Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80127 |
| ensemblid | ENSG00000119636.16 |
| hgncid | 19855 |
| symbol | BBOF1 |
| name | basal body orientation factor 1 |
| refseq_nuc | NM_025057.3 |
| refseq_prot | NP_079333.2 |
| ensembl_nuc | ENST00000394009.5 |
| ensembl_prot | ENSP00000377577.3 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 74019349 |
| end | 74066092 |
| strand | + |
| ver | v1.2 |
| region | chr14:74019349-74066092 |
| region5000 | chr14:74014349-74071092 |
| regionname0 | BBOF1_chr14_74019349_74066092 |
| regionname5000 | BBOF1_chr14_74014349_74071092 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 529 | 111 | 18 | 16 | 53 | 3 | 21 | 41 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(524): Show |
chr14 | 74014349 | 74071092 |
| a0002 | 1/0 | 529 | 103 | 37 | 23 | 27 | 8 | 7 | 21 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(524): Show |
chr14 | 74014349 | 74071092 |
| a0003 | 0/1 | 529 | 80 | 3 | 9 | 63 | 1 | 3 | 50 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(524): Show |
chr14 | 74014349 | 74071092 |
| a0004 | 0/0 | 529 | 56 | 9 | 22 | 15 | 2 | 8 | 11 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(524): Show |
chr14 | 74014349 | 74071092 |
| a0005 | 0/0 | 529 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(524): Show |
chr14 | 74014349 | 74071092 |
| a0006 | 0/0 | 529 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(524): Show |
chr14 | 74014349 | 74071092 |
| a0007 | 0/0 | 529 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(524): Show |
chr14 | 74014349 | 74071092 |
| a0008 | 0/0 | 529 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(524): Show |
chr14 | 74014349 | 74071092 |
| a0009 | 0/0 | 529 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(524): Show |
chr14 | 74014349 | 74071092 |
| a0010 | 0/0 | 529 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(524): Show |
chr14 | 74014349 | 74071092 |
| a0011 | 0/0 | 431 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(426): Show |
chr14 | 74014349 | 74071092 |
| a0012 | 0/0 | 529 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(524): Show |
chr14 | 74014349 | 74071092 |
| a0013 | 0/0 | 529 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(524): Show |
chr14 | 74014349 | 74071092 |
| a0014 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(524): Show |
chr14 | 74014349 | 74071092 |
| a0015 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | MPSKG others(524): Show |
chr14 | 74014349 | 74071092 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1587 | 111 | 18 | 16 | 53 | 3 | 21 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0002c0002 | 1/0 | 1587 | 102 | 37 | 22 | 27 | 8 | 7 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0002c0016 | 0/0 | 1587 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0003c0003 | 0/1 | 1587 | 79 | 3 | 9 | 62 | 1 | 3 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0003c0015 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0004c0004 | 0/0 | 1587 | 46 | 0 | 22 | 15 | 2 | 7 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0004c0007 | 0/0 | 1587 | 7 | 7 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0004c0009 | 0/0 | 1587 | 3 | 2 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0005c0006 | 0/0 | 1587 | 11 | 9 | 2 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0006c0005 | 0/0 | 1587 | 11 | 11 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0007c0008 | 0/0 | 1587 | 3 | 3 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0008c0012 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0009c0010 | 0/0 | 1587 | 2 | 0 | 0 | 2 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0010c0011 | 0/0 | 1587 | 2 | 0 | 0 | 2 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0011c0018 | 0/0 | 1295 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1290): Show |
chr14 | 74014349 | 74071092 | ||
| a0012c0014 | 0/0 | 1587 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0013c0017 | 0/0 | 1587 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0014c0019 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 | ||
| a0015c0013 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | ATGCC others(1582): Show |
chr14 | 74014349 | 74071092 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 3113 | 60 | 1 | 9 | 39 | 2 | 9 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0001c0001t0003 | 0/0 | 3113 | 48 | 17 | 6 | 13 | 0 | 12 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0001c0001t0011 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0001c0001t0012 | 0/0 | 3113 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0001c0001t0013 | 0/0 | 3113 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0002c0002t0001 | 1/0 | 3113 | 99 | 34 | 22 | 27 | 8 | 7 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0002c0002t0010 | 0/0 | 3113 | 2 | 2 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0002c0002t0014 | 0/0 | 3113 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0002c0016t0001 | 0/0 | 3113 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0003c0003t0001 | 0/1 | 3113 | 77 | 2 | 9 | 61 | 1 | 3 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0003c0003t0003 | 0/0 | 3113 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0003c0003t0015 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0003c0015t0001 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0004c0004t0004 | 0/0 | 3113 | 46 | 0 | 22 | 15 | 2 | 7 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0004c0007t0003 | 0/0 | 3113 | 7 | 7 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0004c0009t0007 | 0/0 | 3113 | 3 | 2 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0005c0006t0001 | 0/0 | 3113 | 7 | 6 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0005c0006t0006 | 0/0 | 3113 | 4 | 3 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0006c0005t0003 | 0/0 | 3113 | 2 | 2 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0006c0005t0005 | 0/0 | 3113 | 5 | 5 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0006c0005t0008 | 0/0 | 3114 | 3 | 3 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3109): Show |
chr14 | 74014349 | 74071092 |
| a0006c0005t0016 | 0/0 | 3113 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0007c0008t0001 | 0/0 | 3113 | 3 | 3 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0008c0012t0009 | 0/0 | 3113 | 2 | 2 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0009c0010t0001 | 0/0 | 3113 | 2 | 0 | 0 | 2 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0010c0011t0002 | 0/0 | 3113 | 2 | 0 | 0 | 2 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0011c0018t0003 | 0/0 | 2821 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(2816): Show |
chr14 | 74014349 | 74071092 |
| a0012c0014t0001 | 0/0 | 3113 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0013c0017t0001 | 0/0 | 3113 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0014c0019t0002 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| a0015c0013t0001 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | GCTCT others(3108): Show |
chr14 | 74014349 | 74071092 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0002g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0011g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0012g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0001c0001t0013g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0010g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0010g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0002t0014g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0002c0016t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0003t0015g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0003c0015t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0004t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0007t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0007t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0007t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0007t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0007t0003g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0007t0003g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0007t0003g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0009t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0009t0007g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0004c0009t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0005c0006t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0005c0006t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0005c0006t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0005c0006t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0005c0006t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0005c0006t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0005c0006t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0005c0006t0006g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0005c0006t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0005c0006t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0005c0006t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0006c0005t0003g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0006c0005t0003g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0006c0005t0005g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0006c0005t0005g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0006c0005t0005g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0006c0005t0005g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0006c0005t0005g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0006c0005t0008g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0006c0005t0008g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0006c0005t0008g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0006c0005t0016g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0007c0008t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0007c0008t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0007c0008t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0008c0012t0009g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0008c0012t0009g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0009c0010t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0009c0010t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0010c0011t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0010c0011t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0011c0018t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0012c0014t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0013c0017t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0014c0019t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| a0015c0013t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0237 | EUR | GBR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00099 | hp2 | a0001 | c0001 | t0012 | g0160 | EUR | GBR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0245 | EUR | GBR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0244 | EUR | GBR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0250 | EUR | FIN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00280 | hp2 | a0004 | c0004 | t0004 | g0101 | EUR | FIN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00323 | hp1 | a0004 | c0004 | t0004 | g0114 | EUR | FIN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0056 | EUR | FIN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00423 | hp2 | a0003 | c0003 | t0001 | g0020 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00438 | hp1 | a0003 | c0003 | t0001 | g0013 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00544 | hp2 | a0003 | c0003 | t0001 | g0024 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0057 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00639 | hp1 | a0004 | c0004 | t0004 | g0002 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0240 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0264 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0328 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00673 | hp2 | a0003 | c0003 | t0001 | g0078 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0207 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0347 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0289 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00741 | hp1 | a0004 | c0004 | t0004 | g0089 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01069 | hp2 | a0003 | c0003 | t0001 | g0047 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0211 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01070 | hp2 | a0004 | c0004 | t0004 | g0127 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01071 | hp1 | a0004 | c0004 | t0004 | g0002 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0068 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0267 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0141 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0234 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01099 | hp2 | a0004 | c0004 | t0004 | g0096 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01106 | hp2 | a0004 | c0004 | t0004 | g0119 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0303 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01109 | hp2 | a0005 | c0006 | t0006 | g0193 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0316 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01167 | hp2 | a0004 | c0004 | t0004 | g0092 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0366 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01168 | hp2 | a0004 | c0004 | t0004 | g0095 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01169 | hp1 | a0004 | c0004 | t0004 | g0126 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0220 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01192 | hp1 | a0003 | c0003 | t0001 | g0076 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0212 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01243 | hp1 | a0005 | c0006 | t0001 | g0131 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0191 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0249 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01256 | hp1 | a0004 | c0004 | t0004 | g0104 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01256 | hp2 | a0003 | c0003 | t0001 | g0060 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01257 | hp1 | a0004 | c0004 | t0004 | g0118 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0248 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0260 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01258 | hp2 | a0003 | c0003 | t0001 | g0037 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01261 | hp1 | a0004 | c0004 | t0004 | g0108 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0257 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01346 | hp1 | a0004 | c0004 | t0004 | g0117 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0286 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0331 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01433 | hp1 | a0004 | c0004 | t0004 | g0102 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01496 | hp1 | a0001 | c0001 | t0013 | g0302 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0070 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0336 | EUR | IBS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0251 | EUR | IBS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0247 | EUR | IBS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0246 | EUR | IBS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01884 | hp1 | a0008 | c0012 | t0009 | g0377 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0144 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01928 | hp1 | a0004 | c0004 | t0004 | g0124 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01928 | hp2 | a0003 | c0003 | t0001 | g0011 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01934 | hp1 | a0004 | c0004 | t0004 | g0105 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0270 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01943 | hp1 | a0003 | c0003 | t0001 | g0012 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01943 | hp2 | a0004 | c0004 | t0004 | g0093 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0281 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0265 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01981 | hp1 | a0004 | c0004 | t0004 | g0091 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0346 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02015 | hp1 | a0003 | c0003 | t0001 | g0050 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02015 | hp2 | a0009 | c0010 | t0001 | g0055 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02027 | hp1 | a0003 | c0003 | t0001 | g0064 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02040 | hp2 | a0004 | c0004 | t0004 | g0097 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0231 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02055 | hp2 | a0006 | c0005 | t0005 | g0373 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02071 | hp1 | a0001 | c0001 | t0011 | g0317 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02071 | hp2 | a0004 | c0004 | t0004 | g0106 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02083 | hp1 | a0003 | c0003 | t0001 | g0022 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0079 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02129 | hp2 | a0004 | c0004 | t0004 | g0100 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02135 | hp1 | a0003 | c0003 | t0001 | g0077 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0352 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0304 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02145 | hp2 | a0004 | c0007 | t0003 | g0361 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0268 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02148 | hp2 | a0004 | c0004 | t0004 | g0087 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | CDX | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | CDX | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02165 | hp1 | a0003 | c0003 | t0001 | g0040 | EAS | CDX | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02165 | hp2 | a0004 | c0004 | t0004 | g0094 | EAS | CDX | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02257 | hp1 | a0006 | c0005 | t0005 | g0371 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0261 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0198 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0288 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02300 | hp1 | a0004 | c0004 | t0004 | g0103 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02300 | hp2 | a0004 | c0004 | t0004 | g0122 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0253 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02451 | hp2 | a0006 | c0005 | t0008 | g0380 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02523 | hp1 | a0003 | c0003 | t0001 | g0049 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0217 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02572 | hp2 | a0004 | c0009 | t0007 | g0140 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02602 | hp1 | a0011 | c0018 | t0003 | g0175 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02602 | hp2 | a0004 | c0004 | t0004 | g0099 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02622 | hp1 | a0002 | c0002 | t0010 | g0362 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0299 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0146 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0215 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02647 | hp2 | a0004 | c0009 | t0007 | g0138 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02683 | hp1 | a0012 | c0014 | t0001 | g0204 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0214 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02698 | hp1 | a0003 | c0003 | t0001 | g0045 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0157 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0192 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02717 | hp2 | a0002 | c0002 | t0010 | g0363 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02723 | hp1 | a0003 | c0003 | t0001 | g0190 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02723 | hp2 | a0006 | c0005 | t0005 | g0369 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0243 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02735 | hp2 | a0004 | c0004 | t0004 | g0109 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02738 | hp1 | a0004 | c0004 | t0004 | g0123 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0330 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02809 | hp1 | a0004 | c0007 | t0003 | g0007 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02809 | hp2 | a0004 | c0007 | t0003 | g0006 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02818 | hp2 | a0006 | c0005 | t0003 | g0375 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02886 | hp1 | a0006 | c0005 | t0005 | g0372 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0263 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02895 | hp2 | a0005 | c0006 | t0001 | g0134 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02897 | hp1 | a0005 | c0006 | t0001 | g0132 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0262 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0199 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02922 | hp2 | a0007 | c0008 | t0001 | g0216 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02965 | hp1 | a0006 | c0005 | t0003 | g0374 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0203 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0255 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02970 | hp2 | a0006 | c0005 | t0008 | g0378 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02976 | hp1 | a0007 | c0008 | t0001 | g0273 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0298 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0044 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0154 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03041 | hp1 | a0004 | c0007 | t0003 | g0004 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03041 | hp2 | a0003 | c0003 | t0003 | g0189 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0272 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0219 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03130 | hp1 | a0004 | c0007 | t0003 | g0005 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0147 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03139 | hp2 | a0008 | c0012 | t0009 | g0376 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03195 | hp2 | a0005 | c0006 | t0006 | g0196 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03209 | hp2 | a0006 | c0005 | t0008 | g0379 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0276 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0367 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0200 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03453 | hp2 | a0005 | c0006 | t0006 | g0194 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03486 | hp1 | a0005 | c0006 | t0001 | g0136 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0232 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0318 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03491 | hp2 | a0004 | c0004 | t0004 | g0115 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03492 | hp1 | a0004 | c0004 | t0004 | g0120 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0206 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0142 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03540 | hp2 | a0005 | c0006 | t0001 | g0135 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0148 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0295 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0167 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0205 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0178 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0327 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03831 | hp1 | a0003 | c0003 | t0001 | g0014 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0342 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03927 | hp1 | a0004 | c0004 | t0004 | g0128 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0350 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03942 | hp1 | a0004 | c0004 | t0004 | g0116 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0165 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0290 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG04184 | hp2 | a0004 | c0009 | t0007 | g0139 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0179 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG04204 | hp1 | a0013 | c0017 | t0001 | g0351 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0170 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0266 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0173 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0274 | AFR | YRI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0145 | AFR | YRI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18612 | hp1 | a0003 | c0003 | t0001 | g0038 | EAS | CHB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | CHB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18906 | hp1 | a0005 | c0006 | t0001 | g0133 | AFR | YRI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18906 | hp2 | a0005 | c0006 | t0006 | g0195 | AFR | YRI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18940 | hp1 | a0014 | c0019 | t0002 | g0291 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18940 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18941 | hp2 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18942 | hp1 | a0003 | c0003 | t0001 | g0028 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18942 | hp2 | a0004 | c0004 | t0004 | g0107 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18946 | hp2 | a0003 | c0003 | t0001 | g0023 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18948 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18950 | hp1 | a0003 | c0003 | t0001 | g0382 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18953 | hp1 | a0015 | c0013 | t0001 | g0017 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18954 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18956 | hp1 | a0003 | c0003 | t0001 | g0039 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18957 | hp2 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18959 | hp2 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18960 | hp1 | a0003 | c0003 | t0001 | g0052 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18961 | hp1 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18961 | hp2 | a0004 | c0004 | t0004 | g0129 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18962 | hp2 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18963 | hp1 | a0010 | c0011 | t0002 | g0314 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18963 | hp2 | a0003 | c0003 | t0001 | g0074 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0065 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18966 | hp1 | a0009 | c0010 | t0001 | g0041 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18966 | hp2 | a0003 | c0003 | t0001 | g0053 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18967 | hp2 | a0004 | c0004 | t0004 | g0088 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18972 | hp2 | a0004 | c0004 | t0004 | g0111 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18975 | hp2 | a0003 | c0003 | t0001 | g0084 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18979 | hp1 | a0003 | c0003 | t0001 | g0018 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18979 | hp2 | a0003 | c0003 | t0001 | g0030 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18983 | hp1 | a0003 | c0003 | t0001 | g0081 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18984 | hp1 | a0003 | c0003 | t0001 | g0066 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18985 | hp2 | a0003 | c0003 | t0001 | g0054 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18986 | hp1 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18988 | hp2 | a0003 | c0003 | t0001 | g0086 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18990 | hp1 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18991 | hp2 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18997 | hp1 | a0004 | c0004 | t0004 | g0130 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18997 | hp2 | a0003 | c0015 | t0001 | g0059 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA18999 | hp2 | a0003 | c0003 | t0001 | g0034 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19001 | hp2 | a0003 | c0003 | t0001 | g0058 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0033 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19003 | hp1 | a0004 | c0004 | t0004 | g0113 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0085 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19007 | hp2 | a0010 | c0011 | t0002 | g0337 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19009 | hp1 | a0003 | c0003 | t0001 | g0021 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19010 | hp2 | a0004 | c0004 | t0004 | g0112 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19012 | hp1 | a0003 | c0003 | t0001 | g0069 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0269 | AFR | LWK | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0296 | AFR | LWK | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0242 | AFR | LWK | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19043 | hp2 | a0004 | c0007 | t0003 | g0364 | AFR | LWK | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19055 | hp1 | a0003 | c0003 | t0001 | g0061 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19057 | hp2 | a0003 | c0003 | t0001 | g0043 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19060 | hp1 | a0003 | c0003 | t0001 | g0036 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0071 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19062 | hp1 | a0003 | c0003 | t0001 | g0035 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19062 | hp2 | a0004 | c0004 | t0004 | g0110 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19065 | hp2 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19070 | hp1 | a0003 | c0003 | t0001 | g0029 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19070 | hp2 | a0004 | c0004 | t0004 | g0098 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19076 | hp2 | a0003 | c0003 | t0015 | g0027 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19080 | hp2 | a0003 | c0003 | t0001 | g0063 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19081 | hp1 | a0003 | c0003 | t0001 | g0082 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19081 | hp2 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19082 | hp1 | a0003 | c0003 | t0001 | g0062 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19082 | hp2 | a0004 | c0004 | t0004 | g0125 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19084 | hp2 | a0003 | c0003 | t0001 | g0072 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19086 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19086 | hp2 | a0004 | c0004 | t0004 | g0121 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0067 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19090 | hp1 | a0003 | c0003 | t0001 | g0083 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19091 | hp1 | a0003 | c0003 | t0001 | g0031 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0368 | AFR | YRI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0301 | AFR | YRI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA20129 | hp1 | a0006 | c0005 | t0005 | g0370 | AFR | ASW | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0239 | AFR | ASW | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0345 | EUR | TSI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0252 | EUR | TSI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01123 | hp1 | a0004 | c0004 | t0004 | g0090 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG01123 | hp2 | a0002 | c0016 | t0001 | g0218 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02486 | hp1 | a0005 | c0006 | t0001 | g0137 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02486 | hp2 | a0006 | c0005 | t0016 | g0381 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02559 | hp1 | a0007 | c0008 | t0001 | g0213 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0275 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0143 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0197 | AFR | USA | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| HG06807 | hp2 | a0004 | c0007 | t0003 | g0365 | AFR | USA | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0254 | AFR | USA | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0271 | AFR | USA | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA21309 | hp1 | a0002 | c0002 | t0014 | g0238 | AFR | LWK | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | LWK | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0075 | REF | REF | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0236 | REF | REF | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74022956 | A | T | 1 | a0014 | 1 | NA18940.hp1 | stop_gained | HIGH | c.97A>T | p.Lys33* | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 227/3113 | 97/1590 | 33/529 | chr14 | 74022956 | |||
| chr14:74022958 | G | T | 1 | a0014 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.99G>T | p.Lys33Asn | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 229/3113 | 99/1590 | 33/529 | chr14 | 74022958 | |||
| chr14:74022959 | G | A | 1 | a0014 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.100G>A | p.Ala34Thr | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 230/3113 | 100/1590 | 34/529 | chr14 | 74022959 | |||
| chr14:74022962 | A | G | 1 | a0014 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.103A>G | p.Asn35Asp | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 233/3113 | 103/1590 | 35/529 | chr14 | 74022962 | |||
| chr14:74022966 | C | T | 1 | a0014 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.107C>T | p.Ala36Val | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 237/3113 | 107/1590 | 36/529 | chr14 | 74022966 | |||
| chr14:74022992 | G | T | 1 | a0005 | 11 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(8): Show |
missense_variant | MODERATE | c.133G>T | p.Val45Phe | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 263/3113 | 133/1590 | 45/529 | chr14 | 74022992 | |||
| chr14:74023032 | G | A | 4 | a0003 a0009 a0012 others(1): Show |
84 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
missense_variant | MODERATE | c.173G>A | p.Arg58Gln | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 303/3113 | 173/1590 | 58/529 | chr14 | 74023032 | |||
| chr14:74023079 | A | C | 2 | a0006 a0008 |
13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
missense_variant | MODERATE | c.220A>C | p.Met74Leu | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 350/3113 | 220/1590 | 74/529 | chr14 | 74023079 | |||
| chr14:74034152 | T | A | 1 | a0015 | 1 | NA18953.hp1 | missense_variant | MODERATE | c.476T>A | p.Val159Glu | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/12 | 606/3113 | 476/1590 | 159/529 | chr14 | 74034152 | |||
| chr14:74040617 | G | A | 1 | a0006 | 11 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
missense_variant | MODERATE | c.548G>A | p.Arg183Lys | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/12 | 678/3113 | 548/1590 | 183/529 | chr14 | 74040617 | |||
| chr14:74040629 | G | T | 1 | a0010 | 2 | NA18963.hp1 NA19007.hp2 |
missense_variant | MODERATE | c.560G>T | p.Arg187Ile | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/12 | 690/3113 | 560/1590 | 187/529 | chr14 | 74040629 | |||
| chr14:74047971 | A | T | 11 | a0001 a0003 a0004 others(8): Show |
277 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(274): Show |
missense_variant | MODERATE | c.689A>T | p.Asp230Val | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/12 | 819/3113 | 689/1590 | 230/529 | chr14 | 74047971 | |||
| chr14:74049917 | G | C | 1 | a0012 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1008G>C | p.Gln336His | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/12 | 1138/3113 | 1008/1590 | 336/529 | chr14 | 74049917 | |||
| chr14:74050077 | A | G | 1 | a0013 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.1168A>G | p.Asn390Asp | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/12 | 1298/3113 | 1168/1590 | 390/529 | chr14 | 74050077 | |||
| chr14:74050177 | T | C | 1 | a0007 | 3 | HG02559.hp1 HG02922.hp2 HG02976.hp1 |
missense_variant | MODERATE | c.1268T>C | p.Leu423Pro | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/12 | 1398/3113 | 1268/1590 | 423/529 | chr14 | 74050177 | |||
| chr14:74050188 | G | A | 1 | a0009 | 2 | HG02015.hp2 NA18966.hp1 |
missense_variant | MODERATE | c.1279G>A | p.Glu427Lys | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/12 | 1409/3113 | 1279/1590 | 427/529 | chr14 | 74050188 | |||
| chr14:74053659 | GGCCTCCC others(9771): Show |
G | 1 | a0011 | 1 | HG02602.hp1 | exon_loss_variant | HIGH | c.1287-1913_1579-124 others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr14 | 74053659 | ||||||
| chr14:74057166 | A | G | 3 | a0001 a0010 a0014 |
114 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
missense_variant | MODERATE | c.1486A>G | p.Lys496Glu | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/12 | 1616/3113 | 1486/1590 | 496/529 | chr14 | 74057166 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74022961 | C | T | 1 | a0014c0019 | 1 | NA18940.hp1 | synonymous_variant | LOW | c.102C>T | p.Ala34Ala | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 232/3113 | 102/1590 | 34/529 | chr14 | 74022961 | |||
| chr14:74046113 | C | A | 1 | a0002c0016 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.630C>A | p.Ala210Ala | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/12 | 760/3113 | 630/1590 | 210/529 | chr14 | 74046113 | |||
| chr14:74048014 | C | T | 1 | a0004c0009 | 3 | HG02572.hp2 HG02647.hp2 HG04184.hp2 |
synonymous_variant | LOW | c.732C>T | p.Asp244Asp | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/12 | 862/3113 | 732/1590 | 244/529 | chr14 | 74048014 | |||
| chr14:74049794 | G | A | 1 | a0004c0004 | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
synonymous_variant | LOW | c.885G>A | p.Leu295Leu | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/12 | 1015/3113 | 885/1590 | 295/529 | chr14 | 74049794 | |||
| chr14:74050157 | C | T | 1 | a0003c0015 | 1 | NA18997.hp2 | synonymous_variant | LOW | c.1248C>T | p.Thr416Thr | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/12 | 1378/3113 | 1248/1590 | 416/529 | chr14 | 74050157 | |||
| chr14:74057246 | G | A | 6 | a0001c0001 a0004c0007 a0004c0009 others(3): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
synonymous_variant | LOW | c.1566G>A | p.Gln522Gln | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/12 | 1696/3113 | 1566/1590 | 522/529 | chr14 | 74057246 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74019376 | G | C | 1 | a0005c0006t0006 | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-103G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/12 | chr14 | 74019376 | |||||||
| chr14:74019399 | C | T | 1 | a0006c0005t0016 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/12 | 80 | chr14 | 74019399 | ||||||
| chr14:74064781 | T | C | 1 | a0008c0012t0009 | 2 | HG01884.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*82T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 82 | chr14 | 74064781 | ||||||
| chr14:74064782 | T | G | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(12): Show |
137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*83T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 83 | chr14 | 74064782 | ||||||
| chr14:74064870 | G | A | 1 | a0002c0002t0014 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*171G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 171 | chr14 | 74064870 | ||||||
| chr14:74065450 | A | AT | 1 | a0006c0005t0008 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*754dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 755 | INFO_REALIGN_3_PRIME | chr14 | 74065450 | |||||
| chr14:74065582 | C | A | 1 | a0001c0001t0011 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*883C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 883 | chr14 | 74065582 | ||||||
| chr14:74065584 | A | C | 1 | a0001c0001t0013 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*885A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 885 | chr14 | 74065584 | ||||||
| chr14:74065724 | A | T | 2 | a0006c0005t0005 a0006c0005t0016 |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1025A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 1025 | chr14 | 74065724 | ||||||
| chr14:74065820 | A | C | 4 | a0001c0001t0002 a0001c0001t0011 a0010c0011t0002 others(1): Show |
64 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1121A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 1121 | chr14 | 74065820 | ||||||
| chr14:74065828 | G | A | 1 | a0004c0004t0004 | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1129G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 1129 | chr14 | 74065828 | ||||||
| chr14:74065831 | T | C | 1 | a0004c0009t0007 | 3 | HG02572.hp2 HG02647.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1132T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 1132 | chr14 | 74065831 | ||||||
| chr14:74065986 | T | A | 1 | a0002c0002t0010 | 2 | HG02622.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1287T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 1287 | chr14 | 74065986 | ||||||
| chr14:74066000 | A | C | 1 | a0001c0001t0012 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1301A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 1301 | chr14 | 74066000 | ||||||
| chr14:74066081 | T | C | 1 | a0003c0003t0015 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1382T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 1382 | chr14 | 74066081 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74019738 | A | G | 1 | a0003c0003t0001g0382 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.56+204A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74019738 | |||||||
| chr14:74019766 | G | T | 13 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0005g0369 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.56+232G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74019766 | |||||||
| chr14:74019767 | A | T | 13 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0005g0369 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.56+233A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74019767 | |||||||
| chr14:74019921 | T | C | 5 | a0006c0005t0005g0369 a0006c0005t0005g0370 a0006c0005t0005g0371 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+387T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74019921 | |||||||
| chr14:74020064 | A | G | 1 | a0002c0002t0001g0368 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.56+530A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020064 | |||||||
| chr14:74020094 | A | G | 78 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(75): Show |
79 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.56+560A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020094 | |||||||
| chr14:74020142 | A | G | 1 | a0002c0002t0001g0290 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.56+608A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020142 | |||||||
| chr14:74020238 | A | G | 1 | a0002c0002t0001g0289 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.56+704A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020238 | |||||||
| chr14:74020243 | AT | A | 286 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(283): Show |
288 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.56+719delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 74020243 | ||||||
| chr14:74020266 | C | G | 2 | a0001c0001t0002g0366 a0001c0001t0002g0367 |
2 | HG01168.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.56+732C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020266 | |||||||
| chr14:74020455 | CAGTG | C | 7 | a0002c0002t0001g0197 a0002c0002t0001g0198 a0002c0002t0001g0199 others(4): Show |
7 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+925_56+928delGA others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 74020455 | ||||||
| chr14:74020505 | CT | C | 92 | a0002c0002t0001g0197 a0002c0002t0001g0198 a0002c0002t0001g0199 others(89): Show |
92 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.56+983delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 74020505 | ||||||
| chr14:74020560 | A | G | 4 | a0005c0006t0006g0193 a0005c0006t0006g0194 a0005c0006t0006g0195 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.56+1026A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020560 | |||||||
| chr14:74020567 | G | A | 73 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(70): Show |
74 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.56+1033G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020567 | |||||||
| chr14:74020584 | A | G | 1 | a0002c0002t0001g0288 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.56+1050A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020584 | |||||||
| chr14:74020608 | A | G | 1 | a0002c0002t0001g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.56+1074A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020608 | |||||||
| chr14:74020660 | C | T | 84 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(81): Show |
84 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.56+1126C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020660 | |||||||
| chr14:74020818 | G | A | 73 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(70): Show |
74 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.56+1284G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020818 | |||||||
| chr14:74020889 | A | G | 72 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(69): Show |
73 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.56+1355A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020889 | |||||||
| chr14:74020890 | A | G | 1 | a0014c0019t0002g0291 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.56+1356A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020890 | |||||||
| chr14:74020894 | A | G | 1 | a0014c0019t0002g0291 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.56+1360A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020894 | |||||||
| chr14:74020985 | C | G | 4 | a0005c0006t0006g0193 a0005c0006t0006g0194 a0005c0006t0006g0195 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.56+1451C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020985 | |||||||
| chr14:74021100 | A | C | 5 | a0003c0003t0001g0082 a0003c0003t0001g0083 a0003c0003t0001g0084 others(2): Show |
5 | NA18975.hp2 NA18988.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+1566A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021100 | |||||||
| chr14:74021317 | G | T | 3 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 |
3 | NA18983.hp2 NA18991.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.57-1599G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021317 | |||||||
| chr14:74021403 | T | C | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.57-1513T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021403 | |||||||
| chr14:74021465 | C | A | 11 | a0005c0006t0001g0131 a0005c0006t0001g0132 a0005c0006t0001g0133 others(8): Show |
11 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.57-1451C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021465 | |||||||
| chr14:74021581 | CTT | C | 7 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(4): Show |
7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.57-1334_57-1333del others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021581 | |||||||
| chr14:74021839 | G | A | 6 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0143 others(3): Show |
6 | HG01081.hp1 HG01884.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.57-1077G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021839 | |||||||
| chr14:74021886 | G | C | 2 | a0002c0002t0001g0205 a0002c0002t0001g0206 |
2 | HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.57-1030G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021886 | |||||||
| chr14:74021907 | T | C | 1 | a0014c0019t0002g0291 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.57-1009T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021907 | |||||||
| chr14:74021914 | G | GA | 6 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 others(3): Show |
6 | HG00735.hp1 HG03688.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.57-990dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 74021914 | ||||||
| chr14:74021944 | G | A | 1 | a0001c0001t0003g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.57-972G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021944 | |||||||
| chr14:74022211 | A | T | 12 | a0002c0002t0001g0001 a0002c0002t0001g0277 a0002c0002t0001g0278 others(9): Show |
14 | HG01358.hp1 HG01952.hp1 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.57-705A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022211 | |||||||
| chr14:74022289 | T | G | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.57-627T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022289 | |||||||
