Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8315 |
| ensemblid | ENSG00000089234.16 |
| hgncid | 1099 |
| symbol | BRAP |
| name | BRCA1 associated protein |
| refseq_nuc | NM_006768.5 |
| refseq_prot | NP_006759.3 |
| ensembl_nuc | ENST00000419234.9 |
| ensembl_prot | ENSP00000403524.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 111642146 |
| end | 111685956 |
| strand | - |
| ver | v1.2 |
| region | chr12:111642146-111685956 |
| region5000 | chr12:111637146-111690956 |
| regionname0 | BRAP_chr12_111642146_111685956 |
| regionname5000 | BRAP_chr12_111637146_111690956 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 592 | 363 | 90 | 61 | 160 | 8 | 42 | 132 | BRAP_chr12_111637146_111690956 | BRAP | MSVSL others(587): Show |
chr12 | 111637146 | 111690956 |
| a0002 | 0/0 | 592 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | MSVSL others(587): Show |
chr12 | 111637146 | 111690956 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1776 | 325 | 81 | 60 | 132 | 8 | 42 | BRAP_chr12_111637146_111690956 | BRAP | ATGAG others(1771): Show |
chr12 | 111637146 | 111690956 | ||
| a0001c0002 | 0/0 | 1776 | 27 | 0 | 0 | 27 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | ATGAG others(1771): Show |
chr12 | 111637146 | 111690956 | ||
| a0001c0003 | 0/0 | 1776 | 6 | 6 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | ATGAG others(1771): Show |
chr12 | 111637146 | 111690956 | ||
| a0001c0004 | 0/0 | 1776 | 2 | 1 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | ATGAG others(1771): Show |
chr12 | 111637146 | 111690956 | ||
| a0001c0006 | 0/0 | 1776 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | ATGAG others(1771): Show |
chr12 | 111637146 | 111690956 | ||
| a0001c0007 | 0/0 | 1776 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | ATGAG others(1771): Show |
chr12 | 111637146 | 111690956 | ||
| a0001c0008 | 0/0 | 1776 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | ATGAG others(1771): Show |
chr12 | 111637146 | 111690956 | ||
| a0002c0005 | 0/0 | 1776 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | ATGAG others(1771): Show |
chr12 | 111637146 | 111690956 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3996 | 316 | 79 | 59 | 128 | 8 | 41 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0001t0003 | 0/0 | 3996 | 2 | 0 | 0 | 2 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0001t0005 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0001t0006 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0001t0007 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0001t0008 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0001t0009 | 0/0 | 3996 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0001t0010 | 0/1 | 3996 | 1 | 0 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0001t0011 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0002t0001 | 0/0 | 3996 | 26 | 0 | 0 | 26 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0002t0004 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTGGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0003t0002 | 0/0 | 3996 | 6 | 6 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0004t0002 | 0/0 | 3996 | 2 | 1 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0006t0001 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0007t0001 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0001c0008t0001 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| a0002c0005t0001 | 0/0 | 3996 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | GTTGT others(3991): Show |
chr12 | 111637146 | 111690956 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0003 | 0/0 | 6 | 2 | 4 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0008 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0307 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0008g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0009g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0010g0306 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0001t0011g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0003t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0003t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0003t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0003t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0003t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0004t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0004t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0006t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0007t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0001c0008t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| a0002c0005t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0311 | EUR | GBR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | FIN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0304 | EUR | FIN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | CHS | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | CHS | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00738 | hp1 | a0001 | c0001 | t0009 | g0310 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01496 | hp2 | a0002 | c0005 | t0001 | g0251 | AMR | CLM | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01943 | hp2 | a0001 | c0004 | t0002 | g0223 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02257 | hp1 | a0001 | c0003 | t0002 | g0228 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0277 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0225 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0227 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02965 | hp1 | a0001 | c0004 | t0002 | g0222 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0245 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0226 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03453 | hp1 | a0001 | c0008 | t0001 | g0201 | AFR | MSL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0244 | AFR | MSL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | STU | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | YRI | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18968 | hp2 | a0001 | c0001 | t0008 | g0183 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18973 | hp1 | a0001 | c0002 | t0004 | g0031 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18985 | hp1 | a0001 | c0001 | t0011 | g0071 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19030 | hp1 | a0001 | c0003 | t0002 | g0224 | AFR | LWK | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19083 | hp1 | a0001 | c0007 | t0001 | g0298 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ASW | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0229 | AFR | ASW | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | GIH | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | GIH | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0231 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | USA | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | USA | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | USA | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | USA | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0010 | g0306 | REF | REF | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0307 | REF | REF | BRAP_chr12_111637146_111690956 | BRAP | chr12 | 111637146 | 111690956 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111683305 | C | T | 1 | a0002 | 1 | HG01496.hp2 | missense_variant&splice_region_variant | MODERATE | c.85G>A | p.Gly29Arg | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/12 | 249/3996 | 85/1779 | 29/592 | chr12 | 111683305 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111650001 | C | T | 2 | a0001c0003 a0001c0004 |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
synonymous_variant | LOW | c.1353G>A | p.Lys451Lys | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/12 | 1517/3996 | 1353/1779 | 451/592 | chr12 | 111650001 | |||
| chr12:111659295 | G | A | 1 | a0001c0007 | 1 | NA19083.hp1 | synonymous_variant | LOW | c.1023C>T | p.Val341Val | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 8/12 | 1187/3996 | 1023/1779 | 341/592 | chr12 | 111659295 | |||
| chr12:111659298 | A | G | 1 | a0001c0006 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1020T>C | p.Tyr340Tyr | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 8/12 | 1184/3996 | 1020/1779 | 340/592 | chr12 | 111659298 | |||
| chr12:111665785 | G | A | 2 | a0001c0003 a0001c0004 |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
splice_region_variant&synonymous_variant | LOW | c.750C>T | p.Gly250Gly | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/12 | 914/3996 | 750/1779 | 250/592 | chr12 | 111665785 | |||
| chr12:111672685 | T | C | 1 | a0001c0002 | 27 | HG00438.hp1 HG00544.hp2 HG02132.hp2 others(24): Show |
synonymous_variant | LOW | c.723A>G | p.Arg241Arg | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/12 | 887/3996 | 723/1779 | 241/592 | chr12 | 111672685 | |||
| chr12:111679205 | A | G | 2 | a0001c0003 a0001c0004 |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
synonymous_variant | LOW | c.579T>C | p.Ile193Ile | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/12 | 743/3996 | 579/1779 | 193/592 | chr12 | 111679205 | |||
| chr12:111683264 | G | A | 1 | a0001c0003 | 6 | HG02257.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
synonymous_variant | LOW | c.126C>T | p.Ala42Ala | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/12 | 290/3996 | 126/1779 | 42/592 | chr12 | 111683264 | |||
| chr12:111683306 | G | A | 1 | a0001c0008 | 1 | HG03453.hp1 | splice_region_variant&synonymous_variant | LOW | c.84C>T | p.Ala28Ala | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/12 | 248/3996 | 84/1779 | 28/592 | chr12 | 111683306 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111642242 | G | C | 1 | a0001c0001t0006 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1957C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 12/12 | 1957 | chr12 | 111642242 | ||||||
| chr12:111642296 | A | T | 2 | a0001c0003t0002 a0001c0004t0002 |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1903T>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 12/12 | 1903 | chr12 | 111642296 | ||||||
| chr12:111642542 | T | G | 1 | a0001c0001t0007 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1657A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 12/12 | 1657 | chr12 | 111642542 | ||||||
| chr12:111642679 | T | C | 1 | a0001c0001t0008 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1520A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 12/12 | 1520 | chr12 | 111642679 | ||||||
| chr12:111642865 | T | C | 1 | a0001c0001t0009 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1334A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 12/12 | 1334 | chr12 | 111642865 | ||||||
| chr12:111643098 | A | G | 2 | a0001c0003t0002 a0001c0004t0002 |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1101T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 12/12 | 1101 | chr12 | 111643098 | ||||||
| chr12:111643491 | C | T | 1 | a0001c0001t0005 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*708G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 12/12 | 708 | chr12 | 111643491 | ||||||
| chr12:111643612 | T | C | 1 | a0001c0001t0011 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*587A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 12/12 | 587 | chr12 | 111643612 | ||||||
| chr12:111643780 | G | T | 1 | a0001c0001t0003 | 2 | NA18979.hp1 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*419C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 12/12 | 419 | chr12 | 111643780 | ||||||
| chr12:111685954 | A | C | 1 | a0001c0002t0004 | 1 | NA18973.hp1 | 5_prime_UTR_variant | MODIFIER | c.-162T>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/12 | 162 | chr12 | 111685954 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111644660 | T | A | 1 | a0001c0001t0001g0312 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1416-98A>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111644660 | |||||||
| chr12:111644677 | C | T | 9 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0211 others(6): Show |
9 | HG01884.hp2 HG02976.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.1416-115G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111644677 | |||||||
| chr12:111644689 | C | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1416-127G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111644689 | |||||||
| chr12:111644786 | C | T | 1 | a0001c0002t0001g0172 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1416-224G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111644786 | |||||||
