | A | 1 | a0001c0001t0002g0243 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1518-16687G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165802998 | |||||||
| chr3:165803043 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0229 others(2): Show |
9 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1518-16732T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165803043 | |||||||
| chr3:165803088 | A | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0154 a0001c0001t0001g0179 others(1): Show |
5 | NA18956.hp2 NA18957.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-16777T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165803088 | |||||||
| chr3:165803411 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0179 a0001c0005t0001g0143 |
4 | NA18956.hp2 NA18957.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.1518-17100T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165803411 | |||||||
| chr3:165803443 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01346.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1518-17132T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165803443 | |||||||
| chr3:165803653 | A | T | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1518-17342T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165803653 | |||||||
| chr3:165803698 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1518-17387A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165803698 | |||||||
| chr3:165803833 | C | T | 1 | a0001c0001t0003g0092 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1518-17522G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165803833 | |||||||
| chr3:165803834 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0039 others(5): Show |
11 | HG02015.hp2 NA18939.hp1 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.1518-17523C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165803834 | |||||||
| chr3:165803893 | C | T | 1 | a0002c0002t0002g0104 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1518-17582G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165803893 | |||||||
| chr3:165804017 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1518-17706T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165804017 | |||||||
| chr3:165804028 | G | C | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1518-17717C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165804028 | |||||||
| chr3:165804056 | G | GA | 89 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.1518-17746dupT | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165804056 | |||||||
| chr3:165804155 | T | C | 3 | a0002c0002t0008g0120 a0002c0002t0008g0121 a0002c0002t0008g0122 |
3 | HG02055.hp1 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1518-17844A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165804155 | |||||||
| chr3:165804317 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1518-18006T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165804317 | |||||||
| chr3:165804578 | G | A | 2 | a0001c0001t0001g0023 a0001c0005t0001g0143 |
3 | NA18956.hp2 NA18957.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1518-18267C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165804578 | |||||||
| chr3:165804604 | C | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(8): Show |
19 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.1518-18293G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165804604 | |||||||
| chr3:165804717 | A | G | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1518-18406T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165804717 | |||||||
| chr3:165804816 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
171 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.1518-18505G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165804816 | |||||||
| chr3:165804925 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1518-18614C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165804925 | |||||||
| chr3:165805081 | C | A | 1 | a0001c0001t0002g0242 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1518-18770G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165805081 | |||||||
| chr3:165805279 | A | G | 1 | a0001c0001t0001g0030 | 2 | HG01192.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1518-18968T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165805279 | |||||||
| chr3:165805406 | A | T | 4 | a0003c0003t0005g0018 a0003c0003t0005g0112 a0003c0003t0005g0113 others(1): Show |
5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-19095T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165805406 | |||||||
| chr3:165805528 | A | C | 14 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0235 others(11): Show |
17 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1518-19217T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165805528 | |||||||
| chr3:165805597 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1518-19286A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165805597 | |||||||
| chr3:165805775 | T | C | 1 | a0001c0001t0003g0092 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1518-19464A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165805775 | |||||||
| chr3:165805878 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1518-19567G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165805878 | |||||||
| chr3:165806089 | C | T | 5 | a0001c0001t0003g0052 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-19778G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165806089 | |||||||
| chr3:165806243 | C | T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0191 others(2): Show |
7 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.1518-19932G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165806243 | |||||||
| chr3:165806368 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1518-20057C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165806368 | |||||||
| chr3:165806451 | G | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
171 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.1518-20140C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165806451 | |||||||
| chr3:165806479 | C | T | 3 | a0002c0002t0008g0120 a0002c0002t0008g0121 a0002c0002t0008g0122 |
3 | HG02055.hp1 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1518-20168G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165806479 | |||||||
| chr3:165806523 | A | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0134 |
3 | HG00140.hp1 HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1518-20212T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165806523 | |||||||
| chr3:165806536 | C | T | 1 | a0001c0001t0003g0053 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1518-20225G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165806536 | |||||||
| chr3:165806584 | GA | G | 4 | a0003c0003t0005g0018 a0003c0003t0005g0112 a0003c0003t0005g0113 others(1): Show |
5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-20274delT | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165806584 | |||||||
| chr3:165806895 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(126): Show |
159 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.1518-20584G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165806895 | |||||||
| chr3:165806913 | T | G | 1 | a0001c0001t0001g0172 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1518-20602A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165806913 | |||||||
| chr3:165807053 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1518-20742G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807053 | |||||||