| chr14:74022306 | C | T | 5 | a0002c0002t0010g0362 a0002c0002t0010g0363 a0004c0007t0003g0361 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.57-610C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022306 | |||||||
| chr14:74022310 | G | T | 5 | a0002c0002t0010g0362 a0002c0002t0010g0363 a0004c0007t0003g0361 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.57-606G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022310 | |||||||
| chr14:74022337 | C | CAGGAGTT others(4): Show |
1 | a0003c0003t0001g0008 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.57-577_57-567dupGG others(9): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 74022337 | ||||||
| chr14:74022416 | C | T | 1 | a0004c0004t0004g0130 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.57-500C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022416 | |||||||
| chr14:74022459 | G | A | 7 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0008g0378 others(4): Show |
7 | HG01884.hp1 HG02451.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-457G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022459 | |||||||
| chr14:74022462 | G | A | 2 | a0006c0005t0003g0374 a0006c0005t0003g0375 |
2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.57-454G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022462 | |||||||
| chr14:74022465 | T | C | 2 | a0002c0002t0001g0205 a0002c0002t0001g0206 |
2 | HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.57-451T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022465 | |||||||
| chr14:74022467 | G | A | 3 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 |
3 | HG02809.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57-449G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022467 | |||||||
| chr14:74022522 | C | T | 77 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(74): Show |
78 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.57-394C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022522 | |||||||
| chr14:74022523 | G | A | 1 | a0003c0003t0001g0009 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.57-393G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022523 | |||||||
| chr14:74022541 | A | T | 78 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(75): Show |
79 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.57-375A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022541 | |||||||
| chr14:74022552 | GA | G | 7 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0143 others(4): Show |
7 | HG01081.hp1 HG01884.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-354delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 74022552 | ||||||
| chr14:74022645 | A | G | 3 | a0006c0005t0008g0378 a0006c0005t0008g0379 a0006c0005t0008g0380 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.57-271A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022645 | |||||||
| chr14:74022710 | T | C | 1 | a0003c0003t0001g0010 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.57-206T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022710 | |||||||
| chr14:74022711 | C | T | 1 | a0003c0003t0001g0010 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.57-205C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022711 | |||||||
| chr14:74023299 | T | G | 5 | a0002c0002t0010g0362 a0002c0002t0010g0363 a0004c0007t0003g0361 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+155T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023299 | |||||||
| chr14:74023342 | C | T | 40 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(37): Show |
40 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.285+198C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023342 | |||||||
| chr14:74023448 | T | C | 1 | a0002c0002t0001g0208 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.285+304T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023448 | |||||||
| chr14:74023553 | C | T | 5 | a0002c0002t0010g0362 a0002c0002t0010g0363 a0004c0007t0003g0361 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+409C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023553 | |||||||
| chr14:74023573 | A | T | 2 | a0006c0005t0003g0374 a0006c0005t0003g0375 |
2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.285+429A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023573 | |||||||
| chr14:74023658 | G | A | 1 | a0002c0002t0001g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.285+514G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023658 | |||||||
| chr14:74023745 | G | A | 5 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0002c0002t0001g0147 others(2): Show |
5 | HG02258.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+601G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023745 | |||||||
| chr14:74023841 | G | A | 2 | a0003c0003t0001g0011 a0003c0003t0001g0012 |
2 | HG01928.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.285+697G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023841 | |||||||
| chr14:74023857 | A | G | 5 | a0002c0002t0010g0362 a0002c0002t0010g0363 a0004c0007t0003g0361 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+713A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023857 | |||||||
| chr14:74023920 | C | T | 1 | a0003c0003t0001g0081 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.285+776C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023920 | |||||||
| chr14:74023925 | C | CA | 11 | a0001c0001t0002g0297 a0001c0001t0003g0298 a0001c0001t0003g0299 others(8): Show |
11 | HG00438.hp1 HG01109.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+799dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74023925 | ||||||
| chr14:74023925 | CA | C | 8 | a0001c0001t0002g0356 a0001c0001t0002g0357 a0001c0001t0003g0188 others(5): Show |
8 | HG02451.hp2 HG02976.hp1 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+799delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74023925 | ||||||
| chr14:74023961 | G | A | 7 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(4): Show |
7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+817G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023961 | |||||||
| chr14:74024230 | T | A | 1 | a0002c0002t0001g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.285+1086T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024230 | |||||||
| chr14:74024349 | G | A | 5 | a0006c0005t0005g0369 a0006c0005t0005g0370 a0006c0005t0005g0371 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+1205G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024349 | |||||||
| chr14:74024362 | G | A | 84 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(81): Show |
84 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.285+1218G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024362 | |||||||
| chr14:74024414 | T | G | 6 | a0006c0005t0005g0369 a0006c0005t0005g0370 a0006c0005t0005g0371 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+1270T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024414 | |||||||
| chr14:74024418 | G | C | 64 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(61): Show |
65 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.285+1274G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024418 | |||||||
| chr14:74024419 | G | A | 1 | a0001c0001t0002g0305 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.285+1275G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024419 | |||||||
| chr14:74024542 | C | T | 2 | a0002c0002t0001g0271 a0002c0002t0001g0272 |
2 | HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.285+1398C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024542 | |||||||
| chr14:74024550 | C | T | 2 | a0001c0001t0002g0354 a0001c0001t0002g0355 |
2 | NA18954.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.285+1406C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024550 | |||||||
| chr14:74024557 | C | T | 5 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0002c0002t0001g0147 others(2): Show |
5 | HG02258.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+1413C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024557 | |||||||
| chr14:74024582 | A | G | 14 | a0005c0006t0001g0131 a0005c0006t0001g0132 a0005c0006t0001g0133 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.285+1438A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024582 | |||||||
| chr14:74024627 | G | A | 1 | a0001c0001t0003g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.285+1483G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024627 | |||||||
| chr14:74024713 | G | A | 1 | a0003c0003t0001g0014 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.285+1569G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024713 | |||||||
| chr14:74024748 | G | T | 2 | a0006c0005t0003g0374 a0006c0005t0003g0375 |
2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.285+1604G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024748 | |||||||
| chr14:74024932 | T | G | 12 | a0001c0001t0002g0306 a0001c0001t0002g0307 a0001c0001t0002g0308 others(9): Show |
12 | HG00408.hp1 HG02083.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.285+1788T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024932 | |||||||
| chr14:74024948 | A | G | 1 | a0003c0003t0001g0008 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.285+1804A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024948 | |||||||
| chr14:74025023 | C | T | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.285+1879C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74025023 | |||||||
| chr14:74025127 | A | G | 2 | a0003c0003t0001g0190 a0003c0003t0001g0191 |
2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.285+1983A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74025127 | |||||||
| chr14:74025159 | C | T | 11 | a0005c0006t0001g0131 a0005c0006t0001g0132 a0005c0006t0001g0133 others(8): Show |
11 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+2015C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74025159 | |||||||
| chr14:74025163 | A | G | 5 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0002c0002t0001g0147 others(2): Show |
5 | HG02258.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+2019A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74025163 | |||||||
| chr14:74025565 | A | C | 1 | a0002c0002t0001g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.285+2421A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74025565 | |||||||
| chr14:74025905 | T | TG | 82 | a0001c0001t0003g0152 a0002c0002t0001g0212 a0003c0003t0001g0008 others(79): Show |
82 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.285+2769dupG | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74025905 | ||||||
| chr14:74025906 | G | A | 7 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0008g0378 others(4): Show |
7 | HG01884.hp1 HG02451.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+2762G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74025906 | |||||||
| chr14:74025907 | G | C | 1 | a0001c0001t0003g0151 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.285+2763G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74025907 | |||||||
| chr14:74026140 | C | CA | 66 | a0001c0001t0002g0315 a0002c0002t0001g0197 a0002c0002t0001g0198 others(63): Show |
67 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.285+3010dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74026140 | ||||||
| chr14:74026140 | C | CAA | 7 | a0005c0006t0001g0131 a0005c0006t0001g0132 a0005c0006t0001g0133 others(4): Show |
7 | HG01243.hp1 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+3009_285+3010d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74026140 | ||||||
| chr14:74026140 | CA | C | 7 | a0001c0001t0002g0312 a0001c0001t0002g0313 a0001c0001t0003g0188 others(4): Show |
7 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+3010delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74026140 | ||||||
| chr14:74026153 | A | G | 5 | a0002c0002t0010g0362 a0002c0002t0010g0363 a0004c0007t0003g0361 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+3009A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026153 | |||||||
| chr14:74026263 | G | A | 5 | a0002c0002t0010g0362 a0002c0002t0010g0363 a0004c0007t0003g0361 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-2921G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026263 | |||||||
| chr14:74026271 | A | G | 64 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(61): Show |
65 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.286-2913A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026271 | |||||||
| chr14:74026310 | T | G | 63 | a0002c0002t0001g0197 a0002c0002t0001g0198 a0002c0002t0001g0199 others(60): Show |
64 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.286-2874T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026310 | |||||||
| chr14:74026444 | C | CA | 165 | a0001c0001t0002g0003 a0001c0001t0002g0293 a0001c0001t0002g0294 others(162): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.286-2716dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74026444 | ||||||
| chr14:74026444 | C | CAA | 19 | a0001c0001t0002g0292 a0001c0001t0002g0297 a0001c0001t0002g0316 others(16): Show |
19 | HG00741.hp1 HG01167.hp1 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.286-2717_286-2716d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74026444 | ||||||
| chr14:74026444 | CA | C | 12 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0003g0184 others(9): Show |
12 | HG01934.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.286-2716delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74026444 | ||||||
| chr14:74026505 | A | T | 1 | a0003c0003t0001g0008 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.286-2679A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026505 | |||||||
| chr14:74026509 | T | A | 1 | a0003c0003t0001g0008 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.286-2675T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026509 | |||||||
| chr14:74026511 | A | T | 1 | a0003c0003t0001g0008 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.286-2673A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026511 | |||||||
| chr14:74026538 | T | C | 224 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(221): Show |
226 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.286-2646T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026538 | |||||||
| chr14:74026702 | A | G | 7 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(4): Show |
7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.286-2482A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026702 | |||||||
| chr14:74026791 | A | T | 1 | a0003c0003t0001g0008 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.286-2393A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026791 | |||||||
| chr14:74026820 | G | A | 1 | a0001c0001t0002g0319 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.286-2364G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026820 | |||||||
| chr14:74026930 | GAA | G | 78 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(75): Show |
79 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.286-2243_286-2242d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74026930 | ||||||
| chr14:74026931 | A | G | 1 | a0004c0004t0004g0130 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.286-2253A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026931 | |||||||
| chr14:74026989 | A | T | 28 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0155 others(25): Show |
28 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.286-2195A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026989 | |||||||
| chr14:74027082 | C | CT | 177 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(174): Show |
178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.286-2080dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027082 | ||||||
| chr14:74027082 | C | CTT | 37 | a0001c0001t0003g0155 a0001c0001t0003g0176 a0001c0001t0003g0177 others(34): Show |
37 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.286-2081_286-2080d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027082 | ||||||
| chr14:74027082 | CT | C | 60 | a0001c0001t0002g0003 a0001c0001t0002g0293 a0001c0001t0002g0294 others(57): Show |
61 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.286-2080delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027082 | ||||||
| chr14:74027082 | CTTT | C | 15 | a0003c0003t0001g0009 a0003c0003t0001g0023 a0003c0003t0001g0024 others(12): Show |
15 | HG00544.hp2 NA18940.hp2 NA18942.hp1 others(12): Show |
intron_variant | MODIFIER | c.286-2082_286-2080d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027082 | ||||||
| chr14:74027203 | A | G | 1 | a0001c0001t0002g0319 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.286-1981A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027203 | |||||||
| chr14:74027271 | A | G | 381 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(378): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.286-1913A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027271 | |||||||
| chr14:74027304 | C | A | 1 | a0004c0004t0004g0090 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.286-1880C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027304 | |||||||
| chr14:74027378 | C | T | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.286-1806C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027378 | |||||||
| chr14:74027385 | C | CT | 125 | a0001c0001t0002g0003 a0001c0001t0002g0293 a0001c0001t0002g0312 others(122): Show |
126 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.286-1773dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027385 | ||||||
| chr14:74027385 | C | CTT | 51 | a0001c0001t0002g0294 a0001c0001t0002g0297 a0001c0001t0002g0305 others(48): Show |
51 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.286-1774_286-1773d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027385 | ||||||
| chr14:74027385 | C | CTTT | 8 | a0001c0001t0002g0292 a0001c0001t0002g0309 a0001c0001t0002g0311 others(5): Show |
8 | HG00408.hp1 HG02895.hp1 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.286-1775_286-1773d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027385 | ||||||
| chr14:74027385 | CT | C | 43 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0147 others(40): Show |
44 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.286-1773delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027385 | ||||||
| chr14:74027385 | CTT | C | 13 | a0002c0002t0001g0197 a0002c0002t0001g0198 a0002c0002t0001g0199 others(10): Show |
13 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.286-1774_286-1773d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027385 | ||||||
| chr14:74027385 | CTTT | C | 6 | a0004c0007t0003g0004 a0005c0006t0001g0132 a0005c0006t0001g0133 others(3): Show |
6 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-1775_286-1773d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027385 | ||||||
| chr14:74027449 | T | C | 2 | a0008c0012t0009g0376 a0008c0012t0009g0377 |
2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.286-1735T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027449 | |||||||
| chr14:74027604 | G | T | 1 | a0002c0002t0001g0235 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.286-1580G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027604 | |||||||
| chr14:74027734 | A | G | 78 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(75): Show |
79 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.286-1450A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027734 | |||||||
| chr14:74027736 | C | G | 1 | a0003c0003t0001g0031 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.286-1448C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027736 | |||||||
| chr14:74027911 | T | TACAAGAA others(6): Show |
1 | a0001c0001t0002g0315 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.286-1272_286-1271i others(15): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027911 | ||||||
| chr14:74027915 | C | A | 1 | a0001c0001t0002g0315 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.286-1269C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027915 | |||||||
| chr14:74027918 | G | A | 1 | a0001c0001t0002g0315 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.286-1266G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027918 | |||||||
| chr14:74027933 | G | T | 1 | a0005c0006t0006g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.286-1251G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027933 | |||||||
| chr14:74028347 | C | T | 3 | a0004c0009t0007g0138 a0004c0009t0007g0139 a0004c0009t0007g0140 |
3 | HG02572.hp2 HG02647.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.286-837C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028347 | |||||||
| chr14:74028387 | C | G | 78 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(75): Show |
79 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.286-797C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028387 | |||||||
| chr14:74028467 | T | TAC | 39 | a0001c0001t0003g0153 a0001c0001t0003g0154 a0001c0001t0003g0157 others(36): Show |
39 | HG00544.hp1 HG00673.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.286-673_286-672dup others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | ||||||
| chr14:74028467 | T | TACAC | 17 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0001c0001t0003g0151 others(14): Show |
17 | HG00408.hp2 HG01074.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.286-675_286-672dup others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | ||||||
| chr14:74028467 | T | TACACAC | 4 | a0001c0001t0003g0152 a0001c0001t0003g0158 a0001c0001t0003g0181 others(1): Show |
4 | HG02486.hp2 HG03831.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-677_286-672dup others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | ||||||
| chr14:74028467 | T | TACACACA others(3): Show |
1 | a0001c0001t0003g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.286-681_286-672dup others(10): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | ||||||
| chr14:74028467 | T | TACACACA others(5): Show |
1 | a0001c0001t0003g0275 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.286-683_286-672dup others(12): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | ||||||
| chr14:74028467 | TAC | T | 28 | a0001c0001t0003g0159 a0001c0001t0003g0161 a0001c0001t0003g0162 others(25): Show |
28 | HG00099.hp2 HG00438.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.286-673_286-672del others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | ||||||
| chr14:74028467 | TACAC | T | 79 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(76): Show |
82 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.286-675_286-672del others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | ||||||
| chr14:74028467 | TACACAC | T | 11 | a0002c0002t0001g0230 a0002c0002t0001g0264 a0002c0002t0001g0289 others(8): Show |
11 | HG00558.hp1 HG00642.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.286-677_286-672del others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | ||||||
| chr14:74028467 | TACACACA others(1): Show |
T | 4 | a0002c0002t0001g0197 a0002c0002t0001g0285 a0002c0016t0001g0218 others(1): Show |
4 | HG01123.hp2 HG02818.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-679_286-672del others(8): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | ||||||
| chr14:74028467 | TACACACA others(5): Show |
T | 5 | a0004c0007t0003g0007 a0005c0006t0006g0193 a0005c0006t0006g0194 others(2): Show |
5 | HG01109.hp2 HG02809.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-683_286-672del others(12): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | ||||||
| chr14:74028467 | TACACACA others(7): Show |
T | 1 | a0002c0002t0001g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286-685_286-672del others(14): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | ||||||
| chr14:74028467 | TACACACA others(9): Show |
T | 14 | a0002c0002t0001g0208 a0002c0002t0001g0210 a0002c0002t0001g0211 others(11): Show |
14 | HG01070.hp1 HG01192.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.286-687_286-672del others(16): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | ||||||
| chr14:74028467 | TACACACA others(13): Show |
T | 12 | a0001c0001t0002g0306 a0001c0001t0002g0307 a0001c0001t0002g0308 others(9): Show |
12 | HG00408.hp1 HG02083.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.286-691_286-672del others(20): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | ||||||
| chr14:74028503 | C | G | 5 | a0002c0002t0010g0362 a0002c0002t0010g0363 a0004c0007t0003g0361 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-681C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028503 | |||||||