| chr12:111644841 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1416-279G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111644841 | |||||||
| chr12:111644842 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1416-280G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111644842 | |||||||
| chr12:111644844 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1416-282G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111644844 | |||||||
| chr12:111644845 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1416-283G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111644845 | |||||||
| chr12:111644883 | A | G | 3 | a0001c0001t0001g0061 a0001c0001t0001g0073 a0001c0008t0001g0201 |
3 | HG03453.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1416-321T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111644883 | |||||||
| chr12:111644932 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1416-370A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111644932 | |||||||
| chr12:111644988 | C | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1416-426G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111644988 | |||||||
| chr12:111645005 | T | C | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1416-443A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111645005 | |||||||
| chr12:111645130 | G | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1416-568C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111645130 | |||||||
| chr12:111645357 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1416-795C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111645357 | |||||||
| chr12:111645358 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0252 others(7): Show |
17 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1416-796G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111645358 | |||||||
| chr12:111645415 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1416-853T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111645415 | |||||||
| chr12:111645596 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0114 a0001c0001t0001g0125 others(1): Show |
6 | HG02965.hp2 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1416-1034G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111645596 | |||||||
| chr12:111645680 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1416-1118C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111645680 | |||||||
| chr12:111645814 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0214 |
2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1416-1252G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111645814 | |||||||
| chr12:111645830 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1416-1268T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111645830 | |||||||
| chr12:111645859 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0248 |
3 | HG02109.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1416-1297C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111645859 | |||||||
| chr12:111645887 | G | C | 1 | a0001c0006t0001g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1416-1325C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111645887 | |||||||
| chr12:111645981 | T | C | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1416-1419A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111645981 | |||||||
| chr12:111646079 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1416-1517A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111646079 | |||||||
| chr12:111646277 | C | A | 1 | a0001c0001t0006g0245 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1416-1715G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111646277 | |||||||
| chr12:111646704 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1416-2142G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111646704 | |||||||
| chr12:111646792 | C | A | 1 | a0001c0001t0001g0037 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1416-2230G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111646792 | |||||||
| chr12:111647030 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1416-2468G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111647030 | |||||||
| chr12:111647362 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1415+2577C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111647362 | |||||||
| chr12:111647373 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | NA18967.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1415+2566T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111647373 | |||||||
| chr12:111647424 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1415+2515C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111647424 | |||||||
| chr12:111647692 | T | C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(30): Show |
49 | HG00438.hp1 HG00544.hp2 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.1415+2247A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111647692 | |||||||
| chr12:111647820 | C | T | 35 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0065 others(32): Show |
38 | HG01081.hp2 HG01099.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1415+2119G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111647820 | |||||||
| chr12:111648075 | G | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1415+1864C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111648075 | |||||||
| chr12:111648295 | T | C | 83 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(80): Show |
91 | HG00099.hp1 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1415+1644A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111648295 | |||||||
| chr12:111648315 | C | G | 9 | a0001c0001t0001g0291 a0001c0003t0002g0224 a0001c0003t0002g0225 others(6): Show |
9 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1415+1624G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111648315 | |||||||
| chr12:111648385 | GGGTGGAT others(307): Show |
G | 1 | a0001c0001t0001g0187 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1415+1240_1415+155 others(4): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111648385 | |||||||
| chr12:111648410 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1415+1529C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111648410 | |||||||
| chr12:111648466 | A | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1415+1473T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111648466 | |||||||
| chr12:111648489 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0128 a0001c0001t0001g0185 |
3 | HG02602.hp2 HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1415+1450C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111648489 | |||||||
| chr12:111648567 | G | A | 1 | a0001c0006t0001g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1415+1372C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111648567 | |||||||
| chr12:111648567 | G | C | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1415+1372C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111648567 | |||||||
| chr12:111648629 | G | C | 1 | a0001c0001t0001g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1415+1310C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111648629 | |||||||
| chr12:111648699 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(197): Show |
237 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(234): Show |
intron_variant | MODIFIER | c.1415+1240T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111648699 | |||||||
| chr12:111648724 | G | A | 1 | a0002c0005t0001g0251 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1415+1215C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111648724 | |||||||
| chr12:111648770 | CA | C | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1415+1168delT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111648770 | |||||||
| chr12:111649006 | C | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(197): Show |
237 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(234): Show |
intron_variant | MODIFIER | c.1415+933G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111649006 | |||||||
| chr12:111649021 | C | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1415+918G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111649021 | |||||||
| chr12:111649021 | C | CA | 7 | a0001c0001t0001g0078 a0001c0001t0001g0092 a0001c0001t0001g0105 others(4): Show |
7 | HG00597.hp2 HG02738.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1415+917dupT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111649021 | |||||||
| chr12:111649024 | A | C | 1 | a0001c0001t0001g0111 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1415+915T>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111649024 | |||||||
| chr12:111649178 | A | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1415+761T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111649178 | |||||||
| chr12:111649586 | G | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0066 |
2 | NA19081.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1415+353C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111649586 | |||||||
| chr12:111649737 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0295 |
2 | NA18941.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1415+202C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111649737 | |||||||
| chr12:111649784 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1415+155C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 11/11 | chr12 | 111649784 | |||||||
| chr12:111650296 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1312-254G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111650296 | |||||||
| chr12:111650370 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1312-328T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111650370 | |||||||
| chr12:111650422 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0304 |
2 | HG00323.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1312-380G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111650422 | |||||||
| chr12:111650436 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1312-394A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111650436 | |||||||
| chr12:111650450 | G | C | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-408C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111650450 | |||||||
| chr12:111650485 | C | T | 2 | a0001c0001t0001g0208 a0001c0003t0002g0229 |
2 | HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1312-443G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111650485 | |||||||
| chr12:111650947 | C | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-905G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111650947 | |||||||
| chr12:111650962 | T | G | 1 | a0001c0003t0002g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1312-920A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111650962 | |||||||
| chr12:111651056 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1312-1014T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651056 | |||||||
| chr12:111651150 | CCAGGGAT others(50): Show |
C | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1165_1312-110 others(61): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651150 | |||||||
| chr12:111651208 | C | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1166G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651208 | |||||||
| chr12:111651210 | C | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1168G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651210 | |||||||
| chr12:111651216 | G | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1174C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651216 | |||||||
| chr12:111651217 | C | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1175G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651217 | |||||||
| chr12:111651218 | A | ATAT | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1177_1312-117 others(7): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651218 | |||||||
| chr12:111651219 | C | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1177G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651219 | |||||||
| chr12:111651222 | G | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1180C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651222 | |||||||
| chr12:111651223 | C | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1181G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651223 | |||||||
| chr12:111651225 | T | TTAA | 5 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
