Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 65980 |
| ensemblid | ENSG00000028310.18 |
| hgncid | 25818 |
| symbol | BRD9 |
| name | bromodomain containing 9 |
| refseq_nuc | NM_023924.5 |
| refseq_prot | NP_076413.3 |
| ensembl_nuc | ENST00000467963.6 |
| ensembl_prot | ENSP00000419765.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 863741 |
| end | 892801 |
| strand | - |
| ver | v1.2 |
| region | chr5:863741-892801 |
| region5000 | chr5:858741-897801 |
| regionname0 | BRD9_chr5_863741_892801 |
| regionname5000 | BRD9_chr5_858741_897801 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 597 | 346 | 83 | 70 | 139 | 9 | 43 | 97 | BRD9_chr5_858741_897801 | BRD9 | MGKKH others(592): Show |
chr5 | 858741 | 897801 |
| a0002 | 0/0 | 597 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | MGKKH others(592): Show |
chr5 | 858741 | 897801 |
| a0003 | 0/0 | 597 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | BRD9_chr5_858741_897801 | BRD9 | MGKKH others(592): Show |
chr5 | 858741 | 897801 |
| a0004 | 0/0 | 597 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | MGKKH others(592): Show |
chr5 | 858741 | 897801 |
| a0005 | 0/0 | 597 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | MGKKH others(592): Show |
chr5 | 858741 | 897801 |
| a0006 | 0/0 | 597 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | MGKKH others(592): Show |
chr5 | 858741 | 897801 |
| a0007 | 0/0 | 597 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | MGKKH others(592): Show |
chr5 | 858741 | 897801 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1791 | 314 | 62 | 63 | 138 | 9 | 40 | BRD9_chr5_858741_897801 | BRD9 | ATGGG others(1786): Show |
chr5 | 858741 | 897801 | ||
| a0001c0002 | 0/0 | 1791 | 20 | 12 | 6 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | ATGGG others(1786): Show |
chr5 | 858741 | 897801 | ||
| a0001c0004 | 0/0 | 1791 | 7 | 6 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | ATGGG others(1786): Show |
chr5 | 858741 | 897801 | ||
| a0001c0005 | 0/0 | 1791 | 3 | 3 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | ATGGG others(1786): Show |
chr5 | 858741 | 897801 | ||
| a0001c0008 | 0/0 | 1791 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | ATGGG others(1786): Show |
chr5 | 858741 | 897801 | ||
| a0001c0013 | 0/0 | 1791 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | ATGGG others(1786): Show |
chr5 | 858741 | 897801 | ||
| a0002c0003 | 0/0 | 1791 | 9 | 8 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | ATGGG others(1786): Show |
chr5 | 858741 | 897801 | ||
| a0002c0012 | 0/0 | 1791 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | ATGGG others(1786): Show |
chr5 | 858741 | 897801 | ||
| a0003c0006 | 0/0 | 1791 | 3 | 0 | 0 | 3 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | ATGGG others(1786): Show |
chr5 | 858741 | 897801 | ||
| a0004c0007 | 0/0 | 1791 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | ATGGG others(1786): Show |
chr5 | 858741 | 897801 | ||
| a0005c0009 | 0/0 | 1791 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | ATGGG others(1786): Show |
chr5 | 858741 | 897801 | ||
| a0006c0011 | 0/0 | 1791 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | ATGGG others(1786): Show |
chr5 | 858741 | 897801 | ||
| a0007c0010 | 0/0 | 1791 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | ATGGG others(1786): Show |
chr5 | 858741 | 897801 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2665 | 240 | 34 | 61 | 97 | 9 | 37 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0001t0002 | 0/0 | 2665 | 57 | 18 | 0 | 37 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0001t0005 | 0/0 | 2665 | 5 | 4 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0001t0007 | 0/0 | 2665 | 5 | 5 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0001t0011 | 0/0 | 2665 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0001t0013 | 0/0 | 2665 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0001t0014 | 0/0 | 2665 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0001t0015 | 0/0 | 2665 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0001t0016 | 0/0 | 2665 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0001t0017 | 0/0 | 2665 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0002t0002 | 0/0 | 2665 | 6 | 3 | 3 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0002t0004 | 0/0 | 2665 | 5 | 0 | 3 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0002t0006 | 0/0 | 2665 | 5 | 5 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0002t0009 | 0/0 | 2673 | 4 | 4 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2668): Show |
chr5 | 858741 | 897801 |
| a0001c0004t0003 | 0/0 | 2665 | 7 | 6 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0005t0002 | 0/0 | 2665 | 3 | 3 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0008t0001 | 0/0 | 2665 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0001c0013t0001 | 0/0 | 2665 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0002c0003t0008 | 0/0 | 2664 | 4 | 4 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2659): Show |
chr5 | 858741 | 897801 |
| a0002c0003t0010 | 0/0 | 2664 | 3 | 3 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2659): Show |
chr5 | 858741 | 897801 |
| a0002c0003t0012 | 0/0 | 2664 | 2 | 1 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2659): Show |
chr5 | 858741 | 897801 |
| a0002c0012t0008 | 0/0 | 2664 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2659): Show |
chr5 | 858741 | 897801 |
| a0003c0006t0001 | 0/0 | 2665 | 3 | 0 | 0 | 3 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0004c0007t0001 | 0/0 | 2665 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0005c0009t0001 | 0/0 | 2665 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0006c0011t0001 | 0/0 | 2665 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| a0007c0010t0001 | 0/0 | 2665 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | GTTTC others(2660): Show |
chr5 | 858741 | 897801 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 48 | 3 | 9 | 30 | 1 | 4 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0002 | 0/0 | 22 | 0 | 7 | 12 | 0 | 3 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0006 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0017 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0003 | 0/0 | 15 | 0 | 0 | 14 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0004 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0005g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0007g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0007g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0011g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0013g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0014g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0015g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0016g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0001t0017g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0002t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0002t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0002t0004g0011 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0002t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0002t0006g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0002t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0002t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0002t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0002t0009g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0002t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0004t0003g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0004t0003g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0004t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0005t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0005t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0005t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0008t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0001c0013t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0002c0003t0008g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0002c0003t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0002c0003t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0002c0003t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0002c0003t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0002c0003t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0002c0003t0010g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0002c0003t0012g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0002c0003t0012g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0002c0012t0008g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0003c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0003c0006t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0003c0006t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0004c0007t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0005c0009t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0006c0011t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| a0007c0010t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0054 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0152 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01175 | hp1 | a0001 | c0002 | t0004 | g0011 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01192 | hp2 | a0001 | c0001 | t0013 | g0056 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01243 | hp1 | a0001 | c0004 | t0003 | g0039 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01261 | hp2 | a0002 | c0003 | t0012 | g0066 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01433 | hp2 | a0001 | c0002 | t0004 | g0052 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | IBS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01884 | hp1 | a0002 | c0003 | t0008 | g0183 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01891 | hp2 | a0001 | c0002 | t0009 | g0020 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02040 | hp2 | a0001 | c0001 | t0011 | g0022 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02083 | hp2 | a0001 | c0001 | t0011 | g0022 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02129 | hp2 | a0001 | c0001 | t0016 | g0165 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02132 | hp2 | a0001 | c0001 | t0014 | g0109 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02148 | hp1 | a0001 | c0002 | t0004 | g0011 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02258 | hp2 | a0001 | c0001 | t0017 | g0110 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02280 | hp2 | a0002 | c0003 | t0010 | g0051 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02300 | hp1 | a0005 | c0009 | t0001 | g0072 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0048 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0047 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02723 | hp2 | a0002 | c0003 | t0008 | g0186 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02735 | hp2 | a0001 | c0002 | t0004 | g0011 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02738 | hp2 | a0001 | c0001 | t0015 | g0070 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02809 | hp2 | a0001 | c0005 | t0002 | g0080 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0048 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02818 | hp2 | a0001 | c0002 | t0009 | g0177 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02886 | hp1 | a0001 | c0005 | t0002 | g0086 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0047 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02965 | hp2 | a0001 | c0004 | t0003 | g0012 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03041 | hp1 | a0002 | c0003 | t0008 | g0185 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03098 | hp2 | a0001 | c0004 | t0003 | g0012 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03139 | hp1 | a0002 | c0003 | t0008 | g0184 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03139 | hp2 | a0002 | c0003 | t0012 | g0065 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03195 | hp1 | a0001 | c0004 | t0003 | g0012 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03195 | hp2 | a0001 | c0002 | t0006 | g0179 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03209 | hp1 | a0002 | c0012 | t0008 | g0182 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03453 | hp2 | a0001 | c0002 | t0006 | g0046 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0151 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03516 | hp1 | a0001 | c0002 | t0006 | g0178 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03516 | hp2 | a0001 | c0002 | t0009 | g0020 | AFR | ESN | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03579 | hp2 | a0001 | c0004 | t0003 | g0039 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03654 | hp1 | a0001 | c0013 | t0001 | g0172 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03669 | hp2 | a0006 | c0011 | t0001 | g0108 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18522 | hp2 | a0001 | c0004 | t0003 | g0012 | AFR | YRI | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18950 | hp1 | a0003 | c0006 | t0001 | g0101 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18974 | hp2 | a0004 | c0007 | t0001 | g0024 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18997 | hp1 | a0003 | c0006 | t0001 | g0100 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19043 | hp2 | a0001 | c0005 | t0002 | g0088 | AFR | LWK | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19058 | hp1 | a0003 | c0006 | t0001 | g0077 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19058 | hp2 | a0001 | c0008 | t0001 | g0063 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19059 | hp1 | a0004 | c0007 | t0001 | g0024 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0181 | AFR | YRI | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA19240 | hp2 | a0001 | c0002 | t0009 | g0020 | AFR | YRI | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA20129 | hp1 | a0001 | c0002 | t0006 | g0046 | AFR | ASW | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ASW | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA20752 | hp2 | a0007 | c0010 | t0001 | g0096 | EUR | TSI | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | GIH | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA20905 | hp2 | a0001 | c0002 | t0004 | g0011 | SAS | GIH | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02486 | hp1 | a0001 | c0002 | t0006 | g0180 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02486 | hp2 | a0001 | c0004 | t0003 | g0150 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG02559 | hp2 | a0002 | c0003 | t0010 | g0049 | AFR | ACB | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG03471 | hp2 | a0002 | c0003 | t0010 | g0050 | AFR | MSL | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | USA | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | USA | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0017 | REF | REF | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | BRD9_chr5_858741_897801 | BRD9 | chr5 | 858741 | 897801 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:865498 | C | T | 1 | a0006 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.1609G>A | p.Ala537Thr | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/16 | 1753/2665 | 1609/1794 | 537/597 | chr5 | 865498 | |||
