Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 1620 |
|---|---|
| ensemblid | ENSG00000078725.13 |
| hgncid | 2687 |
| symbol | BRINP1 |
| name | BMP/retinoic acid inducible neural specific 1 |
| refseq_nuc | NM_014618.3 |
| refseq_prot | NP_055433.2 |
| ensembl_nuc | ENST00000265922.8 |
| ensembl_prot | ENSP00000265922.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 119166629 |
| end | 119369435 |
| strand | - |
| ver | v1.2 |
| region | chr9:119166629-119369435 |
| region5000 | chr9:119161629-119374435 |
| regionname0 | BRINP1_chr9_119166629_119369435 |
| regionname5000 | BRINP1_chr9_119161629_119374435 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 761 | 231 | 78 | 57 | 56 | 12 | 26 | 34 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0002 | 0/0 | 761 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0003 | 0/0 | 761 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0004 | 0/0 | 761 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2286 | 88 | 17 | 20 | 27 | 6 | 16 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| c0002 | 0/0 | 2286 | 70 | 7 | 21 | 27 | 5 | 10 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| c0003 | 0/0 | 2286 | 45 | 37 | 7 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| c0004 | 0/0 | 2286 | 10 | 7 | 3 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| c0005 | 0/0 | 2286 | 5 | 5 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| c0006 | 0/0 | 2286 | 5 | 4 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| c0007 | 0/0 | 2286 | 4 | 0 | 4 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| c0008 | 0/0 | 2286 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| c0009 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| c0010 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| c0011 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| c0012 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| c0013 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| c0014 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| c0015 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 886 | 198 | 59 | 50 | 52 | 11 | 25 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| t0002 | 0/0 | 886 | 17 | 16 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| t0003 | 0/0 | 886 | 12 | 1 | 9 | 0 | 1 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| t0004 | 0/0 | 886 | 3 | 0 | 0 | 3 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| t0005 | 0/0 | 886 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| t0006 | 0/0 | 886 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| t0007 | 1/0 | 886 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| t0008 | 0/0 | 886 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| t0009 | 0/0 | 916 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0080 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2286 | 88 | 17 | 20 | 27 | 6 | 16 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0002 | 0/0 | 2286 | 70 | 7 | 21 | 27 | 5 | 10 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0003 | 0/0 | 2286 | 45 | 37 | 7 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0004 | 0/0 | 2286 | 10 | 7 | 3 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0005 | 0/0 | 2286 | 5 | 5 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0006 | 0/0 | 2286 | 5 | 4 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0007 | 0/0 | 2286 | 4 | 0 | 4 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0009 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0010 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0014 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0015 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0002c0012 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0002c0013 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0003c0008 | 0/0 | 2286 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0004c0011 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3171 | 76 | 12 | 18 | 24 | 6 | 15 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0001t0002 | 0/0 | 3171 | 5 | 5 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0001t0003 | 0/0 | 3171 | 3 | 0 | 2 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0001t0004 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0001t0005 | 0/0 | 3171 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0001t0007 | 1/0 | 3171 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0002t0001 | 0/0 | 3171 | 58 | 4 | 16 | 24 | 4 | 10 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0002t0002 | 0/0 | 3171 | 2 | 2 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0002t0003 | 0/0 | 3171 | 7 | 1 | 5 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0002t0004 | 0/0 | 3171 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0002t0006 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0003t0001 | 0/0 | 3171 | 36 | 29 | 6 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0003t0002 | 0/0 | 3171 | 7 | 6 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0003t0008 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0003t0009 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0004t0001 | 0/0 | 3171 | 9 | 6 | 3 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0004t0002 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0005t0001 | 0/0 | 3171 | 4 | 4 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0005t0002 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0006t0001 | 0/0 | 3171 | 4 | 3 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0006t0002 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0007t0001 | 0/0 | 3171 | 4 | 0 | 4 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0009t0001 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0010t0001 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0014t0003 | 0/0 | 3171 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0001c0015t0001 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0002c0012t0001 | 0/0 | 3171 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0002c0013t0003 | 0/0 | 3171 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0003c0008t0001 | 0/0 | 3171 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| a0004c0011t0001 | 0/0 | 3171 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | copy fasta | chr9 | 119161629 | 119374435 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0080 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0001t0007g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0002t0006g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0003t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0004t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0005t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0005t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0005t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0006t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0006t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0006t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0006t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0006t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0007t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0007t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0007t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0007t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0009t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0010t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0014t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0001c0015t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0002c0012t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0002c0013t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0003c0008t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0003c0008t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| a0004c0011t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | GBR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0012 | EUR | GBR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0029 | EUR | GBR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0105 | EUR | FIN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00423 | hp1 | a0001 | c0002 | t0004 | g0118 | EAS | CHS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | CHS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0182 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0181 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00738 | hp1 | a0001 | c0014 | t0003 | g0004 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0144 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0026 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0028 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01074 | hp2 | a0002 | c0012 | t0001 | g0063 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0031 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01099 | hp2 | a0001 | c0007 | t0001 | g0083 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01109 | hp1 | a0001 | c0003 | t0002 | g0233 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01169 | hp1 | a0001 | c0007 | t0001 | g0082 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01169 | hp2 | a0001 | c0004 | t0001 | g0164 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01175 | hp2 | a0001 | c0007 | t0001 | g0052 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0183 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | PUR | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01255 | hp1 | a0001 | c0007 | t0001 | g0038 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01256 | hp1 | a0004 | c0011 | t0001 | g0125 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0207 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0166 | EUR | IBS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0050 | EUR | IBS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0051 | EUR | IBS | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01884 | hp1 | a0001 | c0003 | t0009 | g0214 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0208 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01891 | hp2 | a0001 | c0003 | t0008 | g0185 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0007 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0155 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0180 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0175 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CDX | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0060 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02293 | hp1 | a0002 | c0013 | t0003 | g0006 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02523 | hp1 | a0001 | c0010 | t0001 | g0098 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | KHV | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02572 | hp2 | a0001 | c0003 | t0002 | g0230 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0187 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0198 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02622 | hp1 | a0001 | c0006 | t0001 | g0018 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0210 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0209 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0189 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0188 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02886 | hp2 | a0001 | c0005 | t0002 | g0236 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0041 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02896 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02897 | hp1 | a0001 | c0006 | t0002 | g0225 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0040 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0227 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0085 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02970 | hp2 | a0001 | c0006 | t0001 | g0019 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02976 | hp1 | a0001 | c0004 | t0002 | g0232 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0190 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0197 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0122 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0042 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0016 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03195 | hp2 | a0001 | c0009 | t0001 | g0191 | AFR | ESN | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0211 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03225 | hp2 | a0001 | c0005 | t0001 | g0192 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0221 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03453 | hp2 | a0001 | c0005 | t0001 | g0199 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0074 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0213 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0057 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0224 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0222 | AFR | GWD | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0201 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0094 | AFR | MSL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0179 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0169 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0049 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0079 | SAS | BEB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0226 | AFR | YRI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | YRI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18612 | hp2 | a0003 | c0008 | t0001 | g0174 | EAS | CHB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | CHB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18747 | hp2 | a0003 | c0008 | t0001 | g0091 | EAS | CHB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | YRI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0178 | AFR | YRI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18969 | hp1 | a0001 | c0002 | t0004 | g0030 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0217 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19002 | hp1 | a0001 | c0002 | t0006 | g0013 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0215 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19030 | hp1 | a0001 | c0003 | t0002 | g0223 | AFR | LWK | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0177 | AFR | LWK | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19070 | hp2 | a0001 | c0015 | t0001 | g0133 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0073 | AFR | YRI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0186 | AFR | YRI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0107 | AFR | ASW | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ASW | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | TSI | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01123 | hp1 | a0001 | c0006 | t0001 | g0021 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | CLM | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0193 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0072 | AFR | ACB | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG06807 | hp1 | a0001 | c0003 | t0002 | g0228 | AFR | USA | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0151 | AFR | USA | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | USA | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA20300 | hp2 | a0001 | c0006 | t0001 | g0017 | AFR | USA | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0139 | AFR | LWK | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0080 | REF | REF | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0014 | REF | REF | BRINP1_chr9_119161629_119374435 | BRINP1 | chr9 | 119161629 | 119374435 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:119208791
|
C | T | 1 | a0002 | 2 | HG01074.hp2 HG02293.hp1 |
missense_variant | MODERATE | c.1073G>A | p.Arg358His | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/8 | 1503/3171 | 1073/2286 | 358/761 | chr9 | 119208791 | ||
| chr9:119214069
|
A | T | 1 | a0004 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.772T>A | p.Tyr258Asn | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/8 | 1202/3171 | 772/2286 | 258/761 | chr9 | 119214069 | ||
| chr9:119242167
|
C | A | 1 | a0003 | 2 | NA18612.hp2 NA18747.hp2 |
missense_variant | MODERATE | c.459G>T | p.Lys153Asn | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/8 | 889/3171 | 459/2286 | 153/761 | chr9 | 119242167 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:119167297
|
T | C | 4 | a0001c0003a0001c0004a0001c0009others(1): Show | 57 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(54): Show |
synonymous_variant | LOW | c.2073A>G | p.Ser691Ser | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 8/8 | 2503/3171 | 2073/2286 | 691/761 | chr9 | 119167297 | ||
| chr9:119168029
|
G | A | 2 | a0001c0007a0001c0014 | 5 | HG00738.hp1 HG01099.hp2 HG01169.hp1 others(2): Show |
synonymous_variant | LOW | c.1341C>T | p.Cys447Cys | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 8/8 | 1771/3171 | 1341/2286 | 447/761 | chr9 | 119168029 | ||
| chr9:119168110
|
C | T | 2 | a0001c0005a0001c0006 | 10 | HG01123.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
synonymous_variant | LOW | c.1260G>A | p.Thr420Thr | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 8/8 | 1690/3171 | 1260/2286 | 420/761 | chr9 | 119168110 | ||
| chr9:119238677
|
C | T | 1 | a0001c0010 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.663G>A | p.Thr221Thr | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/8 | 1093/3171 | 663/2286 | 221/761 | chr9 | 119238677 | ||
| chr9:119238722
|
G | A | 7 | a0001c0002a0001c0004a0001c0006others(4): Show | 89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
synonymous_variant | LOW | c.618C>T | p.Ser206Ser | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/8 | 1048/3171 | 618/2286 | 206/761 | chr9 | 119238722 | ||
| chr9:119248994
|
G | A | 1 | a0001c0015 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.375C>T | p.Tyr125Tyr | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/8 | 805/3171 | 375/2286 | 125/761 | chr9 | 119248994 | ||
| chr9:119249072
|
C | T | 1 | a0001c0009 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.297G>A | p.Pro99Pro | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/8 | 727/3171 | 297/2286 | 99/761 | chr9 | 119249072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:119166650
|
T | G | 3 | a0001c0001t0004a0001c0001t0005a0001c0002t0004 | 5 | HG00423.hp1 HG02523.hp2 NA18969.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*434A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 8/8 | 434 | chr9 | 119166650 | |||||
| chr9:119166767
|
T | TTACAATT others(23): Show |
1 | a0001c0003t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*287_*316dupGAAGGG others(24): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 8/8 | 316 | chr9 | 119166767 | |||||
| chr9:119166783
|
A | G | 1 | a0001c0003t0008 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*301T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 8/8 | 301 | chr9 | 119166783 | |||||
| chr9:119167079
|
C | T | 1 | a0001c0001t0005 | 2 | NA18993.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 8/8 | 5 | chr9 | 119167079 | |||||
| chr9:119369093
|
A | C | 23 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(20): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
5_prime_UTR_variant | MODIFIER | c.-88T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/8 | 55738 | chr9 | 119369093 | |||||
| chr9:119369140
|
G | C | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
5_prime_UTR_variant | MODIFIER | c.-135C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/8 | 55785 | chr9 | 119369140 | |||||
| chr9:119369203
|
C | T | 1 | a0001c0002t0006 | 1 | NA19002.hp1 | 5_prime_UTR_variant | MODIFIER | c.-198G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/8 | 55848 | chr9 | 119369203 | |||||
| chr9:119369328
|
C | G | 4 | a0001c0001t0003a0001c0002t0003a0001c0014t0003others(1): Show | 12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-323G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/8 | 55973 | chr9 | 119369328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:119168303
|
G | A | 40 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(37): Show | 40 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1146-79C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168303 | ||||||
| chr9:119168413
|
C | G | 1 | a0001c0002t0001g0036 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1146-189G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168413 | ||||||
| chr9:119168495
|
T | TG | 47 | a0001c0003t0001g0022a0001c0003t0001g0031a0001c0003t0001g0040others(44): Show | 47 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.1146-272dupC | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168495 | ||||||
| chr9:119168600
|
A | ATTGTAAA others(52): Show |
32 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0087others(29): Show | 32 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.1146-435_1146-377d others(61): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168600 | ||||||
| chr9:119168742
|
C | T | 3 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190 | 3 | HG01243.hp1 HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1146-518G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168742 | ||||||
| chr9:119168892
|
A | G | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1146-668T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168892 | ||||||
| chr9:119168924
|
C | T | 1 | a0001c0002t0001g0218 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1146-700G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168924 | ||||||
| chr9:119168936
|
G | T | 8 | a0001c0003t0001g0045a0001c0003t0001g0047a0001c0003t0001g0085others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1146-712C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119168936 | ||||||
| chr9:119169120
|
G | A | 6 | a0001c0003t0001g0031a0001c0003t0001g0144a0001c0003t0001g0166others(3): Show | 6 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146-896C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169120 | ||||||
| chr9:119169150
|
C | T | 1 | a0001c0003t0001g0189 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1146-926G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169150 | ||||||
| chr9:119169154
|
A | G | 34 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-930T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169154 | ||||||
| chr9:119169191
|
T | G | 3 | a0001c0001t0001g0134a0001c0001t0001g0140a0004c0011t0001g0125 | 3 | HG01256.hp1 HG01258.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.1146-967A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169191 | ||||||
| chr9:119169254
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1146-1030C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169254 | ||||||
| chr9:119169277
|
G | T | 1 | a0001c0004t0001g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1146-1053C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169277 | ||||||
| chr9:119169351
|
A | T | 34 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-1127T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169351 | ||||||
| chr9:119169363
|
G | T | 34 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-1139C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169363 | ||||||
| chr9:119169368
|
T | C | 34 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-1144A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169368 | ||||||
| chr9:119169371
|
C | T | 34 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-1147G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169371 | ||||||
| chr9:119169398
|
C | CCT | 32 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(29): Show | 32 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1146-1175_1146-117 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169398 | ||||||
| chr9:119169400
|
A | C | 32 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(29): Show | 32 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1146-1176T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169400 | ||||||
| chr9:119169470
|
C | G | 1 | a0001c0006t0002g0225 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1146-1246G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169470 | ||||||
| chr9:119169471
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1146-1247C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169471 | ||||||
| chr9:119169510
|
G | A | 160 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1146-1286C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169510 | ||||||
| chr9:119169543
|
C | T | 33 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(30): Show | 33 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1146-1319G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169543 | ||||||
| chr9:119169560
|
G | A | 34 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-1336C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169560 | ||||||
| chr9:119169600
|
C | T | 1 | a0001c0002t0001g0203 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1146-1376G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169600 | ||||||
| chr9:119169672
|
G | C | 1 | a0001c0001t0001g0111 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1146-1448C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169672 | ||||||
| chr9:119169789
|
C | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-1565G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169789 | ||||||
| chr9:119169858
|
G | C | 34 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-1634C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169858 | ||||||
| chr9:119169864
|
AG | A | 3 | a0001c0003t0001g0045a0001c0003t0001g0047a0001c0003t0001g0213 | 3 | HG02451.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1146-1641delC | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169864 | ||||||
| chr9:119169880
|
G | C | 34 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-1656C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169880 | ||||||
| chr9:119169906
|
T | C | 35 | a0001c0001t0002g0234a0001c0003t0001g0022a0001c0003t0001g0042others(32): Show | 35 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1146-1682A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169906 | ||||||
| chr9:119169923
|
A | G | 1 | a0001c0001t0002g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1146-1699T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169923 | ||||||
| chr9:119169927
|
G | A | 1 | a0001c0001t0002g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1146-1703C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169927 | ||||||
| chr9:119169937
|
AAACT | A | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-1717_1146-171 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119169937 | ||||||
| chr9:119170064
|
A | T | 34 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0046others(31): Show | 34 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.1146-1840T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170064 | ||||||
| chr9:119170074
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1146-1850G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170074 | ||||||
| chr9:119170113
|
G | A | 7 | a0001c0003t0001g0020a0001c0003t0001g0178a0001c0003t0002g0223others(4): Show | 7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-1889C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170113 | ||||||
| chr9:119170169
|
G | A | 1 | a0001c0002t0001g0135 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1146-1945C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170169 | ||||||
| chr9:119170231
|
A | G | 34 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-2007T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170231 | ||||||
| chr9:119170246
|
G | T | 1 | a0001c0002t0001g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1146-2022C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170246 | ||||||
| chr9:119170344
|
C | G | 1 | a0001c0003t0008g0185 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1146-2120G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170344 | ||||||
| chr9:119170351
|
C | T | 32 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(29): Show | 32 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1146-2127G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170351 | ||||||
| chr9:119170352
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0204 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1146-2128C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170352 | ||||||
| chr9:119170357
|
G | A | 1 | a0001c0003t0008g0185 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1146-2133C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170357 | ||||||
| chr9:119170472
|
G | A | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1146-2248C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170472 | ||||||
| chr9:119170499
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1146-2275T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170499 | ||||||
| chr9:119170500
|
T | C | 1 | a0002c0013t0003g0006 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1146-2276A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170500 | ||||||
| chr9:119170569
|
C | T | 110 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.1146-2345G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170569 | ||||||
| chr9:119170649
|
T | C | 56 | a0001c0001t0001g0023a0001c0001t0001g0053a0001c0001t0001g0081others(53): Show | 56 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1146-2425A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170649 | ||||||
| chr9:119170776
|
A | G | 148 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1146-2552T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170776 | ||||||
| chr9:119170777
|
G | A | 146 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1146-2553C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170777 | ||||||
| chr9:119170784
|
C | T | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1146-2560G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170784 | ||||||
| chr9:119170785
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0003g0009 | 3 | HG00741.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1146-2561C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170785 | ||||||
| chr9:119170883
|
G | A | 14 | a0001c0003t0001g0020a0001c0003t0001g0040a0001c0003t0001g0041others(11): Show | 14 | HG01169.hp2 HG01243.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1146-2659C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170883 | ||||||
| chr9:119170917
|
A | C | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-2693T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170917 | ||||||
| chr9:119170934
|