5 | HG02622.hp1 HG02897.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312-1186_1312-118 others(7): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651225 | |||||||
| chr12:111651225 | T | TTAATAA | 65 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
73 | HG00099.hp1 HG00597.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.1312-1189_1312-118 others(10): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651225 | |||||||
| chr12:111651225 | T | TTAATAAT others(2): Show |
12 | a0001c0001t0001g0058 a0001c0001t0001g0076 a0001c0001t0001g0093 others(9): Show |
12 | HG00735.hp1 HG01081.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1312-1192_1312-118 others(13): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651225 | |||||||
| chr12:111651225 | T | TTAATAAT others(5): Show |
6 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0079 others(3): Show |
6 | HG02132.hp1 HG02523.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.1312-1195_1312-118 others(16): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651225 | |||||||
| chr12:111651225 | T | TTAATAAT others(11): Show |
1 | a0001c0001t0001g0181 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1312-1201_1312-118 others(22): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651225 | |||||||
| chr12:111651225 | TTAA | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(98): Show |
131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1312-1186_1312-118 others(7): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651225 | |||||||
| chr12:111651226 | T | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1184A>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651226 | |||||||
| chr12:111651227 | A | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1185T>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651227 | |||||||
| chr12:111651230 | A | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1188T>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651230 | |||||||
| chr12:111651233 | A | AT | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1192_1312-119 others(5): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651233 | |||||||
| chr12:111651256 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(61): Show |
89 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1312-1214A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651256 | |||||||
| chr12:111651261 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1312-1219G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651261 | |||||||
| chr12:111651264 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1312-1222C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651264 | |||||||
| chr12:111651394 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1312-1352G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651394 | |||||||
| chr12:111651459 | C | T | 22 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0116 others(19): Show |
22 | HG01993.hp1 HG02074.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.1312-1417G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651459 | |||||||
| chr12:111651474 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1312-1432A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651474 | |||||||
| chr12:111651529 | A | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1487T>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651529 | |||||||
| chr12:111651536 | C | CA | 9 | a0001c0001t0001g0313 a0001c0003t0002g0224 a0001c0003t0002g0225 others(6): Show |
9 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1312-1495dupT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651536 | |||||||
| chr12:111651635 | C | CT | 12 | a0001c0001t0001g0048 a0001c0001t0001g0079 a0001c0001t0001g0103 others(9): Show |
12 | HG00544.hp1 HG01934.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.1312-1594dupA | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651635 | |||||||
| chr12:111651635 | C | CTTT | 7 | a0001c0003t0002g0225 a0001c0003t0002g0226 a0001c0003t0002g0227 others(4): Show |
7 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1312-1596_1312-159 others(7): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651635 | |||||||
| chr12:111651635 | CT | C | 13 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0050 others(10): Show |
13 | HG00323.hp1 HG01169.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1312-1594delA | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651635 | |||||||
| chr12:111651715 | A | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-1673T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651715 | |||||||
| chr12:111651882 | C | T | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0238 others(1): Show |
4 | HG01243.hp1 HG02630.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312-1840G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651882 | |||||||
| chr12:111651887 | C | T | 1 | a0001c0003t0002g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1312-1845G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651887 | |||||||
| chr12:111651965 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1312-1923C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111651965 | |||||||
| chr12:111652218 | C | A | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1312-2176G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111652218 | |||||||
| chr12:111652276 | T | G | 1 | a0001c0001t0001g0221 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1312-2234A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111652276 | |||||||
| chr12:111652293 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1312-2251C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111652293 | |||||||
| chr12:111652371 | C | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1312-2329G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111652371 | |||||||
| chr12:111652632 | C | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-2590G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111652632 | |||||||
| chr12:111652772 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1312-2730C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111652772 | |||||||
| chr12:111652960 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1311+2606A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111652960 | |||||||
| chr12:111652975 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(160): Show |
199 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.1311+2591G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111652975 | |||||||
| chr12:111653010 | A | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(198): Show |
238 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(235): Show |
intron_variant | MODIFIER | c.1311+2556T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111653010 | |||||||
| chr12:111653440 | G | A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG01099.hp1 HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1311+2126C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111653440 | |||||||
| chr12:111653552 | C | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0042 others(11): Show |
15 | HG00140.hp2 HG00738.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1311+2014G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111653552 | |||||||
| chr12:111653597 | A | G | 1 | a0001c0001t0001g0311 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1311+1969T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111653597 | |||||||
| chr12:111653665 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0073 a0001c0008t0001g0201 |
3 | HG03453.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1311+1901C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111653665 | |||||||
| chr12:111653678 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1311+1888C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111653678 | |||||||
| chr12:111653785 | C | G | 1 | a0001c0001t0001g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1311+1781G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111653785 | |||||||
| chr12:111653905 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1311+1661A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111653905 | |||||||
| chr12:111654052 | A | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1311+1514T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654052 | |||||||
| chr12:111654149 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1311+1417G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654149 | |||||||
| chr12:111654270 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1311+1296A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654270 | |||||||
| chr12:111654317 | C | CT | 7 | a0001c0001t0001g0036 a0001c0001t0001g0122 a0001c0001t0001g0213 others(4): Show |
7 | HG00544.hp1 HG01175.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1311+1248dupA | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654317 | |||||||
| chr12:111654317 | CTTT | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0033 others(6): Show |
10 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1311+1246_1311+124 others(7): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654317 | |||||||
| chr12:111654333 | T | G | 1 | a0001c0001t0001g0237 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1311+1233A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654333 | |||||||
| chr12:111654472 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1311+1094G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654472 | |||||||
| chr12:111654506 | GGGTTTC | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1311+1054_1311+105 others(10): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654506 | |||||||
| chr12:111654576 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1311+990T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654576 | |||||||
| chr12:111654658 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1311+908C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654658 | |||||||
| chr12:111654682 | C | G | 1 | a0001c0001t0001g0134 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1311+884G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654682 | |||||||
| chr12:111654715 | G | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0127 |
2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1311+851C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654715 | |||||||
| chr12:111654752 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0069 |
3 | HG02055.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1311+814T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654752 | |||||||
| chr12:111654761 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0085 a0001c0001t0001g0087 others(2): Show |
6 | NA18946.hp1 NA18950.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1311+805G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654761 | |||||||
| chr12:111654764 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02145.hp1 HG02622.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1311+802G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654764 | |||||||
| chr12:111654794 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0164 |
2 | NA18943.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1311+772G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111654794 | |||||||
| chr12:111655092 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1311+474C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111655092 | |||||||
| chr12:111655110 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1311+456G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111655110 | |||||||
| chr12:111655274 | G | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(160): Show |
199 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.1311+292C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111655274 | |||||||
| chr12:111655334 | TA | T | 82 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
90 | HG00099.hp1 HG00597.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.1311+231delT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 10/11 | chr12 | 111655334 | |||||||
| chr12:111655854 | G | T | 1 | a0001c0001t0001g0268 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1222-199C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111655854 | |||||||
| chr12:111656140 | C | T | 1 | a0001c0001t0005g0277 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1222-485G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111656140 | |||||||