| chr5:870526 | G | A | 1 | a0003 | 3 | NA18950.hp1 NA18997.hp1 NA19058.hp1 |
missense_variant | MODERATE | c.1472C>T | p.Ser491Leu | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/16 | 1616/2665 | 1472/1794 | 491/597 | chr5 | 870526 | |||
| chr5:878428 | C | T | 1 | a0004 | 2 | NA18974.hp2 NA19059.hp1 |
missense_variant | MODERATE | c.1198G>A | p.Asp400Asn | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/16 | 1342/2665 | 1198/1794 | 400/597 | chr5 | 878428 | |||
| chr5:878436 | A | G | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.1190T>C | p.Val397Ala | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/16 | 1334/2665 | 1190/1794 | 397/597 | chr5 | 878436 | |||
| chr5:886629 | C | T | 1 | a0002 | 10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
missense_variant | MODERATE | c.796G>A | p.Ala266Thr | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/16 | 940/2665 | 796/1794 | 266/597 | chr5 | 886629 | |||
| chr5:886668 | C | T | 1 | a0005 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.757G>A | p.Glu253Lys | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/16 | 901/2665 | 757/1794 | 253/597 | chr5 | 886668 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:865448 | C | T | 2 | a0002c0003 a0002c0012 |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
synonymous_variant | LOW | c.1659G>A | p.Leu553Leu | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/16 | 1803/2665 | 1659/1794 | 553/597 | chr5 | 865448 | |||
| chr5:865469 | C | T | 1 | a0001c0005 | 3 | HG02809.hp2 HG02886.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.1638G>A | p.Pro546Pro | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/16 | 1782/2665 | 1638/1794 | 546/597 | chr5 | 865469 | |||
| chr5:870504 | A | G | 4 | a0001c0002 a0001c0004 a0002c0003 others(1): Show |
37 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(34): Show |
synonymous_variant | LOW | c.1494T>C | p.Val498Val | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/16 | 1638/2665 | 1494/1794 | 498/597 | chr5 | 870504 | |||
| chr5:881123 | G | A | 2 | a0002c0003 a0002c0012 |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
synonymous_variant | LOW | c.1026C>T | p.Ala342Ala | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/16 | 1170/2665 | 1026/1794 | 342/597 | chr5 | 881123 | |||
| chr5:881138 | G | A | 1 | a0002c0003 | 9 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(6): Show |
synonymous_variant | LOW | c.1011C>T | p.Ser337Ser | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/16 | 1155/2665 | 1011/1794 | 337/597 | chr5 | 881138 | |||
| chr5:883944 | G | A | 2 | a0002c0003 a0002c0012 |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
synonymous_variant | LOW | c.960C>T | p.Gly320Gly | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/16 | 1104/2665 | 960/1794 | 320/597 | chr5 | 883944 | |||
| chr5:886609 | C | T | 1 | a0001c0004 | 7 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(4): Show |
synonymous_variant | LOW | c.816G>A | p.Pro272Pro | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/16 | 960/2665 | 816/1794 | 272/597 | chr5 | 886609 | |||
| chr5:887418 | G | A | 1 | a0001c0013 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.660C>T | p.Thr220Thr | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/16 | 804/2665 | 660/1794 | 220/597 | chr5 | 887418 | |||
| chr5:887418 | G | C | 2 | a0002c0003 a0002c0012 |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
synonymous_variant | LOW | c.660C>G | p.Thr220Thr | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/16 | 804/2665 | 660/1794 | 220/597 | chr5 | 887418 | |||
| chr5:891258 | C | T | 1 | a0001c0008 | 1 | NA19058.hp2 | synonymous_variant | LOW | c.297G>A | p.Glu99Glu | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/16 | 441/2665 | 297/1794 | 99/597 | chr5 | 891258 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:863745 | G | A | 1 | a0001c0001t0017 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*723C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 723 | chr5 | 863745 | ||||||
| chr5:863938 | A | G | 7 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(4): Show |
84 | HG00609.hp2 HG01081.hp1 HG01099.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*530T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 530 | chr5 | 863938 | ||||||
| chr5:864017 | G | A | 1 | a0001c0002t0009 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*451C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 451 | chr5 | 864017 | ||||||
| chr5:864065 | C | T | 4 | a0002c0003t0008 a0002c0003t0010 a0002c0003t0012 others(1): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*403G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 403 | chr5 | 864065 | ||||||
| chr5:864073 | A | G | 4 | a0002c0003t0008 a0002c0003t0010 a0002c0003t0012 others(1): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*395T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 395 | chr5 | 864073 | ||||||
| chr5:864075 | C | T | 1 | a0001c0001t0016 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 393 | chr5 | 864075 | ||||||
| chr5:864091 | A | G | 4 | a0002c0003t0008 a0002c0003t0010 a0002c0003t0012 others(1): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*377T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 377 | chr5 | 864091 | ||||||
| chr5:864110 | C | T | 1 | a0001c0001t0015 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*358G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 358 | chr5 | 864110 | ||||||
| chr5:864165 | C | T | 1 | a0001c0004t0003 | 7 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*303G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 303 | chr5 | 864165 | ||||||
| chr5:864189 | C | T | 1 | a0001c0001t0014 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*279G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 279 | chr5 | 864189 | ||||||
| chr5:864193 | T | TATGACTC others(1): Show |
1 | a0001c0002t0009 | 4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*267_*274dupGGAGTC others(2): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 274 | chr5 | 864193 | ||||||
| chr5:864216 | AC | A | 4 | a0002c0003t0008 a0002c0003t0010 a0002c0003t0012 others(1): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*251delG | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 251 | chr5 | 864216 | ||||||
| chr5:864351 | G | A | 1 | a0001c0002t0004 | 5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*117C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 117 | chr5 | 864351 | ||||||
| chr5:864464 | A | G | 1 | a0001c0002t0006 | 5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 16/16 | 4 | chr5 | 864464 | ||||||
| chr5:892693 | G | T | 1 | a0001c0001t0013 | 1 | HG01192.hp2 | 5_prime_UTR_variant | MODIFIER | c.-36C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/16 | 36 | chr5 | 892693 | ||||||
| chr5:892714 | A | C | 1 | a0001c0001t0011 | 2 | HG02040.hp2 HG02083.hp2 |
5_prime_UTR_variant | MODIFIER | c.-57T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/16 | 57 | chr5 | 892714 | ||||||
| chr5:892722 | C | T | 1 | a0001c0001t0005 | 5 | HG01099.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-65G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/16 | 65 | chr5 | 892722 | ||||||
| chr5:892731 | C | T | 2 | a0001c0002t0004 a0002c0003t0010 |
8 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-74G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/16 | 74 | chr5 | 892731 | ||||||
| chr5:892746 | G | A | 1 | a0001c0002t0006 | 5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-89C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/16 | 89 | chr5 | 892746 | ||||||
| chr5:892754 | G | A | 3 | a0001c0001t0007 a0002c0003t0008 a0002c0012t0008 |
10 | HG01884.hp1 HG02451.hp2 HG02630.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-97C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/16 | 97 | chr5 | 892754 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:864708 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1694-140A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 864708 | |||||||
| chr5:864813 | T | A | 1 | a0001c0001t0001g0111 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1694-245A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 864813 | |||||||
| chr5:864912 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1694-344A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 864912 | |||||||
| chr5:864940 | C | A | 3 | a0002c0003t0010g0049 a0002c0003t0010g0050 a0002c0003t0010g0051 |
3 | HG02280.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1694-372G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 864940 | |||||||
| chr5:864941 | A | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1694-373T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 864941 | |||||||
| chr5:865175 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1693+239C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 865175 | |||||||
| chr5:865296 | C | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(96): Show |
185 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(182): Show |
intron_variant | MODIFIER | c.1693+118G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 865296 | |||||||
| chr5:865327 | A | G | 7 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(4): Show |
7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+87T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 15/15 | chr5 | 865327 | |||||||
| chr5:865587 | T | C | 1 | a0002c0012t0008g0182 | 1 | HG03209.hp1 | splice_region_variant&intron_variant | LOW | c.1526-6A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865587 | |||||||
| chr5:865781 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1526-200C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865781 | |||||||
| chr5:865855 | G | A | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1526-274C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865855 | |||||||
| chr5:865865 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1526-284G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865865 | |||||||
| chr5:865880 | C | T | 4 | a0001c0001t0002g0004 a0001c0001t0002g0085 a0001c0001t0002g0087 others(1): Show |
15 | HG00609.hp2 HG02080.hp1 NA18962.hp2 others(12): Show |
intron_variant | MODIFIER | c.1526-299G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865880 | |||||||
| chr5:865900 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1526-319C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865900 | |||||||
| chr5:865921 | C | T | 1 | a0002c0003t0010g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1526-340G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865921 | |||||||
| chr5:865948 | G | A | 4 | a0001c0002t0006g0046 a0001c0002t0006g0178 a0001c0002t0006g0179 others(1): Show |
5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1526-367C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 865948 | |||||||
| chr5:866183 | C | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1526-602G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866183 | |||||||
| chr5:866276 | A | G | 1 | a0001c0008t0001g0063 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1526-695T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866276 | |||||||
| chr5:866489 | A | G | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1526-908T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866489 | |||||||
| chr5:866521 | A | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1526-940T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866521 | |||||||
| chr5:866554 | T | C | 3 | a0002c0003t0010g0049 a0002c0003t0010g0050 a0002c0003t0010g0051 |
3 | HG02280.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1526-973A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866554 | |||||||