G | C | 2 | a0001c0001t0001g0146a0001c0002t0001g0169 | 2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1146-2710C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170934 | ||||||
| chr9:119170935
|
A | C | 2 | a0001c0001t0001g0146a0001c0002t0001g0169 | 2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1146-2711T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119170935 | ||||||
| chr9:119171005
|
C | G | 1 | a0001c0001t0001g0080 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1146-2781G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171005 | ||||||
| chr9:119171005
|
C | T | 10 | a0001c0003t0001g0020a0001c0003t0001g0040a0001c0003t0001g0041others(7): Show | 10 | HG01169.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1146-2781G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171005 | ||||||
| chr9:119171006
|
G | A | 32 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(29): Show | 32 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1146-2782C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171006 | ||||||
| chr9:119171049
|
A | G | 34 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-2825T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171049 | ||||||
| chr9:119171052
|
A | ACTAGAAA others(1): Show |
34 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1146-2836_1146-282 others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171052 | ||||||
| chr9:119171078
|
G | A | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1146-2854C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171078 | ||||||
| chr9:119171083
|
A | G | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1146-2859T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171083 | ||||||
| chr9:119171087
|
A | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0126 | 2 | HG01346.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1146-2863T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171087 | ||||||
| chr9:119171243
|
T | C | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1146-3019A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171243 | ||||||
| chr9:119171489
|
C | T | 6 | a0001c0003t0001g0031a0001c0003t0001g0144a0001c0003t0001g0166others(3): Show | 6 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146-3265G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171489 | ||||||
| chr9:119171561
|
T | C | 5 | a0001c0001t0001g0044a0001c0001t0001g0172a0001c0001t0001g0195others(2): Show | 5 | HG02145.hp1 HG02486.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1146-3337A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171561 | ||||||
| chr9:119171614
|
G | T | 4 | a0001c0001t0001g0108a0001c0001t0001g0148a0001c0001t0001g0152others(1): Show | 4 | HG01975.hp1 HG01978.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-3390C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171614 | ||||||
| chr9:119171644
|
T | G | 1 | a0001c0002t0002g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1146-3420A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171644 | ||||||
| chr9:119171736
|
A | C | 29 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(26): Show | 29 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1146-3512T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171736 | ||||||
| chr9:119171738
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0138 | 2 | HG00423.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1146-3514G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171738 | ||||||
| chr9:119171799
|
A | T | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-3575T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171799 | ||||||
| chr9:119171839
|
T | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-3615A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171839 | ||||||
| chr9:119171981
|
C | G | 1 | a0001c0002t0001g0168 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1146-3757G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171981 | ||||||
| chr9:119171986
|
T | G | 3 | a0001c0002t0001g0168a0001c0003t0001g0181a0001c0003t0001g0182 | 3 | HG00639.hp2 HG00735.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1146-3762A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171986 | ||||||
| chr9:119171988
|
C | T | 49 | a0001c0002t0001g0168a0001c0003t0001g0020a0001c0003t0001g0022others(46): Show | 49 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1146-3764G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119171988 | ||||||
| chr9:119172013
|
C | G | 171 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1146-3789G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172013 | ||||||
| chr9:119172049
|
A | C | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1146-3825T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172049 | ||||||
| chr9:119172274
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0002t0006g0013 | 3 | HG00438.hp2 HG01934.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1146-4050G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172274 | ||||||
| chr9:119172276
|
CAATAAAA | C | 4 | a0001c0003t0001g0060a0001c0003t0001g0073a0001c0003t0001g0122others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-4059_1146-405 others(11): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172276 | ||||||
| chr9:119172326
|
A | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-4102T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172326 | ||||||
| chr9:119172349
|
A | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-4125T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172349 | ||||||
| chr9:119172389
|
G | T | 1 | a0001c0003t0001g0107 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1146-4165C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172389 | ||||||
| chr9:119172476
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1146-4252C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172476 | ||||||
| chr9:119172610
|
A | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-4386T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172610 | ||||||
| chr9:119172610
|
A | T | 9 | a0001c0003t0001g0031a0001c0003t0001g0144a0001c0003t0001g0166others(6): Show | 9 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1146-4386T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172610 | ||||||
| chr9:119172613
|
C | T | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-4389G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172613 | ||||||
| chr9:119172630
|
A | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-4406T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172630 | ||||||
| chr9:119172635
|
G | A | 8 | a0001c0003t0001g0031a0001c0003t0001g0144a0001c0003t0001g0166others(5): Show | 8 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1146-4411C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172635 | ||||||
| chr9:119172661
|
A | G | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1146-4437T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172661 | ||||||
| chr9:119172718
|
T | C | 44 | a0001c0001t0001g0044a0001c0003t0001g0020a0001c0003t0001g0022others(41): Show | 44 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1146-4494A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172718 | ||||||
| chr9:119172784
|
C | T | 3 | a0001c0003t0001g0180a0001c0003t0001g0181a0001c0003t0001g0182 | 3 | HG00639.hp2 HG00735.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1146-4560G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172784 | ||||||
| chr9:119172806
|
C | G | 3 | a0001c0003t0001g0022a0001c0003t0001g0181a0001c0003t0001g0182 | 3 | HG00639.hp2 HG00735.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1146-4582G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172806 | ||||||
| chr9:119172807
|
A | G | 49 | a0001c0001t0001g0044a0001c0003t0001g0020a0001c0003t0001g0022others(46): Show | 49 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1146-4583T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172807 | ||||||
| chr9:119172861
|
A | AGGGAAC | 7 | a0001c0003t0001g0020a0001c0003t0001g0178a0001c0003t0002g0223others(4): Show | 7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4638_1146-463 others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172861 | ||||||
| chr9:119172864
|
G | A | 7 | a0001c0003t0001g0020a0001c0003t0001g0178a0001c0003t0002g0223others(4): Show | 7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4640C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172864 | ||||||
| chr9:119172865
|
A | T | 7 | a0001c0003t0001g0020a0001c0003t0001g0178a0001c0003t0002g0223others(4): Show | 7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4641T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172865 | ||||||
| chr9:119172871
|
A | AACAAT | 7 | a0001c0003t0001g0020a0001c0003t0001g0178a0001c0003t0002g0223others(4): Show | 7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4648_1146-464 others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172871 | ||||||
| chr9:119172895
|
C | A | 7 | a0001c0003t0001g0020a0001c0003t0001g0178a0001c0003t0002g0223others(4): Show | 7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4671G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172895 | ||||||
| chr9:119172902
|
G | A | 7 | a0001c0003t0001g0020a0001c0003t0001g0178a0001c0003t0002g0223others(4): Show | 7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4678C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172902 | ||||||
| chr9:119172910
|
A | G | 7 | a0001c0003t0001g0020a0001c0003t0001g0178a0001c0003t0002g0223others(4): Show | 7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4686T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172910 | ||||||
| chr9:119172930
|
C | A | 9 | a0001c0003t0001g0020a0001c0003t0001g0178a0001c0003t0001g0181others(6): Show | 9 | HG00639.hp2 HG00735.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1146-4706G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172930 | ||||||
| chr9:119172932
|
C | T | 3 | a0001c0003t0001g0020a0001c0004t0001g0164a0001c0004t0001g0177 | 3 | HG01169.hp2 HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1146-4708G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172932 | ||||||
| chr9:119172933
|
C | G | 7 | a0001c0003t0001g0020a0001c0003t0001g0178a0001c0003t0002g0223others(4): Show | 7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4709G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172933 | ||||||
| chr9:119172935
|
T | G | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1146-4711A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172935 | ||||||
| chr9:119172942
|
T | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-4718A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172942 | ||||||
| chr9:119172980
|
T | C | 10 | a0001c0003t0001g0020a0001c0003t0001g0040a0001c0003t0001g0041others(7): Show | 10 | HG01169.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1146-4756A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172980 | ||||||
| chr9:119172997
|
C | T | 7 | a0001c0003t0001g0020a0001c0003t0001g0178a0001c0003t0002g0223others(4): Show | 7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4773G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119172997 | ||||||
| chr9:119173000
|
C | T | 7 | a0001c0003t0001g0020a0001c0003t0001g0178a0001c0003t0002g0223others(4): Show | 7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-4776G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173000 | ||||||
| chr9:119173019
|
G | A | 154 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1146-4795C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173019 | ||||||
| chr9:119173290
|
G | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-5066C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173290 | ||||||
| chr9:119173336
|
C | T | 5 | a0001c0003t0001g0094a0001c0003t0001g0186a0001c0003t0002g0226others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146-5112G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173336 | ||||||
| chr9:119173454
|
C | T | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-5230G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173454 | ||||||
| chr9:119173471
|
T | G | 1 | a0001c0001t0001g0212 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1146-5247A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173471 | ||||||
| chr9:119173538
|
A | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-5314T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173538 | ||||||
| chr9:119173570
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1146-5346C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173570 | ||||||
| chr9:119173651
|
C | A | 166 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.1146-5427G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173651 | ||||||
| chr9:119173668
|
G | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-5444C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173668 | ||||||
| chr9:119173679
|
G | A | 3 | a0001c0001t0001g0163a0001c0003t0001g0181a0001c0003t0001g0182 | 3 | HG00639.hp2 HG00735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1146-5455C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173679 | ||||||
| chr9:119173713
|
G | T | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-5489C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173713 | ||||||
| chr9:119173837
|
G | A | 10 | a0001c0005t0001g0192a0001c0005t0001g0199a0001c0005t0001g0201others(7): Show | 10 | HG01123.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1146-5613C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173837 | ||||||
| chr9:119173903
|
A | G | 21 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0064others(18): Show | 21 | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1146-5679T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173903 | ||||||
| chr9:119173906
|
T | TAATA | 70 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0044others(67): Show | 70 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.1146-5683_1146-568 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173906 | ||||||
| chr9:119173913
|
G | T | 1 | a0001c0007t0001g0083 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1146-5689C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173913 | ||||||
| chr9:119173967
|
C | T | 4 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187others(1): Show | 4 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-5743G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119173967 | ||||||
| chr9:119174008
|
A | C | 6 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146-5784T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174008 | ||||||
| chr9:119174010
|
C | T | 7 | a0001c0001t0001g0158a0001c0002t0001g0202a0001c0002t0001g0203others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1146-5786G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174010 | ||||||
| chr9:119174017
|
C | CCTAAAAC others(15): Show |
127 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0037others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1146-5794_1146-579 others(26): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174017 | ||||||
| chr9:119174052
|
G | A | 4 | a0001c0001t0002g0220a0001c0001t0002g0229a0001c0003t0001g0181others(1): Show | 4 | HG00639.hp2 HG00735.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-5828C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174052 | ||||||
| chr9:119174096
|
T | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-5872A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174096 | ||||||
| chr9:119174110
|
A | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-5886T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174110 | ||||||
| chr9:119174121
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1146-5897G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174121 | ||||||
| chr9:119174347
|
C | T | 17 | a0001c0003t0001g0042a0001c0003t0001g0060a0001c0003t0001g0073others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1146-6123G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174347 | ||||||
| chr9:119174358
|
A | G | 49 | a0001c0001t0001g0044a0001c0003t0001g0020a0001c0003t0001g0022others(46): Show | 49 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1146-6134T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174358 | ||||||
| chr9:119174550
|
G | T | 233 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1146-6326C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174550 | ||||||
| chr9:119174560
|
A | G | 49 | a0001c0001t0001g0044a0001c0003t0001g0020a0001c0003t0001g0022others(46): Show | 49 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1146-6336T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174560 | ||||||
| chr9:119174647
|
G | T | 35 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0046others(32): Show | 35 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.1146-6423C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174647 | ||||||
| chr9:119174680
|
C | T | 3 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0009t0001g0191 | 3 | HG02809.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1146-6456G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174680 | ||||||
| chr9:119174739
|
T | A | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1146-6515A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174739 | ||||||
| chr9:119174835
|
G | T | 57 | a0001c0001t0001g0044a0001c0001t0002g0220a0001c0001t0002g0229others(54): Show | 57 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.1146-6611C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174835 | ||||||
| chr9:119174853
|
C | A | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-6629G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174853 | ||||||
| chr9:119174861
|
G | A | 3 | a0001c0003t0001g0193a0001c0003t0002g0224a0001c0004t0001g0015 | 3 | HG02109.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1146-6637C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174861 | ||||||
| chr9:119174861
|
G | T | 3 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0009t0001g0191 | 3 | HG02809.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1146-6637C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174861 | ||||||
| chr9:119174884
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1146-6660C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119174884 | ||||||
| chr9:119175005
|
A | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-6781T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175005 | ||||||
| chr9:119175049
|
A | G | 49 | a0001c0001t0001g0044a0001c0003t0001g0020a0001c0003t0001g0022others(46): Show | 49 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1146-6825T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175049 | ||||||
| chr9:119175106
|
TTAAAG | T | 80 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0037others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1146-6887_1146-688 others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175106 | ||||||
| chr9:119175111
|
G | A | 2 | a0001c0001t0005g0215a0001c0001t0005g0217 | 2 | NA18993.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1146-6887C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175111 | ||||||
| chr9:119175113
|
AAAG | A | 4 | a0001c0002t0006g0013a0001c0003t0001g0178a0001c0003t0002g0223others(1): Show | 4 | HG06807.hp1 NA18906.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-6892_1146-689 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175113 | ||||||
| chr9:119175114
|
A | T | 13 | a0001c0001t0001g0044a0001c0003t0001g0020a0001c0003t0001g0040others(10): Show | 13 | HG01169.hp2 HG01243.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1146-6890T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175114 | ||||||
| chr9:119175115
|
AGTAT | A | 13 | a0001c0001t0001g0044a0001c0003t0001g0020a0001c0003t0001g0040others(10): Show | 13 | HG01169.hp2 HG01243.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1146-6895_1146-689 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175115 | ||||||
| chr9:119175119
|
T | A | 5 | a0001c0003t0001g0178a0001c0003t0002g0223a0001c0003t0002g0228others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1146-6895A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175119 | ||||||
| chr9:119175119
|
T | TA | 31 | a0001c0003t0001g0022a0001c0003t0001g0045a0001c0003t0001g0047others(28): Show | 31 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1146-6896dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175119 | ||||||
| chr9:119175119
|
TA | T | 7 | a0001c0003t0001g0031a0001c0003t0001g0144a0001c0003t0001g0166others(4): Show | 7 | HG00741.hp2 HG01074.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-6896delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175119 | ||||||
| chr9:119175120
|
A | AGTAT | 2 | a0001c0004t0001g0026a0001c0004t0001g0028 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1146-6897_1146-689 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175120 | ||||||
| chr9:119175121
|
AAAAAAAA others(7): Show |
A | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-6911_1146-689 others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175121 | ||||||
| chr9:119175135
|
C | CA | 11 | a0001c0001t0001g0120a0001c0001t0001g0123a0001c0002t0001g0024others(8): Show | 11 | HG00280.hp1 HG01169.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1146-6912dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175135 | ||||||
| chr9:119175217
|
C | G | 47 | a0001c0001t0001g0044a0001c0003t0001g0020a0001c0003t0001g0022others(44): Show | 47 | HG01109.hp1 HG01169.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.1146-6993G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175217 | ||||||
| chr9:119175228
|
T | G | 46 | a0001c0003t0001g0020a0001c0003t0001g0022a0001c0003t0001g0040others(43): Show | 46 | HG01109.hp1 HG01169.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.1146-7004A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175228 | ||||||
| chr9:119175237
|
A | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-7013T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175237 | ||||||
| chr9:119175472
|
TAACA | T | 2 | a0001c0003t0001g0031a0001c0003t0002g0228 | 2 | HG01099.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1146-7252_1146-724 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175472 | ||||||
| chr9:119175493
|
A | T | 32 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(29): Show | 32 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1146-7269T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175493 | ||||||
| chr9:119175712
|
C | A | 6 | a0001c0003t0001g0031a0001c0003t0001g0144a0001c0003t0001g0166others(3): Show | 6 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146-7488G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119175712 | ||||||
| chr9:119176103
|
T | C | 7 | a0001c0003t0001g0020a0001c0003t0001g0178a0001c0003t0002g0223others(4): Show | 7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-7879A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119176103 | ||||||
| chr9:119176857
|
C | T | 1 | a0001c0002t0001g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1146-8633G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119176857 | ||||||
| chr9:119176893
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1146-8669T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119176893 | ||||||
| chr9:119177163
|
T | C | 1 | a0001c0002t0001g0127 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1146-8939A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119177163 | ||||||
| chr9:119177321
|
G | A | 2 | a0001c0002t0001g0155a0001c0002t0003g0003 | 2 | HG01070.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1146-9097C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119177321 | ||||||
| chr9:119177393
|
G | A | 9 | a0001c0001t0001g0081a0001c0001t0003g0008a0001c0002t0001g0155others(6): Show | 9 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1146-9169C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119177393 | ||||||
| chr9:119177549
|
A | C | 1 | a0001c0002t0001g0154 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1146-9325T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119177549 | ||||||
| chr9:119177564
|
G | C | 1 | a0001c0001t0002g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1146-9340C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119177564 | ||||||
| chr9:119177750
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1146-9526G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119177750 | ||||||
| chr9:119177935
|
T | C | 32 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(29): Show | 32 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1146-9711A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119177935 | ||||||
| chr9:119178212
|
G | T | 174 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1146-9988C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119178212 | ||||||
| chr9:119178318
|
G | A | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1146-10094C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119178318 | ||||||
| chr9:119178399
|
G | T | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-10175C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119178399 | ||||||
| chr9:119178425
|
T | TTG | 3 | a0001c0002t0001g0145a0001c0002t0001g0149a0001c0002t0001g0218 | 3 | NA18948.hp2 NA18966.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1146-10203_1146-10 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119178425 | ||||||
| chr9:119178538
|
A | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-10314T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119178538 | ||||||
| chr9:119178785
|
G | C | 42 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0045others(39): Show | 42 | HG01109.hp1 HG01123.hp1 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.1146-10561C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119178785 | ||||||
| chr9:119178885
|
G | GAAAT | 4 | a0001c0003t0001g0060a0001c0003t0001g0073a0001c0003t0001g0122others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-10665_1146-10 others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119178885 | ||||||
| chr9:119179251
|
C | T | 1 | a0001c0003t0002g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1146-11027G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119179251 | ||||||
| chr9:119179332
|
G | A | 1 | a0001c0004t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1146-11108C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119179332 | ||||||
| chr9:119179343
|
G | A | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1146-11119C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119179343 | ||||||
| chr9:119179356
|
G | A | 4 | a0001c0003t0001g0060a0001c0003t0001g0073a0001c0003t0001g0122others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-11132C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119179356 | ||||||
| chr9:119179366
|
G | A | 2 | a0001c0002t0001g0070a0001c0002t0001g0071 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1146-11142C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119179366 | ||||||
| chr9:119179542
|
G | C | 1 | a0001c0003t0001g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1146-11318C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119179542 | ||||||
| chr9:119180132
|
G | A | 1 | a0001c0001t0002g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1146-11908C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180132 | ||||||
| chr9:119180247
|
A | C | 3 | a0001c0003t0001g0060a0001c0003t0001g0073a0001c0003t0001g0122 | 3 | HG02258.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1146-12023T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180247 | ||||||
| chr9:119180364
|
C | T | 4 | a0001c0001t0001g0172a0001c0001t0001g0195a0001c0001t0001g0200others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-12140G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180364 | ||||||
| chr9:119180441
|
CTGTTCTT others(6): Show |
C | 1 | a0001c0002t0001g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1146-12230_1146-12 others(19): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180441 | ||||||
| chr9:119180473
|
CTGTGCAT others(1): Show |
C | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-12257_1146-12 others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180473 | ||||||
| chr9:119180478
|
CATGTGTG others(1): Show |
C | 4 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187others(1): Show | 4 | HG01169.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-12262_1146-12 others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180478 | ||||||
| chr9:119180478
|
CATGTGTG others(3): Show |
C | 17 | a0001c0001t0001g0044a0001c0003t0001g0020a0001c0003t0001g0031others(14): Show | 17 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1146-12264_1146-12 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180478 | ||||||
| chr9:119180478
|
CATGTGTG others(5): Show |
C | 29 | a0001c0003t0001g0022a0001c0003t0001g0042a0001c0003t0001g0060others(26): Show | 29 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1146-12266_1146-12 others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180478 | ||||||
| chr9:119180479
|
A | ATG | 7 | a0001c0001t0001g0065a0001c0001t0001g0103a0001c0001t0001g0108others(4): Show | 7 | HG00280.hp1 HG01175.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1146-12257_1146-12 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180479 | ||||||
| chr9:119180479
|
ATG | A | 25 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(22): Show | 25 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1146-12257_1146-12 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180479 | ||||||
| chr9:119180479
|
ATGTG | A | 61 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(58): Show | 61 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1146-12259_1146-12 others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180479 | ||||||
| chr9:119180479
|
ATGTGTG | A | 12 | a0001c0001t0001g0039a0001c0001t0001g0053a0001c0001t0001g0055others(9): Show | 12 | HG00280.hp2 HG01255.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1146-12261_1146-12 others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180479 | ||||||
| chr9:119180479
|
ATGTGTGT others(1): Show |
A | 4 | a0001c0001t0002g0220a0001c0001t0002g0229a0001c0002t0001g0036others(1): Show | 4 | HG01358.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-12263_1146-12 others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180479 | ||||||
| chr9:119180479
|
ATGTGTGT others(3): Show |
A | 6 | a0001c0001t0001g0172a0001c0001t0001g0195a0001c0001t0001g0200others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1146-12265_1146-12 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180479 | ||||||
| chr9:119180479
|
ATGTGTGT others(5): Show |