| chr14:74028507 | C | A | 16 | a0001c0001t0002g0294 a0001c0001t0002g0297 a0001c0001t0002g0318 others(13): Show |
16 | HG01109.hp1 HG01981.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.286-677C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028507 | |||||||
| chr14:74028509 | C | A | 86 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(83): Show |
87 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.286-675C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028509 | |||||||
| chr14:74028509 | C | CAA | 55 | a0003c0003t0001g0009 a0003c0003t0001g0011 a0003c0003t0001g0013 others(52): Show |
55 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.286-674_286-673ins others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028509 | ||||||
| chr14:74028509 | C | T | 16 | a0001c0001t0002g0294 a0001c0001t0002g0297 a0001c0001t0002g0318 others(13): Show |
16 | HG01109.hp1 HG01981.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.286-675C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028509 | |||||||
| chr14:74028511 | C | G | 18 | a0001c0001t0002g0294 a0001c0001t0002g0297 a0001c0001t0002g0318 others(15): Show |
18 | HG01109.hp1 HG01981.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.286-673C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028511 | |||||||
| chr14:74028511 | C | T | 141 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(138): Show |
142 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.286-673C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028511 | |||||||
| chr14:74028513 | A | C | 1 | a0001c0001t0003g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.286-671A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028513 | |||||||
| chr14:74028513 | A | G | 141 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(138): Show |
142 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.286-671A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028513 | |||||||
| chr14:74028513 | AAT | A | 18 | a0001c0001t0002g0294 a0001c0001t0002g0297 a0001c0001t0002g0318 others(15): Show |
18 | HG01109.hp1 HG01981.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.286-669_286-668del others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028513 | ||||||
| chr14:74028515 | T | A | 142 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(139): Show |
143 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.286-669T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028515 | |||||||
| chr14:74028515 | T | TAGAA | 64 | a0001c0001t0003g0296 a0001c0001t0003g0298 a0001c0001t0003g0299 others(61): Show |
65 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.286-666_286-665ins others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028515 | ||||||
| chr14:74028638 | G | A | 2 | a0003c0003t0001g0030 a0003c0003t0001g0034 |
2 | NA18979.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.286-546G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028638 | |||||||
| chr14:74028731 | CAG | C | 3 | a0003c0003t0001g0053 a0003c0003t0001g0054 a0003c0003t0001g0069 |
3 | NA18966.hp2 NA18985.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.286-450_286-449del others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028731 | ||||||
| chr14:74028744 | T | C | 2 | a0008c0012t0009g0376 a0008c0012t0009g0377 |
2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.286-440T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028744 | |||||||
| chr14:74028751 | C | T | 3 | a0006c0005t0008g0378 a0006c0005t0008g0379 a0006c0005t0008g0380 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.286-433C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028751 | |||||||
| chr14:74028763 | C | T | 2 | a0001c0001t0003g0153 a0001c0001t0003g0154 |
2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.286-421C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028763 | |||||||
| chr14:74028766 | T | C | 1 | a0002c0002t0001g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.286-418T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028766 | |||||||
| chr14:74028777 | C | T | 5 | a0002c0002t0010g0362 a0002c0002t0010g0363 a0004c0007t0003g0361 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-407C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028777 | |||||||
| chr14:74028831 | C | T | 2 | a0002c0002t0001g0231 a0002c0002t0001g0237 |
2 | HG00099.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.286-353C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028831 | |||||||
| chr14:74028948 | C | CCACA | 40 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(37): Show |
40 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.286-219_286-216dup others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028948 | ||||||
| chr14:74028948 | CCA | C | 226 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(223): Show |
228 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.286-217_286-216del others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028948 | ||||||
| chr14:74029375 | T | C | 1 | a0001c0001t0003g0159 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.351+126T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74029375 | |||||||
| chr14:74029458 | G | A | 7 | a0002c0002t0001g0197 a0002c0002t0001g0198 a0002c0002t0001g0199 others(4): Show |
7 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+209G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74029458 | |||||||
| chr14:74029617 | A | G | 266 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(263): Show |
268 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.351+368A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74029617 | |||||||
| chr14:74029636 | C | T | 1 | a0001c0001t0002g0343 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.351+387C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74029636 | |||||||
| chr14:74029682 | C | CA | 47 | a0001c0001t0002g0343 a0001c0001t0003g0151 a0001c0001t0003g0152 others(44): Show |
47 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.351+448dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74029682 | ||||||
| chr14:74029682 | CA | C | 6 | a0003c0003t0001g0019 a0003c0003t0001g0052 a0003c0003t0001g0074 others(3): Show |
6 | HG02572.hp2 HG02647.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+448delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74029682 | ||||||
| chr14:74029780 | A | G | 4 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0229 others(1): Show |
4 | NA18952.hp2 NA19010.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+531A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74029780 | |||||||
| chr14:74030079 | A | G | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.351+830A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030079 | |||||||
| chr14:74030082 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.351+833C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030082 | |||||||
| chr14:74030527 | G | A | 7 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(4): Show |
7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+1278G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030527 | |||||||
| chr14:74030686 | G | A | 1 | a0001c0001t0002g0311 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.351+1437G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030686 | |||||||
| chr14:74030760 | G | A | 64 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(61): Show |
65 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.351+1511G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030760 | |||||||
| chr14:74030855 | T | G | 1 | a0008c0012t0009g0377 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+1606T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030855 | |||||||
| chr14:74030859 | T | A | 1 | a0001c0001t0002g0354 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.351+1610T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030859 | |||||||
| chr14:74030860 | A | T | 1 | a0001c0001t0002g0354 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.351+1611A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030860 | |||||||
| chr14:74030921 | C | CAT | 3 | a0002c0002t0001g0252 a0002c0002t0001g0255 a0002c0002t0001g0276 |
3 | HG02970.hp1 HG03239.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.351+1690_351+1691d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030921 | ||||||
| chr14:74030921 | CAT | C | 205 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(202): Show |
207 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.351+1690_351+1691d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030921 | ||||||
| chr14:74030931 | T | G | 2 | a0002c0002t0010g0362 a0002c0002t0010g0363 |
2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.351+1682T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030931 | |||||||
| chr14:74030933 | T | G | 9 | a0001c0001t0002g0320 a0001c0001t0003g0158 a0001c0001t0003g0174 others(6): Show |
9 | HG00408.hp2 HG01069.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+1684T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030933 | |||||||
| chr14:74030933 | T | TAG | 7 | a0001c0001t0003g0153 a0001c0001t0003g0154 a0001c0001t0003g0182 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+1685_351+1686i others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030933 | ||||||
| chr14:74030933 | T | TAGAG | 18 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0155 others(15): Show |
18 | HG00099.hp2 HG00544.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.351+1685_351+1686i others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030933 | ||||||
| chr14:74030935 | T | G | 69 | a0001c0001t0002g0320 a0001c0001t0002g0321 a0001c0001t0002g0328 others(66): Show |
69 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.351+1686T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030935 | |||||||
| chr14:74030935 | T | TAG | 4 | a0001c0001t0003g0157 a0001c0001t0003g0183 a0001c0001t0003g0274 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+1687_351+1688i others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030935 | ||||||
| chr14:74030935 | T | TAGAG | 7 | a0001c0001t0003g0159 a0001c0001t0003g0166 a0001c0001t0003g0167 others(4): Show |
7 | HG00438.hp2 HG03669.hp1 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+1687_351+1688i others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030935 | ||||||
| chr14:74030937 | T | G | 176 | a0001c0001t0002g0003 a0001c0001t0002g0293 a0001c0001t0002g0297 others(173): Show |
177 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.351+1688T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030937 | |||||||
| chr14:74030937 | T | TAG | 6 | a0001c0001t0003g0156 a0002c0002t0001g0242 a0002c0016t0001g0218 others(3): Show |
6 | HG01074.hp2 HG01123.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+1689_351+1690i others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030937 | ||||||
| chr14:74030939 | T | G | 297 | a0001c0001t0002g0003 a0001c0001t0002g0293 a0001c0001t0002g0294 others(294): Show |
300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.351+1690T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030939 | |||||||
| chr14:74030939 | TAG | T | 5 | a0003c0003t0001g0051 a0003c0003t0001g0086 a0003c0015t0001g0059 others(2): Show |
5 | HG02738.hp1 HG02818.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+1702_351+1703d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030939 | ||||||
| chr14:74030941 | G | T | 1 | a0002c0002t0001g0230 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.351+1692G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030941 | |||||||
| chr14:74031012 | G | A | 2 | a0001c0001t0003g0162 a0001c0001t0003g0168 |
2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.351+1763G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031012 | |||||||
| chr14:74031119 | C | CTT | 6 | a0001c0001t0002g0354 a0002c0002t0010g0362 a0002c0002t0010g0363 others(3): Show |
6 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+1881_351+1882d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74031119 | ||||||
| chr14:74031119 | C | CTTT | 72 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(69): Show |
73 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.351+1880_351+1882d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74031119 | ||||||
| chr14:74031140 | G | C | 7 | a0001c0001t0003g0298 a0001c0001t0003g0299 a0001c0001t0003g0300 others(4): Show |
7 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+1891G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031140 | |||||||
| chr14:74031350 | C | T | 73 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(70): Show |
74 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.351+2101C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031350 | |||||||
| chr14:74031370 | C | T | 2 | a0004c0004t0004g0115 a0004c0004t0004g0120 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.351+2121C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031370 | |||||||
| chr14:74031499 | T | A | 3 | a0003c0003t0001g0042 a0003c0003t0001g0043 a0003c0003t0001g0082 |
3 | NA19057.hp2 NA19081.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.351+2250T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031499 | |||||||
| chr14:74031512 | T | A | 1 | a0001c0001t0012g0160 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.351+2263T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031512 | |||||||
| chr14:74031589 | G | C | 2 | a0002c0002t0001g0219 a0002c0002t0001g0232 |
2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.351+2340G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031589 | |||||||
| chr14:74031630 | G | A | 229 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(226): Show |
231 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.351+2381G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031630 | |||||||
| chr14:74031655 | A | G | 229 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(226): Show |
231 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.352-2373A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031655 | |||||||
| chr14:74031845 | T | A | 1 | a0001c0001t0003g0151 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.352-2183T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031845 | |||||||
| chr14:74031945 | G | A | 5 | a0002c0002t0010g0362 a0002c0002t0010g0363 a0004c0007t0003g0361 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-2083G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031945 | |||||||
| chr14:74032092 | A | G | 1 | a0004c0004t0004g0109 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.352-1936A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032092 | |||||||
| chr14:74032118 | A | AT | 96 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0001c0001t0003g0152 others(93): Show |
96 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.352-1885dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74032118 | ||||||
| chr14:74032118 | A | ATT | 14 | a0002c0002t0001g0192 a0003c0003t0001g0011 a0003c0003t0001g0014 others(11): Show |
14 | HG01243.hp2 HG01928.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.352-1886_352-1885d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74032118 | ||||||
| chr14:74032118 | AT | A | 8 | a0001c0001t0002g0354 a0002c0002t0001g0208 a0002c0002t0001g0223 others(5): Show |
8 | HG01257.hp2 HG01258.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.352-1885delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74032118 | ||||||
| chr14:74032118 | ATT | A | 10 | a0001c0001t0002g0305 a0001c0001t0002g0340 a0001c0001t0002g0349 others(7): Show |
10 | HG02135.hp2 HG02145.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.352-1886_352-1885d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74032118 | ||||||
| chr14:74032118 | ATTT | A | 65 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(62): Show |
66 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.352-1887_352-1885d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74032118 | ||||||
| chr14:74032126 | T | A | 36 | a0004c0004t0004g0089 a0004c0004t0004g0090 a0004c0004t0004g0091 others(33): Show |
36 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.352-1902T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032126 | |||||||
| chr14:74032133 | T | A | 9 | a0004c0004t0004g0089 a0004c0004t0004g0099 a0004c0004t0004g0100 others(6): Show |
9 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.352-1895T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032133 | |||||||
| chr14:74032148 | C | A | 2 | a0003c0003t0001g0037 a0003c0003t0001g0060 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.352-1880C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032148 | |||||||
| chr14:74032212 | C | T | 3 | a0004c0004t0004g0090 a0004c0004t0004g0103 a0004c0004t0004g0108 |
3 | HG01123.hp1 HG01261.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.352-1816C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032212 | |||||||
| chr14:74032257 | G | A | 1 | a0004c0007t0003g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.352-1771G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032257 | |||||||
| chr14:74032450 | A | T | 8 | a0003c0003t0001g0039 a0003c0003t0001g0050 a0003c0003t0001g0053 others(5): Show |
8 | HG00673.hp2 HG02015.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-1578A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032450 | |||||||
| chr14:74032489 | C | CT | 127 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(124): Show |
128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.352-1525dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74032489 | ||||||
| chr14:74032491 | T | C | 1 | a0002c0002t0001g0146 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.352-1537T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032491 | |||||||
| chr14:74032553 | G | A | 1 | a0001c0001t0002g0328 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.352-1475G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032553 | |||||||
| chr14:74032727 | C | T | 41 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(38): Show |
41 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.352-1301C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032727 | |||||||
| chr14:74032854 | G | A | 11 | a0001c0001t0003g0298 a0001c0001t0003g0299 a0001c0001t0003g0301 others(8): Show |
11 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.352-1174G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032854 | |||||||
| chr14:74033216 | AT | A | 59 | a0003c0003t0003g0189 a0004c0004t0004g0002 a0004c0004t0004g0087 others(56): Show |
60 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.352-805delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74033216 | ||||||
| chr14:74033227 | A | G | 7 | a0003c0003t0001g0018 a0003c0003t0001g0026 a0003c0003t0001g0032 others(4): Show |
7 | NA18940.hp2 NA18959.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.352-801A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033227 | |||||||
| chr14:74033256 | A | T | 4 | a0002c0002t0001g0242 a0002c0002t0001g0255 a0002c0002t0001g0269 others(1): Show |
4 | HG01123.hp2 HG02970.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-772A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033256 | |||||||
| chr14:74033268 | A | G | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.352-760A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033268 | |||||||
| chr14:74033280 | A | G | 3 | a0004c0009t0007g0138 a0004c0009t0007g0139 a0004c0009t0007g0140 |
3 | HG02572.hp2 HG02647.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.352-748A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033280 | |||||||
| chr14:74033421 | T | C | 1 | a0004c0004t0004g0090 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.352-607T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033421 | |||||||
| chr14:74033491 | A | C | 2 | a0008c0012t0009g0376 a0008c0012t0009g0377 |
2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.352-537A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033491 | |||||||
| chr14:74033564 | C | T | 1 | a0004c0004t0004g0126 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.352-464C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033564 | |||||||
| chr14:74033779 | T | G | 1 | a0004c0004t0004g0128 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.352-249T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033779 | |||||||
| chr14:74033808 | G | A | 1 | a0003c0003t0001g0011 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.352-220G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033808 | |||||||
| chr14:74033827 | T | C | 114 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(111): Show |
115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.352-201T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033827 | |||||||
| chr14:74033845 | G | A | 3 | a0004c0004t0004g0094 a0004c0004t0004g0106 a0004c0004t0004g0107 |
3 | HG02071.hp2 HG02165.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.352-183G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033845 | |||||||
| chr14:74033882 | A | T | 114 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(111): Show |
115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.352-146A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033882 | |||||||
| chr14:74033883 | T | A | 114 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(111): Show |
115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.352-145T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033883 | |||||||
| chr14:74033888 | A | C | 6 | a0005c0006t0001g0131 a0005c0006t0001g0132 a0005c0006t0001g0133 others(3): Show |
6 | HG01243.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.352-140A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033888 | |||||||
| chr14:74033918 | G | A | 40 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(37): Show |
40 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.352-110G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033918 | |||||||
| chr14:74034239 | A | G | 1 | a0004c0004t0004g0100 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.495+68A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74034239 | |||||||
| chr14:74034331 | A | C | 132 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(129): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.495+160A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74034331 | |||||||
| chr14:74034481 | A | G | 3 | a0004c0009t0007g0138 a0004c0009t0007g0139 a0004c0009t0007g0140 |
3 | HG02572.hp2 HG02647.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.495+310A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74034481 | |||||||
| chr14:74034566 | G | A | 1 | a0002c0002t0001g0256 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.495+395G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74034566 | |||||||
| chr14:74034747 | C | G | 149 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(146): Show |
150 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.495+576C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74034747 | |||||||
| chr14:74034833 | G | A | 6 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0002c0002t0001g0246 others(3): Show |
6 | HG00639.hp2 HG01261.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.495+662G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74034833 | |||||||
| chr14:74034963 | G | A | 83 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(80): Show |
83 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.495+792G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74034963 | |||||||
| chr14:74035009 | T | C | 81 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(78): Show |
81 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.495+838T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035009 | |||||||
| chr14:74035077 | A | G | 276 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(273): Show |
278 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.495+906A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035077 | |||||||
| chr14:74035138 | T | C | 2 | a0006c0005t0003g0374 a0006c0005t0003g0375 |
2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.495+967T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035138 | |||||||
| chr14:74035226 | TA | T | 51 | a0002c0002t0001g0001 a0002c0002t0001g0205 a0002c0002t0001g0206 others(48): Show |
53 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.495+1065delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035226 | ||||||
| chr14:74035290 | A | C | 275 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(272): Show |
277 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.495+1119A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035290 | |||||||