| chr5:866602 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1526-1021G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866602 | |||||||
| chr5:866603 | G | A | 49 | a0001c0001t0001g0045 a0001c0001t0002g0003 a0001c0001t0002g0004 others(46): Show |
99 | HG00609.hp2 HG01081.hp1 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1526-1022C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866603 | |||||||
| chr5:866761 | A | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1526-1180T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866761 | |||||||
| chr5:866856 | A | T | 69 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0133 others(66): Show |
119 | HG00609.hp2 HG01081.hp1 HG01099.hp1 others(116): Show |
intron_variant | MODIFIER | c.1526-1275T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 866856 | |||||||
| chr5:867138 | G | A | 1 | a0002c0003t0010g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1526-1557C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867138 | |||||||
| chr5:867154 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1526-1573C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867154 | |||||||
| chr5:867213 | G | C | 41 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0007 others(38): Show |
84 | HG00609.hp2 HG01081.hp1 HG01099.hp1 others(81): Show |
intron_variant | MODIFIER | c.1526-1632C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867213 | |||||||
| chr5:867487 | G | A | 1 | a0001c0001t0001g0016 | 3 | HG02132.hp1 NA18950.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1526-1906C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867487 | |||||||
| chr5:867490 | A | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0161 a0001c0001t0001g0164 others(2): Show |
8 | HG01192.hp1 HG01981.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1526-1909T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867490 | |||||||
| chr5:867564 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1526-1983G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867564 | |||||||
| chr5:867745 | C | T | 1 | a0003c0006t0001g0100 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1526-2164G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867745 | |||||||
| chr5:867879 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0073 |
2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1526-2298C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 867879 | |||||||
| chr5:868453 | C | T | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1525+2020G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 868453 | |||||||
| chr5:868570 | T | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1525+1903A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 868570 | |||||||
| chr5:868626 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1525+1847A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 868626 | |||||||
| chr5:868686 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1525+1787G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 868686 | |||||||
| chr5:868731 | G | A | 1 | a0001c0001t0001g0017 | 2 | HG00323.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1525+1742C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 868731 | |||||||
| chr5:868924 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1525+1549G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 868924 | |||||||
| chr5:869301 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1525+1172T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869301 | |||||||
| chr5:869309 | G | A | 7 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(4): Show |
13 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1525+1164C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869309 | |||||||
| chr5:869431 | C | T | 21 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(18): Show |
32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1525+1042G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869431 | |||||||
| chr5:869450 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1525+1023A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869450 | |||||||
| chr5:869467 | A | C | 17 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(14): Show |
23 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1525+1006T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869467 | |||||||
| chr5:869514 | C | CAAGTCTC others(7): Show |
10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1525+945_1525+958d others(16): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869514 | |||||||
| chr5:869733 | T | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1525+740A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869733 | |||||||
| chr5:869752 | G | T | 2 | a0001c0002t0009g0020 a0001c0002t0009g0177 |
4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525+721C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869752 | |||||||
| chr5:869764 | G | A | 1 | a0002c0003t0010g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1525+709C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869764 | |||||||
| chr5:869806 | C | T | 4 | a0001c0002t0006g0046 a0001c0002t0006g0178 a0001c0002t0006g0179 others(1): Show |
5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525+667G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869806 | |||||||
| chr5:869861 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1525+612T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869861 | |||||||
| chr5:869873 | G | A | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1525+600C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 869873 | |||||||
| chr5:870072 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1525+401G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 870072 | |||||||
| chr5:870179 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0113 a0001c0001t0001g0114 |
4 | HG00323.hp2 HG01070.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525+294C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 870179 | |||||||
| chr5:870181 | T | C | 1 | a0001c0001t0002g0090 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1525+292A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 870181 | |||||||
| chr5:870339 | G | T | 2 | a0001c0002t0009g0020 a0001c0002t0009g0177 |
4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525+134C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 870339 | |||||||
| chr5:870341 | C | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1525+132G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 870341 | |||||||
| chr5:870440 | A | G | 21 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(18): Show |
32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1525+33T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 14/15 | chr5 | 870440 | |||||||
| chr5:870625 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0098 others(2): Show |
7 | HG00323.hp1 HG00738.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1423-50G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 870625 | |||||||
| chr5:870725 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1423-150C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 870725 | |||||||
| chr5:870811 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1423-236G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 870811 | |||||||
| chr5:870828 | G | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG02056.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1423-253C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 870828 | |||||||
| chr5:870990 | C | CT | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1423-416dupA | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 870990 | |||||||
| chr5:870999 | ACT | A | 2 | a0001c0002t0009g0020 a0001c0002t0009g0177 |
4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1423-426_1423-425d others(4): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 870999 | |||||||
| chr5:871018 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1423-443C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 871018 | |||||||
| chr5:871018 | G | C | 3 | a0003c0006t0001g0077 a0003c0006t0001g0100 a0003c0006t0001g0101 |
3 | NA18950.hp1 NA18997.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1423-443C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 871018 | |||||||
| chr5:871066 | T | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0148 |
3 | HG00099.hp1 HG03704.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1422+460A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 871066 | |||||||
| chr5:871069 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1422+457G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 871069 | |||||||
| chr5:871233 | T | C | 21 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(18): Show |
32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1422+293A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 871233 | |||||||
| chr5:871483 | T | C | 21 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(18): Show |
32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1422+43A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 13/15 | chr5 | 871483 | |||||||
| chr5:871657 | T | C | 7 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(4): Show |
13 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1384-93A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 871657 | |||||||
| chr5:871790 | G | A | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-226C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 871790 | |||||||
| chr5:871842 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1384-278C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 871842 | |||||||
| chr5:872001 | G | T | 1 | a0001c0001t0005g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1384-437C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872001 | |||||||
| chr5:872052 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(5): Show |
16 | HG00140.hp2 HG00741.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.1384-488G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872052 | |||||||
| chr5:872053 | G | A | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-489C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872053 | |||||||
| chr5:872087 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0105 others(2): Show |
13 | HG00544.hp1 HG00558.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.1384-523C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872087 | |||||||
| chr5:872105 | T | TGGGCC | 3 | a0001c0005t0002g0080 a0001c0005t0002g0086 a0001c0005t0002g0088 |
3 | HG02809.hp2 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1384-546_1384-542d others(7): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872105 | |||||||
| chr5:872111 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1384-547C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872111 | |||||||
| chr5:872148 | C | T | 6 | a0001c0002t0006g0046 a0001c0002t0006g0178 a0001c0002t0006g0179 others(3): Show |
9 | HG01891.hp2 HG02486.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1384-584G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872148 | |||||||
| chr5:872151 | G | A | 1 | a0002c0012t0008g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1384-587C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872151 | |||||||
| chr5:872160 | G | A | 1 | a0002c0003t0010g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1384-596C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872160 | |||||||
| chr5:872194 | T | C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | HG02976.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1384-630A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872194 | |||||||
| chr5:872195 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1384-631C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872195 | |||||||
| chr5:872239 | A | G | 3 | a0001c0001t0002g0031 a0001c0001t0002g0125 a0001c0001t0002g0126 |
4 | HG02257.hp2 HG02258.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384-675T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872239 | |||||||
| chr5:872251 | C | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-687G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872251 | |||||||
| chr5:872252 | G | A | 1 | a0001c0002t0004g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1384-688C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872252 | |||||||
| chr5:872314 | A | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-750T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872314 | |||||||
| chr5:872324 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1384-760C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872324 | |||||||
| chr5:872471 | A | G | 4 | a0001c0002t0006g0046 a0001c0002t0006g0178 a0001c0002t0006g0179 others(1): Show |
5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1384-907T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872471 | |||||||
| chr5:872506 | G | A | 4 | a0001c0002t0006g0046 a0001c0002t0006g0178 a0001c0002t0006g0179 others(1): Show |
5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1384-942C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872506 | |||||||
| chr5:872515 | G | C | 1 | a0001c0005t0002g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1384-951C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872515 | |||||||