| chr3:165807072 | G | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(109): Show |
139 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.1518-20761C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807072 | |||||||
| chr3:165807201 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1518-20890G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807201 | |||||||
| chr3:165807230 | A | G | 1 | a0001c0001t0003g0084 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1518-20919T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807230 | |||||||
| chr3:165807517 | G | GATTT | 18 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0027 others(15): Show |
22 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1518-21210_1518-21 others(10): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807517 | |||||||
| chr3:165807546 | A | T | 4 | a0001c0001t0003g0141 a0001c0001t0007g0136 a0001c0001t0007g0137 others(1): Show |
4 | HG02970.hp1 HG02970.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1518-21235T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807546 | |||||||
| chr3:165807550 | T | A | 2 | a0001c0001t0001g0129 a0001c0001t0003g0139 |
2 | HG00642.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1518-21239A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807550 | |||||||
| chr3:165807552 | A | T | 14 | a0001c0001t0001g0129 a0001c0001t0003g0007 a0001c0001t0003g0040 others(11): Show |
16 | HG00642.hp2 HG02559.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1518-21241T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807552 | |||||||
| chr3:165807556 | A | T | 1 | a0001c0001t0007g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1518-21245T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807556 | |||||||
| chr3:165807610 | G | C | 2 | a0002c0002t0002g0067 a0002c0002t0002g0068 |
2 | NA18975.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1518-21299C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807610 | |||||||
| chr3:165807645 | C | T | 1 | a0001c0001t0002g0032 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1518-21334G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807645 | |||||||
| chr3:165807649 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1518-21338C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807649 | |||||||
| chr3:165807750 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1518-21439C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807750 | |||||||
| chr3:165807880 | A | G | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0213 |
3 | HG00621.hp1 HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1518-21569T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807880 | |||||||
| chr3:165807967 | T | G | 1 | a0001c0001t0001g0220 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1517+21550A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807967 | |||||||
| chr3:165807973 | G | GT | 5 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0174 others(2): Show |
8 | HG01257.hp1 HG01261.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1517+21543dupA | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807973 | |||||||
| chr3:165807992 | G | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0176 a0001c0001t0001g0177 |
4 | HG02040.hp2 HG02155.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1517+21525C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165807992 | |||||||
| chr3:165808070 | G | T | 1 | a0002c0002t0002g0056 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1517+21447C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165808070 | |||||||
| chr3:165808074 | C | CA | 4 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1517+21442dupT | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165808074 | |||||||
| chr3:165808129 | G | T | 1 | a0001c0001t0003g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1517+21388C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165808129 | |||||||
| chr3:165808154 | T | G | 4 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0117 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517+21363A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165808154 | |||||||
| chr3:165808351 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(4): Show |
9 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1517+21166A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165808351 | |||||||
| chr3:165808782 | G | A | 243 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(240): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1517+20735C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165808782 | |||||||
| chr3:165808818 | A | G | 9 | a0001c0001t0001g0114 a0001c0001t0002g0006 a0001c0001t0002g0019 others(6): Show |
12 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1517+20699T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165808818 | |||||||
| chr3:165809056 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0048 |
3 | HG02258.hp1 HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1517+20461T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165809056 | |||||||
| chr3:165809083 | T | C | 4 | a0002c0002t0002g0107 a0002c0002t0002g0108 a0002c0002t0002g0109 others(1): Show |
4 | NA18968.hp1 NA18982.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517+20434A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165809083 | |||||||
| chr3:165809102 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(4): Show |
9 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1517+20415A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165809102 | |||||||
| chr3:165809146 | T | C | 9 | a0001c0001t0001g0114 a0001c0001t0002g0006 a0001c0001t0002g0019 others(6): Show |
12 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1517+20371A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165809146 | |||||||
| chr3:165809246 | G | A | 14 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0235 others(11): Show |
17 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1517+20271C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165809246 | |||||||
| chr3:165809262 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1517+20255C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165809262 | |||||||
| chr3:165809591 | C | A | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1517+19926G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165809591 | |||||||
| chr3:165809605 | TTGTATTA others(7): Show |
T | 1 | a0001c0001t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1517+19898_1517+19 others(20): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165809605 | |||||||
| chr3:165809785 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(126): Show |
159 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.1517+19732A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165809785 | |||||||
| chr3:165809952 | C | T | 1 | a0002c0002t0002g0062 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1517+19565G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165809952 | |||||||
| chr3:165810178 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1517+19339A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165810178 | |||||||
| chr3:165810666 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1517+18851A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165810666 | |||||||
| chr3:165810949 | C | A | 9 | a0001c0001t0001g0114 a0001c0001t0002g0006 a0001c0001t0002g0019 others(6): Show |
12 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1517+18568G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165810949 | |||||||