| chr12:111656162 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1222-507C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111656162 | |||||||
| chr12:111656163 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA19004.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1222-508A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111656163 | |||||||
| chr12:111656363 | T | C | 1 | a0001c0003t0002g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1222-708A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111656363 | |||||||
| chr12:111656587 | T | C | 1 | a0001c0006t0001g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1222-932A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111656587 | |||||||
| chr12:111656604 | A | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222-949T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111656604 | |||||||
| chr12:111656614 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1222-959C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111656614 | |||||||
| chr12:111656631 | C | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222-976G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111656631 | |||||||
| chr12:111656641 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1222-986A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111656641 | |||||||
| chr12:111656703 | A | G | 30 | a0001c0001t0001g0027 a0001c0001t0001g0207 a0001c0001t0001g0208 others(27): Show |
31 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1222-1048T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111656703 | |||||||
| chr12:111656747 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1222-1092A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111656747 | |||||||
| chr12:111656798 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG01099.hp1 HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1222-1143T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111656798 | |||||||
| chr12:111656962 | A | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(168): Show |
207 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.1222-1307T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111656962 | |||||||
| chr12:111656998 | T | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0033 others(6): Show |
10 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1222-1343A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111656998 | |||||||
| chr12:111657105 | G | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222-1450C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111657105 | |||||||
| chr12:111657155 | T | C | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02683.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1222-1500A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111657155 | |||||||
| chr12:111657160 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1222-1505G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111657160 | |||||||
| chr12:111657196 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1221+1540T>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111657196 | |||||||
| chr12:111657205 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0059 |
2 | HG02145.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1221+1531T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111657205 | |||||||
| chr12:111657247 | T | A | 2 | a0001c0004t0002g0222 a0001c0004t0002g0223 |
2 | HG01943.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1221+1489A>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111657247 | |||||||
| chr12:111657377 | A | T | 1 | a0001c0001t0001g0296 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1221+1359T>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111657377 | |||||||
| chr12:111657760 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1221+976A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111657760 | |||||||
| chr12:111657796 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0190 |
3 | NA18960.hp2 NA18967.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1221+940A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111657796 | |||||||
| chr12:111657814 | G | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(74): Show |
105 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1221+922C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111657814 | |||||||
| chr12:111657917 | T | G | 1 | a0001c0001t0001g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1221+819A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111657917 | |||||||
| chr12:111658117 | A | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1221+619T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111658117 | |||||||
| chr12:111658303 | A | AT | 7 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
8 | HG00597.hp2 HG01891.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1221+432dupA | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111658303 | |||||||
| chr12:111658369 | C | T | 30 | a0001c0001t0001g0027 a0001c0001t0001g0207 a0001c0001t0001g0208 others(27): Show |
31 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1221+367G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111658369 | |||||||
| chr12:111658411 | T | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
281 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(278): Show |
intron_variant | MODIFIER | c.1221+325A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111658411 | |||||||
| chr12:111658429 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1221+307C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111658429 | |||||||
| chr12:111658485 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(74): Show |
105 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1221+251G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111658485 | |||||||
| chr12:111658633 | C | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0083 |
2 | NA18945.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1221+103G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 9/11 | chr12 | 111658633 | |||||||
| chr12:111659193 | A | T | 1 | a0001c0001t0001g0254 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1111+14T>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 8/11 | chr12 | 111659193 | |||||||
| chr12:111659351 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG00140.hp1 | splice_region_variant&intron_variant | LOW | c.973-6C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 7/11 | chr12 | 111659351 | |||||||
| chr12:111659405 | G | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0260 |
3 | HG03710.hp1 HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.973-60C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 7/11 | chr12 | 111659405 | |||||||
| chr12:111659585 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.973-240A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 7/11 | chr12 | 111659585 | |||||||
| chr12:111659634 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.973-289T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 7/11 | chr12 | 111659634 | |||||||
| chr12:111659731 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.973-386A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 7/11 | chr12 | 111659731 | |||||||
| chr12:111659904 | AAAAACAA others(3): Show |
A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0214 |
2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.973-569_973-560del others(10): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 7/11 | chr12 | 111659904 | |||||||
| chr12:111660073 | C | CAAAA | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.972+523_972+526dup others(4): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 7/11 | chr12 | 111660073 | |||||||
| chr12:111660084 | G | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.972+516C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 7/11 | chr12 | 111660084 | |||||||
| chr12:111660174 | AT | A | 9 | a0001c0001t0001g0191 a0001c0003t0002g0224 a0001c0003t0002g0225 others(6): Show |
9 | HG01884.hp1 HG01943.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.972+425delA | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 7/11 | chr12 | 111660174 | |||||||
| chr12:111660185 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.972+415C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 7/11 | chr12 | 111660185 | |||||||
| chr12:111660188 | G | C | 1 | a0001c0001t0001g0295 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.972+412C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 7/11 | chr12 | 111660188 | |||||||
| chr12:111660388 | A | T | 22 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0116 others(19): Show |
22 | HG01993.hp1 HG02074.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.972+212T>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 7/11 | chr12 | 111660388 | |||||||
| chr12:111660481 | T | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0070 others(1): Show |
4 | HG00099.hp1 HG01175.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.972+119A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 7/11 | chr12 | 111660481 | |||||||
| chr12:111660555 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.972+45T>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 7/11 | chr12 | 111660555 | |||||||
| chr12:111660732 | A | G | 9 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0033 others(6): Show |
10 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.897-57T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111660732 | |||||||
| chr12:111660971 | G | C | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.897-296C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111660971 | |||||||
| chr12:111660982 | ATTT | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.897-310_897-308del others(3): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111660982 | |||||||
| chr12:111661016 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.897-341C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111661016 | |||||||
| chr12:111661262 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.897-587C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111661262 | |||||||
| chr12:111661279 | G | GTT | 7 | a0001c0001t0001g0105 a0001c0003t0002g0224 a0001c0003t0002g0225 others(4): Show |
7 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.897-606_897-605dup others(2): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111661279 | |||||||
| chr12:111661436 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.897-761G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111661436 | |||||||
| chr12:111661441 | A | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(198): Show |
238 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(235): Show |
intron_variant | MODIFIER | c.897-766T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111661441 | |||||||
| chr12:111661463 | G | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.897-788C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111661463 | |||||||
| chr12:111661559 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.897-884C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111661559 | |||||||
| chr12:111661713 | G | GT | 97 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(94): Show |
104 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(101): Show |
intron_variant | MODIFIER | c.897-1039dupA | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111661713 | |||||||
| chr12:111661713 | G | GTT | 22 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0037 others(19): Show |
23 | HG00597.hp2 HG00735.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.897-1040_897-1039d others(4): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111661713 | |||||||
| chr12:111661713 | G | T | 1 | a0001c0001t0001g0215 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.897-1038C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111661713 | |||||||
| chr12:111661715 | T | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(81): Show |
112 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.897-1040A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111661715 | |||||||
| chr12:111661897 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.897-1222C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111661897 | |||||||
| chr12:111661963 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.897-1288G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111661963 | |||||||
| chr12:111662024 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.897-1349G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111662024 | |||||||