| chr5:872515 | G | T | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-951C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872515 | |||||||
| chr5:872641 | G | C | 3 | a0002c0003t0010g0049 a0002c0003t0010g0050 a0002c0003t0010g0051 |
3 | HG02280.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1384-1077C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872641 | |||||||
| chr5:872650 | T | G | 21 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(18): Show |
32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1384-1086A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872650 | |||||||
| chr5:872693 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG02056.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1384-1129G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872693 | |||||||
| chr5:872707 | A | T | 1 | a0001c0001t0001g0005 | 9 | HG00544.hp1 HG00558.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1384-1143T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872707 | |||||||
| chr5:872962 | A | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-1398T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 872962 | |||||||
| chr5:873033 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-1469G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873033 | |||||||
| chr5:873107 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-1543C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873107 | |||||||
| chr5:873222 | T | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-1658A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873222 | |||||||
| chr5:873237 | C | T | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-1673G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873237 | |||||||
| chr5:873336 | T | C | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-1772A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873336 | |||||||
| chr5:873476 | A | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0016g0165 |
10 | HG01070.hp2 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1384-1912T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873476 | |||||||
| chr5:873484 | T | C | 1 | a0001c0001t0002g0125 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1384-1920A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873484 | |||||||
| chr5:873591 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(39): Show |
78 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1384-2027G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873591 | |||||||
| chr5:873669 | C | G | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-2105G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873669 | |||||||
| chr5:873683 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(82): Show |
166 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(163): Show |
intron_variant | MODIFIER | c.1384-2119T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873683 | |||||||
| chr5:873745 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-2181G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873745 | |||||||
| chr5:873788 | A | T | 3 | a0001c0004t0003g0012 a0001c0004t0003g0039 a0001c0004t0003g0150 |
7 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1384-2224T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873788 | |||||||
| chr5:873805 | T | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-2241A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873805 | |||||||
| chr5:873806 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-2242C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873806 | |||||||
| chr5:873833 | G | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+2268C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873833 | |||||||
| chr5:873886 | G | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
15 | HG00140.hp2 HG00741.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1383+2215C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873886 | |||||||
| chr5:873904 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1383+2197C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873904 | |||||||
| chr5:873907 | G | A | 1 | a0001c0001t0007g0047 | 2 | HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1383+2194C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873907 | |||||||
| chr5:873995 | T | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+2106A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 873995 | |||||||
| chr5:874047 | A | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+2054T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874047 | |||||||
| chr5:874068 | C | T | 1 | a0001c0001t0001g0019 | 3 | HG01123.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1383+2033G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874068 | |||||||
| chr5:874148 | C | CCTAGA | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1948_1383+195 others(9): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874148 | |||||||
| chr5:874324 | T | TA | 3 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0152 |
5 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1383+1776dupT | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874324 | |||||||
| chr5:874362 | G | A | 6 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0152 others(3): Show |
12 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1383+1739C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874362 | |||||||
| chr5:874391 | T | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1710A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874391 | |||||||
| chr5:874402 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1699G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874402 | |||||||
| chr5:874479 | G | A | 1 | a0001c0002t0002g0151 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1383+1622C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874479 | |||||||
| chr5:874610 | C | A | 1 | a0002c0012t0008g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1383+1491G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874610 | |||||||
| chr5:874645 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1383+1456T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874645 | |||||||
| chr5:874658 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1443C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874658 | |||||||
| chr5:874750 | C | T | 2 | a0002c0003t0010g0050 a0002c0003t0010g0051 |
2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1383+1351G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874750 | |||||||
| chr5:874788 | C | T | 7 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(4): Show |
13 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1383+1313G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874788 | |||||||
| chr5:874873 | C | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(27): Show |
66 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1383+1228G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874873 | |||||||
| chr5:874930 | G | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1171C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874930 | |||||||
| chr5:874937 | G | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1164C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874937 | |||||||
| chr5:874977 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1383+1124A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 874977 | |||||||
| chr5:875144 | G | A | 4 | a0001c0002t0006g0046 a0001c0002t0006g0178 a0001c0002t0006g0179 others(1): Show |
5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1383+957C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875144 | |||||||
| chr5:875338 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1383+763C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875338 | |||||||
| chr5:875347 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+754G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875347 | |||||||
| chr5:875349 | C | CA | 5 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0004t0003g0012 others(2): Show |
11 | HG01081.hp1 HG01168.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1383+751_1383+752i others(3): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875349 | |||||||
| chr5:875349 | C | CT | 8 | a0001c0001t0001g0061 a0001c0001t0001g0141 a0001c0001t0001g0143 others(5): Show |
8 | HG02055.hp2 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1383+751dupA | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875349 | |||||||
| chr5:875349 | CT | C | 11 | a0001c0001t0001g0028 a0002c0003t0008g0183 a0002c0003t0008g0184 others(8): Show |
12 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1383+751delA | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875349 | |||||||
| chr5:875373 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+728C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875373 | |||||||
| chr5:875379 | G | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0104 |
6 | HG00408.hp1 HG00673.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1383+722C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875379 | |||||||
| chr5:875474 | A | T | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1383+627T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875474 | |||||||
| chr5:875505 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1383+596C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875505 | |||||||
| chr5:875889 | G | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(22): Show |
58 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1383+212C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875889 | |||||||
| chr5:875946 | C | T | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1383+155G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875946 | |||||||
| chr5:875961 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1383+140G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875961 | |||||||
| chr5:875973 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1383+128G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875973 | |||||||
| chr5:875981 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+120G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875981 | |||||||
| chr5:875998 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0041 others(2): Show |
10 | HG02109.hp2 HG02145.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+103G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 875998 | |||||||
| chr5:876010 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+91C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 876010 | |||||||
| chr5:876046 | G | A | 12 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0002c0003t0008g0183 others(9): Show |
13 | HG00738.hp1 HG01069.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1383+55C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 876046 | |||||||
| chr5:876064 | G | C | 1 | a0007c0010t0001g0096 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1383+37C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 876064 | |||||||
| chr5:876072 | C | T | 10 | a0001c0001t0001g0142 a0001c0002t0002g0037 a0001c0002t0002g0038 others(7): Show |
18 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1383+29G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 876072 | |||||||
| chr5:876077 | A | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+24T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 876077 | |||||||
| chr5:876082 | C | T | 2 | a0003c0006t0001g0100 a0003c0006t0001g0101 |
2 | NA18950.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1383+19G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 876082 | |||||||
| chr5:876087 | C | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+14G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 12/15 | chr5 | 876087 | |||||||
| chr5:876224 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0120 others(2): Show |
6 | HG02280.hp1 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1272-12C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876224 | |||||||
| chr5:876262 | G | A | 1 | a0002c0003t0010g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1272-50C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876262 | |||||||
| chr5:876317 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0079 |
3 | HG02109.hp2 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1272-105G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876317 | |||||||
| chr5:876321 | G | C | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272-109C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876321 | |||||||
| chr5:876347 | T | G | 29 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0133 others(26): Show |
38 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.1272-135A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876347 | |||||||
| chr5:876421 | G | A | 3 | a0001c0005t0002g0080 a0001c0005t0002g0086 a0001c0005t0002g0088 |
3 | HG02809.hp2 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1272-209C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876421 | |||||||
| chr5:876518 | G | A | 1 | a0003c0006t0001g0077 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1272-306C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876518 | |||||||
| chr5:876588 | T | A | 1 | a0001c0001t0002g0093 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1272-376A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876588 | |||||||