| chr14:74035298 | A | G | 40 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(37): Show |
40 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.495+1127A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035298 | |||||||
| chr14:74035377 | C | T | 3 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 |
3 | HG02809.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.495+1206C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035377 | |||||||
| chr14:74035413 | C | CT | 18 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0143 others(15): Show |
18 | HG00735.hp1 HG01081.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.495+1263dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035413 | ||||||
| chr14:74035413 | CT | C | 141 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(138): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.495+1263delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035413 | ||||||
| chr14:74035413 | CTT | C | 19 | a0001c0001t0002g0333 a0001c0001t0003g0149 a0001c0001t0003g0150 others(16): Show |
19 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.495+1262_495+1263d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035413 | ||||||
| chr14:74035413 | CTTT | C | 8 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(5): Show |
8 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.495+1261_495+1263d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035413 | ||||||
| chr14:74035453 | A | G | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.495+1282A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035453 | |||||||
| chr14:74035480 | G | A | 4 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1309G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035480 | |||||||
| chr14:74035527 | G | A | 2 | a0003c0003t0001g0190 a0003c0003t0001g0191 |
2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.495+1356G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035527 | |||||||
| chr14:74035542 | C | T | 95 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(92): Show |
95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.495+1371C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035542 | |||||||
| chr14:74035567 | A | G | 3 | a0007c0008t0001g0213 a0007c0008t0001g0216 a0007c0008t0001g0273 |
3 | HG02559.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.495+1396A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035567 | |||||||
| chr14:74035578 | C | G | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.495+1407C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035578 | |||||||
| chr14:74035584 | A | AT | 22 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(19): Show |
22 | HG00735.hp1 HG01109.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.495+1441dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035584 | A | ATTT | 39 | a0001c0001t0002g0313 a0001c0001t0002g0331 a0001c0001t0003g0149 others(36): Show |
39 | HG00099.hp2 HG00408.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.495+1439_495+1441d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035584 | A | ATTTT | 56 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(53): Show |
57 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.495+1438_495+1441d others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035584 | A | ATTTTT | 15 | a0001c0001t0002g0297 a0001c0001t0002g0306 a0001c0001t0002g0316 others(12): Show |
15 | HG00423.hp1 HG00735.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.495+1437_495+1441d others(7): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035584 | A | ATTTTTTT others(3): Show |
4 | a0004c0007t0003g0361 a0006c0005t0005g0369 a0006c0005t0005g0370 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1432_495+1441d others(12): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035584 | A | ATTTTTTT others(4): Show |
2 | a0006c0005t0005g0373 a0006c0005t0016g0381 |
2 | HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.495+1431_495+1441d others(13): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035584 | A | ATTTTTTT others(5): Show |
1 | a0006c0005t0003g0374 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.495+1430_495+1441d others(14): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035584 | A | ATTTTTTT others(6): Show |
1 | a0006c0005t0005g0372 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.495+1429_495+1441d others(15): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035584 | A | ATTTTTTT others(8): Show |
1 | a0006c0005t0003g0375 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.495+1427_495+1441d others(17): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035584 | A | ATTTTTTT others(11): Show |
2 | a0004c0007t0003g0004 a0004c0007t0003g0006 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.495+1424_495+1441d others(20): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035584 | A | ATTTTTTT others(12): Show |
1 | a0004c0007t0003g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.495+1423_495+1441d others(21): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035584 | A | ATTTTTTT others(21): Show |
1 | a0006c0005t0008g0380 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.495+1414_495+1441d others(30): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035584 | A | ATTTTTTT others(22): Show |
2 | a0006c0005t0008g0378 a0006c0005t0008g0379 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.495+1441_495+1442i others(31): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035584 | AT | A | 114 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0143 others(111): Show |
115 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.495+1441delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035584 | ATTTTTTT others(4): Show |
A | 1 | a0004c0007t0003g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.495+1431_495+1441d others(13): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | ||||||
| chr14:74035712 | C | T | 1 | a0002c0002t0001g0201 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+1541C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035712 | |||||||
| chr14:74035792 | C | A | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.495+1621C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035792 | |||||||
| chr14:74035810 | C | T | 11 | a0001c0001t0002g0339 a0004c0007t0003g0004 a0004c0007t0003g0005 others(8): Show |
11 | HG00673.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.495+1639C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035810 | |||||||
| chr14:74035854 | A | T | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.495+1683A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035854 | |||||||
| chr14:74035856 | TCACA | T | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.495+1686_495+1689d others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035856 | |||||||
| chr14:74035903 | G | A | 1 | a0006c0005t0016g0381 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.495+1732G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035903 | |||||||
| chr14:74036062 | C | CT | 12 | a0002c0002t0001g0001 a0002c0002t0001g0277 a0002c0002t0001g0278 others(9): Show |
14 | HG01358.hp1 HG01884.hp1 HG03139.hp2 others(11): Show |
intron_variant | MODIFIER | c.495+1902dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036062 | ||||||
| chr14:74036062 | CT | C | 8 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+1902delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036062 | ||||||
| chr14:74036118 | C | T | 114 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(111): Show |
115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.495+1947C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036118 | |||||||
| chr14:74036135 | AACCTCC | A | 8 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+1971_495+1976d others(8): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036135 | ||||||
| chr14:74036174 | G | C | 84 | a0002c0002t0001g0261 a0003c0003t0001g0008 a0003c0003t0001g0009 others(81): Show |
84 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.495+2003G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036174 | |||||||
| chr14:74036184 | T | G | 3 | a0006c0005t0008g0378 a0006c0005t0008g0379 a0006c0005t0008g0380 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.495+2013T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036184 | |||||||
| chr14:74036210 | C | T | 3 | a0007c0008t0001g0213 a0007c0008t0001g0216 a0007c0008t0001g0273 |
3 | HG02559.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.495+2039C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036210 | |||||||
| chr14:74036498 | C | T | 2 | a0006c0005t0003g0374 a0006c0005t0003g0375 |
2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.495+2327C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036498 | |||||||
| chr14:74036630 | A | G | 376 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(373): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.495+2459A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036630 | |||||||
| chr14:74036683 | C | CA | 275 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0297 others(272): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.495+2530dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036683 | ||||||
| chr14:74036683 | C | CAA | 46 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0342 others(43): Show |
46 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(43): Show |
intron_variant | MODIFIER | c.495+2529_495+2530d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036683 | ||||||
| chr14:74036683 | CA | C | 44 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(41): Show |
45 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.495+2530delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036683 | ||||||
| chr14:74036701 | A | G | 1 | a0004c0007t0003g0361 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.495+2530A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036701 | |||||||
| chr14:74036702 | G | A | 1 | a0006c0005t0003g0375 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.495+2531G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036702 | |||||||
| chr14:74036782 | G | A | 48 | a0002c0002t0001g0001 a0002c0002t0001g0205 a0002c0002t0001g0206 others(45): Show |
50 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.495+2611G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036782 | |||||||
| chr14:74036905 | T | G | 4 | a0005c0006t0006g0193 a0005c0006t0006g0194 a0005c0006t0006g0195 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+2734T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036905 | |||||||
| chr14:74036952 | ATCTTTTT others(12): Show |
A | 8 | a0006c0005t0005g0369 a0006c0005t0005g0370 a0006c0005t0005g0371 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.495+2795_495+2813d others(21): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036952 | ||||||
| chr14:74036954 | CTTTTTTT others(13): Show |
C | 2 | a0004c0009t0007g0138 a0004c0009t0007g0140 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.495+2795_495+2814d others(22): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036954 | ||||||
| chr14:74036955 | TTTTTTTT others(11): Show |
T | 3 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0016g0381 |
3 | HG02486.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.495+2795_495+2812d others(20): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036955 | ||||||
| chr14:74036973 | C | CT | 20 | a0002c0002t0001g0222 a0002c0002t0001g0233 a0002c0002t0001g0289 others(17): Show |
20 | HG00738.hp1 HG01192.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.495+2819dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036973 | ||||||
| chr14:74037009 | G | A | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.495+2838G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037009 | |||||||
| chr14:74037119 | C | T | 4 | a0002c0002t0001g0147 a0002c0002t0001g0148 a0002c0002t0001g0192 others(1): Show |
4 | HG02717.hp1 HG03139.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+2948C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037119 | |||||||
| chr14:74037156 | G | T | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.495+2985G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037156 | |||||||
| chr14:74037226 | G | A | 16 | a0001c0001t0003g0155 a0001c0001t0003g0158 a0001c0001t0003g0159 others(13): Show |
16 | HG00099.hp2 HG00438.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.495+3055G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037226 | |||||||
| chr14:74037232 | C | T | 1 | a0004c0004t0004g0117 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.495+3061C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037232 | |||||||
| chr14:74037274 | C | CT | 35 | a0001c0001t0003g0152 a0001c0001t0003g0161 a0001c0001t0003g0162 others(32): Show |
35 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.495+3130dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037274 | ||||||
| chr14:74037274 | CT | C | 72 | a0001c0001t0002g0003 a0001c0001t0002g0293 a0001c0001t0002g0294 others(69): Show |
73 | HG00323.hp1 HG00642.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.495+3130delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037274 | ||||||
| chr14:74037274 | CTT | C | 9 | a0001c0001t0002g0316 a0001c0001t0002g0318 a0001c0001t0002g0322 others(6): Show |
9 | HG01167.hp1 HG01346.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.495+3129_495+3130d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037274 | ||||||
| chr14:74037274 | CTTTTTTT others(1): Show |
C | 11 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0005g0369 others(8): Show |
11 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.495+3123_495+3130d others(10): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037274 | ||||||
| chr14:74037274 | CTTTTTTT others(3): Show |
C | 12 | a0003c0003t0003g0189 a0005c0006t0001g0131 a0005c0006t0001g0132 others(9): Show |
12 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.495+3121_495+3130d others(12): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037274 | ||||||
| chr14:74037274 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0320 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.495+3120_495+3130d others(13): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037274 | ||||||
| chr14:74037274 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0308 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.495+3118_495+3130d others(15): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037274 | ||||||
| chr14:74037326 | C | T | 95 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(92): Show |
95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.495+3155C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037326 | |||||||
| chr14:74037364 | T | C | 1 | a0006c0005t0003g0374 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.495+3193T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037364 | |||||||
| chr14:74037439 | C | T | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.496-3126C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037439 | |||||||
| chr14:74037459 | A | AT | 8 | a0003c0003t0001g0033 a0003c0003t0001g0190 a0003c0003t0001g0191 others(5): Show |
8 | HG01109.hp2 HG01243.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.496-3090dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037459 | ||||||
| chr14:74037459 | AT | A | 26 | a0001c0001t0002g0325 a0001c0001t0002g0334 a0002c0002t0001g0147 others(23): Show |
26 | HG00423.hp1 HG01243.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.496-3090delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037459 | ||||||
| chr14:74037629 | A | G | 4 | a0001c0001t0002g0321 a0001c0001t0002g0328 a0001c0001t0002g0346 others(1): Show |
4 | HG00642.hp2 HG00735.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-2936A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037629 | |||||||
| chr14:74037800 | A | G | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.496-2765A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037800 | |||||||
| chr14:74038021 | A | ACCACTTA others(1): Show |
285 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(282): Show |
287 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.496-2542_496-2541i others(10): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74038021 | ||||||
| chr14:74038088 | T | C | 1 | a0002c0002t0001g0225 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.496-2477T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038088 | |||||||
| chr14:74038100 | C | T | 3 | a0006c0005t0008g0378 a0006c0005t0008g0379 a0006c0005t0008g0380 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.496-2465C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038100 | |||||||
| chr14:74038120 | G | A | 8 | a0003c0003t0003g0189 a0005c0006t0001g0131 a0005c0006t0001g0132 others(5): Show |
8 | HG01243.hp1 HG02486.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.496-2445G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038120 | |||||||
| chr14:74038225 | T | A | 81 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(78): Show |
81 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.496-2340T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038225 | |||||||
| chr14:74038278 | A | T | 1 | a0001c0001t0002g0338 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.496-2287A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038278 | |||||||
| chr14:74038366 | T | C | 114 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(111): Show |
115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.496-2199T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038366 | |||||||
| chr14:74038554 | T | G | 1 | a0009c0010t0001g0055 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.496-2011T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038554 | |||||||
| chr14:74038784 | G | A | 283 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(280): Show |
285 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.496-1781G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038784 | |||||||
| chr14:74038790 | G | A | 1 | a0001c0001t0002g0308 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.496-1775G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038790 | |||||||
| chr14:74038989 | C | A | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.496-1576C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038989 | |||||||
| chr14:74038989 | C | T | 1 | a0001c0001t0003g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.496-1576C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038989 | |||||||
| chr14:74039045 | C | T | 275 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(272): Show |
277 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.496-1520C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039045 | |||||||
| chr14:74039117 | C | T | 3 | a0005c0006t0006g0194 a0005c0006t0006g0195 a0005c0006t0006g0196 |
3 | HG03195.hp2 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.496-1448C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039117 | |||||||
| chr14:74039282 | A | G | 2 | a0008c0012t0009g0376 a0008c0012t0009g0377 |
2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.496-1283A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039282 | |||||||
| chr14:74039309 | A | C | 3 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 |
3 | HG02809.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.496-1256A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039309 | |||||||
| chr14:74039392 | T | A | 81 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(78): Show |
81 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.496-1173T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039392 | |||||||
| chr14:74039538 | C | T | 2 | a0005c0006t0001g0134 a0005c0006t0001g0135 |
2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.496-1027C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039538 | |||||||
| chr14:74039595 | A | AT | 272 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(269): Show |
274 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.496-956dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74039595 | ||||||
| chr14:74039624 | C | T | 1 | a0008c0012t0009g0376 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.496-941C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039624 | |||||||
| chr14:74039679 | C | T | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.496-886C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039679 | |||||||
| chr14:74039713 | C | T | 11 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0001c0001t0003g0295 others(8): Show |
11 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.496-852C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039713 | |||||||
| chr14:74039742 | C | T | 286 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(283): Show |
288 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.496-823C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039742 | |||||||
| chr14:74039830 | C | A | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.496-735C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039830 | |||||||
| chr14:74040012 | T | A | 9 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0001c0001t0003g0298 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.496-553T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74040012 | |||||||
| chr14:74040060 | TCA | T | 114 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(111): Show |
115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.496-503_496-502del others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74040060 | ||||||
| chr14:74040115 | C | T | 1 | a0011c0018t0003g0175 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.496-450C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74040115 | |||||||
| chr14:74040279 | G | A | 11 | a0002c0002t0001g0207 a0002c0002t0001g0248 a0002c0002t0001g0249 others(8): Show |
11 | HG00280.hp1 HG00735.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.496-286G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74040279 | |||||||
| chr14:74040414 | G | A | 3 | a0004c0009t0007g0138 a0004c0009t0007g0139 a0004c0009t0007g0140 |
3 | HG02572.hp2 HG02647.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.496-151G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74040414 | |||||||
| chr14:74040659 | G | C | 1 | a0003c0003t0001g0040 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.576+14G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74040659 | |||||||
| chr14:74040971 | G | A | 6 | a0006c0005t0005g0369 a0006c0005t0005g0370 a0006c0005t0005g0371 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+326G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74040971 | |||||||
| chr14:74041004 | G | A | 6 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(3): Show |
6 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+359G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041004 | |||||||
| chr14:74041056 | G | T | 95 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(92): Show |
95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.576+411G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041056 | |||||||
| chr14:74041072 | C | T | 12 | a0003c0003t0003g0189 a0005c0006t0001g0131 a0005c0006t0001g0132 others(9): Show |
12 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.576+427C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041072 | |||||||
| chr14:74041213 | G | T | 6 | a0006c0005t0005g0369 a0006c0005t0005g0370 a0006c0005t0005g0371 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+568G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041213 | |||||||
| chr14:74041282 | G | A | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.576+637G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041282 | |||||||
| chr14:74041465 | T | G | 1 | a0001c0001t0003g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.576+820T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041465 | |||||||
| chr14:74041480 | ATAAT | A | 8 | a0001c0001t0002g0315 a0001c0001t0002g0316 a0001c0001t0002g0326 others(5): Show |
8 | HG00673.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.576+839_576+842del others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74041480 | ||||||
| chr14:74041644 | C | T | 11 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0005g0369 others(8): Show |
11 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.576+999C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041644 | |||||||
| chr14:74041756 | G | A | 11 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0005g0369 others(8): Show |
11 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.576+1111G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041756 | |||||||