| chr3:165810984 | T | A | 1 | a0002c0002t0002g0101 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1517+18533A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165810984 | |||||||
| chr3:165811097 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1517+18420T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165811097 | |||||||
| chr3:165811175 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1517+18342T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165811175 | |||||||
| chr3:165811234 | A | G | 1 | a0002c0002t0004g0002 | 5 | HG01256.hp1 HG01258.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1517+18283T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165811234 | |||||||
| chr3:165811262 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(4): Show |
9 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1517+18255T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165811262 | |||||||
| chr3:165811283 | A | T | 1 | a0002c0002t0002g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1517+18234T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165811283 | |||||||
| chr3:165811323 | A | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1517+18194T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165811323 | |||||||
| chr3:165811367 | A | T | 1 | a0002c0002t0002g0097 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1517+18150T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165811367 | |||||||
| chr3:165811389 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01346.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1517+18128T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165811389 | |||||||
| chr3:165811433 | A | AGT | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1517+18082_1517+18 others(8): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165811433 | |||||||
| chr3:165811667 | T | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(4): Show |
9 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1517+17850A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165811667 | |||||||
| chr3:165811723 | T | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0115 others(4): Show |
10 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1517+17794A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165811723 | |||||||
| chr3:165811825 | G | A | 1 | a0002c0002t0002g0062 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1517+17692C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165811825 | |||||||
| chr3:165811908 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1517+17609G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165811908 | |||||||
| chr3:165812074 | C | T | 1 | a0001c0001t0003g0033 | 2 | HG01255.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1517+17443G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812074 | |||||||
| chr3:165812151 | C | T | 4 | a0003c0003t0005g0018 a0003c0003t0005g0112 a0003c0003t0005g0113 others(1): Show |
5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1517+17366G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812151 | |||||||
| chr3:165812235 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1517+17282G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812235 | |||||||
| chr3:165812236 | T | A | 1 | a0001c0001t0001g0175 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1517+17281A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812236 | |||||||
| chr3:165812286 | A | AT | 216 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(213): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1517+17230dupA | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812286 | |||||||
| chr3:165812344 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1517+17173G>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812344 | |||||||
| chr3:165812363 | C | T | 1 | a0002c0002t0002g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1517+17154G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812363 | |||||||
| chr3:165812499 | C | G | 1 | a0001c0001t0003g0079 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1517+17018G>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812499 | |||||||
| chr3:165812555 | T | C | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1517+16962A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812555 | |||||||
| chr3:165812615 | G | A | 1 | a0001c0001t0003g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1517+16902C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812615 | |||||||
| chr3:165812646 | A | T | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1517+16871T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812646 | |||||||
| chr3:165812718 | T | C | 1 | a0002c0002t0009g0102 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1517+16799A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812718 | |||||||
| chr3:165812724 | C | A | 3 | a0001c0001t0003g0072 a0001c0001t0003g0082 a0001c0001t0003g0083 |
3 | NA18983.hp1 NA18984.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1517+16793G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812724 | |||||||
| chr3:165812847 | T | A | 9 | a0001c0001t0001g0114 a0001c0001t0002g0006 a0001c0001t0002g0019 others(6): Show |
12 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1517+16670A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812847 | |||||||
| chr3:165812870 | G | A | 3 | a0002c0002t0008g0120 a0002c0002t0008g0121 a0002c0002t0008g0122 |
3 | HG02055.hp1 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1517+16647C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812870 | |||||||
| chr3:165812872 | G | T | 3 | a0002c0002t0008g0120 a0002c0002t0008g0121 a0002c0002t0008g0122 |
3 | HG02055.hp1 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1517+16645C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812872 | |||||||
| chr3:165812959 | A | G | 36 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0002c0002t0002g0005 others(33): Show |
39 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1517+16558T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165812959 | |||||||
| chr3:165813037 | C | A | 1 | a0001c0001t0002g0117 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1517+16480G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165813037 | |||||||
| chr3:165813060 | TC | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(126): Show |
159 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.1517+16456delG | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165813060 | |||||||
| chr3:165813071 | T | C | 1 | a0002c0002t0002g0103 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1517+16446A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165813071 | |||||||
| chr3:165813139 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1517+16378C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165813139 | |||||||
| chr3:165813142 | G | C | 1 | a0002c0002t0004g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1517+16375C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165813142 | |||||||
| chr3:165813438 | C | A | 3 | a0002c0002t0008g0120 a0002c0002t0008g0121 a0002c0002t0008g0122 |
3 | HG02055.hp1 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1517+16079G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165813438 | |||||||
| chr3:165813449 | G | C | 7 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0002c0002t0002g0054 others(4): Show |
7 | HG01346.hp1 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1517+16068C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165813449 | |||||||