| chr12:111662267 | G | T | 1 | a0001c0001t0001g0037 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.897-1592C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111662267 | |||||||
| chr12:111662349 | A | C | 1 | a0001c0001t0001g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.897-1674T>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111662349 | |||||||
| chr12:111662472 | C | T | 1 | a0001c0006t0001g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.897-1797G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111662472 | |||||||
| chr12:111662566 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.897-1891T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111662566 | |||||||
| chr12:111662798 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.897-2123C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111662798 | |||||||
| chr12:111662945 | T | TA | 20 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0043 others(17): Show |
21 | HG00140.hp2 HG00738.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.897-2271dupT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111662945 | |||||||
| chr12:111662951 | A | C | 3 | a0001c0002t0001g0022 a0001c0002t0001g0051 a0001c0002t0001g0173 |
4 | HG00438.hp1 HG00544.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.897-2276T>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111662951 | |||||||
| chr12:111662954 | A | C | 4 | a0001c0001t0001g0104 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG01099.hp1 HG01175.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.897-2279T>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111662954 | |||||||
| chr12:111662957 | A | C | 7 | a0001c0003t0002g0225 a0001c0003t0002g0226 a0001c0003t0002g0227 others(4): Show |
7 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.897-2282T>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111662957 | |||||||
| chr12:111662958 | A | C | 1 | a0001c0003t0002g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.897-2283T>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111662958 | |||||||
| chr12:111662960 | AC | A | 7 | a0001c0003t0002g0225 a0001c0003t0002g0226 a0001c0003t0002g0227 others(4): Show |
7 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.897-2286delG | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111662960 | |||||||
| chr12:111662961 | C | A | 1 | a0001c0003t0002g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.897-2286G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111662961 | |||||||
| chr12:111662969 | T | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
283 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(280): Show |
intron_variant | MODIFIER | c.897-2294A>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111662969 | |||||||
| chr12:111663216 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG02622.hp1 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.896+2423C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111663216 | |||||||
| chr12:111663230 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.896+2409C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111663230 | |||||||
| chr12:111663576 | A | ATCTC | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.896+2059_896+2062d others(6): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111663576 | |||||||
| chr12:111663799 | T | C | 8 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0239 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.896+1840A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111663799 | |||||||
| chr12:111663931 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.896+1708A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111663931 | |||||||
| chr12:111664013 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.896+1626T>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111664013 | |||||||
| chr12:111664054 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.896+1585G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111664054 | |||||||
| chr12:111664344 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.896+1295T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111664344 | |||||||
| chr12:111664357 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.896+1282C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111664357 | |||||||
| chr12:111664423 | T | C | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.896+1216A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111664423 | |||||||
| chr12:111664713 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.896+926G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111664713 | |||||||
| chr12:111664730 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.896+909C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111664730 | |||||||
| chr12:111664875 | G | C | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.896+764C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111664875 | |||||||
| chr12:111664949 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.896+690C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111664949 | |||||||
| chr12:111665081 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.896+558A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111665081 | |||||||
| chr12:111665262 | T | G | 1 | a0001c0001t0001g0254 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.896+377A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111665262 | |||||||
| chr12:111665344 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(198): Show |
238 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(235): Show |
intron_variant | MODIFIER | c.896+295G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111665344 | |||||||
| chr12:111665442 | A | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.896+197T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111665442 | |||||||
| chr12:111665509 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.896+130C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 6/11 | chr12 | 111665509 | |||||||
| chr12:111665854 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.748-67A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111665854 | |||||||
| chr12:111666570 | G | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-783C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111666570 | |||||||
| chr12:111666793 | C | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-1006G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111666793 | |||||||
| chr12:111666849 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.748-1062A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111666849 | |||||||
| chr12:111666880 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG01099.hp1 HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.748-1093G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111666880 | |||||||
| chr12:111666944 | A | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(74): Show |
105 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.748-1157T>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111666944 | |||||||
| chr12:111667024 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.748-1237C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667024 | |||||||
| chr12:111667592 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.748-1805A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667592 | |||||||
| chr12:111667633 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.748-1846T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667633 | |||||||
| chr12:111667698 | C | CA | 9 | a0001c0001t0001g0120 a0001c0001t0001g0260 a0001c0001t0001g0264 others(6): Show |
9 | HG01167.hp2 HG01168.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.748-1912dupT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0059 a0001c0001t0001g0239 |
2 | HG02280.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.748-1922_748-1912d others(13): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0064 a0001c0001t0001g0143 |
2 | HG03688.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.748-1923_748-1912d others(14): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0146 a0001c0001t0009g0310 |
2 | HG00738.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.748-1924_748-1912d others(15): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(7): Show |
6 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0045 others(3): Show |
8 | HG00140.hp2 HG00738.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-1925_748-1912d others(16): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(8): Show |
35 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0020 others(32): Show |
42 | HG01256.hp1 HG01884.hp1 HG01975.hp1 others(39): Show |
intron_variant | MODIFIER | c.748-1926_748-1912d others(17): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(9): Show |
45 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(42): Show |
63 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.748-1927_748-1912d others(18): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(10): Show |
18 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0054 others(15): Show |
20 | HG01168.hp1 HG02074.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.748-1928_748-1912d others(19): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(11): Show |
27 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0024 others(24): Show |
30 | HG00735.hp1 HG01099.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-1929_748-1912d others(20): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(12): Show |
31 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(28): Show |
35 | HG00099.hp1 HG00597.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.748-1930_748-1912d others(21): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(13): Show |
15 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0053 others(12): Show |
17 | HG01175.hp2 HG01891.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.748-1931_748-1912d others(22): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(14): Show |
8 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0063 others(5): Show |
8 | HG01175.hp1 HG01361.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-1932_748-1912d others(23): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(15): Show |
5 | a0001c0001t0001g0096 a0001c0001t0001g0207 a0001c0001t0001g0209 others(2): Show |
5 | HG02280.hp1 HG02559.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-1933_748-1912d others(24): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(16): Show |
5 | a0001c0001t0001g0072 a0001c0001t0001g0082 a0001c0001t0001g0139 others(2): Show |
5 | HG02129.hp2 HG02886.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-1934_748-1912d others(25): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(17): Show |
4 | a0001c0001t0001g0052 a0001c0001t0001g0067 a0001c0001t0001g0106 others(1): Show |
4 | HG01167.hp1 HG03225.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-1912_748-1911i others(26): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.748-1912_748-1911i others(27): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(19): Show |
1 | a0001c0001t0001g0235 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.748-1912_748-1911i others(28): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(20): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0125 |
5 | HG02965.hp2 HG06807.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-1912_748-1911i others(29): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(21): Show |
3 | a0001c0001t0001g0114 a0001c0001t0001g0181 a0001c0001t0001g0214 |
3 | HG02970.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.748-1912_748-1911i others(30): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(22): Show |
3 | a0001c0001t0001g0068 a0001c0001t0001g0097 a0001c0001t0001g0099 |
3 | HG02258.hp2 NA18959.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.748-1912_748-1911i others(31): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(23): Show |
3 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0237 |
3 | HG01081.hp1 HG01891.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.748-1912_748-1911i others(32): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0069 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.748-1912_748-1911i others(33): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(26): Show |
2 | a0001c0001t0001g0050 a0001c0001t0001g0130 |
2 | HG04204.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.748-1912_748-1911i others(35): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(27): Show |