| chr14:74041932 | G | A | 12 | a0003c0003t0003g0189 a0005c0006t0001g0131 a0005c0006t0001g0132 others(9): Show |
12 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.576+1287G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041932 | |||||||
| chr14:74042037 | AAAC | A | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.576+1413_576+1415d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042037 | ||||||
| chr14:74042090 | G | A | 95 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(92): Show |
95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.576+1445G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042090 | |||||||
| chr14:74042155 | A | G | 40 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(37): Show |
40 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.576+1510A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042155 | |||||||
| chr14:74042272 | C | T | 1 | a0005c0006t0006g0193 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.576+1627C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042272 | |||||||
| chr14:74042320 | G | A | 40 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(37): Show |
40 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.576+1675G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042320 | |||||||
| chr14:74042436 | C | T | 1 | a0001c0001t0003g0172 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.576+1791C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042436 | |||||||
| chr14:74042535 | C | T | 1 | a0002c0002t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.576+1890C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042535 | |||||||
| chr14:74042563 | C | T | 1 | a0001c0001t0002g0342 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.576+1918C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042563 | |||||||
| chr14:74042674 | C | T | 218 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(215): Show |
219 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.576+2029C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042674 | |||||||
| chr14:74042698 | C | A | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.576+2053C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042698 | |||||||
| chr14:74042716 | A | G | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.576+2071A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042716 | |||||||
| chr14:74042837 | C | T | 1 | a0003c0003t0001g0023 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.576+2192C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042837 | |||||||
| chr14:74042859 | C | G | 1 | a0001c0001t0002g0366 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.576+2214C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042859 | |||||||
| chr14:74042871 | CACACACA others(1): Show |
C | 5 | a0006c0005t0005g0369 a0006c0005t0005g0370 a0006c0005t0005g0371 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+2234_576+2241d others(10): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042871 | ||||||
| chr14:74042873 | CACACAG | C | 6 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0008g0378 others(3): Show |
6 | HG02451.hp2 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+2234_576+2239d others(8): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042873 | ||||||
| chr14:74042879 | G | GAC | 89 | a0001c0001t0003g0182 a0001c0001t0003g0185 a0001c0001t0003g0274 others(86): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.576+2265_576+2266d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | ||||||
| chr14:74042879 | G | GACAC | 12 | a0001c0001t0003g0156 a0002c0002t0001g0198 a0002c0002t0001g0199 others(9): Show |
12 | HG01074.hp2 HG01934.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.576+2263_576+2266d others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | ||||||
| chr14:74042879 | G | GACACAC | 39 | a0002c0002t0001g0202 a0003c0003t0001g0042 a0003c0003t0001g0065 others(36): Show |
40 | HG00280.hp2 HG00639.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.576+2261_576+2266d others(8): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | ||||||
| chr14:74042879 | G | GACACACA others(1): Show |
6 | a0004c0004t0004g0095 a0004c0004t0004g0114 a0004c0004t0004g0126 others(3): Show |
6 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.576+2259_576+2266d others(10): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | ||||||
| chr14:74042879 | GAC | G | 46 | a0001c0001t0002g0305 a0001c0001t0003g0151 a0001c0001t0003g0152 others(43): Show |
46 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.576+2265_576+2266d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | ||||||
| chr14:74042879 | GACAC | G | 76 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(73): Show |
77 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.576+2263_576+2266d others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | ||||||
| chr14:74042879 | GACACAC | G | 13 | a0001c0001t0003g0150 a0001c0001t0003g0295 a0003c0003t0003g0189 others(10): Show |
13 | HG01243.hp1 HG02258.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.576+2261_576+2266d others(8): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | ||||||
| chr14:74042879 | GACACACA others(1): Show |
G | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.576+2259_576+2266d others(10): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | ||||||
| chr14:74042887 | C | G | 2 | a0006c0005t0003g0374 a0006c0005t0003g0375 |
2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.576+2242C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042887 | |||||||
| chr14:74042889 | C | G | 4 | a0006c0005t0008g0378 a0006c0005t0008g0379 a0006c0005t0008g0380 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+2244C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042889 | |||||||
| chr14:74042891 | C | G | 5 | a0006c0005t0005g0369 a0006c0005t0005g0370 a0006c0005t0005g0371 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+2246C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042891 | |||||||
| chr14:74042895 | C | G | 2 | a0006c0005t0003g0374 a0006c0005t0003g0375 |
2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.576+2250C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042895 | |||||||
| chr14:74042957 | A | G | 230 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(227): Show |
231 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.576+2312A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042957 | |||||||
| chr14:74043187 | T | C | 1 | a0003c0003t0001g0064 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.576+2542T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043187 | |||||||
| chr14:74043208 | A | G | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.576+2563A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043208 | |||||||
| chr14:74043245 | A | G | 1 | a0004c0004t0004g0128 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.576+2600A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043245 | |||||||
| chr14:74043249 | A | G | 8 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+2604A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043249 | |||||||
| chr14:74043253 | T | A | 1 | a0002c0002t0001g0148 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.576+2608T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043253 | |||||||
| chr14:74043269 | G | T | 2 | a0006c0005t0003g0374 a0006c0005t0003g0375 |
2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.576+2624G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043269 | |||||||
| chr14:74043273 | A | G | 285 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(282): Show |
287 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.576+2628A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043273 | |||||||
| chr14:74043279 | G | A | 1 | a0006c0005t0003g0375 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.576+2634G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043279 | |||||||
| chr14:74043302 | G | C | 1 | a0003c0003t0001g0077 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.576+2657G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043302 | |||||||
| chr14:74043533 | G | A | 3 | a0006c0005t0008g0378 a0006c0005t0008g0379 a0006c0005t0008g0380 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.577-2527G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043533 | |||||||
| chr14:74043543 | C | T | 5 | a0002c0002t0001g0197 a0003c0003t0001g0047 a0003c0003t0001g0068 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.577-2517C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043543 | |||||||
| chr14:74043551 | C | T | 4 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0008c0012t0009g0376 others(1): Show |
4 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-2509C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043551 | |||||||
| chr14:74043556 | C | CA | 76 | a0001c0001t0002g0352 a0001c0001t0003g0150 a0001c0001t0003g0152 others(73): Show |
78 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.577-2476dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74043556 | ||||||
| chr14:74043556 | CA | C | 65 | a0001c0001t0002g0003 a0001c0001t0002g0293 a0001c0001t0002g0306 others(62): Show |
66 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.577-2476delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74043556 | ||||||
| chr14:74043556 | CAA | C | 73 | a0002c0002t0001g0199 a0002c0002t0001g0200 a0002c0002t0001g0201 others(70): Show |
73 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.577-2477_577-2476d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74043556 | ||||||
| chr14:74043556 | CAAA | C | 10 | a0003c0003t0003g0189 a0005c0006t0001g0131 a0005c0006t0001g0132 others(7): Show |
10 | HG01243.hp1 HG02486.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.577-2478_577-2476d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74043556 | ||||||
| chr14:74043557 | A | C | 3 | a0004c0004t0004g0089 a0004c0004t0004g0114 a0004c0004t0004g0119 |
3 | HG00323.hp1 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.577-2503A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043557 | |||||||
| chr14:74043587 | C | G | 3 | a0006c0005t0008g0378 a0006c0005t0008g0379 a0006c0005t0008g0380 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.577-2473C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043587 | |||||||
| chr14:74043666 | C | A | 1 | a0003c0003t0001g0052 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.577-2394C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043666 | |||||||
| chr14:74043776 | G | T | 1 | a0002c0002t0001g0225 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.577-2284G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043776 | |||||||
| chr14:74043784 | C | T | 1 | a0003c0003t0001g0076 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.577-2276C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043784 | |||||||
| chr14:74043881 | T | G | 2 | a0008c0012t0009g0376 a0008c0012t0009g0377 |
2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.577-2179T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043881 | |||||||
| chr14:74043905 | T | C | 7 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(4): Show |
7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.577-2155T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043905 | |||||||
| chr14:74043909 | G | A | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.577-2151G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043909 | |||||||
| chr14:74044021 | G | A | 10 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(7): Show |
10 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.577-2039G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044021 | |||||||
| chr14:74044170 | C | T | 6 | a0006c0005t0005g0369 a0006c0005t0005g0370 a0006c0005t0005g0371 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.577-1890C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044170 | |||||||
| chr14:74044180 | A | C | 1 | a0002c0002t0001g0266 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.577-1880A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044180 | |||||||
| chr14:74044193 | C | T | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.577-1867C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044193 | |||||||
| chr14:74044195 | G | A | 1 | a0011c0018t0003g0175 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.577-1865G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044195 | |||||||
| chr14:74044239 | CTGTCTCA others(17): Show |
C | 2 | a0006c0005t0003g0374 a0006c0005t0003g0375 |
2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.577-1819_577-1796d others(26): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74044239 | ||||||
| chr14:74044260 | A | AAAAT | 4 | a0001c0001t0002g0320 a0004c0007t0003g0361 a0004c0007t0003g0364 others(1): Show |
4 | HG01069.hp1 HG02145.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-1781_577-1778d others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74044260 | ||||||
| chr14:74044403 | A | T | 1 | a0001c0001t0002g0346 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.577-1657A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044403 | |||||||
| chr14:74044421 | C | G | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.577-1639C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044421 | |||||||
| chr14:74044475 | C | CT | 224 | a0001c0001t0002g0318 a0001c0001t0002g0322 a0001c0001t0003g0159 others(221): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.577-1569dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74044475 | ||||||
| chr14:74044475 | C | CTT | 129 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(126): Show |
130 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.577-1570_577-1569d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74044475 | ||||||
| chr14:74044476 | T | TC | 8 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-1584_577-1583i others(3): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044476 | |||||||
| chr14:74044508 | G | A | 21 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(18): Show |
21 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.577-1552G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044508 | |||||||
| chr14:74044523 | C | T | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.577-1537C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044523 | |||||||
| chr14:74044651 | C | T | 4 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-1409C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044651 | |||||||
| chr14:74044704 | T | C | 1 | a0004c0004t0004g0092 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.577-1356T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044704 | |||||||
| chr14:74044762 | C | G | 3 | a0001c0001t0003g0184 a0001c0001t0003g0186 a0001c0001t0003g0187 |
3 | HG02615.hp1 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.577-1298C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044762 | |||||||
| chr14:74044869 | G | A | 21 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(18): Show |
21 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.577-1191G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044869 | |||||||
| chr14:74045030 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.577-1030G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045030 | |||||||
| chr14:74045087 | C | G | 4 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-973C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045087 | |||||||
| chr14:74045127 | A | G | 1 | a0004c0007t0003g0365 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.577-933A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045127 | |||||||
| chr14:74045172 | T | C | 1 | a0008c0012t0009g0376 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.577-888T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045172 | |||||||
| chr14:74045175 | T | C | 95 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(92): Show |
95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.577-885T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045175 | |||||||
| chr14:74045232 | A | G | 7 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(4): Show |
7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.577-828A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045232 | |||||||
| chr14:74045302 | A | ATTCTT | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.577-756_577-755ins others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74045302 | ||||||
| chr14:74045371 | G | A | 46 | a0002c0002t0001g0209 a0004c0004t0004g0002 a0004c0004t0004g0087 others(43): Show |
47 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.577-689G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045371 | |||||||
| chr14:74045496 | C | A | 230 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(227): Show |
231 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.577-564C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045496 | |||||||
| chr14:74045686 | T | A | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.577-374T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045686 | |||||||
| chr14:74045995 | T | C | 285 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(282): Show |
287 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.577-65T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045995 | |||||||
| chr14:74046218 | C | G | 1 | a0007c0008t0001g0216 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.647+88C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046218 | |||||||
| chr14:74046402 | CATCCAGG others(2): Show |
C | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.647+282_647+290del others(9): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74046402 | ||||||
| chr14:74046530 | A | T | 8 | a0003c0003t0003g0189 a0005c0006t0001g0131 a0005c0006t0001g0132 others(5): Show |
8 | HG01243.hp1 HG02486.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.647+400A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046530 | |||||||
| chr14:74046533 | T | C | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.647+403T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046533 | |||||||
| chr14:74046543 | T | C | 1 | a0001c0001t0002g0330 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.647+413T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046543 | |||||||
| chr14:74046643 | G | C | 1 | a0003c0003t0001g0048 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.647+513G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046643 | |||||||
| chr14:74046644 | A | C | 1 | a0003c0003t0001g0048 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.647+514A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046644 | |||||||
| chr14:74046647 | A | C | 1 | a0003c0003t0001g0048 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.647+517A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046647 | |||||||
| chr14:74046648 | T | C | 1 | a0003c0003t0001g0048 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.647+518T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046648 | |||||||
| chr14:74046849 | C | T | 2 | a0003c0003t0001g0190 a0003c0003t0001g0191 |
2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.647+719C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046849 | |||||||
| chr14:74046937 | G | A | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.647+807G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046937 | |||||||
| chr14:74046939 | G | A | 1 | a0003c0003t0001g0012 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.647+809G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046939 | |||||||
| chr14:74047407 | C | CTTTA | 112 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0143 others(109): Show |
112 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.648-487_648-484dup others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74047407 | ||||||
| chr14:74047407 | C | CTTTATTT others(1): Show |
29 | a0002c0002t0001g0199 a0002c0002t0001g0200 a0002c0002t0001g0201 others(26): Show |
29 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.648-491_648-484dup others(8): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74047407 | ||||||
| chr14:74047407 | C | CTTTATTT others(5): Show |
13 | a0002c0002t0001g0198 a0002c0002t0001g0224 a0002c0002t0001g0225 others(10): Show |
13 | HG02258.hp1 HG02486.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.648-495_648-484dup others(12): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74047407 | ||||||
| chr14:74047407 | C | CTTTATTT others(9): Show |
1 | a0002c0002t0001g0223 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.648-499_648-484dup others(16): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74047407 | ||||||
| chr14:74047407 | C | CTTTATTT others(13): Show |
1 | a0003c0003t0001g0078 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.648-503_648-484dup others(20): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74047407 | ||||||
| chr14:74047407 | CTTTA | C | 13 | a0002c0002t0001g0147 a0002c0002t0001g0148 a0002c0002t0001g0192 others(10): Show |
13 | HG00558.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.648-487_648-484del others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74047407 | ||||||
| chr14:74047413 | T | TTATG | 34 | a0001c0001t0002g0321 a0001c0001t0002g0328 a0001c0001t0002g0346 others(31): Show |
34 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.648-514_648-513ins others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74047413 | ||||||
| chr14:74047417 | T | G | 79 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(76): Show |
80 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.648-513T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74047417 | |||||||
| chr14:74047463 | C | G | 2 | a0006c0005t0003g0374 a0006c0005t0003g0375 |
2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.648-467C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74047463 | |||||||
| chr14:74047594 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.648-336C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74047594 | |||||||
| chr14:74047595 | G | A | 3 | a0006c0005t0008g0378 a0006c0005t0008g0379 a0006c0005t0008g0380 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.648-335G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74047595 | |||||||
| chr14:74047685 | C | T | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.648-245C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74047685 | |||||||
| chr14:74047899 | C | A | 1 | a0002c0002t0001g0266 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.648-31C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74047899 | |||||||
| chr14:74048152 | A | G | 1 | a0001c0001t0002g0309 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.792+78A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74048152 | |||||||
| chr14:74048180 | A | T | 2 | a0006c0005t0003g0374 a0006c0005t0003g0375 |
2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.792+106A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74048180 | |||||||
| chr14:74048375 | T | G | 2 | a0002c0002t0001g0244 a0002c0002t0001g0289 |
2 | HG00140.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.792+301T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74048375 | |||||||
| chr14:74048380 | C | T | 2 | a0006c0005t0003g0374 a0006c0005t0003g0375 |
2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.792+306C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74048380 | |||||||
| chr14:74048881 | G | T | 2 | a0002c0002t0001g0269 a0003c0003t0001g0066 |
2 | NA18984.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.792+807G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74048881 | |||||||
| chr14:74048951 | C | T | 1 | a0002c0002t0001g0220 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.793-751C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74048951 | |||||||
| chr14:74048957 | T | C | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.793-745T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74048957 | |||||||
| chr14:74049018 | A | C | 7 | a0002c0002t0001g0214 a0002c0002t0001g0239 a0002c0002t0001g0240 others(4): Show |
7 | HG00639.hp2 HG01261.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.793-684A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74049018 | |||||||
| chr14:74049030 | G | A | 1 | a0003c0003t0001g0069 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.793-672G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74049030 | |||||||
| chr14:74049120 | C | A | 1 | a0002c0002t0001g0368 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.793-582C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74049120 | |||||||