| chr3:165813562 | C | T | 1 | a0001c0001t0001g0020 | 2 | NA18985.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1517+15955G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165813562 | |||||||
| chr3:165813701 | A | G | 1 | a0001c0001t0003g0140 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1517+15816T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165813701 | |||||||
| chr3:165813701 | A | T | 1 | a0001c0001t0003g0053 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1517+15816T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165813701 | |||||||
| chr3:165813838 | A | G | 1 | a0002c0002t0002g0062 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1517+15679T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165813838 | |||||||
| chr3:165813908 | A | G | 4 | a0003c0003t0005g0018 a0003c0003t0005g0112 a0003c0003t0005g0113 others(1): Show |
5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1517+15609T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165813908 | |||||||
| chr3:165814218 | A | AT | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1517+15298dupA | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165814218 | |||||||
| chr3:165814467 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1517+15050G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165814467 | |||||||
| chr3:165814525 | G | A | 9 | a0001c0001t0001g0114 a0001c0001t0002g0006 a0001c0001t0002g0019 others(6): Show |
12 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1517+14992C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165814525 | |||||||
| chr3:165814571 | A | G | 1 | a0002c0002t0008g0121 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517+14946T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165814571 | |||||||
| chr3:165814620 | A | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(202): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1517+14897T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165814620 | |||||||
| chr3:165814744 | T | G | 6 | a0002c0002t0002g0005 a0002c0002t0002g0095 a0002c0002t0002g0096 others(3): Show |
8 | NA18944.hp2 NA18945.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.1517+14773A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165814744 | |||||||
| chr3:165814864 | C | G | 1 | a0001c0001t0003g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1517+14653G>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165814864 | |||||||
| chr3:165815127 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1517+14390G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165815127 | |||||||
| chr3:165815247 | GA | G | 40 | a0001c0001t0001g0059 a0001c0001t0003g0091 a0002c0002t0002g0005 others(37): Show |
49 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1517+14269delT | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165815247 | |||||||
| chr3:165815247 | GAA | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(154): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1517+14268_1517+14 others(8): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165815247 | |||||||
| chr3:165815379 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1517+14138T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165815379 | |||||||
| chr3:165815821 | C | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1517+13696G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165815821 | |||||||
| chr3:165815953 | T | C | 1 | a0001c0001t0002g0243 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1517+13564A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165815953 | |||||||
| chr3:165816121 | T | C | 4 | a0003c0003t0005g0018 a0003c0003t0005g0112 a0003c0003t0005g0113 others(1): Show |
5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1517+13396A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165816121 | |||||||
| chr3:165816163 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(217): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1517+13354C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165816163 | |||||||
| chr3:165816194 | C | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0174 others(1): Show |
7 | HG01257.hp1 HG01261.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1517+13323G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165816194 | |||||||
| chr3:165816410 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0194 others(3): Show |
9 | HG00738.hp2 HG01175.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1517+13107C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165816410 | |||||||
| chr3:165816479 | G | A | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1517+13038C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165816479 | |||||||
| chr3:165816484 | ATG | A | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1517+13031_1517+13 others(8): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165816484 | |||||||
| chr3:165816561 | T | A | 8 | a0001c0001t0001g0044 a0001c0001t0001g0193 a0001c0001t0001g0196 others(5): Show |
8 | HG00423.hp2 HG02015.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.1517+12956A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165816561 | |||||||
| chr3:165816922 | C | A | 5 | a0001c0001t0006g0221 a0001c0001t0006g0222 a0001c0001t0006g0223 others(2): Show |
5 | HG01433.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1517+12595G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165816922 | |||||||
| chr3:165817267 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1517+12250T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165817267 | |||||||
| chr3:165817325 | G | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(195): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1517+12192C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165817325 | |||||||
| chr3:165817569 | A | G | 9 | a0001c0001t0001g0114 a0001c0001t0002g0006 a0001c0001t0002g0019 others(6): Show |
12 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1517+11948T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165817569 | |||||||
| chr3:165817656 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1517+11861C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165817656 | |||||||
| chr3:165817711 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1517+11806C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165817711 | |||||||
| chr3:165817713 | T | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(8): Show |
19 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.1517+11804A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165817713 | |||||||
| chr3:165817797 | A | G | 1 | a0002c0002t0002g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1517+11720T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165817797 | |||||||
| chr3:165817998 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(4): Show |
9 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1517+11519T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165817998 | |||||||
| chr3:165818530 | A | C | 2 | a0002c0002t0002g0095 a0002c0002t0002g0096 |
2 | NA18988.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1517+10987T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165818530 | |||||||
| chr3:165818560 | A | C | 1 | a0002c0002t0002g0060 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1517+10957T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165818560 | |||||||
| chr3:165818617 | A | G | 1 | a0001c0001t0003g0091 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1517+10900T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165818617 | |||||||
| chr3:165818813 | G | A | 7 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0002c0002t0002g0054 others(4): Show |