A | 10 | a0001c0001t0001g0153a0001c0005t0001g0192a0001c0005t0001g0201others(7): Show | 10 | HG01123.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1146-12267_1146-12 others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180479 | ||||||
| chr9:119180482
|
T | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-12258A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180482 | ||||||
| chr9:119180545
|
T | C | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1146-12321A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180545 | ||||||
| chr9:119180581
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1146-12357G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180581 | ||||||
| chr9:119180647
|
C | A | 1 | a0001c0007t0001g0083 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1146-12423G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180647 | ||||||
| chr9:119180712
|
C | T | 5 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146-12488G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119180712 | ||||||
| chr9:119181122
|
C | T | 1 | a0001c0002t0001g0119 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1146-12898G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119181122 | ||||||
| chr9:119181156
|
C | T | 1 | a0001c0003t0002g0226 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1146-12932G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119181156 | ||||||
| chr9:119181192
|
G | A | 1 | a0001c0003t0002g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1146-12968C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119181192 | ||||||
| chr9:119181209
|
A | G | 1 | a0002c0013t0003g0006 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1146-12985T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119181209 | ||||||
| chr9:119181358
|
G | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-13134C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119181358 | ||||||
| chr9:119181495
|
C | T | 1 | a0001c0003t0001g0207 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1146-13271G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119181495 | ||||||
| chr9:119181714
|
C | T | 7 | a0001c0003t0001g0020a0001c0003t0001g0178a0001c0003t0002g0223others(4): Show | 7 | HG01169.hp2 HG02572.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1146-13490G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119181714 | ||||||
| chr9:119182292
|
G | A | 4 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0003t0001g0031others(1): Show | 4 | HG01099.hp1 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-14068C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119182292 | ||||||
| chr9:119182500
|
G | T | 3 | a0001c0003t0001g0193a0001c0003t0002g0224a0001c0004t0001g0015 | 3 | HG02109.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1146-14276C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119182500 | ||||||
| chr9:119182529
|
G | A | 1 | a0001c0003t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1146-14305C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119182529 | ||||||
| chr9:119182562
|
T | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-14338A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119182562 | ||||||
| chr9:119182747
|
T | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-14523A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119182747 | ||||||
| chr9:119182795
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1146-14571G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119182795 | ||||||
| chr9:119182970
|
C | G | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1146-14746G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119182970 | ||||||
| chr9:119183037
|
G | A | 2 | a0001c0003t0002g0224a0001c0004t0001g0015 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1146-14813C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183037 | ||||||
| chr9:119183228
|
T | A | 1 | a0001c0001t0001g0153 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1146-15004A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183228 | ||||||
| chr9:119183339
|
A | T | 1 | a0001c0001t0001g0055 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1146-15115T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183339 | ||||||
| chr9:119183497
|
C | T | 2 | a0001c0001t0001g0170a0001c0002t0001g0114 | 2 | HG00544.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1146-15273G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183497 | ||||||
| chr9:119183615
|
C | G | 1 | a0001c0010t0001g0098 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1146-15391G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183615 | ||||||
| chr9:119183730
|
A | G | 2 | a0001c0003t0001g0186a0001c0003t0002g0233 | 2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1146-15506T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183730 | ||||||
| chr9:119183745
|
T | A | 1 | a0001c0004t0001g0164 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1146-15521A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183745 | ||||||
| chr9:119183912
|
T | C | 1 | a0001c0002t0001g0075 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1146-15688A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119183912 | ||||||
| chr9:119184159
|
A | G | 8 | a0001c0002t0001g0079a0001c0003t0001g0031a0001c0003t0001g0166others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1146-15935T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184159 | ||||||
| chr9:119184189
|
T | A | 4 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-15965A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184189 | ||||||
| chr9:119184232
|
G | C | 64 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0067others(61): Show | 64 | HG00140.hp1 HG00544.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1146-16008C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184232 | ||||||
| chr9:119184382
|
G | A | 3 | a0001c0003t0001g0209a0001c0004t0001g0016a0001c0004t0002g0232 | 3 | HG02717.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1146-16158C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184382 | ||||||
| chr9:119184387
|
G | A | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-16163C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184387 | ||||||
| chr9:119184458
|
G | A | 3 | a0001c0003t0001g0085a0001c0003t0001g0198a0001c0003t0001g0208 | 3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1146-16234C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184458 | ||||||
| chr9:119184537
|
A | G | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1146-16313T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184537 | ||||||
| chr9:119184736
|
A | G | 14 | a0001c0001t0002g0220a0001c0001t0002g0229a0001c0003t0001g0042others(11): Show | 14 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1146-16512T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184736 | ||||||
| chr9:119184749
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1146-16525A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184749 | ||||||
| chr9:119184765
|
A | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-16541T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184765 | ||||||
| chr9:119184936
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1146-16712G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184936 | ||||||
| chr9:119184944
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1146-16720T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184944 | ||||||
| chr9:119184984
|
G | T | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-16760C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119184984 | ||||||
| chr9:119185085
|
G | A | 3 | a0001c0003t0001g0085a0001c0003t0001g0198a0001c0003t0001g0208 | 3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1146-16861C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185085 | ||||||
| chr9:119185190
|
A | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-16966T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185190 | ||||||
| chr9:119185345
|
T | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-17121A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185345 | ||||||
| chr9:119185447
|
G | A | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-17223C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185447 | ||||||
| chr9:119185585
|
C | T | 2 | a0001c0001t0001g0167a0001c0002t0001g0057 | 2 | HG02683.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1146-17361G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185585 | ||||||
| chr9:119185700
|
G | A | 1 | a0001c0001t0002g0231 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1146-17476C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185700 | ||||||
| chr9:119185708
|
T | A | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-17484A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185708 | ||||||
| chr9:119185766
|
C | G | 14 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0055others(11): Show | 14 | HG00099.hp1 HG01074.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1146-17542G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185766 | ||||||
| chr9:119185773
|
T | C | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1146-17549A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185773 | ||||||
| chr9:119185841
|
C | T | 4 | a0001c0003t0001g0189a0001c0003t0001g0193a0001c0003t0001g0197others(1): Show | 4 | HG02109.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-17617G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185841 | ||||||
| chr9:119185963
|
T | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1146-17739A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119185963 | ||||||
| chr9:119186506
|
C | T | 1 | a0001c0002t0001g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1146-18282G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119186506 | ||||||
| chr9:119186846
|
C | T | 1 | a0001c0003t0001g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1146-18622G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119186846 | ||||||
| chr9:119186853
|
G | A | 1 | a0001c0002t0001g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1146-18629C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119186853 | ||||||
| chr9:119186859
|
G | T | 2 | a0001c0003t0001g0166a0001c0010t0001g0098 | 2 | HG01515.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1146-18635C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119186859 | ||||||
| chr9:119187029
|
T | C | 14 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0055others(11): Show | 14 | HG00099.hp1 HG01074.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1146-18805A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187029 | ||||||
| chr9:119187062
|
G | C | 1 | a0001c0010t0001g0098 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1146-18838C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187062 | ||||||
| chr9:119187117
|
T | G | 4 | a0001c0003t0001g0189a0001c0003t0001g0193a0001c0003t0001g0197others(1): Show | 4 | HG02109.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146-18893A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187117 | ||||||
| chr9:119187144
|
G | A | 1 | a0001c0003t0002g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1146-18920C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187144 | ||||||
| chr9:119187483
|
T | C | 1 | a0001c0003t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1146-19259A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187483 | ||||||
| chr9:119187566
|
CTT | C | 25 | a0001c0001t0001g0172a0001c0001t0001g0195a0001c0001t0001g0200others(22): Show | 25 | HG01109.hp1 HG01169.hp2 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.1146-19344_1146-19 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187566 | ||||||
| chr9:119187627
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0109 | 2 | HG01256.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1146-19403A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187627 | ||||||
| chr9:119187949
|
T | A | 2 | a0001c0003t0001g0193a0001c0003t0001g0211 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1146-19725A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119187949 | ||||||
| chr9:119188137
|
G | C | 1 | a0001c0001t0002g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1146-19913C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119188137 | ||||||
| chr9:119188189
|
AC | A | 37 | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0054others(34): Show | 37 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1146-19966delG | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119188189 | ||||||
| chr9:119188196
|
C | T | 1 | a0001c0001t0002g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1146-19972G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119188196 | ||||||
| chr9:119188242
|
A | G | 3 | a0001c0003t0001g0209a0001c0005t0001g0192a0001c0005t0001g0210 | 3 | HG02622.hp2 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1146-20018T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119188242 | ||||||
| chr9:119188300
|
T | A | 1 | a0001c0002t0001g0110 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1146-20076A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119188300 | ||||||
| chr9:119188443
|
T | G | 5 | a0001c0003t0001g0189a0001c0003t0001g0193a0001c0003t0001g0197others(2): Show | 5 | HG02109.hp2 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146-20219A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119188443 | ||||||
| chr9:119188771
|
G | A | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1145+19948C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119188771 | ||||||
| chr9:119189072
|
A | G | 5 | a0001c0003t0001g0189a0001c0003t0001g0193a0001c0003t0001g0197others(2): Show | 5 | HG02109.hp2 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1145+19647T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119189072 | ||||||
| chr9:119189100
|
A | G | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1145+19619T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119189100 | ||||||
| chr9:119189214
|
C | T | 83 | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0043others(80): Show | 83 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1145+19505G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119189214 | ||||||
| chr9:119189341
|
A | G | 181 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1145+19378T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119189341 | ||||||
| chr9:119189374
|
G | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0080others(1): Show | 4 | HG00735.hp1 HG01256.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145+19345C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119189374 | ||||||
| chr9:119189691
|
A | C | 1 | a0001c0002t0001g0075 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1145+19028T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119189691 | ||||||
| chr9:119189735
|
C | T | 83 | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0043others(80): Show | 83 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1145+18984G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119189735 | ||||||
| chr9:119190058
|
T | C | 31 | a0001c0001t0001g0172a0001c0001t0001g0195a0001c0001t0001g0200others(28): Show | 31 | HG01109.hp1 HG01169.hp2 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.1145+18661A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190058 | ||||||
| chr9:119190143
|
A | T | 7 | a0001c0003t0001g0209a0001c0005t0001g0192a0001c0005t0001g0199others(4): Show | 7 | HG02622.hp2 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1145+18576T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190143 | ||||||
| chr9:119190185
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1145+18534C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190185 | ||||||
| chr9:119190412
|
T | TA | 8 | a0001c0003t0001g0042a0001c0003t0001g0060a0001c0003t0001g0073others(5): Show | 8 | HG02258.hp2 HG02922.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1145+18306dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190412 | ||||||
| chr9:119190412
|
TA | T | 52 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0046others(49): Show | 52 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.1145+18306delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190412 | ||||||
| chr9:119190427
|
T | A | 8 | a0001c0003t0001g0042a0001c0003t0001g0060a0001c0003t0001g0073others(5): Show | 8 | HG02258.hp2 HG02922.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1145+18292A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190427 | ||||||
| chr9:119190568
|
C | A | 1 | a0001c0003t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1145+18151G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190568 | ||||||
| chr9:119190649
|
A | C | 1 | a0001c0003t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1145+18070T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119190649 | ||||||
| chr9:119191154
|
A | G | 1 | a0001c0003t0002g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1145+17565T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191154 | ||||||
| chr9:119191294
|
C | G | 1 | a0001c0001t0001g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1145+17425G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191294 | ||||||
| chr9:119191323
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1145+17396A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191323 | ||||||
| chr9:119191349
|
C | G | 1 | a0001c0002t0001g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1145+17370G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191349 | ||||||
| chr9:119191491
|
C | A | 5 | a0001c0003t0001g0189a0001c0003t0001g0193a0001c0003t0001g0197others(2): Show | 5 | HG02109.hp2 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1145+17228G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191491 | ||||||
| chr9:119191561
|
G | A | 1 | a0001c0003t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1145+17158C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191561 | ||||||
| chr9:119191668
|
T | G | 1 | a0001c0002t0004g0118 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1145+17051A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191668 | ||||||
| chr9:119191786
|
G | A | 26 | a0001c0001t0001g0172a0001c0001t0001g0195a0001c0001t0001g0200others(23): Show | 26 | HG01109.hp1 HG01169.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.1145+16933C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191786 | ||||||
| chr9:119191800
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1145+16919C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191800 | ||||||
| chr9:119191922
|
C | G | 8 | a0001c0003t0001g0085a0001c0003t0001g0181a0001c0003t0001g0182others(5): Show | 8 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1145+16797G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119191922 | ||||||
| chr9:119192140
|
C | A | 3 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0009t0001g0191 | 3 | HG02809.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1145+16579G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192140 | ||||||
| chr9:119192145
|
A | G | 1 | a0001c0002t0006g0013 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1145+16574T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192145 | ||||||
| chr9:119192176
|
C | T | 2 | a0001c0002t0001g0149a0001c0002t0001g0218 | 2 | NA18966.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1145+16543G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192176 | ||||||
| chr9:119192193
|
G | T | 7 | a0001c0003t0001g0094a0001c0003t0001g0186a0001c0003t0002g0226others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1145+16526C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192193 | ||||||
| chr9:119192410
|
C | T | 83 | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0043others(80): Show | 83 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1145+16309G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192410 | ||||||
| chr9:119192415
|
C | T | 16 | a0001c0001t0001g0172a0001c0001t0001g0195a0001c0001t0001g0200others(13): Show | 16 | HG01109.hp1 HG01169.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1145+16304G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192415 | ||||||
| chr9:119192616
|
G | A | 83 | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0043others(80): Show | 83 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1145+16103C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192616 | ||||||
| chr9:119192640
|
A | T | 83 | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0043others(80): Show | 83 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1145+16079T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192640 | ||||||
| chr9:119192676
|
A | G | 2 | a0001c0002t0001g0070a0001c0002t0001g0071 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1145+16043T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192676 | ||||||
| chr9:119192837
|
G | A | 1 | a0001c0014t0003g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1145+15882C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192837 | ||||||
| chr9:119192933
|
C | T | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1145+15786G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119192933 | ||||||
| chr9:119193044
|
A | C | 1 | a0001c0002t0001g0105 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1145+15675T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193044 | ||||||
| chr9:119193052
|
T | C | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1145+15667A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193052 | ||||||
| chr9:119193147
|
A | T | 5 | a0001c0003t0001g0189a0001c0003t0001g0193a0001c0003t0001g0197others(2): Show | 5 | HG02109.hp2 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1145+15572T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193147 | ||||||
| chr9:119193296
|
T | C | 7 | a0001c0001t0001g0212a0001c0002t0001g0202a0001c0002t0001g0203others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1145+15423A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193296 | ||||||
| chr9:119193566
|
G | A | 81 | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0043others(78): Show | 81 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1145+15153C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193566 | ||||||
| chr9:119193653
|
T | C | 1 | a0001c0002t0001g0025 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1145+15066A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193653 | ||||||
| chr9:119193731
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1145+14988C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193731 | ||||||
| chr9:119193798
|
G | A | 81 | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0043others(78): Show | 81 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1145+14921C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119193798 | ||||||
| chr9:119194271
|
A | G | 31 | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0054others(28): Show | 31 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1145+14448T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119194271 | ||||||
| chr9:119194557
|
G | A | 1 | a0001c0003t0002g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1145+14162C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119194557 | ||||||
| chr9:119194709
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1145+14010G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119194709 | ||||||
| chr9:119194761
|
T | C | 3 | a0001c0002t0001g0024a0001c0002t0001g0075a0001c0002t0001g0127 | 3 | HG02698.hp1 HG03239.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1145+13958A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119194761 | ||||||
| chr9:119194809
|
C | A | 1 | a0001c0001t0001g0065 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1145+13910G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119194809 | ||||||
| chr9:119194851
|
C | T | 1 | a0001c0003t0002g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1145+13868G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119194851 | ||||||
| chr9:119195067
|
T | A | 1 | a0001c0002t0004g0030 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1145+13652A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119195067 | ||||||
| chr9:119195169
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1145+13550C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119195169 | ||||||
| chr9:119195328
|
T | G | 24 | a0001c0001t0001g0172a0001c0001t0001g0195a0001c0001t0001g0200others(21): Show | 24 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1145+13391A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119195328 | ||||||
| chr9:119195702
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1145+13017G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119195702 | ||||||
| chr9:119196164
|
A | G | 4 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0003t0001g0211others(1): Show | 4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145+12555T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119196164 | ||||||
| chr9:119196639
|
C | G | 51 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0032others(48): Show | 51 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1145+12080G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119196639 | ||||||
| chr9:119196882
|
G | A | 2 | a0001c0003t0001g0107a0001c0003t0001g0139 | 2 | NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1145+11837C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119196882 | ||||||
| chr9:119197088
|
G | A | 3 | a0001c0003t0001g0085a0001c0003t0001g0198a0001c0003t0001g0208 | 3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1145+11631C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119197088 | ||||||
| chr9:119197262
|
G | A | 3 | a0001c0003t0001g0085a0001c0003t0001g0198a0001c0003t0001g0208 | 3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1145+11457C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119197262 | ||||||
| chr9:119197292
|
C | T | 3 | a0001c0004t0001g0026a0001c0004t0001g0028a0001c0004t0001g0072 | 3 | HG01069.hp1 HG01071.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1145+11427G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119197292 | ||||||
| chr9:119197473
|
A | G | 3 | a0001c0003t0001g0085a0001c0003t0001g0198a0001c0003t0001g0208 | 3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1145+11246T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119197473 | ||||||
| chr9:119197710
|
C | CAT | 198 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1145+11008_1145+11 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119197710 | ||||||
| chr9:119197759
|
G | A | 5 | a0001c0001t0002g0235a0001c0003t0001g0042a0001c0003t0001g0060others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145+10960C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119197759 | ||||||
| chr9:119197785
|
G | A | 7 | a0001c0003t0001g0209a0001c0003t0002g0223a0001c0003t0009g0214others(4): Show | 7 | HG01884.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1145+10934C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119197785 | ||||||
| chr9:119198236
|
G | A | 1 | a0001c0003t0001g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1145+10483C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198236 | ||||||
| chr9:119198382
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1145+10337G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198382 | ||||||
| chr9:119198473
|
T | C | 1 | a0001c0003t0002g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1145+10246A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198473 | ||||||
| chr9:119198484
|
A | G | 6 | a0001c0002t0001g0093a0001c0004t0001g0015a0001c0004t0001g0016others(3): Show | 6 | HG01169.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1145+10235T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198484 | ||||||
| chr9:119198556
|
G | A | 1 | a0001c0003t0001g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1145+10163C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198556 | ||||||
| chr9:119198579
|
A | C | 7 | a0001c0003t0001g0209a0001c0003t0002g0223a0001c0003t0009g0214others(4): Show | 7 | HG01884.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1145+10140T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198579 | ||||||
| chr9:119198672
|
ATT | A | 154 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0061others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1145+10045_1145+10 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198672 | ||||||
| chr9:119198672
|
ATTT | A | 36 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(33): Show | 36 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.1145+10044_1145+10 others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198672 | ||||||
| chr9:119198681
|
T | A | 51 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0032others(48): Show | 51 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1145+10038A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198681 | ||||||
| chr9:119198721
|
G | C | 1 | a0001c0002t0001g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1145+9998C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198721 | ||||||
| chr9:119198806
|
G | A | 1 | a0001c0003t0002g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1145+9913C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198806 | ||||||
| chr9:119198893
|
G | T | 32 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0132others(29): Show | 32 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1145+9826C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198893 | ||||||
| chr9:119198961
|
C | T | 1 | a0001c0002t0001g0196 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1145+9758G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119198961 | ||||||
| chr9:119199346
|
C | T | 39 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(36): Show | 39 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.1145+9373G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119199346 | ||||||
| chr9:119199618
|
G | A | 25 | a0001c0001t0001g0172a0001c0001t0001g0195a0001c0001t0001g0200others(22): Show | 25 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1145+9101C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119199618 | ||||||
| chr9:119199749
|
G | A | 2 | a0003c0008t0001g0091a0003c0008t0001g0174 | 2 | NA18612.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1145+8970C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119199749 | ||||||
| chr9:119199762
|
T | C | 34 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0132others(31): Show | 34 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1145+8957A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119199762 | ||||||