| chr5:876594 | C | T | 7 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(4): Show |
13 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1272-382G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876594 | |||||||
| chr5:876721 | A | C | 1 | a0001c0001t0001g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1272-509T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876721 | |||||||
| chr5:876755 | C | G | 9 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(6): Show |
9 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1272-543G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876755 | |||||||
| chr5:876791 | A | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272-579T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876791 | |||||||
| chr5:876851 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272-639C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876851 | |||||||
| chr5:876865 | C | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272-653G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876865 | |||||||
| chr5:876888 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272-676C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876888 | |||||||
| chr5:876911 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1272-699C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876911 | |||||||
| chr5:876911 | G | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272-699C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876911 | |||||||
| chr5:876961 | C | A | 1 | a0001c0001t0002g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1272-749G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 876961 | |||||||
| chr5:877048 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1272-836G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877048 | |||||||
| chr5:877073 | G | A | 8 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(5): Show |
8 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272-861C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877073 | |||||||
| chr5:877152 | A | G | 7 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0133 others(4): Show |
8 | HG02280.hp1 HG02818.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272-940T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877152 | |||||||
| chr5:877213 | G | A | 4 | a0002c0003t0010g0049 a0002c0003t0010g0050 a0002c0003t0010g0051 others(1): Show |
4 | HG02280.hp2 HG02559.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272-1001C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877213 | |||||||
| chr5:877238 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272-1026G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877238 | |||||||
| chr5:877344 | G | A | 9 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(6): Show |
9 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1271+1011C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877344 | |||||||
| chr5:877377 | G | A | 21 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(18): Show |
32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1271+978C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877377 | |||||||
| chr5:877567 | A | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0098 |
2 | HG00738.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1271+788T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877567 | |||||||
| chr5:877584 | C | A | 2 | a0001c0002t0009g0020 a0001c0002t0009g0177 |
4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1271+771G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877584 | |||||||
| chr5:877635 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+720G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877635 | |||||||
| chr5:877667 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1271+688C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877667 | |||||||
| chr5:877701 | A | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+654T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877701 | |||||||
| chr5:877724 | T | G | 1 | a0001c0001t0002g0124 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1271+631A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877724 | |||||||
| chr5:877734 | G | A | 4 | a0001c0002t0006g0046 a0001c0002t0006g0178 a0001c0002t0006g0179 others(1): Show |
5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271+621C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877734 | |||||||
| chr5:877742 | T | A | 1 | a0001c0001t0001g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1271+613A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877742 | |||||||
| chr5:877779 | T | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+576A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877779 | |||||||
| chr5:877785 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1271+570G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877785 | |||||||
| chr5:877924 | A | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+431T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877924 | |||||||
| chr5:877937 | C | T | 11 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0133 others(8): Show |
18 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1271+418G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877937 | |||||||
| chr5:877942 | C | G | 1 | a0002c0003t0010g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1271+413G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877942 | |||||||
| chr5:877967 | G | C | 1 | a0002c0003t0010g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1271+388C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 877967 | |||||||
| chr5:878018 | A | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+337T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878018 | |||||||
| chr5:878033 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1271+322C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878033 | |||||||
| chr5:878068 | T | C | 21 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(18): Show |
32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1271+287A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878068 | |||||||
| chr5:878145 | A | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+210T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878145 | |||||||
| chr5:878238 | A | C | 3 | a0002c0003t0010g0049 a0002c0003t0010g0050 a0002c0003t0010g0051 |
3 | HG02280.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1271+117T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878238 | |||||||
| chr5:878271 | G | A | 1 | a0001c0001t0001g0030 | 2 | NA18962.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1271+84C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878271 | |||||||
| chr5:878281 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1271+74C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878281 | |||||||
| chr5:878284 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1271+71T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878284 | |||||||
| chr5:878289 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1271+66T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878289 | |||||||
| chr5:878290 | C | G | 1 | a0001c0001t0001g0036 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1271+65G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878290 | |||||||
| chr5:878306 | A | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+49T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878306 | |||||||
| chr5:878333 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1271+22C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878333 | |||||||
| chr5:878334 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1271+21G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 11/15 | chr5 | 878334 | |||||||
| chr5:878492 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18959.hp1 | splice_region_variant&intron_variant | LOW | c.1139-5C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878492 | |||||||
| chr5:878550 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1139-63G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878550 | |||||||
| chr5:878632 | A | G | 25 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(22): Show |
37 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.1139-145T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878632 | |||||||
| chr5:878642 | T | G | 15 | a0001c0001t0001g0169 a0001c0002t0006g0046 a0001c0002t0006g0178 others(12): Show |
16 | HG01261.hp2 HG01884.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.1139-155A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878642 | |||||||
| chr5:878645 | C | A | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1139-158G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878645 | |||||||
| chr5:878684 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG01106.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1139-197A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878684 | |||||||
| chr5:878685 | T | G | 1 | a0002c0003t0008g0185 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1139-198A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878685 | |||||||
| chr5:878758 | T | C | 6 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0152 others(3): Show |
12 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1139-271A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878758 | |||||||
| chr5:878768 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1139-281G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878768 | |||||||
| chr5:878808 | A | G | 1 | a0001c0004t0003g0039 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1139-321T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878808 | |||||||
| chr5:878820 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1139-333G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878820 | |||||||
| chr5:878827 | A | G | 2 | a0001c0001t0011g0022 a0001c0002t0002g0151 |
3 | HG02040.hp2 HG02083.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1139-340T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878827 | |||||||
| chr5:878838 | C | T | 1 | a0001c0005t0002g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1139-351G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878838 | |||||||
| chr5:878985 | A | G | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1139-498T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878985 | |||||||
| chr5:878990 | C | CA | 11 | a0001c0002t0002g0151 a0002c0003t0008g0183 a0002c0003t0008g0184 others(8): Show |
11 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1139-504dupT | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 878990 | |||||||
| chr5:879017 | G | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1139-530C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879017 | |||||||
| chr5:879064 | A | AC | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1139-578_1139-577i others(3): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879064 | |||||||
| chr5:879068 | A | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1139-581T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879068 | |||||||
| chr5:879069 | A | C | 1 | a0001c0002t0009g0177 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1139-582T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879069 | |||||||
| chr5:879107 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1139-620C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879107 | |||||||
| chr5:879308 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1138+486A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879308 | |||||||
| chr5:879321 | C | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0148 a0002c0003t0010g0049 others(3): Show |
7 | HG00099.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1138+473G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879321 | |||||||
| chr5:879339 | G | A | 30 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0007 others(27): Show |
67 | HG00609.hp2 HG01099.hp1 HG01192.hp2 others(64): Show |
intron_variant | MODIFIER | c.1138+455C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879339 | |||||||
| chr5:879357 | T | C | 1 | a0001c0004t0003g0012 | 4 | HG02965.hp2 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1138+437A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879357 | |||||||
| chr5:879391 | T | C | 49 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0133 others(46): Show |
91 | HG00609.hp2 HG01081.hp1 HG01099.hp1 others(88): Show |
intron_variant | MODIFIER | c.1138+403A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879391 | |||||||
| chr5:879392 | G | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0062 a0001c0001t0002g0078 others(2): Show |
11 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1138+402C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879392 | |||||||
| chr5:879398 | T | G | 55 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0133 others(52): Show |
99 | HG00609.hp2 HG01081.hp1 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1138+396A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879398 | |||||||
| chr5:879414 | G | A | 2 | a0001c0001t0002g0058 a0001c0001t0002g0091 |
2 | NA18980.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1138+380C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879414 | |||||||
| chr5:879450 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1138+344C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879450 | |||||||