| chr14:74049208 | T | C | 10 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(7): Show |
10 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.793-494T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74049208 | |||||||
| chr14:74049364 | A | G | 2 | a0001c0001t0003g0301 a0001c0001t0003g0303 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.793-338A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74049364 | |||||||
| chr14:74049379 | T | TA | 281 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(278): Show |
283 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.793-313dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 74049379 | ||||||
| chr14:74049535 | A | C | 1 | a0006c0005t0008g0380 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.793-167A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74049535 | |||||||
| chr14:74049640 | C | T | 1 | a0013c0017t0001g0351 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.793-62C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74049640 | |||||||
| chr14:74050209 | TTTA | T | 5 | a0006c0005t0005g0369 a0006c0005t0005g0370 a0006c0005t0005g0371 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1286+22_1286+24del others(3): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74050209 | ||||||
| chr14:74050309 | G | T | 8 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286+114G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050309 | |||||||
| chr14:74050403 | C | T | 8 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0005g0369 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1286+208C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050403 | |||||||
| chr14:74050451 | T | C | 8 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0005g0369 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1286+256T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050451 | |||||||
| chr14:74050529 | T | A | 3 | a0002c0002t0001g0249 a0002c0002t0001g0250 a0002c0002t0001g0268 |
3 | HG00280.hp1 HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1286+334T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050529 | |||||||
| chr14:74050535 | A | G | 3 | a0001c0001t0003g0165 a0001c0001t0003g0173 a0001c0001t0003g0179 |
3 | HG04115.hp1 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1286+340A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050535 | |||||||
| chr14:74050543 | C | A | 1 | a0004c0004t0004g0103 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1286+348C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050543 | |||||||
| chr14:74050584 | A | G | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1286+389A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050584 | |||||||
| chr14:74050674 | C | T | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1286+479C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050674 | |||||||
| chr14:74051042 | G | A | 21 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(18): Show |
21 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1286+847G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051042 | |||||||
| chr14:74051070 | C | T | 1 | a0001c0001t0002g0338 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1286+875C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051070 | |||||||
| chr14:74051116 | T | C | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1286+921T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051116 | |||||||
| chr14:74051117 | T | A | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1286+922T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051117 | |||||||
| chr14:74051137 | GGGAGGCT others(1394): Show |
G | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1286+965_1286+2365 others(3): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74051137 | ||||||
| chr14:74051201 | G | A | 8 | a0002c0002t0001g0223 a0002c0002t0001g0224 a0002c0002t0001g0225 others(5): Show |
8 | HG02155.hp1 NA18612.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1286+1006G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051201 | |||||||
| chr14:74051215 | G | C | 132 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(129): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1286+1020G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051215 | |||||||
| chr14:74051327 | C | T | 5 | a0006c0005t0005g0369 a0006c0005t0005g0370 a0006c0005t0005g0371 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1286+1132C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051327 | |||||||
| chr14:74051365 | A | T | 1 | a0003c0003t0001g0056 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1286+1170A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051365 | |||||||
| chr14:74051370 | A | G | 132 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(129): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1286+1175A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051370 | |||||||
| chr14:74051394 | C | T | 1 | a0002c0002t0001g0146 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1286+1199C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051394 | |||||||
| chr14:74052174 | C | T | 3 | a0006c0005t0008g0378 a0006c0005t0008g0379 a0006c0005t0008g0380 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1286+1979C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74052174 | |||||||
| chr14:74052357 | C | A | 2 | a0001c0001t0003g0301 a0001c0001t0003g0303 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1286+2162C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74052357 | |||||||
| chr14:74052644 | C | CA | 19 | a0001c0001t0003g0188 a0003c0003t0001g0052 a0004c0007t0003g0004 others(16): Show |
19 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1286+2462dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74052644 | ||||||
| chr14:74052860 | C | T | 2 | a0002c0002t0001g0255 a0002c0002t0001g0269 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1286+2665C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74052860 | |||||||
| chr14:74052877 | G | T | 8 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286+2682G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74052877 | |||||||
| chr14:74052934 | AGGCTGCA others(9): Show |
A | 375 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(372): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1287-2616_1287-260 others(20): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74052934 | ||||||
| chr14:74053035 | A | T | 3 | a0007c0008t0001g0213 a0007c0008t0001g0216 a0007c0008t0001g0273 |
3 | HG02559.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1287-2549A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053035 | |||||||
| chr14:74053056 | T | C | 25 | a0002c0002t0001g0208 a0002c0002t0001g0209 a0002c0002t0001g0210 others(22): Show |
25 | HG01070.hp1 HG01074.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1287-2528T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053056 | |||||||
| chr14:74053121 | A | T | 2 | a0002c0002t0001g0199 a0002c0002t0001g0201 |
2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1287-2463A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053121 | |||||||
| chr14:74053125 | T | A | 12 | a0003c0003t0003g0189 a0005c0006t0001g0131 a0005c0006t0001g0132 others(9): Show |
12 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1287-2459T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053125 | |||||||
| chr14:74053161 | C | A | 1 | a0004c0004t0004g0118 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1287-2423C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053161 | |||||||
| chr14:74053222 | C | T | 1 | a0001c0001t0002g0352 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1287-2362C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053222 | |||||||
| chr14:74053273 | C | T | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1287-2311C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053273 | |||||||
| chr14:74053373 | A | C | 9 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0001c0001t0003g0298 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1287-2211A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053373 | |||||||
| chr14:74053390 | T | C | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1287-2194T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053390 | |||||||
| chr14:74053607 | A | G | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1287-1977A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053607 | |||||||
| chr14:74053957 | A | C | 229 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(226): Show |
230 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1287-1627A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053957 | |||||||
| chr14:74054036 | G | A | 113 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(110): Show |
114 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1287-1548G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054036 | |||||||
| chr14:74054037 | G | C | 7 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(4): Show |
7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-1547G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054037 | |||||||
| chr14:74054127 | C | T | 63 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(60): Show |
64 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1287-1457C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054127 | |||||||
| chr14:74054168 | G | A | 63 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(60): Show |
64 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1287-1416G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054168 | |||||||
| chr14:74054212 | A | G | 229 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(226): Show |
230 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1287-1372A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054212 | |||||||
| chr14:74054305 | T | C | 134 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(131): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1287-1279T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054305 | |||||||
| chr14:74054385 | G | GT | 8 | a0002c0002t0001g0215 a0002c0002t0001g0220 a0002c0002t0001g0234 others(5): Show |
8 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1287-1188dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74054385 | ||||||
| chr14:74054385 | G | T | 1 | a0003c0003t0001g0051 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1287-1199G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054385 | |||||||
| chr14:74054410 | G | A | 1 | a0002c0002t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1287-1174G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054410 | |||||||
| chr14:74054415 | G | C | 1 | a0001c0001t0003g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1287-1169G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054415 | |||||||
| chr14:74054430 | G | A | 83 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(80): Show |
83 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1287-1154G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054430 | |||||||
| chr14:74054441 | C | T | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1287-1143C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054441 | |||||||
| chr14:74054442 | G | T | 95 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(92): Show |
95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1287-1142G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054442 | |||||||
| chr14:74054634 | C | T | 2 | a0001c0001t0002g0358 a0001c0001t0002g0360 |
2 | NA18983.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1287-950C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054634 | |||||||
| chr14:74054652 | C | T | 1 | a0006c0005t0016g0381 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1287-932C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054652 | |||||||
| chr14:74054678 | C | CT | 195 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(192): Show |
196 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1287-889dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74054678 | ||||||
| chr14:74054678 | C | CTT | 9 | a0003c0003t0001g0080 a0003c0003t0003g0189 a0005c0006t0001g0131 others(6): Show |
9 | HG01243.hp1 HG02486.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1287-890_1287-889d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74054678 | ||||||
| chr14:74054678 | CT | C | 12 | a0002c0002t0001g0203 a0002c0002t0001g0214 a0002c0002t0001g0242 others(9): Show |
12 | HG00323.hp1 HG01123.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1287-889delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74054678 | ||||||
| chr14:74054747 | G | A | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1287-837G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054747 | |||||||
| chr14:74054867 | C | T | 2 | a0003c0003t0001g0064 a0003c0003t0001g0382 |
2 | HG02027.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1287-717C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054867 | |||||||
| chr14:74054870 | C | T | 1 | a0002c0002t0001g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1287-714C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054870 | |||||||
| chr14:74054899 | G | A | 3 | a0001c0001t0002g0334 a0001c0001t0002g0335 a0002c0002t0001g0269 |
3 | NA18953.hp2 NA18960.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1287-685G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054899 | |||||||
| chr14:74055106 | T | C | 1 | a0002c0002t0001g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1287-478T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055106 | |||||||
| chr14:74055154 | C | CT | 8 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0143 others(5): Show |
8 | HG01081.hp1 HG01884.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1287-419dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74055154 | ||||||
| chr14:74055170 | C | T | 113 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(110): Show |
114 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1287-414C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055170 | |||||||
| chr14:74055171 | G | A | 1 | a0004c0007t0003g0006 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1287-413G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055171 | |||||||
| chr14:74055211 | C | T | 39 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(36): Show |
39 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1287-373C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055211 | |||||||
| chr14:74055212 | G | A | 1 | a0003c0003t0001g0045 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1287-372G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055212 | |||||||
| chr14:74055220 | C | G | 3 | a0004c0009t0007g0138 a0004c0009t0007g0139 a0004c0009t0007g0140 |
3 | HG02572.hp2 HG02647.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1287-364C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055220 | |||||||
| chr14:74055276 | G | A | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1287-308G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055276 | |||||||
| chr14:74055340 | G | C | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1287-244G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055340 | |||||||
| chr14:74055401 | G | A | 3 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 |
3 | HG02809.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1287-183G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055401 | |||||||
| chr14:74055539 | A | G | 1 | a0009c0010t0001g0055 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1287-45A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055539 | |||||||
| chr14:74055549 | T | C | 2 | a0002c0002t0001g0211 a0002c0002t0001g0212 |
2 | HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1287-35T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055549 | |||||||
| chr14:74055785 | G | A | 2 | a0008c0012t0009g0376 a0008c0012t0009g0377 |
2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1388+100G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74055785 | |||||||
| chr14:74056033 | T | TA | 3 | a0004c0004t0004g0090 a0004c0004t0004g0103 a0004c0004t0004g0122 |
3 | HG01123.hp1 HG02300.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1388+349dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056033 | ||||||
| chr14:74056034 | AT | A | 129 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(126): Show |
130 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1388+364delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056034 | ||||||
| chr14:74056035 | T | A | 144 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(141): Show |
145 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1388+350T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056035 | |||||||
| chr14:74056036 | T | A | 127 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(124): Show |
128 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1388+351T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056036 | |||||||
| chr14:74056192 | C | T | 113 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(110): Show |
114 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1388+507C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056192 | |||||||
| chr14:74056198 | A | AT | 115 | a0001c0001t0002g0003 a0001c0001t0002g0293 a0001c0001t0002g0294 others(112): Show |
117 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1388+533dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056198 | ||||||
| chr14:74056198 | A | ATT | 45 | a0001c0001t0002g0292 a0001c0001t0002g0329 a0001c0001t0002g0330 others(42): Show |
45 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1388+532_1388+533d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056198 | ||||||
| chr14:74056198 | A | ATTT | 77 | a0001c0001t0003g0168 a0001c0001t0003g0172 a0001c0001t0003g0178 others(74): Show |
77 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1388+531_1388+533d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056198 | ||||||
| chr14:74056198 | A | ATTTT | 13 | a0003c0003t0001g0014 a0003c0003t0001g0015 a0003c0003t0001g0016 others(10): Show |
13 | HG02135.hp1 HG02895.hp2 HG02897.hp1 others(10): Show |
intron_variant | MODIFIER | c.1388+530_1388+533d others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056198 | ||||||
| chr14:74056322 | C | G | 1 | a0001c0001t0003g0171 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1389-584C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056322 | |||||||
| chr14:74056324 | C | T | 10 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(7): Show |
10 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1389-582C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056324 | |||||||
| chr14:74056344 | G | C | 229 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(226): Show |
230 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1389-562G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056344 | |||||||
| chr14:74056380 | T | G | 1 | a0002c0002t0001g0290 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1389-526T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056380 | |||||||
| chr14:74056397 | A | G | 8 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0005g0369 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1389-509A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056397 | |||||||
| chr14:74056474 | ACAGG | A | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1389-429_1389-426d others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056474 | ||||||
| chr14:74056752 | G | C | 1 | a0002c0002t0001g0252 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1389-154G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056752 | |||||||
| chr14:74056816 | TA | T | 8 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1389-81delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056816 | ||||||
| chr14:74056836 | A | G | 1 | a0006c0005t0016g0381 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1389-70A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056836 | |||||||
| chr14:74057022 | C | T | 1 | a0002c0002t0001g0225 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1463+42C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 10/11 | chr14 | 74057022 | |||||||
| chr14:74057091 | G | C | 1 | a0001c0001t0002g0305 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1464-53G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 10/11 | chr14 | 74057091 | |||||||
| chr14:74057295 | T | C | 12 | a0003c0003t0001g0015 a0003c0003t0001g0020 a0003c0003t0001g0021 others(9): Show |
12 | HG00423.hp2 HG02165.hp1 NA18975.hp2 others(9): Show |
intron_variant | MODIFIER | c.1578+37T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057295 | |||||||
| chr14:74057454 | T | C | 1 | a0001c0001t0002g0313 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1578+196T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057454 | |||||||
| chr14:74057490 | G | C | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1578+232G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057490 | |||||||
| chr14:74057495 | C | T | 3 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 |
3 | HG02809.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1578+237C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057495 | |||||||
| chr14:74057648 | T | G | 10 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(7): Show |
10 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1578+390T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057648 | |||||||
| chr14:74057826 | A | G | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1578+568A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057826 | |||||||
| chr14:74057962 | T | C | 7 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(4): Show |
7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1578+704T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057962 | |||||||
| chr14:74057990 | G | A | 5 | a0002c0002t0001g0144 a0002c0002t0001g0145 a0002c0002t0001g0146 others(2): Show |
5 | HG01884.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1578+732G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057990 | |||||||
| chr14:74058125 | A | G | 6 | a0006c0005t0005g0369 a0006c0005t0005g0370 a0006c0005t0005g0371 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1578+867A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058125 | |||||||
| chr14:74058151 | C | A | 1 | a0009c0010t0001g0041 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1578+893C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058151 | |||||||
| chr14:74058235 | G | A | 2 | a0006c0005t0003g0374 a0006c0005t0003g0375 |
2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1578+977G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058235 | |||||||
| chr14:74058281 | C | T | 8 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0005g0369 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1578+1023C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058281 | |||||||
| chr14:74058289 | T | C | 1 | a0002c0002t0001g0141 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1578+1031T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058289 | |||||||
| chr14:74058290 | G | A | 4 | a0002c0002t0001g0147 a0002c0002t0001g0148 a0002c0002t0001g0192 others(1): Show |
4 | HG02717.hp1 HG03139.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578+1032G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058290 | |||||||
| chr14:74058318 | C | A | 1 | a0001c0001t0002g0342 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1578+1060C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058318 | |||||||
| chr14:74058340 | ACAACAAC others(19): Show |
A | 10 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(7): Show |
10 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1578+1083_1578+110 others(30): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058340 | |||||||
| chr14:74058344 | C | T | 1 | a0002c0002t0001g0272 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1578+1086C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058344 | |||||||
| chr14:74058448 | G | GA | 173 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(170): Show |
175 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1578+1206dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74058448 | ||||||
| chr14:74058448 | GA | G | 16 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(13): Show |
16 | HG02258.hp1 HG02280.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.1578+1206delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74058448 | ||||||