| chr9:119199796
|
T | C | 19 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0084others(16): Show | 19 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1145+8923A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119199796 | ||||||
| chr9:119199800
|
C | CT | 186 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1145+8918dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119199800 | ||||||
| chr9:119199800
|
C | CTT | 8 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187others(5): Show | 8 | HG01884.hp1 HG02615.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1145+8917_1145+891 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119199800 | ||||||
| chr9:119200241
|
G | A | 1 | a0001c0003t0001g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1145+8478C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200241 | ||||||
| chr9:119200292
|
C | T | 44 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0084others(41): Show | 44 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1145+8427G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200292 | ||||||
| chr9:119200389
|
A | C | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1145+8330T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200389 | ||||||
| chr9:119200612
|
G | A | 146 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1145+8107C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200612 | ||||||
| chr9:119200620
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1145+8099G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200620 | ||||||
| chr9:119200636
|
G | GA | 94 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.1145+8082dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200636 | ||||||
| chr9:119200636
|
GA | G | 25 | a0001c0001t0001g0172a0001c0001t0001g0195a0001c0001t0001g0204others(22): Show | 25 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1145+8082delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200636 | ||||||
| chr9:119200648
|
AAAG | A | 5 | a0001c0001t0002g0235a0001c0003t0001g0042a0001c0003t0001g0060others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145+8068_1145+807 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200648 | ||||||
| chr9:119200710
|
T | C | 2 | a0001c0002t0001g0075a0001c0002t0001g0127 | 2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1145+8009A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200710 | ||||||
| chr9:119200731
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1145+7988C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200731 | ||||||
| chr9:119200918
|
G | A | 6 | a0001c0002t0001g0093a0001c0004t0001g0015a0001c0004t0001g0016others(3): Show | 6 | HG01169.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1145+7801C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200918 | ||||||
| chr9:119200921
|
A | C | 1 | a0001c0001t0001g0076 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1145+7798T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200921 | ||||||
| chr9:119200936
|
A | G | 195 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1145+7783T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119200936 | ||||||
| chr9:119201244
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1145+7475G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119201244 | ||||||
| chr9:119201304
|
A | G | 1 | a0001c0002t0001g0062 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1145+7415T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119201304 | ||||||
| chr9:119202136
|
A | G | 7 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1145+6583T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202136 | ||||||
| chr9:119202196
|
G | T | 10 | a0001c0001t0002g0220a0001c0001t0002g0229a0001c0003t0001g0209others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1145+6523C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202196 | ||||||
| chr9:119202413
|
A | G | 2 | a0001c0003t0001g0073a0001c0003t0001g0122 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1145+6306T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202413 | ||||||
| chr9:119202572
|
T | C | 1 | a0001c0001t0002g0231 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1145+6147A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202572 | ||||||
| chr9:119202574
|
C | A | 2 | a0001c0001t0002g0234a0001c0003t0002g0228 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1145+6145G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202574 | ||||||
| chr9:119202670
|
G | A | 23 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(20): Show | 23 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1145+6049C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202670 | ||||||
| chr9:119202751
|
C | T | 51 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0032others(48): Show | 51 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1145+5968G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202751 | ||||||
| chr9:119202791
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1145+5928G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202791 | ||||||
| chr9:119202962
|
G | A | 23 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(20): Show | 23 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1145+5757C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119202962 | ||||||
| chr9:119203093
|
C | T | 63 | a0001c0001t0001g0044a0001c0001t0001g0099a0001c0001t0001g0100others(60): Show | 63 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.1145+5626G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119203093 | ||||||
| chr9:119203427
|
G | T | 1 | a0001c0001t0002g0231 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1145+5292C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119203427 | ||||||
| chr9:119203894
|
C | T | 1 | a0001c0003t0001g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1145+4825G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119203894 | ||||||
| chr9:119204204
|
T | C | 3 | a0001c0002t0001g0025a0001c0002t0001g0097a0001c0002t0001g0219 | 3 | HG02135.hp2 NA18961.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1145+4515A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119204204 | ||||||
| chr9:119204357
|
C | T | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0173 | 3 | HG03017.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1145+4362G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119204357 | ||||||
| chr9:119204457
|
AATAAATT others(3): Show |
A | 28 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0132others(25): Show | 28 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1145+4252_1145+426 others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119204457 | ||||||
| chr9:119204547
|
G | A | 40 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.1145+4172C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119204547 | ||||||
| chr9:119205176
|
G | A | 194 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1145+3543C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205176 | ||||||
| chr9:119205267
|
C | T | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1145+3452G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205267 | ||||||
| chr9:119205319
|
A | C | 36 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0132others(33): Show | 36 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.1145+3400T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205319 | ||||||
| chr9:119205484
|
A | T | 35 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0132others(32): Show | 35 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1145+3235T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205484 | ||||||
| chr9:119205567
|
A | G | 1 | a0001c0002t0001g0159 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1145+3152T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205567 | ||||||
| chr9:119205626
|
C | A | 23 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(20): Show | 23 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1145+3093G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205626 | ||||||
| chr9:119205645
|
A | G | 128 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.1145+3074T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205645 | ||||||
| chr9:119205679
|
G | A | 105 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.1145+3040C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205679 | ||||||
| chr9:119205827
|
G | T | 51 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0032others(48): Show | 51 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1145+2892C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205827 | ||||||
| chr9:119205858
|
CATG | C | 23 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(20): Show | 23 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1145+2858_1145+286 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205858 | ||||||
| chr9:119205859
|
A | G | 167 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1145+2860T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205859 | ||||||
| chr9:119205917
|
T | C | 128 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.1145+2802A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205917 | ||||||
| chr9:119205995
|
T | TA | 23 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(20): Show | 23 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1145+2723dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119205995 | ||||||
| chr9:119206102
|
A | G | 1 | a0001c0002t0001g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1145+2617T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206102 | ||||||
| chr9:119206110
|
TATCCTCT others(24): Show |
T | 1 | a0001c0001t0001g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1145+2578_1145+260 others(35): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206110 | ||||||
| chr9:119206121
|
G | A | 53 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.1145+2598C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206121 | ||||||
| chr9:119206233
|
C | T | 14 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(11): Show | 14 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1145+2486G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206233 | ||||||
| chr9:119206334
|
C | T | 2 | a0001c0001t0002g0234a0001c0003t0002g0228 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1145+2385G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206334 | ||||||
| chr9:119206383
|
G | A | 7 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1145+2336C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206383 | ||||||
| chr9:119206419
|
C | CA | 34 | a0001c0001t0001g0099a0001c0001t0001g0132a0001c0001t0001g0172others(31): Show | 34 | HG00140.hp2 HG00741.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1145+2299dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206419 | ||||||
| chr9:119206419
|
C | CAA | 24 | a0001c0001t0001g0044a0001c0001t0002g0220a0001c0001t0002g0229others(21): Show | 24 | HG00741.hp1 HG01169.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1145+2298_1145+229 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206419 | ||||||
| chr9:119206419
|
CA | C | 6 | a0001c0001t0001g0067a0001c0001t0002g0231a0001c0002t0001g0032others(3): Show | 6 | HG01069.hp2 HG01070.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1145+2299delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206419 | ||||||
| chr9:119206419
|
CAA | C | 22 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(19): Show | 22 | HG01109.hp2 HG01515.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1145+2298_1145+229 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206419 | ||||||
| chr9:119206419
|
CAAAAAAA others(5): Show |
C | 54 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.1145+2288_1145+229 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206419 | ||||||
| chr9:119206491
|
C | T | 5 | a0001c0001t0002g0235a0001c0003t0001g0042a0001c0003t0001g0060others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145+2228G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206491 | ||||||
| chr9:119206492
|
G | A | 1 | a0001c0002t0001g0116 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1145+2227C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206492 | ||||||
| chr9:119206684
|
T | A | 1 | a0001c0002t0001g0029 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1145+2035A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206684 | ||||||
| chr9:119206785
|
A | G | 128 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.1145+1934T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206785 | ||||||
| chr9:119206837
|
T | C | 5 | a0001c0001t0002g0235a0001c0003t0001g0042a0001c0003t0001g0060others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145+1882A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206837 | ||||||
| chr9:119206842
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0204 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1145+1877C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119206842 | ||||||
| chr9:119207032
|
G | A | 51 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0032others(48): Show | 51 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1145+1687C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119207032 | ||||||
| chr9:119207072
|
G | T | 40 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.1145+1647C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119207072 | ||||||
| chr9:119207235
|
A | G | 1 | a0001c0002t0001g0116 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1145+1484T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119207235 | ||||||
| chr9:119207395
|
G | A | 3 | a0001c0004t0001g0026a0001c0004t0001g0028a0001c0004t0001g0072 | 3 | HG01069.hp1 HG01071.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1145+1324C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119207395 | ||||||
| chr9:119207887
|
C | A | 1 | a0001c0004t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1145+832G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119207887 | ||||||
| chr9:119207983
|
G | A | 2 | a0001c0003t0001g0107a0001c0003t0001g0139 | 2 | NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1145+736C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119207983 | ||||||
| chr9:119208020
|
G | A | 1 | a0001c0002t0003g0011 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1145+699C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119208020 | ||||||
| chr9:119208141
|
T | C | 140 | a0001c0001t0001g0044a0001c0001t0001g0099a0001c0001t0001g0100others(137): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1145+578A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119208141 | ||||||
| chr9:119208225
|
C | T | 63 | a0001c0001t0001g0044a0001c0001t0001g0099a0001c0001t0001g0100others(60): Show | 63 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.1145+494G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119208225 | ||||||
| chr9:119208314
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1145+405G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119208314 | ||||||
| chr9:119208414
|
T | A | 193 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1145+305A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119208414 | ||||||
| chr9:119208601
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1145+118C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 7/7 | chr9 | 119208601 | ||||||
| chr9:119208967
|
G | T | 15 | a0001c0001t0001g0044a0001c0001t0002g0220a0001c0001t0002g0229others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.923-26C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119208967 | ||||||
| chr9:119209152
|
C | T | 3 | a0001c0003t0001g0085a0001c0003t0001g0198a0001c0003t0001g0208 | 3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.923-211G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209152 | ||||||
| chr9:119209219
|
C | T | 4 | a0001c0001t0001g0156a0001c0003t0001g0085a0001c0003t0001g0198others(1): Show | 4 | HG01884.hp2 HG02165.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.923-278G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209219 | ||||||
| chr9:119209359
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0160 | 3 | HG00280.hp2 HG01517.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.923-418G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209359 | ||||||
| chr9:119209492
|
C | T | 1 | a0001c0001t0002g0231 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.923-551G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209492 | ||||||
| chr9:119209500
|
A | C | 1 | a0001c0009t0001g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.923-559T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209500 | ||||||
| chr9:119209501
|
G | C | 1 | a0001c0009t0001g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.923-560C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209501 | ||||||
| chr9:119209575
|
T | TA | 15 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(12): Show | 15 | HG01515.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.923-635dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209575 | ||||||
| chr9:119209577
|
A | AAAAAAAA others(338): Show |
5 | a0001c0001t0002g0235a0001c0003t0001g0042a0001c0003t0001g0060others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.923-637_923-636ins others(345): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209577 | ||||||
| chr9:119209668
|
G | A | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.923-727C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209668 | ||||||
| chr9:119209758
|
C | A | 136 | a0001c0001t0001g0044a0001c0001t0001g0099a0001c0001t0001g0100others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.923-817G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209758 | ||||||
| chr9:119209826
|
G | T | 12 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.923-885C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209826 | ||||||
| chr9:119209891
|
T | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0170 | 2 | HG00544.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.923-950A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209891 | ||||||
| chr9:119209906
|
G | C | 12 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.923-965C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119209906 | ||||||
| chr9:119210082
|
C | T | 68 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(65): Show | 68 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.923-1141G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210082 | ||||||
| chr9:119210147
|
C | T | 3 | a0001c0002t0001g0029a0001c0002t0001g0050a0001c0002t0001g0051 | 3 | HG00140.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.923-1206G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210147 | ||||||
| chr9:119210148
|
T | C | 14 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(11): Show | 14 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.923-1207A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210148 | ||||||
| chr9:119210362
|
T | C | 2 | a0001c0002t0001g0070a0001c0002t0001g0071 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.923-1421A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210362 | ||||||
| chr9:119210393
|
T | C | 5 | a0001c0001t0002g0235a0001c0003t0001g0042a0001c0003t0001g0060others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.923-1452A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210393 | ||||||
| chr9:119210395
|
G | T | 28 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0132others(25): Show | 28 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.923-1454C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210395 | ||||||
| chr9:119210592
|
A | G | 1 | a0001c0004t0001g0074 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.923-1651T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210592 | ||||||
| chr9:119210631
|
G | A | 12 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.923-1690C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210631 | ||||||
| chr9:119210631
|
G | C | 53 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0032others(50): Show | 53 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.923-1690C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210631 | ||||||
| chr9:119210646
|
AG | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204 | 3 | HG02145.hp1 HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.923-1706delC | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210646 | ||||||
| chr9:119210937
|
G | T | 3 | a0001c0003t0001g0085a0001c0003t0001g0198a0001c0003t0001g0208 | 3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.923-1996C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119210937 | ||||||
| chr9:119211138
|
T | C | 15 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(12): Show | 15 | HG01515.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.923-2197A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211138 | ||||||
| chr9:119211149
|
A | C | 52 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0032others(49): Show | 52 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.923-2208T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211149 | ||||||
| chr9:119211164
|
C | CTTTA | 18 | a0001c0001t0001g0039a0001c0001t0001g0061a0001c0001t0001g0090others(15): Show | 18 | HG00738.hp2 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.923-2227_923-2224d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211164 | ||||||
| chr9:119211164
|
CTTTA | C | 75 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0055others(72): Show | 75 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.923-2227_923-2224d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211164 | ||||||
| chr9:119211164
|
CTTTATTT others(1): Show |
C | 5 | a0001c0001t0001g0146a0001c0003t0001g0022a0001c0003t0001g0175others(2): Show | 5 | HG01496.hp1 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.923-2231_923-2224d others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211164 | ||||||
| chr9:119211164
|
CTTTATTT others(9): Show |
C | 15 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(12): Show | 15 | HG01515.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.923-2239_923-2224d others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211164 | ||||||
| chr9:119211212
|
T | A | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.923-2271A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211212 | ||||||
| chr9:119211470
|
T | TAC | 15 | a0001c0001t0001g0044a0001c0001t0002g0220a0001c0001t0002g0229others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.922+2447_922+2448d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211470 | ||||||
| chr9:119211564
|
A | G | 67 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(64): Show | 67 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.922+2355T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211564 | ||||||
| chr9:119211713
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.922+2206G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211713 | ||||||
| chr9:119211740
|
C | T | 67 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(64): Show | 67 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.922+2179G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119211740 | ||||||
| chr9:119212170
|
A | G | 190 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.922+1749T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119212170 | ||||||
| chr9:119212425
|
A | T | 12 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.922+1494T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119212425 | ||||||
| chr9:119212487
|
T | A | 1 | a0004c0011t0001g0125 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.922+1432A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119212487 | ||||||
| chr9:119212577
|
A | T | 1 | a0004c0011t0001g0125 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.922+1342T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119212577 | ||||||
| chr9:119212792
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.922+1127A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119212792 | ||||||
| chr9:119212929
|
C | T | 68 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(65): Show | 68 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.922+990G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119212929 | ||||||
| chr9:119213024
|
AC | A | 15 | a0001c0001t0001g0044a0001c0001t0002g0220a0001c0001t0002g0229others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.922+894delG | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213024 | ||||||
| chr9:119213128
|
C | G | 14 | a0001c0001t0001g0044a0001c0001t0002g0220a0001c0001t0002g0229others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.922+791G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213128 | ||||||
| chr9:119213206
|
C | A | 7 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.922+713G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213206 | ||||||
| chr9:119213231
|
T | A | 29 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0132others(26): Show | 29 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.922+688A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213231 | ||||||
| chr9:119213369
|
A | G | 15 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(12): Show | 15 | HG01515.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.922+550T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213369 | ||||||
| chr9:119213438
|
A | G | 1 | a0001c0001t0002g0231 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.922+481T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213438 | ||||||
| chr9:119213569
|
C | T | 15 | a0001c0001t0001g0044a0001c0001t0002g0220a0001c0001t0002g0229others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.922+350G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213569 | ||||||
| chr9:119213589
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.922+330G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213589 | ||||||
| chr9:119213766
|
G | A | 15 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(12): Show | 15 | HG01515.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.922+153C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213766 | ||||||
| chr9:119213796
|
C | A | 1 | a0004c0011t0001g0125 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.922+123G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213796 | ||||||
| chr9:119213797
|
A | C | 1 | a0004c0011t0001g0125 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.922+122T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 6/7 | chr9 | 119213797 | ||||||
| chr9:119214162
|
G | A | 2 | a0003c0008t0001g0091a0003c0008t0001g0174 | 2 | NA18612.hp2 NA18747.hp2 |
splice_region_variant&intron_variant | LOW | c.686-7C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214162 | ||||||
| chr9:119214167
|
T | C | 1 | a0001c0002t0001g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.686-12A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214167 | ||||||
| chr9:119214373
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0109 | 2 | HG01256.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.686-218C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214373 | ||||||
| chr9:119214580
|
G | A | 66 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(63): Show | 66 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.686-425C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214580 | ||||||
| chr9:119214587
|
T | TA | 6 | a0001c0001t0002g0220a0001c0005t0001g0210a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.686-433dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214587 | ||||||
| chr9:119214587
|
T | TAA | 55 | a0001c0001t0001g0044a0001c0001t0001g0099a0001c0001t0001g0100others(52): Show | 55 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.686-434_686-433dup others(2): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214587 | ||||||
| chr9:119214587
|
T | TAAA | 13 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(10): Show | 13 | HG01109.hp2 HG01169.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.686-435_686-433dup others(3): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214587 | ||||||
| chr9:119214587
|
TA | T | 54 | a0001c0001t0001g0061a0001c0001t0001g0081a0001c0002t0001g0024others(51): Show | 54 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.686-433delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214587 | ||||||
| chr9:119214646
|
T | C | 200 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.686-491A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214646 | ||||||
| chr9:119214918
|
G | A | 2 | a0001c0002t0001g0075a0001c0002t0001g0127 | 2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.686-763C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119214918 | ||||||
| chr9:119215011
|
T | C | 4 | a0001c0001t0002g0235a0001c0003t0001g0060a0001c0003t0001g0073others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.686-856A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119215011 | ||||||
| chr9:119215317
|
G | A | 2 | a0001c0001t0002g0234a0001c0003t0002g0228 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.686-1162C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119215317 | ||||||
| chr9:119215484
|
T | C | 30 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0132others(27): Show | 30 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.686-1329A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119215484 | ||||||
| chr9:119215536
|
A | G | 4 | a0001c0002t0001g0025a0001c0002t0001g0097a0001c0002t0001g0165others(1): Show | 4 | HG02135.hp2 HG03927.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.686-1381T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119215536 | ||||||
| chr9:119215800
|
A | C | 235 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.686-1645T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119215800 | ||||||
| chr9:119215838
|
GAAACCTG others(29): Show |
G | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.686-1719_686-1684d others(38): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119215838 | ||||||
| chr9:119216084
|
T | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0170 | 2 | HG00544.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.686-1929A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216084 | ||||||
| chr9:119216373
|
C | G | 1 | a0001c0002t0001g0135 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.686-2218G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216373 | ||||||
| chr9:119216397
|
C | T | 1 | a0001c0002t0002g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.686-2242G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216397 | ||||||