| chr5:879462 | A | G | 8 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0058 others(5): Show |
23 | HG02027.hp2 HG03927.hp1 NA18943.hp1 others(20): Show |
intron_variant | MODIFIER | c.1138+332T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879462 | |||||||
| chr5:879491 | A | G | 4 | a0001c0002t0006g0046 a0001c0002t0006g0178 a0001c0002t0006g0179 others(1): Show |
5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138+303T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879491 | |||||||
| chr5:879527 | G | A | 7 | a0001c0002t0004g0011 a0001c0002t0004g0052 a0001c0002t0009g0020 others(4): Show |
12 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1138+267C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879527 | |||||||
| chr5:879543 | C | T | 26 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0007 others(23): Show |
59 | HG00609.hp2 HG01099.hp1 HG01192.hp2 others(56): Show |
intron_variant | MODIFIER | c.1138+251G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879543 | |||||||
| chr5:879582 | T | C | 1 | a0001c0002t0009g0020 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1138+212A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879582 | |||||||
| chr5:879597 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1138+197G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879597 | |||||||
| chr5:879622 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1138+172C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879622 | |||||||
| chr5:879655 | T | G | 1 | a0001c0001t0002g0128 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1138+139A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879655 | |||||||
| chr5:879722 | T | C | 6 | a0001c0001t0001g0144 a0001c0002t0004g0011 a0001c0002t0004g0052 others(3): Show |
11 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1138+72A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 10/15 | chr5 | 879722 | |||||||
| chr5:879974 | C | A | 7 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(4): Show |
7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1043-85G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 879974 | |||||||
| chr5:879984 | G | C | 1 | a0001c0001t0002g0129 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1043-95C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 879984 | |||||||
| chr5:879991 | T | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1043-102A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 879991 | |||||||
| chr5:879998 | A | G | 31 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0076 others(28): Show |
43 | HG00639.hp1 HG01081.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.1043-109T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 879998 | |||||||
| chr5:880031 | C | G | 2 | a0001c0002t0002g0038 a0001c0002t0002g0152 |
3 | HG01081.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1043-142G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880031 | |||||||
| chr5:880102 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1043-213C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880102 | |||||||
| chr5:880207 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1043-318G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880207 | |||||||
| chr5:880208 | G | A | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1043-319C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880208 | |||||||
| chr5:880211 | T | C | 11 | a0001c0001t0001g0130 a0002c0003t0008g0183 a0002c0003t0008g0184 others(8): Show |
11 | HG00738.hp1 HG01261.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1043-322A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880211 | |||||||
| chr5:880235 | T | C | 4 | a0001c0002t0006g0046 a0001c0002t0006g0178 a0001c0002t0006g0179 others(1): Show |
5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043-346A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880235 | |||||||
| chr5:880335 | C | G | 9 | a0002c0003t0008g0183 a0002c0003t0008g0185 a0002c0003t0008g0186 others(6): Show |
9 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1043-446G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880335 | |||||||
| chr5:880458 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1043-569C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880458 | |||||||
| chr5:880485 | C | G | 1 | a0001c0001t0002g0085 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1043-596G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880485 | |||||||
| chr5:880498 | T | C | 8 | a0001c0001t0001g0084 a0001c0002t0002g0037 a0001c0002t0002g0038 others(5): Show |
14 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1042+609A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880498 | |||||||
| chr5:880500 | A | C | 10 | a0001c0001t0001g0084 a0001c0002t0002g0037 a0001c0002t0002g0038 others(7): Show |
18 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1042+607T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880500 | |||||||
| chr5:880501 | G | A | 2 | a0001c0002t0009g0020 a0001c0002t0009g0177 |
4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042+606C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880501 | |||||||
| chr5:880538 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0162 others(1): Show |
6 | HG02559.hp1 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042+569G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880538 | |||||||
| chr5:880561 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042+546G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880561 | |||||||
| chr5:880564 | G | A | 1 | a0001c0001t0002g0033 | 2 | NA18974.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.1042+543C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880564 | |||||||
| chr5:880569 | C | T | 1 | a0002c0003t0012g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1042+538G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880569 | |||||||
| chr5:880572 | G | T | 1 | a0001c0001t0001g0083 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1042+535C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880572 | |||||||
| chr5:880578 | G | A | 1 | a0001c0001t0001g0018 | 3 | HG00741.hp1 HG01256.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1042+529C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880578 | |||||||
| chr5:880604 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042+503G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880604 | |||||||
| chr5:880616 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1042+491T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880616 | |||||||
| chr5:880656 | C | T | 2 | a0001c0002t0009g0020 a0001c0002t0009g0177 |
4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042+451G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880656 | |||||||
| chr5:880672 | A | C | 7 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(4): Show |
13 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1042+435T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880672 | |||||||
| chr5:880676 | T | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042+431A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880676 | |||||||
| chr5:880725 | A | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042+382T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880725 | |||||||
| chr5:880768 | T | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042+339A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880768 | |||||||
| chr5:880860 | A | G | 3 | a0001c0001t0002g0157 a0001c0002t0004g0011 a0001c0002t0004g0052 |
6 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042+247T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880860 | |||||||
| chr5:880874 | G | A | 1 | a0001c0001t0007g0048 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1042+233C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880874 | |||||||
| chr5:880889 | C | A | 2 | a0001c0002t0006g0179 a0001c0002t0006g0180 |
2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1042+218G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880889 | |||||||
| chr5:880952 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG00597.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1042+155C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880952 | |||||||
| chr5:880972 | C | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(26): Show |
65 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1042+135G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880972 | |||||||
| chr5:880972 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042+135G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880972 | |||||||
| chr5:880978 | AGGTCG | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0133 others(1): Show |
5 | HG02280.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042+124_1042+128d others(7): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 880978 | |||||||
| chr5:881042 | A | G | 1 | a0001c0001t0002g0035 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1042+65T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 881042 | |||||||
| chr5:881090 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1042+17G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 9/15 | chr5 | 881090 | |||||||
| chr5:881516 | C | T | 3 | a0001c0004t0003g0012 a0001c0004t0003g0039 a0001c0004t0003g0150 |
7 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-334G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881516 | |||||||
| chr5:881532 | C | T | 6 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(3): Show |
6 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-350G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881532 | |||||||
| chr5:881596 | C | T | 8 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0152 others(5): Show |
16 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.967-414G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881596 | |||||||
| chr5:881610 | GATCC | G | 7 | a0001c0001t0005g0021 a0001c0001t0005g0053 a0001c0001t0005g0054 others(4): Show |
10 | HG01099.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.967-432_967-429del others(4): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881610 | |||||||
| chr5:881679 | G | A | 3 | a0001c0001t0001g0131 a0001c0002t0009g0020 a0001c0002t0009g0177 |
5 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.967-497C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881679 | |||||||
| chr5:881763 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.967-581G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881763 | |||||||
| chr5:881795 | G | C | 2 | a0001c0002t0009g0020 a0001c0002t0009g0177 |
4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-613C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881795 | |||||||
| chr5:881855 | G | A | 14 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(11): Show |
21 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.967-673C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881855 | |||||||
| chr5:881908 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.967-726C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 881908 | |||||||
| chr5:882133 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.967-951C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882133 | |||||||
| chr5:882362 | A | T | 2 | a0001c0002t0009g0020 a0001c0002t0009g0177 |
4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-1180T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882362 | |||||||
| chr5:882425 | T | C | 4 | a0001c0002t0006g0046 a0001c0002t0006g0178 a0001c0002t0006g0179 others(1): Show |
5 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.967-1243A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882425 | |||||||
| chr5:882434 | C | T | 4 | a0001c0001t0001g0149 a0002c0003t0010g0049 a0002c0003t0010g0050 others(1): Show |
4 | HG02280.hp2 HG02559.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-1252G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882434 | |||||||
| chr5:882441 | C | G | 1 | a0001c0002t0002g0037 | 2 | HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.967-1259G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882441 | |||||||
| chr5:882471 | C | T | 7 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(4): Show |
7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-1289G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882471 | |||||||
| chr5:882518 | C | T | 1 | a0001c0005t0002g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.967-1336G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882518 | |||||||
| chr5:882524 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.967-1342G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882524 | |||||||
| chr5:882525 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.967-1343C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882525 | |||||||
| chr5:882635 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+1303G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882635 | |||||||
| chr5:882742 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+1196C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882742 | |||||||
| chr5:882750 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.966+1188G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882750 | |||||||
| chr5:882811 | G | C | 1 | a0001c0002t0009g0177 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.966+1127C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882811 | |||||||
| chr5:882829 | T | G | 10 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0133 others(7): Show |