1 | a0001c0001t0001g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.748-1912_748-1911i others(36): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(30): Show |
1 | a0001c0001t0001g0049 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.748-1912_748-1911i others(39): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(39): Show |
1 | a0001c0001t0001g0131 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.748-1912_748-1911i others(48): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(40): Show |
1 | a0001c0001t0001g0046 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.748-1912_748-1911i others(49): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | C | CAAAAAAA others(45): Show |
1 | a0001c0001t0001g0043 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.748-1912_748-1911i others(54): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667698 | CAAAAAAA others(2): Show |
C | 9 | a0001c0001t0001g0144 a0001c0003t0002g0224 a0001c0003t0002g0225 others(6): Show |
9 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.748-1920_748-1912d others(11): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667698 | |||||||
| chr12:111667761 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.748-1974G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667761 | |||||||
| chr12:111667991 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.748-2204C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111667991 | |||||||
| chr12:111668082 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0065 a0001c0001t0001g0179 others(3): Show |
8 | HG01081.hp2 HG01099.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.748-2295G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111668082 | |||||||
| chr12:111668338 | AT | A | 13 | a0001c0001t0001g0131 a0001c0001t0001g0268 a0001c0001t0001g0296 others(10): Show |
13 | HG01943.hp2 HG02257.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.748-2552delA | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111668338 | |||||||
| chr12:111668339 | T | A | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.748-2552A>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111668339 | |||||||
| chr12:111668340 | T | A | 13 | a0001c0001t0001g0131 a0001c0001t0001g0268 a0001c0001t0001g0296 others(10): Show |
13 | HG01943.hp2 HG02257.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.748-2553A>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111668340 | |||||||
| chr12:111668559 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.748-2772A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111668559 | |||||||
| chr12:111668645 | C | CT | 6 | a0001c0001t0001g0207 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG03098.hp2 HG03209.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.748-2859dupA | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111668645 | |||||||
| chr12:111668645 | CTT | C | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-2860_748-2859d others(4): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111668645 | |||||||
| chr12:111668688 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.748-2901C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111668688 | |||||||
| chr12:111668706 | G | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-2919C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111668706 | |||||||
| chr12:111668748 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.748-2961G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111668748 | |||||||
| chr12:111668750 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0107 |
3 | HG02027.hp2 NA18949.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.748-2963C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111668750 | |||||||
| chr12:111668868 | A | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-3081T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111668868 | |||||||
| chr12:111668874 | T | G | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.748-3087A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111668874 | |||||||
| chr12:111668980 | T | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0156 others(1): Show |
6 | HG02109.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-3193A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111668980 | |||||||
| chr12:111669172 | G | C | 11 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.748-3385C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111669172 | |||||||
| chr12:111669299 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.747+3362C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111669299 | |||||||
| chr12:111669311 | C | A | 1 | a0001c0001t0001g0158 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.747+3350G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111669311 | |||||||
| chr12:111669469 | G | A | 1 | a0001c0003t0002g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.747+3192C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111669469 | |||||||
| chr12:111669514 | C | T | 2 | a0001c0001t0001g0278 a0001c0001t0005g0277 |
2 | HG01074.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.747+3147G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111669514 | |||||||
| chr12:111670220 | T | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.747+2441A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111670220 | |||||||
| chr12:111670488 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.747+2173G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111670488 | |||||||
| chr12:111670505 | G | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.747+2156C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111670505 | |||||||
| chr12:111670522 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.747+2139G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111670522 | |||||||
| chr12:111670574 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.747+2087T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111670574 | |||||||
| chr12:111670644 | C | T | 7 | a0001c0001t0001g0262 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
7 | HG01192.hp2 HG01255.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.747+2017G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111670644 | |||||||
| chr12:111670733 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.747+1928C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111670733 | |||||||
| chr12:111670737 | A | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.747+1924T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111670737 | |||||||
| chr12:111670968 | C | T | 1 | a0001c0001t0011g0071 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.747+1693G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111670968 | |||||||
| chr12:111670970 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.747+1691G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111670970 | |||||||
| chr12:111670978 | T | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0033 others(6): Show |
10 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.747+1683A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111670978 | |||||||
| chr12:111671053 | T | C | 9 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0211 others(6): Show |
9 | HG01884.hp2 HG02976.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.747+1608A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671053 | |||||||
| chr12:111671101 | C | CA | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.747+1559dupT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671101 | |||||||
| chr12:111671292 | A | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.747+1369T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671292 | |||||||
| chr12:111671407 | T | C | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.747+1254A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671407 | |||||||
| chr12:111671419 | G | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.747+1242C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671419 | |||||||
| chr12:111671487 | TTGCAGTG others(648): Show |
T | 1 | a0001c0001t0001g0119 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.747+519_747+1173de others(1): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671487 | |||||||
| chr12:111671549 | CCAAAA | C | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.747+1107_747+1111d others(7): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671549 | |||||||
| chr12:111671681 | C | CT | 23 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(20): Show |
23 | HG00597.hp1 HG01361.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.747+979dupA | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671681 | |||||||
| chr12:111671681 | CT | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0160 a0001c0001t0001g0232 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.747+979delA | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671681 | |||||||
| chr12:111671684 | T | TC | 5 | a0001c0003t0002g0224 a0001c0003t0002g0226 a0001c0003t0002g0227 others(2): Show |
5 | HG02257.hp1 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+976_747+977ins others(1): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671684 | |||||||
| chr12:111671783 | T | G | 1 | a0001c0001t0001g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.747+878A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671783 | |||||||
| chr12:111671882 | C | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.747+779G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671882 | |||||||
| chr12:111671909 | T | C | 1 | a0001c0001t0001g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.747+752A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671909 | |||||||
| chr12:111671967 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.747+694C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671967 | |||||||
| chr12:111671975 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.747+686T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111671975 | |||||||
| chr12:111672025 | G | C | 1 | a0001c0001t0001g0029 | 2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.747+636C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111672025 | |||||||
| chr12:111672084 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.747+577A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111672084 | |||||||
| chr12:111672191 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.747+470G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111672191 | |||||||
| chr12:111672224 | A | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.747+437T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111672224 | |||||||
| chr12:111672278 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.747+383G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111672278 | |||||||
| chr12:111672387 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.747+274A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111672387 | |||||||
| chr12:111672622 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.747+39C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 5/11 | chr12 | 111672622 | |||||||
| chr12:111672916 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.634-142G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111672916 | |||||||
| chr12:111673280 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.634-506C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673280 | |||||||
| chr12:111673348 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.634-574A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673348 | |||||||
| chr12:111673360 | C | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.634-586G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673360 | |||||||
| chr12:111673396 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0273 a0001c0001t0001g0274 |
3 | HG01074.hp2 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.634-622G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673396 | |||||||
| chr12:111673508 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.634-734T>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673508 | |||||||
| chr12:111673510 | GA | G | 293 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(290): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.634-737delT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673510 | |||||||
| chr12:111673510 | GAA | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0217 a0001c0001t0001g0253 others(2): Show |