7 | HG01346.hp1 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1517+10704C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165818813 | |||||||
| chr3:165819074 | C | CT | 208 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(205): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1517+10442dupA | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165819074 | |||||||
| chr3:165819074 | C | CTT | 8 | a0001c0001t0001g0150 a0001c0001t0001g0185 a0001c0001t0001g0233 others(5): Show |
8 | HG02080.hp2 HG02572.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1517+10441_1517+10 others(8): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165819074 | |||||||
| chr3:165819224 | G | A | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1517+10293C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165819224 | |||||||
| chr3:165819274 | T | TC | 243 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(240): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1517+10242_1517+10 others(7): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165819274 | |||||||
| chr3:165819324 | C | T | 1 | a0001c0001t0003g0078 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1517+10193G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165819324 | |||||||
| chr3:165819343 | G | T | 1 | a0001c0001t0003g0083 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1517+10174C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165819343 | |||||||
| chr3:165819723 | T | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1517+9794A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165819723 | |||||||
| chr3:165819748 | T | TAGAG | 205 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(202): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1517+9768_1517+976 others(8): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165819748 | |||||||
| chr3:165819949 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02738.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1517+9568A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165819949 | |||||||
| chr3:165820001 | T | TA | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(4): Show |
9 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1517+9515dupT | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165820001 | |||||||
| chr3:165820111 | A | T | 1 | a0001c0001t0003g0077 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1517+9406T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165820111 | |||||||
| chr3:165820202 | T | TG | 129 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(126): Show |
159 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.1517+9314dupC | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165820202 | |||||||
| chr3:165820291 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1517+9226T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165820291 | |||||||
| chr3:165820582 | C | T | 3 | a0001c0001t0007g0136 a0001c0001t0007g0137 a0001c0001t0007g0138 |
3 | HG02970.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1517+8935G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165820582 | |||||||
| chr3:165820637 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1517+8880T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165820637 | |||||||
| chr3:165820680 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(195): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1517+8837C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165820680 | |||||||
| chr3:165821037 | T | TA | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1517+8479dupT | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821037 | |||||||
| chr3:165821236 | A | T | 1 | a0002c0002t0002g0060 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1517+8281T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821236 | |||||||
| chr3:165821267 | T | C | 4 | a0003c0003t0005g0018 a0003c0003t0005g0112 a0003c0003t0005g0113 others(1): Show |
5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1517+8250A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821267 | |||||||
| chr3:165821334 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
100 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1517+8183A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821334 | |||||||
| chr3:165821364 | T | C | 1 | a0002c0002t0002g0069 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1517+8153A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821364 | |||||||
| chr3:165821658 | T | C | 2 | a0001c0001t0002g0236 a0001c0001t0002g0245 |
2 | HG02280.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1517+7859A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821658 | |||||||
| chr3:165821807 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(195): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1517+7710G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821807 | |||||||
| chr3:165821822 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(195): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1517+7695C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821822 | |||||||
| chr3:165821843 | T | G | 2 | a0002c0002t0002g0054 a0002c0002t0002g0055 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1517+7674A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821843 | |||||||
| chr3:165821851 | C | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG02040.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1517+7666G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821851 | |||||||
| chr3:165821916 | TGGTGAA | T | 14 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0235 others(11): Show |
17 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1517+7595_1517+760 others(10): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821916 | |||||||
| chr3:165821923 | A | T | 14 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0235 others(11): Show |
17 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1517+7594T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821923 | |||||||
| chr3:165821928 | T | TTCA | 14 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0235 others(11): Show |
17 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1517+7588_1517+758 others(7): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821928 | |||||||
| chr3:165821929 | A | G | 14 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0235 others(11): Show |
17 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1517+7588T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821929 | |||||||
| chr3:165821933 | A | ACTTG | 14 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0235 others(11): Show |
17 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1517+7583_1517+758 others(8): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821933 | |||||||
| chr3:165821934 | T | A | 14 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0235 others(11): Show |
17 | HG00140.hp2 HG01106.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1517+7583A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165821934 | |||||||
| chr3:165822059 | C | T | 1 | a0002c0002t0008g0120 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1517+7458G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165822059 | |||||||
| chr3:165822154 | A | T | 36 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0002c0002t0002g0005 others(33): Show |
39 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1517+7363T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165822154 | |||||||