11 | HG02280.hp1 HG02572.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.966+1109A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882829 | |||||||
| chr5:882854 | T | A | 1 | a0001c0001t0001g0019 | 3 | HG01123.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.966+1084A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882854 | |||||||
| chr5:882909 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+1029G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882909 | |||||||
| chr5:882944 | G | T | 3 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0152 |
5 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.966+994C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882944 | |||||||
| chr5:882947 | AACCACAA others(24): Show |
A | 7 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(4): Show |
7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+960_966+990del others(31): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882947 | |||||||
| chr5:882950 | C | G | 29 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(26): Show |
65 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.966+988G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882950 | |||||||
| chr5:882999 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.966+939C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 882999 | |||||||
| chr5:883052 | T | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+886A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883052 | |||||||
| chr5:883108 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0079 |
3 | HG02109.hp2 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.966+830G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883108 | |||||||
| chr5:883129 | CCACA | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0133 others(1): Show |
5 | HG02280.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.966+805_966+808del others(4): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883129 | |||||||
| chr5:883172 | C | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+766G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883172 | |||||||
| chr5:883185 | T | G | 7 | a0001c0002t0004g0011 a0001c0002t0004g0052 a0001c0002t0009g0020 others(4): Show |
16 | HG01175.hp1 HG01243.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.966+753A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883185 | |||||||
| chr5:883190 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.966+748A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883190 | |||||||
| chr5:883196 | C | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+742G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883196 | |||||||
| chr5:883204 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+734G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883204 | |||||||
| chr5:883228 | G | T | 1 | a0001c0001t0001g0162 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.966+710C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883228 | |||||||
| chr5:883266 | T | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+672A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883266 | |||||||
| chr5:883509 | T | C | 2 | a0001c0002t0009g0020 a0001c0002t0009g0177 |
4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+429A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883509 | |||||||
| chr5:883522 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(26): Show |
65 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.966+416C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883522 | |||||||
| chr5:883540 | C | T | 2 | a0001c0002t0009g0020 a0001c0002t0009g0177 |
4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+398G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883540 | |||||||
| chr5:883561 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.966+377T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883561 | |||||||
| chr5:883821 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.966+117G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883821 | |||||||
| chr5:883846 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+92C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883846 | |||||||
| chr5:883903 | C | T | 1 | a0003c0006t0001g0077 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.966+35G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 8/15 | chr5 | 883903 | |||||||
| chr5:884136 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(26): Show |
65 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.834-66C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884136 | |||||||
| chr5:884244 | G | A | 11 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(8): Show |
22 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.834-174C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884244 | |||||||
| chr5:884324 | A | C | 11 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(8): Show |
22 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.834-254T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884324 | |||||||
| chr5:884334 | A | G | 1 | a0001c0002t0002g0151 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.834-264T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884334 | |||||||
| chr5:884388 | T | C | 6 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0152 others(3): Show |
12 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.834-318A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884388 | |||||||
| chr5:884523 | T | G | 7 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(4): Show |
13 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.834-453A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884523 | |||||||
| chr5:884569 | T | C | 21 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(18): Show |
32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.834-499A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884569 | |||||||
| chr5:884655 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0076 |
6 | HG00639.hp1 HG01255.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.834-585G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884655 | |||||||
| chr5:884709 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0133 others(1): Show |
5 | HG02280.hp1 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.834-639A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 884709 | |||||||
| chr5:885045 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.834-975G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885045 | |||||||
| chr5:885046 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.834-976G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885046 | |||||||
| chr5:885092 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.834-1022C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885092 | |||||||
| chr5:885203 | A | C | 7 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(4): Show |
7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.834-1133T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885203 | |||||||
| chr5:885237 | C | G | 3 | a0001c0004t0003g0012 a0001c0004t0003g0039 a0001c0004t0003g0150 |
7 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.834-1167G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885237 | |||||||
| chr5:885319 | C | G | 29 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(26): Show |
65 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.834-1249G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885319 | |||||||
| chr5:885321 | A | G | 1 | a0001c0001t0001g0042 | 2 | HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.834-1251T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885321 | |||||||
| chr5:885339 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.833+1253G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885339 | |||||||
| chr5:885426 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.833+1166C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885426 | |||||||
| chr5:885462 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.833+1130A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885462 | |||||||
| chr5:885464 | T | G | 2 | a0001c0002t0009g0020 a0001c0002t0009g0177 |
4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.833+1128A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885464 | |||||||
| chr5:885517 | G | A | 21 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(18): Show |
32 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.833+1075C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885517 | |||||||
| chr5:885529 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.833+1063G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885529 | |||||||
| chr5:885530 | T | A | 1 | a0001c0001t0005g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.833+1062A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885530 | |||||||
| chr5:885533 | A | C | 1 | a0001c0001t0005g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.833+1059T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885533 | |||||||
| chr5:885552 | A | G | 1 | a0001c0002t0009g0020 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.833+1040T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885552 | |||||||
| chr5:885563 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.833+1029G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885563 | |||||||
| chr5:885593 | C | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(26): Show |
65 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.833+999G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885593 | |||||||
| chr5:885607 | T | C | 1 | a0002c0003t0010g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.833+985A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885607 | |||||||
| chr5:885720 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG01106.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.833+872C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885720 | |||||||
| chr5:885792 | T | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.833+800A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885792 | |||||||
| chr5:885796 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.833+796C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885796 | |||||||
| chr5:885799 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.833+793G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885799 | |||||||
| chr5:885802 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.833+790A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885802 | |||||||
| chr5:885850 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.833+742A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885850 | |||||||
| chr5:885935 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.833+657G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885935 | |||||||
| chr5:885950 | C | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.833+642G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 885950 | |||||||
| chr5:886084 | C | T | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.833+508G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 886084 | |||||||
| chr5:886111 | G | A | 11 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(8): Show |
22 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.833+481C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 886111 | |||||||
| chr5:886276 | G | A | 3 | a0001c0001t0001g0138 a0001c0002t0004g0011 a0001c0002t0004g0052 |
6 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.833+316C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 886276 | |||||||
| chr5:886475 | T | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.833+117A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 886475 | |||||||
| chr5:886482 | G | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.833+110C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 886482 | |||||||
| chr5:886574 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.833+18A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 886574 | |||||||
| chr5:886584 | A | G | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.833+8T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 7/15 | chr5 | 886584 | |||||||
| chr5:886891 | G | A | 1 | a0001c0001t0007g0048 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.718-184C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/15 | chr5 | 886891 | |||||||
| chr5:886928 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.718-221C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/15 | chr5 | 886928 | |||||||
| chr5:887013 | A | AGCCACTG others(6): Show |
2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-307_718-306ins others(13): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/15 | chr5 | 887013 | |||||||
| chr5:887062 | T | A | 2 | a0001c0002t0009g0020 a0001c0002t0009g0177 |
4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+299A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/15 | chr5 | 887062 | |||||||
| chr5:887172 | T | C | 3 | a0002c0003t0010g0049 a0002c0003t0010g0050 a0002c0003t0010g0051 |
3 | HG02280.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.717+189A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/15 | chr5 | 887172 | |||||||
| chr5:887211 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.717+150C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 6/15 | chr5 | 887211 | |||||||