7 | HG01168.hp2 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.634-738_634-737del others(2): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673510 | |||||||
| chr12:111673517 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.634-743T>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673517 | |||||||
| chr12:111673543 | C | G | 5 | a0001c0001t0001g0249 a0001c0001t0001g0270 a0001c0001t0001g0271 others(2): Show |
5 | HG01928.hp1 HG01934.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.634-769G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673543 | |||||||
| chr12:111673549 | T | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0033 others(6): Show |
10 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.634-775A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673549 | |||||||
| chr12:111673554 | G | GA | 4 | a0001c0001t0001g0004 a0001c0001t0001g0114 a0001c0001t0001g0125 others(1): Show |
6 | HG02965.hp2 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.634-781dupT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673554 | |||||||
| chr12:111673560 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.634-786T>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673560 | |||||||
| chr12:111673748 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.634-974G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673748 | |||||||
| chr12:111673809 | A | G | 9 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0033 others(6): Show |
10 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.634-1035T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673809 | |||||||
| chr12:111673833 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.634-1059C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673833 | |||||||
| chr12:111673891 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.634-1117G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673891 | |||||||
| chr12:111673913 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG00099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.634-1139G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111673913 | |||||||
| chr12:111674008 | C | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.634-1234G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111674008 | |||||||
| chr12:111674120 | C | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18942.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.634-1346G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111674120 | |||||||
| chr12:111674376 | G | T | 1 | a0001c0006t0001g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.634-1602C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111674376 | |||||||
| chr12:111674535 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.634-1761C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111674535 | |||||||
| chr12:111674778 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.634-2004G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111674778 | |||||||
| chr12:111674855 | G | A | 1 | a0001c0001t0006g0245 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.634-2081C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111674855 | |||||||
| chr12:111674955 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.634-2181G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111674955 | |||||||
| chr12:111675001 | C | T | 3 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 |
3 | HG02572.hp1 HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.634-2227G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111675001 | |||||||
| chr12:111675065 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.634-2291T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111675065 | |||||||
| chr12:111675076 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.634-2302G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111675076 | |||||||
| chr12:111675294 | A | C | 7 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(4): Show |
7 | NA18952.hp2 NA18973.hp2 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.634-2520T>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111675294 | |||||||
| chr12:111675704 | G | A | 84 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(81): Show |
92 | HG00099.hp1 HG00597.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.634-2930C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111675704 | |||||||
| chr12:111675753 | T | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0073 a0001c0008t0001g0201 |
3 | HG03453.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.634-2979A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111675753 | |||||||
| chr12:111675854 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(198): Show |
238 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(235): Show |
intron_variant | MODIFIER | c.634-3080G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111675854 | |||||||
| chr12:111676013 | G | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+3138C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111676013 | |||||||
| chr12:111676046 | T | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(75): Show |
106 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.633+3105A>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111676046 | |||||||
| chr12:111676054 | A | T | 6 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(3): Show |
6 | HG01943.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.633+3097T>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111676054 | |||||||
| chr12:111676292 | A | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+2859T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111676292 | |||||||
| chr12:111676413 | A | G | 2 | a0001c0001t0001g0269 a0001c0001t0001g0302 |
2 | NA18986.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.633+2738T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111676413 | |||||||
| chr12:111676611 | A | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+2540T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111676611 | |||||||
| chr12:111676825 | C | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18942.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.633+2326G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111676825 | |||||||
| chr12:111676841 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.633+2310A>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111676841 | |||||||
| chr12:111676921 | CT | C | 5 | a0001c0001t0001g0262 a0001c0001t0001g0299 a0001c0001t0001g0300 others(2): Show |
5 | HG01255.hp1 HG01496.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.633+2229delA | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111676921 | |||||||
| chr12:111677188 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.633+1963C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111677188 | |||||||
| chr12:111677243 | C | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+1908G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111677243 | |||||||
| chr12:111677320 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.633+1831C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111677320 | |||||||
| chr12:111677321 | T | A | 1 | a0001c0001t0001g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.633+1830A>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111677321 | |||||||
| chr12:111677616 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.633+1535T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111677616 | |||||||
| chr12:111677625 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.633+1526G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111677625 | |||||||
| chr12:111677639 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.633+1512T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111677639 | |||||||
| chr12:111677882 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.633+1269C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111677882 | |||||||
| chr12:111677984 | C | T | 11 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0126 others(8): Show |
11 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.633+1167G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111677984 | |||||||
| chr12:111678081 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.633+1070G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678081 | |||||||
| chr12:111678249 | C | CA | 13 | a0001c0001t0001g0029 a0001c0001t0001g0053 a0001c0001t0001g0059 others(10): Show |
14 | HG01256.hp2 HG01928.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.633+901dupT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678249 | |||||||
| chr12:111678249 | CA | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(77): Show |
108 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.633+901delT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678249 | |||||||
| chr12:111678249 | CAA | C | 13 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(10): Show |
13 | HG01256.hp1 HG01943.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.633+900_633+901del others(2): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678249 | |||||||
| chr12:111678335 | C | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+816G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678335 | |||||||
| chr12:111678355 | C | A | 1 | a0001c0001t0001g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.633+796G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678355 | |||||||
| chr12:111678357 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.633+794G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678357 | |||||||
| chr12:111678380 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18942.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.633+771G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678380 | |||||||
| chr12:111678455 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.633+696C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678455 | |||||||
| chr12:111678474 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.633+677A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678474 | |||||||
| chr12:111678635 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0248 |
3 | HG02109.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.633+516G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678635 | |||||||
| chr12:111678643 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.633+508G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678643 | |||||||
| chr12:111678652 | G | C | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.633+499C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678652 | |||||||
| chr12:111678686 | A | AT | 91 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(88): Show |
119 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.633+464dupA | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678686 | |||||||
| chr12:111678686 | A | ATT | 7 | a0001c0001t0001g0136 a0001c0001t0001g0163 a0001c0001t0001g0164 others(4): Show |
7 | HG02071.hp1 HG02818.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.633+463_633+464dup others(2): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678686 | |||||||
| chr12:111678950 | C | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0248 |
3 | HG02109.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.633+201G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678950 | |||||||
| chr12:111678951 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.633+200G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678951 | |||||||
| chr12:111678972 | C | A | 1 | a0001c0001t0009g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.633+179G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 4/11 | chr12 | 111678972 | |||||||
| chr12:111679378 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0101 a0001c0001t0001g0102 others(2): Show |
5 | HG00735.hp1 HG01081.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.444-38C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111679378 | |||||||
| chr12:111679642 | G | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | HG01891.hp2 HG02280.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.444-302C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111679642 | |||||||
| chr12:111679692 | G | A | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.444-352C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111679692 | |||||||
| chr12:111679832 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.444-492C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111679832 | |||||||