| chr9:119216502
|
A | C | 80 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0132others(77): Show | 80 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.686-2347T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216502 | ||||||
| chr9:119216614
|
C | T | 3 | a0001c0002t0001g0104a0001c0002t0001g0112a0001c0002t0001g0154 | 3 | HG02074.hp2 HG02129.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.686-2459G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216614 | ||||||
| chr9:119216774
|
A | G | 4 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187others(1): Show | 4 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.686-2619T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216774 | ||||||
| chr9:119216875
|
G | A | 1 | a0001c0002t0001g0157 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.686-2720C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216875 | ||||||
| chr9:119216903
|
T | G | 38 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(35): Show | 38 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.686-2748A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216903 | ||||||
| chr9:119216926
|
A | G | 1 | a0001c0001t0002g0231 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.686-2771T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119216926 | ||||||
| chr9:119217314
|
AACACACA others(1): Show |
A | 12 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.686-3167_686-3160d others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217314 | ||||||
| chr9:119217330
|
G | GAC | 19 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(16): Show | 19 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.686-3177_686-3176d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217330 | ||||||
| chr9:119217330
|
GAC | G | 38 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(35): Show | 38 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.686-3177_686-3176d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217330 | ||||||
| chr9:119217345
|
A | G | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.686-3190T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217345 | ||||||
| chr9:119217352
|
G | C | 3 | a0001c0003t0001g0085a0001c0003t0001g0198a0001c0003t0001g0208 | 3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.686-3197C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217352 | ||||||
| chr9:119217521
|
C | T | 118 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.686-3366G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217521 | ||||||
| chr9:119217527
|
A | G | 1 | a0001c0003t0001g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.686-3372T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217527 | ||||||
| chr9:119217581
|
GA | G | 12 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.686-3427delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217581 | ||||||
| chr9:119217676
|
G | A | 19 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(16): Show | 19 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.686-3521C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217676 | ||||||
| chr9:119217710
|
T | G | 20 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0132others(17): Show | 20 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.686-3555A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217710 | ||||||
| chr9:119217865
|
G | C | 1 | a0001c0001t0001g0156 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.686-3710C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119217865 | ||||||
| chr9:119218055
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0005g0215a0001c0001t0005g0217 | 3 | HG00423.hp2 NA18993.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.686-3900C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218055 | ||||||
| chr9:119218064
|
C | T | 21 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0132others(18): Show | 21 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.686-3909G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218064 | ||||||
| chr9:119218069
|
A | C | 118 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.686-3914T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218069 | ||||||
| chr9:119218167
|
T | A | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.686-4012A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218167 | ||||||
| chr9:119218204
|
AT | A | 68 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0044others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.686-4050delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218204 | ||||||
| chr9:119218204
|
ATT | A | 112 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0099others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.686-4051_686-4050d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218204 | ||||||
| chr9:119218204
|
ATTT | A | 8 | a0001c0001t0002g0235a0001c0002t0001g0068a0001c0002t0001g0131others(5): Show | 8 | HG01169.hp1 HG01243.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.686-4052_686-4050d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218204 | ||||||
| chr9:119218297
|
C | T | 20 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0132others(17): Show | 20 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.686-4142G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218297 | ||||||
| chr9:119218308
|
G | A | 74 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0027others(71): Show | 74 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.686-4153C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218308 | ||||||
| chr9:119218395
|
G | A | 20 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0132others(17): Show | 20 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.686-4240C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218395 | ||||||
| chr9:119218511
|
C | T | 5 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.686-4356G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218511 | ||||||
| chr9:119218652
|
G | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0081 | 2 | HG00738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.686-4497C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218652 | ||||||
| chr9:119218746
|
A | AT | 67 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0037others(64): Show | 67 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.686-4592dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218746 | ||||||
| chr9:119218746
|
A | ATT | 11 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.686-4593_686-4592d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218746 | ||||||
| chr9:119218746
|
A | ATTT | 21 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0132others(18): Show | 21 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.686-4594_686-4592d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218746 | ||||||
| chr9:119218746
|
AT | A | 77 | a0001c0001t0001g0134a0001c0002t0001g0024a0001c0002t0001g0025others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.686-4592delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218746 | ||||||
| chr9:119218933
|
C | T | 2 | a0001c0003t0001g0198a0001c0003t0001g0208 | 2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.686-4778G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119218933 | ||||||
| chr9:119219640
|
G | C | 1 | a0001c0004t0001g0164 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.686-5485C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219640 | ||||||
| chr9:119219646
|
T | TGA | 4 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0146others(1): Show | 4 | HG03942.hp1 NA18522.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.686-5493_686-5492d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219646
|
T | TGAGA | 5 | a0001c0001t0001g0150a0001c0001t0001g0194a0001c0003t0002g0227others(2): Show | 5 | HG00438.hp2 HG01109.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.686-5495_686-5492d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219646
|
T | TGAGAGA | 3 | a0001c0001t0001g0078a0001c0001t0001g0172a0001c0002t0001g0143 | 3 | HG01175.hp1 HG01261.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.686-5497_686-5492d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219646
|
T | TGAGAGAG others(9): Show |
1 | a0001c0003t0001g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.686-5507_686-5492d others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219646
|
TGA | T | 25 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0053others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.686-5493_686-5492d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219646
|
TGAGA | T | 27 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0054others(24): Show | 27 | HG01069.hp2 HG01255.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.686-5495_686-5492d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219646
|
TGAGAGA | T | 11 | a0001c0001t0001g0039a0001c0001t0001g0087a0001c0001t0001g0148others(8): Show | 11 | HG01346.hp1 HG01975.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.686-5497_686-5492d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219646
|
TGAGAGAG others(1): Show |
T | 16 | a0001c0001t0001g0076a0001c0001t0001g0117a0001c0001t0001g0121others(13): Show | 16 | HG01106.hp2 HG01123.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.686-5499_686-5492d others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219646
|
TGAGAGAG others(3): Show |
T | 16 | a0001c0001t0001g0044a0001c0001t0001g0195a0001c0002t0001g0105others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.686-5501_686-5492d others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219646
|
TGAGAGAG others(5): Show |
T | 49 | a0001c0001t0002g0220a0001c0001t0002g0229a0001c0002t0001g0024others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.686-5503_686-5492d others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219646
|
TGAGAGAG others(7): Show |
T | 8 | a0001c0001t0001g0200a0001c0001t0003g0008a0001c0003t0001g0094others(5): Show | 8 | HG01891.hp2 HG02683.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.686-5505_686-5492d others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219646
|
TGAGAGAG others(11): Show |
T | 10 | a0001c0001t0001g0132a0001c0001t0001g0212a0001c0001t0003g0009others(7): Show | 10 | HG00741.hp1 HG00741.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.686-5509_686-5492d others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219646
|
TGAGAGAG others(13): Show |
T | 15 | a0001c0002t0001g0093a0001c0002t0001g0202a0001c0002t0001g0203others(12): Show | 15 | HG01109.hp2 HG01169.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.686-5511_686-5492d others(22): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219646
|
TGAGAGAG others(15): Show |
T | 16 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(13): Show | 16 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.686-5513_686-5492d others(24): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219646
|
TGAGAGAG others(17): Show |
T | 3 | a0001c0003t0001g0193a0001c0003t0001g0198a0001c0003t0001g0208 | 3 | HG01884.hp2 HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.686-5515_686-5492d others(26): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219646 | ||||||
| chr9:119219675
|
GAGAGAGA others(14): Show |
G | 1 | a0001c0003t0001g0122 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.686-5541_686-5521d others(23): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219675 | ||||||
| chr9:119219696
|
A | AG | 3 | a0001c0001t0001g0048a0001c0001t0001g0167a0001c0001t0005g0215 | 3 | HG02683.hp1 HG03927.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.686-5542_686-5541i others(3): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219696 | ||||||
| chr9:119219737
|
A | G | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-5582T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219737 | ||||||
| chr9:119219766
|
A | C | 2 | a0001c0002t0001g0092a0001c0002t0001g0110 | 2 | NA18994.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.686-5611T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219766 | ||||||
| chr9:119219838
|
G | T | 3 | a0001c0002t0001g0032a0001c0002t0001g0114a0001c0002t0001g0179 | 3 | HG03669.hp1 NA18940.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.686-5683C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119219838 | ||||||
| chr9:119220092
|
G | A | 24 | a0001c0002t0001g0027a0001c0002t0001g0029a0001c0002t0001g0036others(21): Show | 24 | HG00140.hp2 HG01074.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.686-5937C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220092 | ||||||
| chr9:119220121
|
C | A | 12 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.686-5966G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220121 | ||||||
| chr9:119220274
|
C | A | 19 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(16): Show | 19 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.686-6119G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220274 | ||||||
| chr9:119220303
|
C | T | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.686-6148G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220303 | ||||||
| chr9:119220617
|
C | CAA | 19 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(16): Show | 19 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.686-6464_686-6463d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220617 | ||||||
| chr9:119220617
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0109 | 2 | HG01256.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.686-6462G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220617 | ||||||
| chr9:119220627
|
A | G | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-6472T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220627 | ||||||
| chr9:119220731
|
T | C | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-6576A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220731 | ||||||
| chr9:119220830
|
A | T | 19 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(16): Show | 19 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.686-6675T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220830 | ||||||
| chr9:119220866
|
G | T | 5 | a0001c0003t0001g0094a0001c0003t0001g0151a0001c0003t0001g0186others(2): Show | 5 | HG01891.hp2 HG03579.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.686-6711C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220866 | ||||||
| chr9:119220875
|
AT | A | 2 | a0001c0003t0001g0198a0001c0003t0001g0208 | 2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.686-6721delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119220875 | ||||||
| chr9:119221503
|
C | A | 1 | a0001c0003t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.686-7348G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119221503 | ||||||
| chr9:119221836
|
TAGC | T | 14 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(11): Show | 14 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.686-7684_686-7682d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119221836 | ||||||
| chr9:119221986
|
C | T | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.686-7831G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119221986 | ||||||
| chr9:119222029
|
C | G | 41 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.686-7874G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222029 | ||||||
| chr9:119222069
|
C | T | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.686-7914G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222069 | ||||||
| chr9:119222275
|
A | G | 41 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.686-8120T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222275 | ||||||
| chr9:119222395
|
C | T | 189 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.686-8240G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222395 | ||||||
| chr9:119222588
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.686-8433C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222588 | ||||||
| chr9:119222615
|
A | ACAAGGAA others(10): Show |
18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-8461_686-8460i others(19): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222615 | ||||||
| chr9:119222667
|
T | C | 1 | a0001c0007t0001g0082 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.686-8512A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222667 | ||||||
| chr9:119222690
|
CA | C | 7 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.686-8536delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222690 | ||||||
| chr9:119222822
|
G | A | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.686-8667C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222822 | ||||||
| chr9:119222858
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.686-8703T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119222858 | ||||||
| chr9:119223199
|
T | C | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-9044A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223199 | ||||||
| chr9:119223520
|
C | A | 3 | a0001c0003t0001g0085a0001c0005t0001g0192a0001c0005t0002g0236 | 3 | HG02886.hp2 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.686-9365G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223520 | ||||||
| chr9:119223562
|
T | C | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-9407A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223562 | ||||||
| chr9:119223570
|
C | T | 59 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.686-9415G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223570 | ||||||
| chr9:119223642
|
G | A | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-9487C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223642 | ||||||
| chr9:119223722
|
T | G | 13 | a0001c0001t0001g0044a0001c0003t0001g0085a0001c0003t0001g0180others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.686-9567A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223722 | ||||||
| chr9:119223790
|
G | A | 3 | a0001c0001t0002g0220a0001c0001t0002g0229a0001c0005t0001g0210 | 3 | HG02622.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.686-9635C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223790 | ||||||
| chr9:119223827
|
C | T | 118 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.686-9672G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223827 | ||||||
| chr9:119223929
|
T | C | 1 | a0001c0002t0002g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.686-9774A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223929 | ||||||
| chr9:119223941
|
TATAG | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(3): Show | 6 | HG01261.hp1 HG01496.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.686-9790_686-9787d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223941 | ||||||
| chr9:119223955
|
C | T | 3 | a0001c0001t0002g0220a0001c0001t0002g0229a0001c0005t0001g0210 | 3 | HG02622.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.686-9800G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119223955 | ||||||
| chr9:119224106
|
A | G | 42 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(39): Show | 42 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.686-9951T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119224106 | ||||||
| chr9:119224548
|
T | A | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.686-10393A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119224548 | ||||||
| chr9:119224778
|
C | G | 93 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0027others(90): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.686-10623G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119224778 | ||||||
| chr9:119224873
|
C | T | 1 | a0001c0002t0001g0062 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.686-10718G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119224873 | ||||||
| chr9:119225104
|
T | A | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-10949A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225104 | ||||||
| chr9:119225142
|
C | T | 150 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0084others(147): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.686-10987G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225142 | ||||||
| chr9:119225209
|
C | T | 1 | a0001c0002t0006g0013 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.686-11054G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225209 | ||||||
| chr9:119225266
|
A | G | 128 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0084others(125): Show | 128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.686-11111T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225266 | ||||||
| chr9:119225370
|
A | G | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.686-11215T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225370 | ||||||
| chr9:119225441
|
G | A | 3 | a0001c0001t0002g0220a0001c0001t0002g0229a0001c0005t0001g0210 | 3 | HG02622.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.686-11286C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225441 | ||||||
| chr9:119225709
|
T | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.686-11554A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225709 | ||||||
| chr9:119225896
|
TAAAC | T | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-11745_686-1174 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225896 | ||||||
| chr9:119225922
|
G | A | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-11767C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225922 | ||||||
| chr9:119225965
|
G | A | 1 | a0001c0002t0001g0135 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.686-11810C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119225965 | ||||||
| chr9:119226009
|
T | C | 3 | a0001c0003t0001g0085a0001c0003t0001g0198a0001c0003t0001g0208 | 3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.686-11854A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226009 | ||||||
| chr9:119226072
|
C | T | 192 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.686-11917G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226072 | ||||||
| chr9:119226085
|
A | G | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-11930T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226085 | ||||||
| chr9:119226090
|
TAAGAC | T | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-11940_686-1193 others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226090 | ||||||
| chr9:119226250
|
G | A | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.686-12095C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226250 | ||||||
| chr9:119226437
|
T | A | 192 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.685+12218A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226437 | ||||||
| chr9:119226621
|
T | G | 93 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0027others(90): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.685+12034A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226621 | ||||||
| chr9:119226668
|
GT | G | 190 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.685+11986delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226668 | ||||||
| chr9:119226669
|
T | G | 1 | a0001c0003t0002g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.685+11986A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226669 | ||||||
| chr9:119226686
|
C | T | 12 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.685+11969G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226686 | ||||||
| chr9:119226812
|
G | A | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.685+11843C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119226812 | ||||||
| chr9:119227074
|
A | G | 39 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(36): Show | 39 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.685+11581T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227074 | ||||||
| chr9:119227083
|
CA | C | 4 | a0001c0001t0002g0235a0001c0003t0001g0060a0001c0003t0001g0073others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.685+11571delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227083 | ||||||
| chr9:119227278
|
C | A | 1 | a0001c0001t0002g0235 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.685+11377G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227278 | ||||||
| chr9:119227361
|
T | C | 5 | a0001c0001t0002g0235a0001c0003t0001g0042a0001c0003t0001g0060others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.685+11294A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227361 | ||||||
| chr9:119227533
|
C | T | 1 | a0001c0002t0001g0057 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.685+11122G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227533 | ||||||
| chr9:119227625
|
G | C | 2 | a0001c0002t0001g0075a0001c0002t0001g0127 | 2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.685+11030C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227625 | ||||||
| chr9:119227741
|
T | C | 1 | a0001c0002t0001g0057 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.685+10914A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227741 | ||||||
| chr9:119227771
|
C | T | 1 | a0001c0007t0001g0052 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.685+10884G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227771 | ||||||
| chr9:119227890
|
T | A | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.685+10765A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119227890 | ||||||
| chr9:119228034
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.685+10621G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228034 | ||||||
| chr9:119228036
|
C | T | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.685+10619G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228036 | ||||||
| chr9:119228076
|
G | A | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.685+10579C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228076 | ||||||
| chr9:119228212
|
T | A | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.685+10443A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228212 | ||||||
| chr9:119228223
|
A | T | 127 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0084others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.685+10432T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228223 | ||||||
| chr9:119228224
|
T | A | 127 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0084others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.685+10431A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228224 | ||||||
| chr9:119228231
|
C | T | 1 | a0001c0003t0002g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.685+10424G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228231 | ||||||
| chr9:119228299
|
C | T | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.685+10356G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228299 | ||||||
| chr9:119228307
|
C | A | 1 | a0001c0002t0003g0012 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.685+10348G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228307 | ||||||
| chr9:119228398
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0109 | 2 | HG01256.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.685+10257A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228398 | ||||||
| chr9:119228483
|
TA | T | 58 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.685+10171delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228483 | ||||||
| chr9:119228576
|
T | C | 71 | a0001c0001t0003g0001a0001c0002t0001g0024a0001c0002t0001g0025others(68): Show | 71 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.685+10079A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228576 | ||||||
| chr9:119228625
|
A | G | 6 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.685+10030T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228625 | ||||||
| chr9:119228932
|
T | C | 13 | a0001c0001t0001g0044a0001c0003t0001g0085a0001c0003t0001g0180others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.685+9723A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119228932 | ||||||
| chr9:119229198
|
A | G | 40 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.685+9457T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119229198 | ||||||
| chr9:119229482
|
C | T | 1 | a0001c0002t0001g0161 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.685+9173G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119229482 | ||||||
| chr9:119229668
|
C | CA | 3 | a0001c0003t0001g0085a0001c0003t0001g0198a0001c0003t0001g0208 | 3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.685+8986dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119229668 | ||||||
| chr9:119229673
|
A | G | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.685+8982T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119229673 | ||||||
| chr9:119229863
|
C | T | 126 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0084others(123): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.685+8792G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119229863 | ||||||
| chr9:119229996
|
T | C | 40 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.685+8659A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119229996 | ||||||
| chr9:119230072
|
TGAGAGAG others(19): Show |
T | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.685+8557_685+8582d others(28): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230072 | ||||||
| chr9:119230081
|
T | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0080 | 2 | HG00735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.685+8574A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230081 | ||||||
| chr9:119230186
|
A | G | 18 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.685+8469T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230186 | ||||||
| chr9:119230271
|
C | T | 12 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.685+8384G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230271 | ||||||
| chr9:119230408
|
G | A | 125 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0084others(122): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.685+8247C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230408 | ||||||
| chr9:119230469
|
G | A | 185 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.685+8186C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230469 | ||||||
| chr9:119230480
|
A | G | 189 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.685+8175T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230480 | ||||||
| chr9:119230683
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.685+7972C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119230683 | ||||||
| chr9:119231230
|
T | C | 114 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0123others(111): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.685+7425A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119231230 | ||||||