| chr3:165822466 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1517+7051C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165822466 | |||||||
| chr3:165822708 | A | T | 2 | a0001c0001t0002g0032 a0001c0001t0002g0237 |
3 | HG01891.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1517+6809T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165822708 | |||||||
| chr3:165823012 | T | C | 1 | a0001c0001t0002g0118 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1517+6505A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165823012 | |||||||
| chr3:165823255 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1517+6262A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165823255 | |||||||
| chr3:165823287 | A | G | 1 | a0001c0001t0003g0082 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1517+6230T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165823287 | |||||||
| chr3:165823550 | A | C | 1 | a0001c0001t0002g0236 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1517+5967T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165823550 | |||||||
| chr3:165823607 | C | T | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1517+5910G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165823607 | |||||||
| chr3:165823618 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0178 |
3 | HG02015.hp2 NA18945.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1517+5899A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165823618 | |||||||
| chr3:165823803 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(195): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1517+5714T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165823803 | |||||||
| chr3:165823819 | C | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(195): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1517+5698G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165823819 | |||||||
| chr3:165823934 | CT | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
210 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.1517+5582delA | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165823934 | |||||||
| chr3:165823934 | CTT | C | 46 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(43): Show |
49 | HG00099.hp2 HG00544.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1517+5581_1517+558 others(6): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165823934 | |||||||
| chr3:165824168 | T | A | 1 | a0001c0001t0001g0044 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1517+5349A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165824168 | |||||||
| chr3:165824225 | T | C | 1 | a0002c0002t0002g0069 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1517+5292A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165824225 | |||||||
| chr3:165824336 | A | C | 1 | a0001c0001t0002g0235 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1517+5181T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165824336 | |||||||
| chr3:165824419 | A | G | 1 | a0001c0001t0003g0040 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1517+5098T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165824419 | |||||||
| chr3:165824426 | G | T | 1 | a0001c0001t0003g0033 | 2 | HG01255.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1517+5091C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165824426 | |||||||
| chr3:165824465 | T | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(202): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1517+5052A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165824465 | |||||||
| chr3:165824566 | A | C | 36 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0002c0002t0002g0005 others(33): Show |
39 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1517+4951T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165824566 | |||||||
| chr3:165824568 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | NA18975.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1517+4949G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165824568 | |||||||
| chr3:165824642 | C | T | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1517+4875G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165824642 | |||||||
| chr3:165824667 | C | A | 2 | a0002c0002t0002g0054 a0002c0002t0002g0055 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1517+4850G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165824667 | |||||||
| chr3:165825285 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1517+4232T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165825285 | |||||||
| chr3:165825341 | TA | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(217): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1517+4175delT | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165825341 | |||||||
| chr3:165825632 | G | A | 1 | a0001c0001t0003g0033 | 2 | HG01255.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1517+3885C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165825632 | |||||||
| chr3:165825700 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02738.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1517+3817G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165825700 | |||||||
| chr3:165825806 | T | A | 2 | a0001c0001t0003g0087 a0001c0001t0003g0088 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1517+3711A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165825806 | |||||||
| chr3:165825921 | T | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1517+3596A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165825921 | |||||||
| chr3:165826110 | A | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0119 |
3 | HG02615.hp1 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1517+3407T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165826110 | |||||||
| chr3:165826514 | G | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
115 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.1517+3003C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165826514 | |||||||
| chr3:165826601 | T | C | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1517+2916A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165826601 | |||||||
| chr3:165826701 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1517+2816T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165826701 | |||||||
| chr3:165826886 | A | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(5): Show |
10 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1517+2631T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165826886 | |||||||
| chr3:165826942 | A | G | 3 | a0002c0002t0002g0017 a0002c0002t0002g0056 a0002c0002t0002g0057 |
4 | NA18946.hp1 NA18962.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1517+2575T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165826942 | |||||||
| chr3:165827121 | C | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG00609.hp1 HG02155.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1517+2396G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165827121 | |||||||
| chr3:165827157 | G | A | 1 | a0005c0004t0004g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1517+2360C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165827157 | |||||||
| chr3:165827223 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1517+2294G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165827223 | |||||||
| chr3:165827267 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(4): Show |
9 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1517+2250G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165827267 | |||||||