| chr5:887611 | T | C | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-140A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 887611 | |||||||
| chr5:887687 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.607-216C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 887687 | |||||||
| chr5:887726 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.607-255C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 887726 | |||||||
| chr5:887744 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.607-273C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 887744 | |||||||
| chr5:887787 | G | A | 1 | a0002c0012t0008g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.607-316C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 887787 | |||||||
| chr5:887829 | G | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.607-358C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 887829 | |||||||
| chr5:887993 | T | A | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.607-522A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 887993 | |||||||
| chr5:888051 | C | T | 1 | a0001c0001t0002g0071 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.607-580G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888051 | |||||||
| chr5:888076 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.607-605C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888076 | |||||||
| chr5:888101 | C | T | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.607-630G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888101 | |||||||
| chr5:888173 | G | A | 3 | a0001c0002t0006g0046 a0001c0002t0006g0179 a0001c0002t0006g0180 |
4 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-702C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888173 | |||||||
| chr5:888209 | G | A | 1 | a0001c0004t0003g0039 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.607-738C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888209 | |||||||
| chr5:888285 | G | T | 1 | a0002c0003t0010g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.606+736C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888285 | |||||||
| chr5:888377 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.606+644C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888377 | |||||||
| chr5:888618 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.606+403C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888618 | |||||||
| chr5:888728 | G | A | 1 | a0001c0001t0002g0035 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.606+293C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888728 | |||||||
| chr5:888858 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.606+163C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888858 | |||||||
| chr5:888900 | G | A | 6 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(3): Show |
6 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+121C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888900 | |||||||
| chr5:888953 | G | C | 10 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(7): Show |
10 | HG01261.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.606+68C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888953 | |||||||
| chr5:888976 | C | T | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.606+45G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888976 | |||||||
| chr5:888980 | G | T | 1 | a0001c0001t0015g0070 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.606+41C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 5/15 | chr5 | 888980 | |||||||
| chr5:889189 | C | T | 7 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(4): Show |
7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.462-24G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889189 | |||||||
| chr5:889254 | C | T | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.462-89G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889254 | |||||||
| chr5:889279 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.462-114T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889279 | |||||||
| chr5:889281 | G | A | 11 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(8): Show |
22 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.462-116C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889281 | |||||||
| chr5:889382 | C | A | 4 | a0001c0002t0004g0011 a0001c0002t0004g0052 a0001c0002t0009g0020 others(1): Show |
9 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.461+205G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889382 | |||||||
| chr5:889421 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.461+166A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889421 | |||||||
| chr5:889450 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.461+137C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889450 | |||||||
| chr5:889542 | C | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0154 |
7 | HG02273.hp2 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.461+45G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889542 | |||||||
| chr5:889571 | A | G | 11 | a0001c0002t0006g0046 a0001c0002t0006g0178 a0001c0002t0006g0179 others(8): Show |
12 | HG01261.hp2 HG01884.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.461+16T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889571 | |||||||
| chr5:889579 | C | A | 11 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0151 others(8): Show |
22 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
splice_region_variant&intron_variant | LOW | c.461+8G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 4/15 | chr5 | 889579 | |||||||
| chr5:889679 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.401-32T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889679 | |||||||
| chr5:889808 | C | T | 4 | a0001c0002t0004g0011 a0001c0002t0004g0052 a0001c0002t0009g0020 others(1): Show |
9 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.401-161G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889808 | |||||||
| chr5:889809 | C | G | 4 | a0001c0002t0004g0011 a0001c0002t0004g0052 a0001c0002t0009g0020 others(1): Show |
9 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.401-162G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889809 | |||||||
| chr5:889817 | G | T | 4 | a0001c0002t0004g0011 a0001c0002t0004g0052 a0001c0002t0009g0020 others(1): Show |
9 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.401-170C>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889817 | |||||||
| chr5:889818 | C | T | 4 | a0001c0002t0004g0011 a0001c0002t0004g0052 a0001c0002t0009g0020 others(1): Show |
9 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.401-171G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889818 | |||||||
| chr5:889820 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.401-173C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889820 | |||||||
| chr5:889914 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.401-267A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889914 | |||||||
| chr5:889915 | G | C | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-268C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 889915 | |||||||
| chr5:890009 | T | C | 4 | a0001c0002t0004g0011 a0001c0002t0004g0052 a0001c0002t0009g0020 others(1): Show |
9 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.401-362A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890009 | |||||||
| chr5:890062 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0154 |
7 | HG02273.hp2 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.401-415C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890062 | |||||||
| chr5:890188 | G | A | 2 | a0001c0002t0009g0020 a0001c0002t0009g0177 |
4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-541C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890188 | |||||||
| chr5:890189 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.401-542A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890189 | |||||||
| chr5:890241 | G | A | 11 | a0001c0002t0004g0011 a0001c0002t0004g0052 a0001c0002t0009g0020 others(8): Show |
16 | HG01175.hp1 HG01261.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.401-594C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890241 | |||||||
| chr5:890279 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.401-632T>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890279 | |||||||
| chr5:890314 | C | A | 7 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(4): Show |
7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.401-667G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890314 | |||||||
| chr5:890315 | C | A | 7 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(4): Show |
7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.401-668G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890315 | |||||||
| chr5:890393 | C | T | 2 | a0001c0001t0001g0068 a0004c0007t0001g0024 |
3 | HG02015.hp1 NA18974.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.401-746G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890393 | |||||||
| chr5:890416 | T | C | 1 | a0002c0003t0008g0185 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.400+739A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890416 | |||||||
| chr5:890484 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.400+671G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890484 | |||||||
| chr5:890519 | T | G | 2 | a0001c0002t0004g0011 a0001c0002t0004g0052 |
5 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+636A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890519 | |||||||
| chr5:890596 | T | G | 7 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(4): Show |
7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.400+559A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890596 | |||||||
| chr5:890639 | A | G | 7 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(4): Show |
7 | HG01261.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.400+516T>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890639 | |||||||
| chr5:890773 | T | C | 5 | a0001c0002t0004g0011 a0001c0002t0004g0052 a0002c0003t0010g0049 others(2): Show |
8 | HG01175.hp1 HG01433.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.400+382A>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890773 | |||||||
| chr5:890846 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.400+309G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 890846 | |||||||
| chr5:891015 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.400+140C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 891015 | |||||||
| chr5:891019 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.400+136G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 3/15 | chr5 | 891019 | |||||||
| chr5:891325 | T | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(27): Show |
66 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.268-38A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 2/15 | chr5 | 891325 | |||||||
| chr5:891370 | G | C | 5 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-83C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 2/15 | chr5 | 891370 | |||||||
| chr5:891875 | T | G | 1 | a0001c0001t0005g0055 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-21A>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 891875 | |||||||
| chr5:891921 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.53-67C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 891921 | |||||||
| chr5:891980 | G | C | 4 | a0002c0003t0008g0183 a0002c0003t0008g0184 a0002c0003t0008g0185 others(1): Show |
4 | HG01884.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-126C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 891980 | |||||||
| chr5:892089 | G | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(26): Show |
65 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.53-235C>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892089 | |||||||
| chr5:892124 | A | C | 3 | a0002c0003t0010g0049 a0002c0003t0010g0050 a0002c0003t0010g0051 |
3 | HG02280.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.53-270T>G | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892124 | |||||||
| chr5:892276 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.52+330C>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892276 | |||||||
| chr5:892365 | T | A | 2 | a0001c0002t0009g0020 a0001c0002t0009g0177 |
4 | HG01891.hp2 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+241A>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892365 | |||||||
| chr5:892474 | C | A | 1 | a0002c0003t0008g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.52+132G>T | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892474 | |||||||
| chr5:892501 | GCCAGGAC others(12): Show |
G | 1 | a0001c0001t0011g0022 | 2 | HG02040.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.52+86_52+104delGCA others(16): Show |
BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892501 | |||||||
| chr5:892531 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.52+75G>C | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892531 | |||||||
| chr5:892563 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.52+43G>A | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892563 | |||||||
| chr5:892567 | A | AC | 6 | a0001c0001t0001g0023 a0001c0001t0001g0057 a0001c0001t0001g0059 others(3): Show |
7 | HG01109.hp2 HG01175.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+38dupG | BRD9 | ENSG00000028310.18 | transcript | ENST00000467963.6 | protein_coding | 1/15 | chr5 | 892567 |