| chr9:119231641
|
C | A | 129 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0084others(126): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.685+7014G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119231641 | ||||||
| chr9:119231689
|
G | A | 19 | a0001c0002t0001g0093a0001c0002t0001g0202a0001c0002t0001g0203others(16): Show | 19 | HG01109.hp2 HG01123.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.685+6966C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119231689 | ||||||
| chr9:119231996
|
T | A | 2 | a0001c0001t0001g0134a0004c0011t0001g0125 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.685+6659A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119231996 | ||||||
| chr9:119232010
|
G | A | 1 | a0001c0004t0002g0232 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.685+6645C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232010 | ||||||
| chr9:119232042
|
A | T | 40 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.685+6613T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232042 | ||||||
| chr9:119232144
|
T | C | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.685+6511A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232144 | ||||||
| chr9:119232225
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.685+6430G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232225 | ||||||
| chr9:119232435
|
T | C | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.685+6220A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232435 | ||||||
| chr9:119232622
|
T | C | 128 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0084others(125): Show | 128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.685+6033A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232622 | ||||||
| chr9:119232851
|
A | G | 41 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.685+5804T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232851 | ||||||
| chr9:119232873
|
G | A | 12 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.685+5782C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232873 | ||||||
| chr9:119232908
|
GCCATTAG others(10): Show |
G | 1 | a0001c0002t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.685+5730_685+5746d others(19): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119232908 | ||||||
| chr9:119233012
|
C | A | 1 | a0001c0002t0001g0203 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.685+5643G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119233012 | ||||||
| chr9:119233022
|
C | CT | 127 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0084others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.685+5632dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119233022 | ||||||
| chr9:119233146
|
C | A | 2 | a0001c0003t0001g0209a0001c0003t0002g0223 | 2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.685+5509G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119233146 | ||||||
| chr9:119233339
|
T | A | 12 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.685+5316A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119233339 | ||||||
| chr9:119233427
|
A | G | 1 | a0001c0004t0001g0164 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.685+5228T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119233427 | ||||||
| chr9:119233737
|
A | G | 2 | a0001c0001t0001g0134a0004c0011t0001g0125 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.685+4918T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119233737 | ||||||
| chr9:119234188
|
C | T | 179 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.685+4467G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234188 | ||||||
| chr9:119234371
|
G | A | 1 | a0001c0003t0001g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.685+4284C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234371 | ||||||
| chr9:119234435
|
TTTCA | T | 25 | a0001c0001t0001g0044a0001c0001t0001g0195a0001c0001t0001g0200others(22): Show | 25 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.685+4216_685+4219d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234435 | ||||||
| chr9:119234582
|
T | C | 1 | a0001c0002t0001g0036 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.685+4073A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234582 | ||||||
| chr9:119234590
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.685+4065A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234590 | ||||||
| chr9:119234630
|
G | A | 12 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.685+4025C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234630 | ||||||
| chr9:119234655
|
C | A | 12 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.685+4000G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234655 | ||||||
| chr9:119234676
|
C | T | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.685+3979G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234676 | ||||||
| chr9:119234988
|
A | G | 1 | a0001c0002t0001g0027 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.685+3667T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119234988 | ||||||
| chr9:119235560
|
C | T | 14 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(11): Show | 14 | HG00639.hp2 HG00735.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.685+3095G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119235560 | ||||||
| chr9:119235568
|
T | C | 13 | a0001c0001t0001g0044a0001c0003t0001g0085a0001c0003t0001g0180others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.685+3087A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119235568 | ||||||
| chr9:119235585
|
C | T | 40 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.685+3070G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119235585 | ||||||
| chr9:119235730
|
G | A | 4 | a0001c0001t0001g0090a0001c0001t0001g0130a0001c0001t0001g0156others(1): Show | 4 | HG00544.hp2 HG02135.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.685+2925C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119235730 | ||||||
| chr9:119236036
|
A | T | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.685+2619T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119236036 | ||||||
| chr9:119236257
|
C | A | 1 | a0001c0003t0001g0166 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.685+2398G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119236257 | ||||||
| chr9:119236484
|
T | G | 2 | a0002c0012t0001g0063a0002c0013t0003g0006 | 2 | HG01074.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.685+2171A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119236484 | ||||||
| chr9:119236673
|
C | G | 1 | a0001c0003t0002g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.685+1982G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119236673 | ||||||
| chr9:119236788
|
T | C | 19 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(16): Show | 19 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.685+1867A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119236788 | ||||||
| chr9:119236910
|
A | C | 1 | a0001c0002t0001g0159 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.685+1745T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119236910 | ||||||
| chr9:119237049
|
T | C | 3 | a0001c0002t0001g0104a0001c0002t0001g0112a0001c0002t0001g0154 | 3 | HG02074.hp2 HG02129.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.685+1606A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237049 | ||||||
| chr9:119237289
|
G | A | 41 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.685+1366C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237289 | ||||||
| chr9:119237315
|
T | G | 1 | a0003c0008t0001g0174 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.685+1340A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237315 | ||||||
| chr9:119237346
|
C | CATTATT | 6 | a0001c0002t0001g0157a0001c0003t0001g0040a0001c0003t0001g0041others(3): Show | 6 | HG01884.hp2 HG02129.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.685+1303_685+1308d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | ||||||
| chr9:119237346
|
C | CATTATTA others(2): Show |
6 | a0001c0002t0004g0030a0001c0002t0004g0118a0001c0003t0001g0151others(3): Show | 6 | HG00423.hp1 HG01891.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.685+1300_685+1308d others(11): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | ||||||
| chr9:119237346
|
C | CATTATTA others(5): Show |
14 | a0001c0002t0001g0162a0001c0002t0001g0196a0001c0002t0002g0221others(11): Show | 14 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.685+1297_685+1308d others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | ||||||
| chr9:119237346
|
C | CATTATTA others(8): Show |
51 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0184others(48): Show | 51 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.685+1294_685+1308d others(17): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | ||||||
| chr9:119237346
|
C | CATTATTA others(11): Show |
27 | a0001c0001t0001g0200a0001c0001t0001g0212a0001c0001t0002g0235others(24): Show | 27 | HG01070.hp2 HG01123.hp1 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.685+1291_685+1308d others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | ||||||
| chr9:119237346
|
C | CATTATTA others(14): Show |
3 | a0001c0001t0001g0084a0001c0003t0001g0189a0001c0006t0001g0019 | 3 | HG01261.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.685+1288_685+1308d others(23): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | ||||||
| chr9:119237346
|
CATT | C | 41 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.685+1306_685+1308d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | ||||||
| chr9:119237346
|
CATTATT | C | 26 | a0001c0002t0001g0027a0001c0002t0001g0029a0001c0002t0001g0036others(23): Show | 26 | HG00140.hp2 HG01074.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.685+1303_685+1308d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237346 | ||||||
| chr9:119237375
|
T | TTATTATT others(4): Show |
3 | a0001c0002t0001g0097a0001c0002t0001g0142a0001c0015t0001g0133 | 3 | NA18961.hp2 NA19070.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.685+1279_685+1280i others(13): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237375 | ||||||
| chr9:119237376
|
T | TATTATTA others(6): Show |
1 | a0001c0005t0002g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.685+1278_685+1279i others(15): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237376 | ||||||
| chr9:119237378
|
T | A | 3 | a0001c0002t0001g0097a0001c0002t0001g0142a0001c0015t0001g0133 | 3 | NA18961.hp2 NA19070.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.685+1277A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237378 | ||||||
| chr9:119237487
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0003g0009a0001c0003t0001g0144 | 3 | HG00741.hp1 HG00741.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.685+1168G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237487 | ||||||
| chr9:119237566
|
G | A | 1 | a0001c0002t0001g0159 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.685+1089C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237566 | ||||||
| chr9:119237738
|
T | C | 5 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0099others(2): Show | 5 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.685+917A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237738 | ||||||
| chr9:119237764
|
C | T | 4 | a0001c0002t0001g0093a0001c0004t0001g0015a0001c0004t0001g0164others(1): Show | 4 | HG01169.hp2 HG02965.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.685+891G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237764 | ||||||
| chr9:119237796
|
G | A | 2 | a0001c0003t0001g0186a0001c0003t0008g0185 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.685+859C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119237796 | ||||||
| chr9:119238031
|
T | A | 1 | a0001c0001t0001g0120 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.685+624A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238031 | ||||||
| chr9:119238060
|
G | C | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.685+595C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238060 | ||||||
| chr9:119238185
|
TA | T | 89 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0027others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.685+469delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238185 | ||||||
| chr9:119238334
|
C | T | 2 | a0001c0003t0001g0198a0001c0003t0001g0208 | 2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.685+321G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238334 | ||||||
| chr9:119238339
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.685+316G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238339 | ||||||
| chr9:119238410
|
CCTTA | C | 89 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0027others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.685+241_685+244del others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238410 | ||||||
| chr9:119238553
|
TC | T | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.685+101delG | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238553 | ||||||
| chr9:119238584
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184 | 3 | HG01261.hp1 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.685+71T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 5/7 | chr9 | 119238584 | ||||||
| chr9:119238776
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0109 | 2 | HG01256.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.580-16T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119238776 | ||||||
| chr9:119238868
|
G | A | 12 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.580-108C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119238868 | ||||||
| chr9:119238951
|
G | C | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.580-191C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119238951 | ||||||
| chr9:119239006
|
G | A | 12 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-246C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119239006 | ||||||
| chr9:119239217
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.580-457G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119239217 | ||||||
| chr9:119239436
|
G | A | 178 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.580-676C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119239436 | ||||||
| chr9:119239551
|
T | C | 3 | a0001c0003t0001g0085a0001c0003t0001g0198a0001c0003t0001g0208 | 3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.580-791A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119239551 | ||||||
| chr9:119239777
|
C | T | 14 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(11): Show | 14 | HG00639.hp2 HG00735.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.580-1017G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119239777 | ||||||
| chr9:119239956
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.580-1196C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119239956 | ||||||
| chr9:119239998
|
C | T | 1 | a0001c0004t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.580-1238G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119239998 | ||||||
| chr9:119240105
|
C | T | 54 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.580-1345G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119240105 | ||||||
| chr9:119240140
|
G | A | 2 | a0003c0008t0001g0091a0003c0008t0001g0174 | 2 | NA18612.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.580-1380C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119240140 | ||||||
| chr9:119240612
|
A | T | 13 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(10): Show | 13 | HG00639.hp2 HG00735.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.579+1435T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119240612 | ||||||
| chr9:119240891
|
T | G | 1 | a0001c0001t0002g0231 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.579+1156A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119240891 | ||||||
| chr9:119241025
|
G | A | 4 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187others(1): Show | 4 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+1022C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241025 | ||||||
| chr9:119241141
|
T | C | 12 | a0001c0001t0001g0044a0001c0003t0001g0085a0001c0003t0001g0180others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+906A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241141 | ||||||
| chr9:119241289
|
C | A | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.579+758G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241289 | ||||||
| chr9:119241364
|
C | T | 1 | a0001c0002t0001g0071 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.579+683G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241364 | ||||||
| chr9:119241516
|
G | C | 2 | a0001c0003t0001g0198a0001c0003t0001g0208 | 2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.579+531C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241516 | ||||||
| chr9:119241669
|
G | A | 2 | a0001c0002t0001g0149a0001c0002t0001g0218 | 2 | NA18966.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.579+378C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241669 | ||||||
| chr9:119241750
|
A | G | 39 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(36): Show | 39 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.579+297T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241750 | ||||||
| chr9:119241798
|
T | C | 2 | a0001c0004t0001g0188a0001c0006t0002g0225 | 2 | HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.579+249A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241798 | ||||||
| chr9:119241877
|
T | C | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.579+170A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241877 | ||||||
| chr9:119241894
|
G | A | 12 | a0001c0001t0001g0044a0001c0003t0001g0085a0001c0003t0001g0180others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+153C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 4/7 | chr9 | 119241894 | ||||||
| chr9:119242267
|
GAGGACAG others(4): Show |
G | 72 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0027others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.410-62_410-52delAT others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242267 | ||||||
| chr9:119242538
|
C | T | 41 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(38): Show | 41 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.410-322G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242538 | ||||||
| chr9:119242560
|
A | G | 20 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(17): Show | 20 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.410-344T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242560 | ||||||
| chr9:119242684
|
CT | C | 19 | a0001c0002t0001g0093a0001c0002t0001g0202a0001c0002t0001g0203others(16): Show | 19 | HG01109.hp2 HG01123.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.410-469delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242684 | ||||||
| chr9:119242786
|
G | A | 1 | a0001c0002t0001g0077 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.410-570C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242786 | ||||||
| chr9:119242799
|
T | G | 3 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0009t0001g0191 | 3 | HG02809.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.410-583A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242799 | ||||||
| chr9:119242866
|
T | G | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.410-650A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242866 | ||||||
| chr9:119242979
|
CT | C | 145 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0084others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.410-764delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242979 | ||||||
| chr9:119242982
|
T | C | 20 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0200others(17): Show | 20 | HG00741.hp1 HG00741.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.410-766A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242982 | ||||||
| chr9:119242983
|
T | C | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.410-767A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119242983 | ||||||
| chr9:119243242
|
G | T | 15 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(12): Show | 15 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.410-1026C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119243242 | ||||||
| chr9:119243484
|
T | A | 70 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0027others(67): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.410-1268A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119243484 | ||||||
| chr9:119243682
|
C | T | 115 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.410-1466G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119243682 | ||||||
| chr9:119244225
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.410-2009C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119244225 | ||||||
| chr9:119244391
|
T | A | 1 | a0001c0003t0002g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.410-2175A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119244391 | ||||||
| chr9:119244515
|
G | A | 1 | a0001c0002t0001g0112 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.410-2299C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119244515 | ||||||
| chr9:119244626
|
G | C | 11 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.410-2410C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119244626 | ||||||
| chr9:119244696
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.410-2480T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119244696 | ||||||
| chr9:119244757
|
T | C | 1 | a0001c0003t0001g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.410-2541A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119244757 | ||||||
| chr9:119244793
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.410-2577G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119244793 | ||||||
| chr9:119245194
|
T | TAC | 4 | a0001c0001t0001g0176a0001c0003t0001g0189a0001c0003t0001g0197others(1): Show | 4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.410-2980_410-2979d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245194 | ||||||
| chr9:119245210
|
CACAT | C | 75 | a0001c0001t0001g0023a0001c0001t0001g0163a0001c0001t0003g0001others(72): Show | 75 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.410-2998_410-2995d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245210 | ||||||
| chr9:119245212
|
CAT | C | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.410-2998_410-2997d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245212 | ||||||
| chr9:119245437
|
G | A | 16 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(13): Show | 16 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.410-3221C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245437 | ||||||
| chr9:119245481
|
G | A | 1 | a0001c0002t0001g0218 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.410-3265C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245481 | ||||||
| chr9:119245485
|
T | C | 2 | a0001c0003t0001g0198a0001c0003t0001g0208 | 2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.410-3269A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245485 | ||||||
| chr9:119245532
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0106 | 2 | NA18970.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.410-3316G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245532 | ||||||
| chr9:119245616
|
AT | A | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.409+3343delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245616 | ||||||
| chr9:119245750
|
G | C | 1 | a0001c0003t0002g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.409+3210C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245750 | ||||||
| chr9:119245782
|
G | A | 138 | a0001c0001t0001g0023a0001c0001t0001g0043a0001c0001t0001g0044others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.409+3178C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119245782 | ||||||
| chr9:119246069
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.409+2891T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119246069 | ||||||
| chr9:119246417
|
C | T | 1 | a0001c0002t0001g0049 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.409+2543G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119246417 | ||||||
| chr9:119246456
|
A | G | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.409+2504T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119246456 | ||||||
| chr9:119246533
|
G | A | 45 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(42): Show | 45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.409+2427C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119246533 | ||||||
| chr9:119246627
|
C | T | 1 | a0001c0002t0001g0088 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.409+2333G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119246627 | ||||||
| chr9:119246895
|
G | A | 4 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0005t0001g0192others(1): Show | 4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+2065C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119246895 | ||||||
| chr9:119247302
|
C | CTGGT | 164 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.409+1654_409+1657d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247302 | ||||||
| chr9:119247454
|
C | G | 1 | a0001c0003t0001g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.409+1506G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247454 | ||||||
| chr9:119247487
|
T | TA | 45 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(42): Show | 45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.409+1472dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247487 | ||||||
| chr9:119247496
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.409+1464T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247496 | ||||||
| chr9:119247527
|
C | T | 5 | a0001c0003t0001g0094a0001c0003t0001g0151a0001c0003t0001g0186others(2): Show | 5 | HG01891.hp2 HG02886.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.409+1433G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247527 | ||||||
| chr9:119247528
|
G | C | 1 | a0001c0002t0006g0013 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.409+1432C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247528 | ||||||
| chr9:119247578
|
C | A | 42 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0039others(39): Show | 42 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.409+1382G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247578 | ||||||
| chr9:119247657
|
CA | C | 16 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(13): Show | 16 | HG00741.hp1 HG01515.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.409+1302delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247657 | ||||||
| chr9:119247657
|
CAA | C | 29 | a0001c0001t0001g0163a0001c0001t0002g0235a0001c0002t0001g0027others(26): Show | 29 | HG01074.hp1 HG01099.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.409+1301_409+1302d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247657 | ||||||
| chr9:119247657
|
CAAA | C | 30 | a0001c0001t0001g0043a0001c0001t0001g0078a0001c0001t0001g0084others(27): Show | 30 | HG00140.hp2 HG00280.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.409+1300_409+1302d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247657 | ||||||
| chr9:119247657
|
CAAAA | C | 93 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0035others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.409+1299_409+1302d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247657 | ||||||
| chr9:119247657
|
CAAAAA | C | 43 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0039others(40): Show | 43 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.409+1298_409+1302d others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247657 | ||||||
| chr9:119247657
|
CAAAAAA | C | 16 | a0001c0001t0001g0044a0001c0002t0004g0030a0001c0003t0001g0180others(13): Show | 16 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.409+1297_409+1302d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247657 | ||||||
| chr9:119247698
|
T | C | 7 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187others(4): Show | 7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.409+1262A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247698 | ||||||
| chr9:119247741
|
C | T | 2 | a0001c0002t0001g0145a0001c0015t0001g0133 | 2 | NA18948.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.409+1219G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247741 | ||||||
| chr9:119247842
|
A | G | 231 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.409+1118T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247842 | ||||||
| chr9:119247981
|
C | T | 231 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.409+979G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119247981 | ||||||
| chr9:119248081
|
T | C | 1 | a0001c0002t0001g0036 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.409+879A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119248081 | ||||||
| chr9:119248088
|
T | G | 3 | a0001c0003t0001g0085a0001c0003t0001g0198a0001c0003t0001g0208 | 3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.409+872A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119248088 | ||||||
| chr9:119248099
|
T | C | 14 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.409+861A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 3/7 | chr9 | 119248099 | ||||||
| chr9:119249278
|
G | C | 14 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.219-128C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249278 | ||||||
| chr9:119249751
|
A | C | 167 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.219-601T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249751 | ||||||
| chr9:119249770
|
G | A | 1 | a0001c0014t0003g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.219-620C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249770 | ||||||
| chr9:119249787
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0153 | 2 | HG00544.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.219-637C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249787 | ||||||
| chr9:119249805
|
T | TGGAA | 63 | a0001c0001t0001g0023a0001c0001t0001g0043a0001c0001t0001g0053others(60): Show | 63 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.219-659_219-656dup others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249805 | ||||||
| chr9:119249805
|
T | TGGAAGGA others(1): Show |
58 | a0001c0001t0001g0035a0001c0001t0001g0048a0001c0001t0001g0061others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(55): Show |
intron_variant | MODIFIER | c.219-663_219-656dup others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249805 | ||||||