| chr3:165827363 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1517+2154A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165827363 | |||||||
| chr3:165827397 | A | C | 9 | a0001c0001t0001g0114 a0001c0001t0002g0006 a0001c0001t0002g0019 others(6): Show |
12 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1517+2120T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165827397 | |||||||
| chr3:165827608 | CA | C | 4 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0117 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517+1908delT | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165827608 | |||||||
| chr3:165827691 | A | G | 3 | a0002c0002t0008g0120 a0002c0002t0008g0121 a0002c0002t0008g0122 |
3 | HG02055.hp1 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1517+1826T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165827691 | |||||||
| chr3:165827759 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1517+1758G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165827759 | |||||||
| chr3:165827891 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1517+1626T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165827891 | |||||||
| chr3:165827981 | C | T | 1 | a0001c0001t0003g0072 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1517+1536G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165827981 | |||||||
| chr3:165828042 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1517+1475C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165828042 | |||||||
| chr3:165828242 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1517+1275A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165828242 | |||||||
| chr3:165828495 | G | T | 1 | a0001c0001t0001g0193 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1517+1022C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165828495 | |||||||
| chr3:165828731 | AG | A | 9 | a0001c0001t0001g0114 a0001c0001t0002g0006 a0001c0001t0002g0019 others(6): Show |
12 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1517+785delC | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165828731 | |||||||
| chr3:165828928 | A | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(202): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1517+589T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165828928 | |||||||
| chr3:165828974 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1517+543G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165828974 | |||||||
| chr3:165829179 | T | G | 1 | a0002c0002t0002g0109 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1517+338A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165829179 | |||||||
| chr3:165829420 | C | A | 4 | a0002c0002t0002g0107 a0002c0002t0002g0108 a0002c0002t0002g0109 others(1): Show |
4 | NA18968.hp1 NA18982.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517+97G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165829420 | |||||||
| chr3:165829434 | T | C | 2 | a0001c0001t0003g0089 a0001c0001t0003g0090 |
2 | NA18950.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1517+83A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 2/3 | chr3 | 165829434 | |||||||
| chr3:165831214 | A | G | 8 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0045 others(5): Show |
11 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8-173T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165831214 | |||||||
| chr3:165831312 | T | C | 1 | a0001c0001t0001g0026 | 2 | NA18952.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-8-271A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165831312 | |||||||
| chr3:165831591 | T | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0115 others(4): Show |
10 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-550A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165831591 | |||||||
| chr3:165831890 | A | T | 2 | a0002c0002t0002g0054 a0002c0002t0002g0055 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-8-849T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165831890 | |||||||
| chr3:165831973 | G | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0191 others(1): Show |
6 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-932C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165831973 | |||||||
| chr3:165832057 | C | A | 1 | a0001c0001t0002g0245 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-8-1016G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165832057 | |||||||
| chr3:165832178 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-8-1137A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165832178 | |||||||
| chr3:165832248 | C | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(89): Show |
119 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.-8-1207G>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165832248 | |||||||
| chr3:165832595 | G | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-8-1554C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165832595 | |||||||
| chr3:165832677 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-1636T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165832677 | |||||||
| chr3:165832834 | T | C | 13 | a0001c0001t0003g0007 a0001c0001t0003g0040 a0001c0001t0003g0041 others(10): Show |
15 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.-8-1793A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165832834 | |||||||
| chr3:165833004 | G | A | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-1963C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833004 | |||||||
| chr3:165833188 | A | G | 1 | a0002c0002t0002g0005 | 3 | NA18944.hp2 NA18945.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-8-2147T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833188 | |||||||
| chr3:165833230 | T | C | 7 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG00738.hp1 HG01192.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-2189A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833230 | |||||||
| chr3:165833296 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
90 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.-8-2255A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833296 | |||||||
| chr3:165833355 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-8-2314G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833355 | |||||||
| chr3:165833366 | A | G | 4 | a0003c0003t0005g0018 a0003c0003t0005g0112 a0003c0003t0005g0113 others(1): Show |
5 | HG01496.hp2 HG02055.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2325T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833366 | |||||||
| chr3:165833453 | T | C | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-8-2412A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833453 | |||||||
| chr3:165833472 | G | A | 1 | a0002c0002t0002g0110 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-8-2431C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833472 | |||||||
| chr3:165833489 | G | A | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-8-2448C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833489 | |||||||
| chr3:165833736 | C | A | 1 | a0001c0001t0001g0031 | 2 | NA18973.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-8-2695G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833736 | |||||||
| chr3:165833776 | G | A | 1 | a0001c0001t0003g0091 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-8-2735C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833776 | |||||||
| chr3:165833785 | AT | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(142): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-8-2745delA | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833785 | |||||||