| chr12:111679876 | CA | C | 124 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(121): Show |
134 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.444-537delT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111679876 | |||||||
| chr12:111679876 | CAA | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
213 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.444-538_444-537del others(2): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111679876 | |||||||
| chr12:111679978 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.444-638T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111679978 | |||||||
| chr12:111679985 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.444-645T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111679985 | |||||||
| chr12:111680019 | A | G | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.444-679T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680019 | |||||||
| chr12:111680096 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.444-756T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680096 | |||||||
| chr12:111680117 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.444-777C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680117 | |||||||
| chr12:111680278 | T | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG02622.hp1 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.444-938A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680278 | |||||||
| chr12:111680305 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.444-965G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680305 | |||||||
| chr12:111680317 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.444-977C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680317 | |||||||
| chr12:111680400 | C | T | 1 | a0001c0001t0009g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.444-1060G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680400 | |||||||
| chr12:111680508 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0134 others(2): Show |
7 | HG01256.hp1 HG01258.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.443+1129G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680508 | |||||||
| chr12:111680534 | CA | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
271 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(268): Show |
intron_variant | MODIFIER | c.443+1102delT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680534 | |||||||
| chr12:111680583 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.443+1054G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680583 | |||||||
| chr12:111680618 | G | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0042 others(11): Show |
15 | HG00140.hp2 HG00738.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.443+1019C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680618 | |||||||
| chr12:111680618 | G | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.443+1019C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680618 | |||||||
| chr12:111680694 | AAAAAAAC others(5): Show |
A | 208 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(205): Show |
246 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(243): Show |
intron_variant | MODIFIER | c.443+931_443+942del others(12): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680694 | |||||||
| chr12:111680772 | T | C | 86 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
94 | HG00099.hp1 HG00597.hp2 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.443+865A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680772 | |||||||
| chr12:111680933 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.443+704C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680933 | |||||||
| chr12:111680980 | T | TA | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.443+656dupT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111680980 | |||||||
| chr12:111681118 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.443+519G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111681118 | |||||||
| chr12:111681182 | A | G | 1 | a0001c0001t0001g0263 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443+455T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111681182 | |||||||
| chr12:111681186 | G | T | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.443+451C>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111681186 | |||||||
| chr12:111681236 | G | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0214 |
2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.443+401C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111681236 | |||||||
| chr12:111681367 | T | C | 14 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0021 others(11): Show |
26 | HG00438.hp1 HG00544.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.443+270A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111681367 | |||||||
| chr12:111681402 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.443+235A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111681402 | |||||||
| chr12:111681496 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.443+141A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111681496 | |||||||
| chr12:111681570 | T | C | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.443+67A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111681570 | |||||||
| chr12:111681583 | C | CA | 99 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(96): Show |
108 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.443+53dupT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111681583 | |||||||
| chr12:111681583 | CA | C | 9 | a0001c0001t0001g0052 a0001c0001t0001g0110 a0001c0001t0001g0111 others(6): Show |
9 | HG01099.hp1 HG01175.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.443+53delT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 3/11 | chr12 | 111681583 | |||||||
| chr12:111682366 | C | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(190): Show |
230 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(227): Show |
intron_variant | MODIFIER | c.245-531G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/11 | chr12 | 111682366 | |||||||
| chr12:111682450 | G | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(65): Show |
95 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.245-615C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/11 | chr12 | 111682450 | |||||||
| chr12:111682497 | C | CA | 6 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0250 others(3): Show |
6 | HG02683.hp1 HG03516.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.244+648dupT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/11 | chr12 | 111682497 | |||||||
| chr12:111682497 | CA | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
259 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.244+648delT | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/11 | chr12 | 111682497 | |||||||
| chr12:111682497 | CAA | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0040 others(12): Show |
16 | HG00140.hp2 HG00738.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.244+647_244+648del others(2): Show |
BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/11 | chr12 | 111682497 | |||||||
| chr12:111682514 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.244+632T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/11 | chr12 | 111682514 | |||||||
| chr12:111682705 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.244+441T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/11 | chr12 | 111682705 | |||||||
| chr12:111682725 | A | G | 1 | a0001c0001t0001g0039 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.244+421T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/11 | chr12 | 111682725 | |||||||
| chr12:111682831 | C | T | 1 | a0001c0003t0002g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244+315G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/11 | chr12 | 111682831 | |||||||
| chr12:111682865 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0246 a0001c0001t0001g0247 others(1): Show |
5 | HG02109.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+281A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/11 | chr12 | 111682865 | |||||||
| chr12:111682924 | C | T | 1 | a0001c0006t0001g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.244+222G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/11 | chr12 | 111682924 | |||||||
| chr12:111683092 | T | C | 13 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01167.hp1 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.244+54A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 2/11 | chr12 | 111683092 | |||||||
| chr12:111683517 | A | C | 1 | a0001c0001t0001g0220 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.83-210T>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111683517 | |||||||
| chr12:111683538 | T | C | 4 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(1): Show |
4 | HG02074.hp1 NA18943.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-231A>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111683538 | |||||||
| chr12:111683569 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.83-262G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111683569 | |||||||
| chr12:111683697 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.83-390G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111683697 | |||||||
| chr12:111683761 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.83-454C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111683761 | |||||||
| chr12:111683841 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.83-534G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111683841 | |||||||
| chr12:111684066 | A | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG00099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.83-759T>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111684066 | |||||||
| chr12:111684174 | G | A | 1 | a0001c0003t0002g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.83-867C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111684174 | |||||||
| chr12:111684183 | G | A | 11 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.83-876C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111684183 | |||||||
| chr12:111684412 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.83-1105C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111684412 | |||||||
| chr12:111684663 | G | GT | 9 | a0001c0001t0001g0034 a0001c0003t0002g0224 a0001c0003t0002g0225 others(6): Show |
9 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.82+1047dupA | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111684663 | |||||||
| chr12:111684680 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.82+1031A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111684680 | |||||||
| chr12:111684708 | G | C | 1 | a0001c0001t0001g0219 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.82+1003C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111684708 | |||||||
| chr12:111684867 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.82+844G>A | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111684867 | |||||||
| chr12:111685001 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.82+710G>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111685001 | |||||||
| chr12:111685278 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.82+433C>T | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111685278 | |||||||
| chr12:111685365 | G | C | 8 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0226 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.82+346C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111685365 | |||||||
| chr12:111685396 | T | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0230 |
3 | HG00438.hp2 NA18981.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.82+315A>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111685396 | |||||||
| chr12:111685453 | G | C | 19 | a0001c0001t0001g0027 a0001c0001t0001g0232 a0001c0001t0001g0233 others(16): Show |
20 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.82+258C>G | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111685453 | |||||||
| chr12:111685480 | A | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
282 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(279): Show |
intron_variant | MODIFIER | c.82+231T>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111685480 | |||||||
| chr12:111685620 | C | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.82+91G>C | BRAP | ENSG00000089234.16 | transcript | ENST00000419234.9 | protein_coding | 1/11 | chr12 | 111685620 |