| chr9:119249805
|
T | TGGAAGGA others(5): Show |
27 | a0001c0001t0001g0033a0001c0001t0001g0058a0001c0001t0001g0064others(24): Show | 27 | HG00423.hp1 HG00438.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.219-667_219-656dup others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249805 | ||||||
| chr9:119249805
|
T | TGGAAGGA others(9): Show |
10 | a0001c0001t0001g0055a0001c0001t0001g0106a0001c0001t0001g0160others(7): Show | 10 | HG01109.hp2 HG01169.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.219-671_219-656dup others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249805 | ||||||
| chr9:119249805
|
TGGAAGGA others(5): Show |
T | 1 | a0001c0003t0002g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.219-667_219-656del others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249805 | ||||||
| chr9:119249839
|
G | GAAGGAAG others(5): Show |
2 | a0001c0001t0001g0195a0001c0001t0001g0204 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.219-690_219-689ins others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249839 | ||||||
| chr9:119249839
|
G | GAAGGAAG others(17): Show |
1 | a0001c0001t0001g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.219-690_219-689ins others(24): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249839 | ||||||
| chr9:119249848
|
A | G | 1 | a0001c0009t0001g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.219-698T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249848 | ||||||
| chr9:119249852
|
A | AAGGAAGG others(9): Show |
2 | a0001c0001t0001g0046a0001c0001t0001g0194 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.219-703_219-702ins others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249852 | ||||||
| chr9:119249852
|
A | AAGGAAGG others(1): Show |
2 | a0001c0003t0001g0060a0001c0007t0001g0052 | 2 | HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.219-703_219-702ins others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249852 | ||||||
| chr9:119249852
|
A | G | 4 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0005t0001g0192others(1): Show | 4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-702T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249852 | ||||||
| chr9:119249852
|
AAGGG | A | 18 | a0001c0001t0001g0034a0001c0001t0001g0081a0001c0001t0001g0109others(15): Show | 18 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.219-706_219-703del others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249852 | ||||||
| chr9:119249852
|
AAGGGAGG others(1): Show |
A | 3 | a0001c0001t0001g0090a0001c0001t0001g0120a0001c0001t0002g0229 | 3 | HG02135.hp1 HG03098.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.219-710_219-703del others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249852 | ||||||
| chr9:119249853
|
A | AGGAAGGA others(34): Show |
1 | a0001c0003t0001g0190 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.219-704_219-703ins others(41): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249853 | ||||||
| chr9:119249853
|
A | AGGAAGGA others(30): Show |
1 | a0001c0005t0001g0201 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.219-704_219-703ins others(37): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249853 | ||||||
| chr9:119249853
|
A | AGGAAGGA others(34): Show |
1 | a0001c0003t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-704_219-703ins others(41): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249853 | ||||||
| chr9:119249853
|
A | AGGAAGGA others(26): Show |
3 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0009g0214 | 3 | HG01884.hp1 HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.219-704_219-703ins others(33): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249853 | ||||||
| chr9:119249853
|
A | AGGAAGGA others(30): Show |
1 | a0001c0005t0001g0199 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.219-704_219-703ins others(37): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249853 | ||||||
| chr9:119249853
|
A | AGGAAGGA others(22): Show |
2 | a0001c0003t0001g0209a0001c0003t0002g0224 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.219-704_219-703ins others(29): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249853 | ||||||
| chr9:119249856
|
G | A | 111 | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0039others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.219-706C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249856 | ||||||
| chr9:119249860
|
G | A | 115 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0037others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.219-710C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249860 | ||||||
| chr9:119249860
|
G | GAGGGAGG others(6): Show |
3 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0005t0001g0192 | 3 | HG02809.hp1 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.219-723_219-711dup others(13): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249860 | ||||||
| chr9:119249864
|
G | A | 1 | a0001c0002t0001g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.219-714C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249864 | ||||||
| chr9:119249871
|
G | A | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-721C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249871 | ||||||
| chr9:119249876
|
GA | G | 9 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-727delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249876 | ||||||
| chr9:119249877
|
A | AGGG | 4 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0005t0001g0192others(1): Show | 4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-728_219-727ins others(3): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249877 | ||||||
| chr9:119249877
|
A | AGGGAGGG others(21): Show |
1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.219-728_219-727ins others(28): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249877 | ||||||
| chr9:119249913
|
G | A | 115 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0037others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.219-763C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249913 | ||||||
| chr9:119249916
|
T | TGAAGGGA others(65): Show |
3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-838_219-767dup others(72): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249916 | ||||||
| chr9:119249938
|
A | AAGGGAAG others(69): Show |
2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-864_219-789dup others(76): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119249938 | ||||||
| chr9:119250049
|
A | G | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-899T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250049 | ||||||
| chr9:119250071
|
A | C | 2 | a0001c0002t0001g0093a0001c0004t0001g0015 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.219-921T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250071 | ||||||
| chr9:119250081
|
A | G | 45 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(42): Show | 45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-931T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250081 | ||||||
| chr9:119250082
|
A | G | 45 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(42): Show | 45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-932T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250082 | ||||||
| chr9:119250085
|
G | A | 45 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(42): Show | 45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-935C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250085 | ||||||
| chr9:119250086
|
A | G | 45 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(42): Show | 45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-936T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250086 | ||||||
| chr9:119250090
|
A | G | 45 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(42): Show | 45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-940T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250090 | ||||||
| chr9:119250092
|
GGAAGGA | G | 45 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(42): Show | 45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-948_219-943del others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250092 | ||||||
| chr9:119250102
|
A | G | 45 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(42): Show | 45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-952T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250102 | ||||||
| chr9:119250104
|
A | AGGAAGGA others(9): Show |
1 | a0001c0003t0001g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.219-970_219-955dup others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250104 | ||||||
| chr9:119250104
|
AGGAAGG | A | 45 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(42): Show | 45 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-960_219-955del others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250104 | ||||||
| chr9:119250124
|
AGGAG | A | 3 | a0001c0002t0001g0149a0001c0004t0001g0016a0001c0004t0002g0232 | 3 | HG02976.hp1 HG03195.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.219-978_219-975del others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250124 | ||||||
| chr9:119250168
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.219-1018C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250168 | ||||||
| chr9:119250365
|
T | C | 118 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0037others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.219-1215A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250365 | ||||||
| chr9:119250494
|
A | G | 3 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204 | 3 | HG02145.hp1 HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.219-1344T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250494 | ||||||
| chr9:119250502
|
T | A | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-1352A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250502 | ||||||
| chr9:119250679
|
C | T | 1 | a0001c0003t0001g0208 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.219-1529G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250679 | ||||||
| chr9:119250978
|
G | A | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-1828C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119250978 | ||||||
| chr9:119251244
|
C | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204 | 3 | HG02145.hp1 HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.219-2094G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251244 | ||||||
| chr9:119251361
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.219-2211G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251361 | ||||||
| chr9:119251476
|
T | C | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-2326A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251476 | ||||||
| chr9:119251544
|
T | A | 171 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.219-2394A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251544 | ||||||
| chr9:119251613
|
C | CA | 24 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0056others(21): Show | 24 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.219-2464dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251613 | ||||||
| chr9:119251665
|
G | A | 10 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-2515C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251665 | ||||||
| chr9:119251669
|
A | C | 1 | a0001c0001t0001g0140 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219-2519T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251669 | ||||||
| chr9:119251670
|
C | G | 1 | a0001c0001t0001g0140 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219-2520G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251670 | ||||||
| chr9:119251671
|
A | G | 181 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.219-2521T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251671 | ||||||
| chr9:119251671
|
A | T | 1 | a0001c0001t0001g0140 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219-2521T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251671 | ||||||
| chr9:119251672
|
T | TTA | 171 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.219-2523_219-2522i others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251672 | ||||||
| chr9:119251692
|
T | G | 49 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(46): Show | 49 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.219-2542A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251692 | ||||||
| chr9:119251693
|
AG | A | 173 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.219-2544delC | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251693 | ||||||
| chr9:119251693
|
AGGGG | A | 10 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-2547_219-2544d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251693 | ||||||
| chr9:119251749
|
T | C | 183 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.219-2599A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251749 | ||||||
| chr9:119251750
|
G | C | 1 | a0001c0001t0001g0140 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219-2600C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251750 | ||||||
| chr9:119251968
|
C | G | 3 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204 | 3 | HG02145.hp1 HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.219-2818G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119251968 | ||||||
| chr9:119252033
|
C | T | 3 | a0001c0003t0001g0085a0001c0003t0001g0198a0001c0003t0001g0208 | 3 | HG01884.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.219-2883G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252033 | ||||||
| chr9:119252059
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.219-2909G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252059 | ||||||
| chr9:119252061
|
C | T | 172 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.219-2911G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252061 | ||||||
| chr9:119252161
|
G | A | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-3011C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252161 | ||||||
| chr9:119252477
|
T | C | 1 | a0001c0003t0001g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.219-3327A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252477 | ||||||
| chr9:119252488
|
TTA | T | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-3340_219-3339d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252488 | ||||||
| chr9:119252553
|
C | T | 49 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(46): Show | 49 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.219-3403G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252553 | ||||||
| chr9:119252553
|
CGT | C | 28 | a0001c0001t0001g0163a0001c0001t0002g0234a0001c0001t0002g0235others(25): Show | 28 | HG00140.hp2 HG01074.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.219-3405_219-3404d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252553 | ||||||
| chr9:119252574
|
A | T | 4 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0005t0001g0192others(1): Show | 4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-3424T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252574 | ||||||
| chr9:119252862
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219-3712A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252862 | ||||||
| chr9:119252890
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.219-3740C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252890 | ||||||
| chr9:119252944
|
C | T | 2 | a0001c0003t0001g0193a0001c0003t0001g0211 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.219-3794G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119252944 | ||||||
| chr9:119253110
|
G | C | 2 | a0001c0001t0001g0048a0001c0001t0003g0009 | 2 | HG00741.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.219-3960C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119253110 | ||||||
| chr9:119253137
|
G | C | 3 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204 | 3 | HG02145.hp1 HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.219-3987C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119253137 | ||||||
| chr9:119253548
|
A | T | 1 | a0001c0002t0001g0024 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.219-4398T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119253548 | ||||||
| chr9:119253864
|
A | G | 1 | a0001c0002t0006g0013 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.219-4714T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119253864 | ||||||
| chr9:119253906
|
T | G | 1 | a0001c0001t0001g0140 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219-4756A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119253906 | ||||||
| chr9:119253955
|
T | C | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-4805A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119253955 | ||||||
| chr9:119253983
|
T | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0158 | 2 | HG01069.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.219-4833A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119253983 | ||||||
| chr9:119254013
|
T | G | 1 | a0001c0001t0001g0076 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.219-4863A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254013 | ||||||
| chr9:119254030
|
A | C | 1 | a0001c0002t0006g0013 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.219-4880T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254030 | ||||||
| chr9:119254166
|
A | G | 1 | a0001c0002t0001g0127 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.219-5016T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254166 | ||||||
| chr9:119254315
|
A | G | 29 | a0001c0001t0001g0123a0001c0001t0001g0163a0001c0001t0002g0234others(26): Show | 29 | HG00140.hp2 HG01074.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.219-5165T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254315 | ||||||
| chr9:119254378
|
C | T | 40 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0039others(37): Show | 40 | HG00423.hp2 HG00544.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.219-5228G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254378 | ||||||
| chr9:119254407
|
G | A | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-5257C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254407 | ||||||
| chr9:119254474
|
T | C | 1 | a0001c0002t0001g0116 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.219-5324A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254474 | ||||||
| chr9:119254680
|
G | A | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.219-5530C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254680 | ||||||
| chr9:119254689
|
G | A | 6 | a0001c0001t0001g0048a0001c0001t0001g0212a0001c0001t0003g0008others(3): Show | 6 | HG00741.hp1 HG01515.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-5539C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254689 | ||||||
| chr9:119254811
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.219-5661A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254811 | ||||||
| chr9:119254812
|
G | A | 28 | a0001c0001t0001g0163a0001c0001t0002g0234a0001c0001t0002g0235others(25): Show | 28 | HG00140.hp2 HG01074.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.219-5662C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254812 | ||||||
| chr9:119254950
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.219-5800C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119254950 | ||||||
| chr9:119255080
|
T | TA | 5 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0005t0001g0192others(2): Show | 5 | HG02622.hp2 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-5931dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255080 | ||||||
| chr9:119255184
|
G | T | 9 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(6): Show | 9 | HG00639.hp2 HG00735.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.219-6034C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255184 | ||||||
| chr9:119255512
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.219-6362G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255512 | ||||||
| chr9:119255513
|
G | A | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-6363C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255513 | ||||||
| chr9:119255596
|
G | C | 17 | a0001c0002t0001g0093a0001c0002t0001g0202a0001c0002t0001g0203others(14): Show | 17 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.219-6446C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255596 | ||||||
| chr9:119255615
|
G | T | 214 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.219-6465C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255615 | ||||||
| chr9:119255656
|
C | T | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.219-6506G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255656 | ||||||
| chr9:119255687
|
C | G | 1 | a0001c0002t0001g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.219-6537G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255687 | ||||||
| chr9:119255782
|
C | G | 34 | a0001c0001t0001g0044a0001c0002t0001g0093a0001c0002t0001g0202others(31): Show | 34 | HG01109.hp2 HG01123.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.219-6632G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255782 | ||||||
| chr9:119255815
|
C | T | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-6665G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255815 | ||||||
| chr9:119255835
|
G | C | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-6685C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255835 | ||||||
| chr9:119255897
|
G | C | 4 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0005t0001g0192others(1): Show | 4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-6747C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255897 | ||||||
| chr9:119255904
|
G | A | 14 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.219-6754C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255904 | ||||||
| chr9:119255909
|
C | T | 133 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0037others(130): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.219-6759G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255909 | ||||||
| chr9:119255912
|
G | A | 4 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0005t0001g0192others(1): Show | 4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-6762C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255912 | ||||||
| chr9:119255954
|
C | CA | 7 | a0001c0001t0001g0048a0001c0001t0001g0195a0001c0001t0003g0009others(4): Show | 7 | HG00741.hp1 HG01515.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-6805dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255954 | ||||||
| chr9:119255954
|
CA | C | 24 | a0001c0001t0001g0056a0001c0001t0001g0064a0001c0001t0001g0067others(21): Show | 24 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.219-6805delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255954 | ||||||
| chr9:119255954
|
CAA | C | 83 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.219-6806_219-6805d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255954 | ||||||
| chr9:119255954
|
CAAA | C | 85 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0053others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.219-6807_219-6805d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255954 | ||||||
| chr9:119255954
|
CAAAAAA | C | 10 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-6810_219-6805d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119255954 | ||||||
| chr9:119256013
|
G | A | 1 | a0001c0002t0001g0112 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.219-6863C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256013 | ||||||
| chr9:119256047
|
G | A | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-6897C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256047 | ||||||
| chr9:119256192
|
C | T | 2 | a0001c0003t0001g0193a0001c0003t0001g0211 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.219-7042G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256192 | ||||||
| chr9:119256310
|
T | C | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-7160A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256310 | ||||||
| chr9:119256413
|
G | A | 2 | a0001c0001t0001g0132a0001c0003t0001g0144 | 2 | HG00741.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.219-7263C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256413 | ||||||
| chr9:119256518
|
C | G | 3 | a0001c0001t0001g0053a0001c0001t0001g0069a0001c0002t0001g0196 | 3 | HG00099.hp2 HG00280.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.219-7368G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256518 | ||||||
| chr9:119256526
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.219-7376T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256526 | ||||||
| chr9:119256588
|
T | G | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-7438A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256588 | ||||||
| chr9:119256819
|
TAATC | T | 2 | a0001c0002t0001g0070a0001c0002t0001g0171 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.219-7673_219-7670d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256819 | ||||||
| chr9:119256941
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.219-7791G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119256941 | ||||||
| chr9:119257060
|
T | C | 17 | a0001c0002t0001g0093a0001c0002t0001g0202a0001c0002t0001g0203others(14): Show | 17 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.219-7910A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257060 | ||||||
| chr9:119257156
|
A | T | 4 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0005t0001g0192others(1): Show | 4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-8006T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257156 | ||||||
| chr9:119257217
|
A | G | 1 | a0001c0001t0002g0231 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.219-8067T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257217 | ||||||
| chr9:119257248
|
A | G | 13 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(10): Show | 13 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.219-8098T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257248 | ||||||
| chr9:119257302
|
G | C | 2 | a0001c0001t0001g0172a0001c0003t0002g0226 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.219-8152C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257302 | ||||||
| chr9:119257631
|
A | C | 20 | a0001c0002t0001g0093a0001c0002t0001g0202a0001c0002t0001g0203others(17): Show | 20 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.219-8481T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257631 | ||||||
| chr9:119257781
|
C | T | 17 | a0001c0002t0001g0093a0001c0002t0001g0202a0001c0002t0001g0203others(14): Show | 17 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.219-8631G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257781 | ||||||
| chr9:119257782
|
G | A | 1 | a0001c0002t0001g0029 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.219-8632C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257782 | ||||||
| chr9:119257867
|
A | G | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-8717T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257867 | ||||||
| chr9:119257902
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0148 | 3 | HG01346.hp1 HG01975.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.219-8752G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257902 | ||||||
| chr9:119257918
|
G | C | 1 | a0001c0001t0002g0235 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.219-8768C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257918 | ||||||
| chr9:119257923
|
A | T | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-8773T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119257923 | ||||||
| chr9:119258401
|
G | C | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.219-9251C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258401 | ||||||
| chr9:119258417
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0003g0009 | 2 | HG00741.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.219-9267G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258417 | ||||||
| chr9:119258420
|
T | C | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-9270A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258420 | ||||||
| chr9:119258506
|
T | A | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-9356A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258506 | ||||||
| chr9:119258507
|
G | T | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-9357C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258507 | ||||||
| chr9:119258604
|
G | A | 30 | a0001c0001t0001g0044a0001c0002t0001g0093a0001c0002t0001g0202others(27): Show | 30 | HG01109.hp2 HG01123.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.219-9454C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258604 | ||||||
| chr9:119258615
|
C | T | 43 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(40): Show | 43 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.219-9465G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258615 | ||||||
| chr9:119258618
|
A | G | 2 | a0001c0003t0001g0107a0001c0003t0001g0139 | 2 | NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.219-9468T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258618 | ||||||
| chr9:119258654
|
T | C | 1 | a0001c0002t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.219-9504A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258654 | ||||||
| chr9:119258667
|
G | T | 10 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-9517C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258667 | ||||||
| chr9:119258681
|
G | C | 1 | a0001c0002t0001g0077 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.219-9531C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258681 | ||||||
| chr9:119258923
|
T | G | 1 | a0001c0003t0001g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.219-9773A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119258923 | ||||||
| chr9:119259610
|
G | A | 1 | a0001c0004t0002g0232 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.219-10460C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119259610 | ||||||
| chr9:119259847
|
T | G | 3 | a0001c0003t0001g0045a0001c0003t0001g0047a0001c0003t0001g0213 | 3 | HG02451.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.219-10697A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119259847 | ||||||
| chr9:119260250
|
C | T | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-11100G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119260250 | ||||||
| chr9:119260540
|
G | A | 1 | a0001c0006t0001g0017 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.219-11390C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119260540 | ||||||