| chr3:165833828 | A | G | 1 | a0001c0001t0003g0053 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-8-2787T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833828 | |||||||
| chr3:165833861 | C | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0229 others(2): Show |
9 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-2820G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833861 | |||||||
| chr3:165833961 | A | C | 2 | a0003c0003t0005g0112 a0003c0003t0005g0234 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-8-2920T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165833961 | |||||||
| chr3:165834140 | T | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(5): Show |
10 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-3099A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165834140 | |||||||
| chr3:165834172 | A | G | 1 | a0001c0001t0003g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-3131T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165834172 | |||||||
| chr3:165834213 | CACTTA | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(152): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-9+3096_-9+3100del others(5): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165834213 | |||||||
| chr3:165834581 | C | T | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9+2733G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165834581 | |||||||
| chr3:165834674 | T | C | 1 | a0001c0001t0003g0092 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-9+2640A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165834674 | |||||||
| chr3:165834724 | T | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(161): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-9+2590A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165834724 | |||||||
| chr3:165835028 | G | C | 20 | a0002c0002t0002g0005 a0002c0002t0002g0037 a0002c0002t0002g0094 others(17): Show |
22 | HG00621.hp2 HG02040.hp1 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.-9+2286C>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165835028 | |||||||
| chr3:165835049 | C | A | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(8): Show |
19 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.-9+2265G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165835049 | |||||||
| chr3:165835177 | A | T | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9+2137T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165835177 | |||||||
| chr3:165835196 | C | CTT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(161): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-9+2116_-9+2117dup others(2): Show |
BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165835196 | |||||||
| chr3:165835395 | G | A | 1 | a0002c0002t0002g0111 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-9+1919C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165835395 | |||||||
| chr3:165835486 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(161): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-9+1828G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165835486 | |||||||
| chr3:165835530 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(161): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-9+1784T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165835530 | |||||||
| chr3:165835546 | T | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(161): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-9+1768A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165835546 | |||||||
| chr3:165835755 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-9+1559A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165835755 | |||||||
| chr3:165835799 | G | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(161): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-9+1515C>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165835799 | |||||||
| chr3:165835858 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(161): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-9+1456G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165835858 | |||||||
| chr3:165835876 | A | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(161): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-9+1438T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165835876 | |||||||
| chr3:165835950 | T | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(5): Show |
10 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+1364A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165835950 | |||||||
| chr3:165836072 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(161): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-9+1242T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165836072 | |||||||
| chr3:165836077 | G | A | 1 | a0001c0001t0010g0246 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9+1237C>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165836077 | |||||||
| chr3:165836106 | T | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(161): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-9+1208A>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165836106 | |||||||
| chr3:165836148 | C | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-9+1166G>T | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165836148 | |||||||
| chr3:165836387 | T | G | 1 | a0001c0001t0001g0233 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-9+927A>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165836387 | |||||||
| chr3:165836433 | A | G | 24 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0047 others(21): Show |
30 | HG00140.hp2 HG01106.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.-9+881T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165836433 | |||||||
| chr3:165836530 | A | G | 1 | a0001c0001t0002g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-9+784T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165836530 | |||||||
| chr3:165836740 | A | C | 5 | a0001c0001t0001g0044 a0002c0002t0004g0002 a0002c0002t0004g0003 others(2): Show |
11 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9+574T>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165836740 | |||||||
| chr3:165836779 | T | C | 16 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0235 others(13): Show |
20 | HG00140.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-9+535A>G | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165836779 | |||||||
| chr3:165836937 | A | T | 1 | a0001c0001t0003g0014 | 2 | NA18993.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-9+377T>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165836937 | |||||||
| chr3:165836946 | A | G | 4 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+368T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165836946 | |||||||
| chr3:165836974 | A | G | 1 | a0001c0001t0001g0039 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-9+340T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165836974 | |||||||
| chr3:165837050 | A | G | 4 | a0002c0002t0004g0002 a0002c0002t0004g0003 a0002c0002t0004g0036 others(1): Show |
10 | HG01256.hp1 HG01258.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9+264T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165837050 | |||||||
| chr3:165837100 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-9+214T>C | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165837100 | |||||||
| chr3:165837165 | C | T | 1 | a0002c0002t0002g0037 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-9+149G>A | BCHE | ENSG00000114200.10 | transcript | ENST00000264381.8 | protein_coding | 1/3 | chr3 | 165837165 |