| chr14:74058485 | G | A | 2 | a0004c0009t0007g0138 a0004c0009t0007g0140 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1578+1227G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058485 | |||||||
| chr14:74058596 | C | CT | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1578+1350dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74058596 | ||||||
| chr14:74058708 | A | G | 134 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(131): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1578+1450A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058708 | |||||||
| chr14:74058738 | C | G | 1 | a0003c0003t0001g0075 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1578+1480C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058738 | |||||||
| chr14:74058822 | C | T | 2 | a0001c0001t0003g0301 a0001c0001t0003g0303 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1578+1564C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058822 | |||||||
| chr14:74058952 | C | T | 1 | a0003c0003t0001g0050 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1578+1694C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058952 | |||||||
| chr14:74059019 | G | A | 8 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0005g0369 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1578+1761G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059019 | |||||||
| chr14:74059057 | C | G | 1 | a0002c0002t0001g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1578+1799C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059057 | |||||||
| chr14:74059083 | T | TCAAAAAA others(3): Show |
1 | a0003c0003t0001g0058 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1578+1826_1578+183 others(14): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74059083 | ||||||
| chr14:74059083 | TC | T | 9 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0001c0001t0003g0298 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1578+1826delC | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059083 | |||||||
| chr14:74059084 | C | CA | 33 | a0001c0001t0002g0292 a0001c0001t0002g0307 a0001c0001t0002g0357 others(30): Show |
33 | HG01255.hp2 HG02055.hp2 HG02257.hp1 others(30): Show |
intron_variant | MODIFIER | c.1578+1848dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74059084 | ||||||
| chr14:74059084 | CA | C | 59 | a0001c0001t0002g0315 a0001c0001t0003g0156 a0001c0001t0003g0274 others(56): Show |
60 | HG00280.hp2 HG00639.hp1 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.1578+1848delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74059084 | ||||||
| chr14:74059085 | A | T | 9 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0001c0001t0003g0298 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1578+1827A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059085 | |||||||
| chr14:74059128 | T | C | 4 | a0001c0001t0003g0156 a0001c0001t0003g0185 a0001c0001t0003g0274 others(1): Show |
4 | HG01074.hp2 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578+1870T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059128 | |||||||
| chr14:74059187 | G | A | 1 | a0001c0001t0003g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1578+1929G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059187 | |||||||
| chr14:74059461 | C | T | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1578+2203C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059461 | |||||||
| chr14:74059485 | C | G | 134 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(131): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1578+2227C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059485 | |||||||
| chr14:74059494 | G | A | 134 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(131): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1578+2236G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059494 | |||||||
| chr14:74059610 | G | A | 11 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0005g0369 others(8): Show |
11 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1578+2352G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059610 | |||||||
| chr14:74059626 | C | T | 4 | a0005c0006t0006g0193 a0005c0006t0006g0194 a0005c0006t0006g0195 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578+2368C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059626 | |||||||
| chr14:74059627 | G | A | 8 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1578+2369G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059627 | |||||||
| chr14:74059636 | G | A | 6 | a0006c0005t0005g0369 a0006c0005t0005g0370 a0006c0005t0005g0371 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1578+2378G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059636 | |||||||
| chr14:74059662 | T | C | 4 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578+2404T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059662 | |||||||
| chr14:74059950 | T | C | 1 | a0001c0001t0003g0171 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1578+2692T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059950 | |||||||
| chr14:74060000 | G | A | 63 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(60): Show |
64 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1578+2742G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060000 | |||||||
| chr14:74060075 | G | A | 8 | a0004c0004t0004g0088 a0004c0004t0004g0098 a0004c0004t0004g0110 others(5): Show |
8 | NA18967.hp2 NA18972.hp2 NA19003.hp1 others(5): Show |
intron_variant | MODIFIER | c.1578+2817G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060075 | |||||||
| chr14:74060148 | T | A | 64 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(61): Show |
65 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.1578+2890T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060148 | |||||||
| chr14:74060209 | G | A | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1578+2951G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060209 | |||||||
| chr14:74060239 | A | G | 142 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(139): Show |
143 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1578+2981A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060239 | |||||||
| chr14:74060292 | G | C | 1 | a0008c0012t0009g0376 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1578+3034G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060292 | |||||||
| chr14:74060333 | C | T | 2 | a0009c0010t0001g0041 a0009c0010t0001g0055 |
2 | HG02015.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1578+3075C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060333 | |||||||
| chr14:74060487 | A | G | 113 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(110): Show |
114 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1578+3229A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060487 | |||||||
| chr14:74060500 | G | A | 378 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(375): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.1578+3242G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060500 | |||||||
| chr14:74060646 | C | T | 2 | a0001c0001t0002g0315 a0001c0001t0002g0316 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1578+3388C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060646 | |||||||
| chr14:74060811 | CT | C | 5 | a0006c0005t0005g0369 a0006c0005t0005g0370 a0006c0005t0005g0371 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1578+3557delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74060811 | ||||||
| chr14:74060923 | C | T | 1 | a0006c0005t0003g0374 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1578+3665C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060923 | |||||||
| chr14:74060924 | T | C | 8 | a0002c0002t0001g0223 a0002c0002t0001g0224 a0002c0002t0001g0225 others(5): Show |
8 | HG02155.hp1 NA18612.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1578+3666T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060924 | |||||||
| chr14:74061001 | G | A | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1579-3687G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061001 | |||||||
| chr14:74061294 | C | CATTT | 66 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(63): Show |
67 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.1579-3373_1579-337 others(8): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74061294 | ||||||
| chr14:74061320 | G | T | 134 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(131): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1579-3368G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061320 | |||||||
| chr14:74061321 | A | T | 134 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(131): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1579-3367A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061321 | |||||||
| chr14:74061499 | T | C | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1579-3189T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061499 | |||||||
| chr14:74061585 | CAA | C | 95 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(92): Show |
95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1579-3101_1579-310 others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74061585 | ||||||
| chr14:74061643 | T | C | 1 | a0002c0002t0001g0235 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1579-3045T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061643 | |||||||
| chr14:74061681 | A | G | 1 | a0001c0001t0003g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1579-3007A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061681 | |||||||
| chr14:74061785 | A | C | 1 | a0009c0010t0001g0041 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1579-2903A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061785 | |||||||
| chr14:74061802 | A | T | 2 | a0001c0001t0002g0328 a0001c0001t0002g0347 |
2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1579-2886A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061802 | |||||||
| chr14:74062024 | A | G | 7 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0006 others(4): Show |
7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1579-2664A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062024 | |||||||
| chr14:74062048 | T | TG | 12 | a0002c0002t0001g0231 a0002c0002t0001g0264 a0003c0003t0001g0011 others(9): Show |
12 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579-2637dupG | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062048 | ||||||
| chr14:74062051 | G | GA | 89 | a0001c0001t0002g0003 a0001c0001t0002g0294 a0001c0001t0002g0306 others(86): Show |
90 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1579-2608dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | ||||||
| chr14:74062051 | G | GAA | 33 | a0001c0001t0002g0293 a0001c0001t0002g0297 a0001c0001t0002g0305 others(30): Show |
33 | HG00673.hp1 HG00735.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.1579-2609_1579-260 others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | ||||||
| chr14:74062051 | G | GAAA | 8 | a0001c0001t0002g0292 a0001c0001t0002g0352 a0001c0001t0003g0165 others(5): Show |
8 | HG02135.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1579-2610_1579-260 others(7): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | ||||||
| chr14:74062051 | GA | G | 20 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0143 others(17): Show |
20 | HG01081.hp1 HG02040.hp1 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.1579-2608delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | ||||||
| chr14:74062051 | GAA | G | 47 | a0003c0003t0003g0189 a0004c0004t0004g0002 a0004c0004t0004g0088 others(44): Show |
48 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1579-2609_1579-260 others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | ||||||
| chr14:74062051 | GAAAAA | G | 8 | a0006c0005t0003g0374 a0006c0005t0003g0375 a0006c0005t0005g0369 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1579-2612_1579-260 others(9): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | ||||||
| chr14:74062051 | GAAAAAAA others(3): Show |
G | 2 | a0001c0001t0002g0315 a0001c0001t0002g0316 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1579-2617_1579-260 others(14): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | ||||||
| chr14:74062051 | GAAAAAAA others(5): Show |
G | 3 | a0001c0001t0003g0167 a0004c0007t0003g0006 a0004c0009t0007g0139 |
3 | HG02809.hp2 HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1579-2619_1579-260 others(16): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | ||||||
| chr14:74062051 | GAAAAAAA others(6): Show |
G | 8 | a0004c0007t0003g0004 a0004c0007t0003g0005 a0004c0007t0003g0007 others(5): Show |
8 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1579-2620_1579-260 others(17): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | ||||||
| chr14:74062052 | A | G | 74 | a0002c0002t0001g0237 a0002c0002t0001g0270 a0003c0003t0001g0008 others(71): Show |
74 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1579-2636A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062052 | |||||||
| chr14:74062053 | A | G | 6 | a0003c0015t0001g0059 a0005c0006t0001g0136 a0005c0006t0001g0137 others(3): Show |
6 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1579-2635A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062053 | |||||||
| chr14:74062054 | A | G | 5 | a0003c0003t0003g0189 a0005c0006t0001g0131 a0005c0006t0001g0133 others(2): Show |
5 | HG01243.hp1 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579-2634A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062054 | |||||||
| chr14:74062055 | A | G | 1 | a0005c0006t0001g0132 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1579-2633A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062055 | |||||||
| chr14:74062150 | A | T | 274 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(271): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1579-2538A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062150 | |||||||
| chr14:74062167 | A | G | 1 | a0002c0016t0001g0218 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1579-2521A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062167 | |||||||
| chr14:74062192 | C | T | 1 | a0001c0001t0003g0178 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1579-2496C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062192 | |||||||
| chr14:74062205 | T | A | 1 | a0003c0003t0015g0027 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1579-2483T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062205 | |||||||
| chr14:74062206 | A | T | 1 | a0003c0003t0015g0027 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1579-2482A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062206 | |||||||
| chr14:74062207 | A | T | 1 | a0006c0005t0003g0374 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1579-2481A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062207 | |||||||
| chr14:74062249 | G | C | 50 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0001c0001t0003g0151 others(47): Show |
50 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1579-2439G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062249 | |||||||
| chr14:74062329 | C | T | 1 | a0002c0002t0001g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1579-2359C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062329 | |||||||
| chr14:74062333 | G | A | 1 | a0001c0001t0003g0182 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1579-2355G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062333 | |||||||
| chr14:74062730 | A | G | 63 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(60): Show |
64 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1579-1958A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062730 | |||||||
| chr14:74062776 | C | T | 3 | a0006c0005t0008g0378 a0006c0005t0008g0379 a0006c0005t0008g0380 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1579-1912C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062776 | |||||||
| chr14:74062780 | C | T | 2 | a0004c0009t0007g0138 a0004c0009t0007g0140 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1579-1908C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062780 | |||||||
| chr14:74062797 | T | C | 274 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(271): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1579-1891T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062797 | |||||||
| chr14:74062808 | GA | G | 45 | a0004c0004t0004g0002 a0004c0004t0004g0087 a0004c0004t0004g0088 others(42): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1579-1870delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062808 | ||||||
| chr14:74062820 | C | T | 134 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(131): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1579-1868C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062820 | |||||||
| chr14:74062832 | G | C | 1 | a0002c0002t0014g0238 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1579-1856G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062832 | |||||||
| chr14:74062871 | A | C | 1 | a0015c0013t0001g0017 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1579-1817A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062871 | |||||||
| chr14:74062957 | T | G | 296 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(293): Show |
298 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.1579-1731T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062957 | |||||||
| chr14:74062979 | A | G | 3 | a0006c0005t0008g0378 a0006c0005t0008g0379 a0006c0005t0008g0380 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1579-1709A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062979 | |||||||
| chr14:74062983 | C | T | 3 | a0003c0003t0001g0022 a0003c0003t0001g0048 a0003c0015t0001g0059 |
3 | HG02083.hp1 NA18957.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1579-1705C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062983 | |||||||
| chr14:74063122 | G | T | 2 | a0003c0003t0003g0189 a0005c0006t0001g0137 |
2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1579-1566G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063122 | |||||||
| chr14:74063156 | C | T | 2 | a0003c0003t0001g0037 a0003c0003t0001g0060 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1579-1532C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063156 | |||||||
| chr14:74063164 | C | T | 8 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1579-1524C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063164 | |||||||
| chr14:74063165 | C | T | 95 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(92): Show |
95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1579-1523C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063165 | |||||||
| chr14:74063190 | C | CT | 45 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(42): Show |
45 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1579-1484dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74063190 | ||||||
| chr14:74063190 | CT | C | 49 | a0001c0001t0002g0319 a0003c0003t0001g0012 a0003c0003t0001g0056 others(46): Show |
50 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1579-1484delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74063190 | ||||||
| chr14:74063272 | C | T | 1 | a0002c0002t0001g0252 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1579-1416C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063272 | |||||||
| chr14:74063316 | A | G | 1 | a0013c0017t0001g0351 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1579-1372A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063316 | |||||||
| chr14:74063327 | T | C | 274 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(271): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1579-1361T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063327 | |||||||
| chr14:74063464 | C | T | 4 | a0002c0002t0001g0147 a0002c0002t0001g0148 a0002c0002t0001g0192 others(1): Show |
4 | HG02717.hp1 HG03139.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1579-1224C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063464 | |||||||
| chr14:74063593 | T | C | 114 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(111): Show |
115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1579-1095T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063593 | |||||||
| chr14:74063723 | A | G | 281 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(278): Show |
283 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.1579-965A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063723 | |||||||
| chr14:74063829 | G | T | 1 | a0001c0001t0003g0296 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1579-859G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063829 | |||||||
| chr14:74063865 | CA | C | 263 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(260): Show |
265 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.1579-807delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74063865 | ||||||
| chr14:74063865 | CAA | C | 9 | a0001c0001t0002g0316 a0001c0001t0002g0326 a0001c0001t0002g0354 others(6): Show |
9 | HG01167.hp1 HG01167.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1579-808_1579-807d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74063865 | ||||||
| chr14:74064011 | T | A | 95 | a0003c0003t0001g0008 a0003c0003t0001g0009 a0003c0003t0001g0010 others(92): Show |
95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1579-677T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064011 | |||||||
| chr14:74064225 | G | A | 12 | a0003c0003t0003g0189 a0005c0006t0001g0131 a0005c0006t0001g0132 others(9): Show |
12 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579-463G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064225 | |||||||
| chr14:74064230 | G | A | 4 | a0005c0006t0006g0193 a0005c0006t0006g0194 a0005c0006t0006g0195 others(1): Show |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1579-458G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064230 | |||||||
| chr14:74064263 | A | G | 1 | a0003c0003t0001g0016 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1579-425A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064263 | |||||||
| chr14:74064292 | T | C | 230 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(227): Show |
231 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.1579-396T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064292 | |||||||
| chr14:74064297 | C | CA | 65 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0001c0001t0003g0151 others(62): Show |
65 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1579-377dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74064297 | ||||||
| chr14:74064297 | CA | C | 12 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0319 others(9): Show |
12 | HG03669.hp2 HG03688.hp2 HG03834.hp2 others(9): Show |
intron_variant | MODIFIER | c.1579-377delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74064297 | ||||||
| chr14:74064309 | A | AT | 5 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0171 others(2): Show |
5 | HG01074.hp2 HG01081.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579-379_1579-378i others(3): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064309 | |||||||
| chr14:74064309 | A | T | 10 | a0002c0002t0001g0144 a0002c0002t0001g0145 a0002c0002t0001g0146 others(7): Show |
10 | HG01884.hp2 HG02630.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1579-379A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064309 | |||||||
| chr14:74064311 | AT | A | 142 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0297 others(139): Show |
143 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1579-376delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064311 | |||||||
| chr14:74064312 | T | A | 66 | a0001c0001t0002g0338 a0001c0001t0003g0151 a0001c0001t0003g0153 others(63): Show |
67 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1579-376T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064312 | |||||||
| chr14:74064314 | A | T | 1 | a0003c0003t0001g0051 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1579-374A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064314 | |||||||
| chr14:74064315 | T | A | 59 | a0002c0002t0014g0238 a0003c0003t0001g0008 a0003c0003t0001g0009 others(56): Show |
59 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1579-373T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064315 | |||||||
| chr14:74064352 | C | G | 135 | a0001c0001t0002g0003 a0001c0001t0002g0292 a0001c0001t0002g0293 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1579-336C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064352 | |||||||
| chr14:74064661 | T | C | 3 | a0004c0007t0003g0361 a0004c0007t0003g0364 a0004c0007t0003g0365 |
3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1579-27T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064661 |