| chr9:119260574
|
T | G | 21 | a0001c0002t0001g0093a0001c0002t0001g0202a0001c0002t0001g0203others(18): Show | 21 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.219-11424A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119260574 | ||||||
| chr9:119260581
|
A | G | 2 | a0001c0003t0001g0175a0001c0003t0001g0207 | 2 | HG01496.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.219-11431T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119260581 | ||||||
| chr9:119260838
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0003g0008a0001c0001t0003g0009others(2): Show | 5 | HG00741.hp1 HG01515.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-11688C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119260838 | ||||||
| chr9:119260893
|
G | A | 1 | a0001c0002t0001g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.219-11743C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119260893 | ||||||
| chr9:119260967
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.219-11817A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119260967 | ||||||
| chr9:119261221
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.219-12071C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261221 | ||||||
| chr9:119261258
|
G | A | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-12108C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261258 | ||||||
| chr9:119261283
|
G | T | 2 | a0001c0003t0001g0193a0001c0003t0001g0211 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.219-12133C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261283 | ||||||
| chr9:119261296
|
T | C | 212 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.219-12146A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261296 | ||||||
| chr9:119261380
|
T | C | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-12230A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261380 | ||||||
| chr9:119261516
|
A | C | 18 | a0001c0002t0001g0093a0001c0002t0001g0202a0001c0002t0001g0203others(15): Show | 18 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.219-12366T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261516 | ||||||
| chr9:119261517
|
G | C | 18 | a0001c0002t0001g0093a0001c0002t0001g0202a0001c0002t0001g0203others(15): Show | 18 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.219-12367C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261517 | ||||||
| chr9:119261544
|
C | T | 1 | a0001c0002t0001g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.219-12394G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261544 | ||||||
| chr9:119261788
|
T | C | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-12638A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261788 | ||||||
| chr9:119261861
|
C | T | 10 | a0001c0001t0001g0044a0001c0003t0001g0085a0001c0003t0001g0180others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-12711G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261861 | ||||||
| chr9:119261943
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0158 | 2 | HG01069.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.219-12793A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261943 | ||||||
| chr9:119261945
|
G | A | 1 | a0001c0002t0001g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.219-12795C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119261945 | ||||||
| chr9:119262083
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.219-12933T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262083 | ||||||
| chr9:119262179
|
A | G | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-13029T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262179 | ||||||
| chr9:119262521
|
C | T | 1 | a0001c0003t0008g0185 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.219-13371G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262521 | ||||||
| chr9:119262621
|
G | C | 1 | a0001c0001t0002g0231 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.219-13471C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262621 | ||||||
| chr9:119262632
|
C | A | 1 | a0001c0003t0001g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.219-13482G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262632 | ||||||
| chr9:119262645
|
C | CA | 6 | a0001c0001t0001g0204a0001c0001t0001g0212a0001c0001t0002g0229others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-13496dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262645 | ||||||
| chr9:119262645
|
CA | C | 177 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.219-13496delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262645 | ||||||
| chr9:119262689
|
C | A | 2 | a0001c0003t0001g0198a0001c0003t0001g0208 | 2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.219-13539G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262689 | ||||||
| chr9:119262957
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.219-13807T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262957 | ||||||
| chr9:119262971
|
C | G | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-13821G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262971 | ||||||
| chr9:119262981
|
A | G | 18 | a0001c0002t0001g0093a0001c0002t0001g0202a0001c0002t0001g0203others(15): Show | 18 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.219-13831T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119262981 | ||||||
| chr9:119263106
|
G | T | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-13956C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263106 | ||||||
| chr9:119263158
|
G | A | 13 | a0001c0001t0003g0001a0001c0002t0001g0070a0001c0002t0001g0162others(10): Show | 13 | HG00140.hp1 HG00738.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.219-14008C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263158 | ||||||
| chr9:119263180
|
C | G | 212 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.219-14030G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263180 | ||||||
| chr9:119263472
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.219-14322C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263472 | ||||||
| chr9:119263525
|
T | C | 25 | a0001c0002t0001g0093a0001c0002t0001g0202a0001c0002t0001g0203others(22): Show | 25 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.219-14375A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263525 | ||||||
| chr9:119263544
|
A | G | 36 | a0001c0001t0001g0044a0001c0002t0001g0093a0001c0002t0001g0202others(33): Show | 36 | HG01109.hp2 HG01123.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.219-14394T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263544 | ||||||
| chr9:119263567
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.219-14417A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263567 | ||||||
| chr9:119263601
|
C | CT | 5 | a0001c0001t0001g0048a0001c0001t0001g0204a0001c0003t0001g0186others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-14452dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263601 | ||||||
| chr9:119263601
|
C | CTTT | 94 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0039others(91): Show | 94 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.219-14454_219-1445 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263601 | ||||||
| chr9:119263601
|
C | CTTTT | 77 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0043others(74): Show | 77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.219-14455_219-1445 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263601 | ||||||
| chr9:119263601
|
C | CTTTTT | 25 | a0001c0001t0001g0023a0001c0001t0002g0229a0001c0002t0001g0057others(22): Show | 25 | HG00423.hp1 HG00738.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.219-14456_219-1445 others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263601 | ||||||
| chr9:119263601
|
C | CTTTTTT | 9 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0002g0221others(6): Show | 9 | HG01106.hp1 HG01109.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.219-14457_219-1445 others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263601 | ||||||
| chr9:119263708
|
C | T | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-14558G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263708 | ||||||
| chr9:119263764
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.219-14614G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263764 | ||||||
| chr9:119263845
|
T | C | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.219-14695A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263845 | ||||||
| chr9:119263854
|
C | A | 44 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(41): Show | 44 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.219-14704G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119263854 | ||||||
| chr9:119264085
|
A | T | 1 | a0001c0003t0002g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.219-14935T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119264085 | ||||||
| chr9:119264125
|
T | A | 172 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.219-14975A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119264125 | ||||||
| chr9:119264247
|
C | A | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-15097G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119264247 | ||||||
| chr9:119264421
|
A | T | 10 | a0001c0001t0001g0044a0001c0003t0001g0085a0001c0003t0001g0180others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-15271T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119264421 | ||||||
| chr9:119264717
|
C | T | 1 | a0001c0002t0001g0169 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.219-15567G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119264717 | ||||||
| chr9:119264878
|
G | A | 1 | a0001c0002t0003g0005 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.219-15728C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119264878 | ||||||
| chr9:119265016
|
C | T | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-15866G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265016 | ||||||
| chr9:119265034
|
T | C | 3 | a0001c0002t0001g0070a0001c0002t0001g0171a0001c0002t0003g0002 | 3 | HG01106.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.219-15884A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265034 | ||||||
| chr9:119265065
|
T | C | 3 | a0001c0004t0001g0026a0001c0004t0001g0028a0001c0004t0001g0072 | 3 | HG01069.hp1 HG01071.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.219-15915A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265065 | ||||||
| chr9:119265350
|
G | A | 212 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.219-16200C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265350 | ||||||
| chr9:119265443
|
A | AT | 2 | a0001c0001t0001g0046a0001c0001t0001g0194 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.219-16294dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265443 | ||||||
| chr9:119265445
|
A | T | 171 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.219-16295T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265445 | ||||||
| chr9:119265446
|
A | T | 1 | a0001c0002t0001g0149 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.219-16296T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265446 | ||||||
| chr9:119265591
|
C | T | 3 | a0001c0001t0002g0231a0001c0003t0002g0233a0001c0005t0002g0236 | 3 | HG01109.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.219-16441G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265591 | ||||||
| chr9:119265720
|
A | G | 2 | a0001c0003t0001g0193a0001c0003t0001g0211 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.219-16570T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265720 | ||||||
| chr9:119265733
|
A | T | 215 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.219-16583T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265733 | ||||||
| chr9:119265808
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.219-16658C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265808 | ||||||
| chr9:119265869
|
C | T | 10 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-16719G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265869 | ||||||
| chr9:119265882
|
G | A | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-16732C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119265882 | ||||||
| chr9:119266266
|
C | T | 2 | a0001c0003t0001g0193a0001c0003t0001g0211 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.219-17116G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119266266 | ||||||
| chr9:119266345
|
G | A | 1 | a0001c0002t0004g0118 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.219-17195C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119266345 | ||||||
| chr9:119266511
|
G | T | 13 | a0001c0001t0003g0001a0001c0002t0001g0070a0001c0002t0001g0162others(10): Show | 13 | HG00140.hp1 HG00738.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.219-17361C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119266511 | ||||||
| chr9:119266674
|
C | T | 4 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0005t0001g0192others(1): Show | 4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-17524G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119266674 | ||||||
| chr9:119266681
|
C | T | 79 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(76): Show | 79 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.219-17531G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119266681 | ||||||
| chr9:119266810
|
T | A | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-17660A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119266810 | ||||||
| chr9:119267095
|
T | C | 1 | a0001c0002t0003g0005 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.219-17945A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267095 | ||||||
| chr9:119267382
|
C | A | 5 | a0001c0001t0002g0231a0001c0003t0001g0193a0001c0003t0001g0211others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-18232G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267382 | ||||||
| chr9:119267402
|
A | G | 52 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(49): Show | 52 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.219-18252T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267402 | ||||||
| chr9:119267428
|
T | A | 52 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(49): Show | 52 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.219-18278A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267428 | ||||||
| chr9:119267445
|
G | A | 1 | a0001c0003t0001g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.219-18295C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267445 | ||||||
| chr9:119267584
|
C | T | 1 | a0003c0008t0001g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.219-18434G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267584 | ||||||
| chr9:119267601
|
A | T | 1 | a0001c0003t0002g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.219-18451T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267601 | ||||||
| chr9:119267612
|
G | A | 9 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-18462C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267612 | ||||||
| chr9:119267636
|
C | CAATA | 51 | a0001c0001t0001g0023a0001c0001t0001g0080a0001c0001t0001g0081others(48): Show | 51 | HG00280.hp1 HG00423.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.219-18490_219-1848 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267636 | ||||||
| chr9:119267636
|
C | CAATAAAT others(1): Show |
22 | a0001c0001t0001g0065a0001c0001t0001g0103a0001c0001t0001g0153others(19): Show | 22 | HG00544.hp2 HG01109.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.219-18494_219-1848 others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267636 | ||||||
| chr9:119267636
|
C | CAATAAAT others(5): Show |
1 | a0001c0015t0001g0133 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.219-18498_219-1848 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267636 | ||||||
| chr9:119267636
|
CAATA | C | 26 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0053others(23): Show | 26 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.219-18490_219-1848 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267636 | ||||||
| chr9:119267636
|
CAATAAAT others(1): Show |
C | 19 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(16): Show | 19 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-18494_219-1848 others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267636 | ||||||
| chr9:119267636
|
CAATAAAT others(5): Show |
C | 3 | a0001c0004t0001g0016a0001c0004t0002g0232a0001c0006t0001g0017 | 3 | HG02976.hp1 HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.219-18498_219-1848 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267636 | ||||||
| chr9:119267636
|
CAATAAAT others(17): Show |
C | 46 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(43): Show | 46 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.219-18510_219-1848 others(28): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267636 | ||||||
| chr9:119267733
|
A | G | 1 | a0001c0002t0001g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.219-18583T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267733 | ||||||
| chr9:119267786
|
G | A | 26 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0002t0001g0027others(23): Show | 26 | HG00140.hp2 HG01074.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.219-18636C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267786 | ||||||
| chr9:119267798
|
C | T | 46 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(43): Show | 46 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.219-18648G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267798 | ||||||
| chr9:119267900
|
G | C | 46 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(43): Show | 46 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.219-18750C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267900 | ||||||
| chr9:119267989
|
T | C | 17 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(14): Show | 17 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.219-18839A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119267989 | ||||||
| chr9:119268052
|
A | G | 219 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.219-18902T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268052 | ||||||
| chr9:119268088
|
C | A | 5 | a0001c0001t0002g0231a0001c0003t0001g0193a0001c0003t0001g0211others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-18938G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268088 | ||||||
| chr9:119268199
|
C | T | 1 | a0001c0005t0002g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.219-19049G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268199 | ||||||
| chr9:119268201
|
T | C | 209 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.219-19051A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268201 | ||||||
| chr9:119268243
|
A | AATATAGA others(3): Show |
1 | a0001c0001t0001g0124 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.219-19094_219-1909 others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268243 | ||||||
| chr9:119268243
|
A | AATATAGA others(7): Show |
2 | a0001c0001t0001g0054a0001c0001t0001g0103 | 2 | HG03834.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.219-19094_219-1909 others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268243 | ||||||
| chr9:119268247
|
A | AATAG | 3 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0004t0002g0232 | 3 | HG00738.hp2 HG01106.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.219-19101_219-1909 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268247 | ||||||
| chr9:119268247
|
A | G | 5 | a0001c0001t0001g0054a0001c0001t0001g0103a0001c0001t0001g0124others(2): Show | 5 | HG00639.hp1 HG02698.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-19097T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268247 | ||||||
| chr9:119268247
|
AATAG | A | 66 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0044others(63): Show | 66 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.219-19101_219-1909 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268247 | ||||||
| chr9:119268247
|
AATAGATA others(1): Show |
A | 21 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0056others(18): Show | 21 | HG00438.hp2 HG00735.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.219-19105_219-1909 others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268247 | ||||||
| chr9:119268247
|
AATAGATA others(5): Show |
A | 2 | a0001c0001t0001g0067a0001c0003t0002g0227 | 2 | HG01069.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.219-19109_219-1909 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268247 | ||||||
| chr9:119268285
|
T | C | 3 | a0001c0001t0001g0054a0001c0001t0001g0103a0001c0001t0001g0163 | 3 | HG03017.hp1 HG03834.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.219-19135A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | ||||||
| chr9:119268285
|
T | TAGAC | 4 | a0001c0001t0001g0132a0001c0002t0001g0027a0001c0002t0001g0068others(1): Show | 4 | HG01243.hp2 HG04184.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-19136_219-1913 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | ||||||
| chr9:119268285
|
T | TAGATAGA others(1): Show |
9 | a0001c0001t0001g0039a0001c0001t0001g0102a0001c0001t0001g0148others(6): Show | 9 | HG00280.hp1 HG01255.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.219-19136_219-1913 others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | ||||||
| chr9:119268285
|
T | TAGATAGA others(5): Show |
72 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0053others(69): Show | 72 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.219-19136_219-1913 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | ||||||
| chr9:119268285
|
T | TAGATAGA others(9): Show |
21 | a0001c0001t0001g0023a0001c0001t0001g0069a0001c0001t0001g0090others(18): Show | 21 | HG00099.hp2 HG01099.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.219-19136_219-1913 others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | ||||||
| chr9:119268285
|
T | TAGATAGA others(13): Show |
1 | a0001c0002t0003g0012 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.219-19136_219-1913 others(24): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | ||||||
| chr9:119268285
|
T | TAGATAGA others(13): Show |
7 | a0001c0001t0001g0080a0001c0001t0001g0153a0001c0002t0001g0070others(4): Show | 7 | HG01257.hp1 HG01258.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-19136_219-1913 others(24): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | ||||||
| chr9:119268285
|
T | TAGATAGA others(17): Show |
2 | a0001c0002t0001g0088a0001c0002t0001g0131 | 2 | NA18747.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.219-19136_219-1913 others(28): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268285 | ||||||
| chr9:119268289
|
T | C | 1 | a0001c0002t0003g0002 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.219-19139A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268289 | ||||||
| chr9:119268289
|
T | TAGATAGA others(5): Show |
2 | a0001c0001t0001g0170a0001c0003t0001g0198 | 2 | HG00544.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.219-19140_219-1913 others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268289 | ||||||
| chr9:119268289
|
T | TAGATAGA others(9): Show |
2 | a0001c0003t0001g0208a0001c0014t0003g0004 | 2 | HG00738.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.219-19140_219-1913 others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268289 | ||||||
| chr9:119268345
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.219-19195G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268345 | ||||||
| chr9:119268495
|
G | T | 1 | a0001c0002t0001g0077 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.219-19345C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268495 | ||||||
| chr9:119268538
|
A | C | 52 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(49): Show | 52 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.219-19388T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268538 | ||||||
| chr9:119268693
|
G | A | 2 | a0001c0004t0001g0016a0001c0004t0002g0232 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-19543C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268693 | ||||||
| chr9:119268705
|
G | A | 157 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0037others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.219-19555C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119268705 | ||||||
| chr9:119269090
|
C | G | 4 | a0001c0001t0002g0231a0001c0003t0001g0211a0001c0003t0002g0233others(1): Show | 4 | HG01109.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-19940G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269090 | ||||||
| chr9:119269159
|
A | G | 4 | a0001c0001t0002g0231a0001c0003t0001g0211a0001c0003t0002g0233others(1): Show | 4 | HG01109.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-20009T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269159 | ||||||
| chr9:119269224
|
TCACTATT others(7): Show |
T | 1 | a0001c0004t0001g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.219-20088_219-2007 others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269224 | ||||||
| chr9:119269225
|
C | T | 208 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.219-20075G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269225 | ||||||
| chr9:119269239
|
C | T | 1 | a0001c0004t0001g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.219-20089G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269239 | ||||||
| chr9:119269270
|
A | C | 1 | a0001c0002t0001g0168 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.219-20120T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269270 | ||||||
| chr9:119269325
|
T | C | 52 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(49): Show | 52 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.219-20175A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269325 | ||||||
| chr9:119269399
|
T | C | 2 | a0003c0008t0001g0091a0003c0008t0001g0174 | 2 | NA18612.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.219-20249A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269399 | ||||||
| chr9:119269443
|
T | C | 3 | a0001c0002t0001g0114a0001c0003t0001g0040a0001c0003t0001g0041 | 3 | HG02896.hp1 HG02897.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.219-20293A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269443 | ||||||
| chr9:119269449
|
T | A | 1 | a0001c0002t0001g0168 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.219-20299A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269449 | ||||||
| chr9:119269503
|
T | C | 9 | a0001c0001t0001g0044a0001c0003t0001g0085a0001c0003t0001g0180others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-20353A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269503 | ||||||
| chr9:119269625
|
A | C | 1 | a0001c0003t0001g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.219-20475T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269625 | ||||||
| chr9:119269752
|
C | T | 4 | a0001c0001t0002g0231a0001c0003t0001g0211a0001c0003t0002g0233others(1): Show | 4 | HG01109.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-20602G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269752 | ||||||
| chr9:119269822
|
G | A | 6 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0004t0001g0016others(3): Show | 6 | HG02809.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-20672C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269822 | ||||||
| chr9:119269824
|
A | G | 5 | a0001c0001t0002g0231a0001c0003t0001g0193a0001c0003t0001g0211others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-20674T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269824 | ||||||
| chr9:119269837
|
T | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.219-20687A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269837 | ||||||
| chr9:119269868
|
A | AC | 209 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.219-20719_219-2071 others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119269868 | ||||||
| chr9:119270108
|
G | A | 6 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0004t0001g0016others(3): Show | 6 | HG02809.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-20958C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270108 | ||||||
| chr9:119270205
|
T | C | 207 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.219-21055A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270205 | ||||||
| chr9:119270206
|
G | A | 6 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0004t0001g0016others(3): Show | 6 | HG02809.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-21056C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270206 | ||||||
| chr9:119270324
|
C | T | 5 | a0001c0001t0002g0231a0001c0003t0001g0193a0001c0003t0001g0211others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-21174G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270324 | ||||||
| chr9:119270329
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.219-21179G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270329 | ||||||
| chr9:119270397
|
T | A | 6 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0004t0001g0016others(3): Show | 6 | HG02809.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-21247A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270397 | ||||||
| chr9:119270449
|
T | C | 47 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0043others(44): Show | 47 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.219-21299A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270449 | ||||||
| chr9:119270658
|
A | G | 209 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.219-21508T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270658 | ||||||
| chr9:119270666
|
T | C | 151 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0037others(148): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.219-21516A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270666 | ||||||
| chr9:119270804
|
A | G | 3 | a0001c0001t0002g0231a0001c0003t0002g0233a0001c0005t0002g0236 | 3 | HG01109.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.219-21654T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270804 | ||||||
| chr9:119270896
|
A | C | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-21746T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119270896 | ||||||
| chr9:119271029
|
A | G | 5 | a0001c0001t0002g0231a0001c0003t0001g0193a0001c0003t0001g0211others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-21879T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271029 | ||||||
| chr9:119271188
|
C | T | 150 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0037others(147): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.219-22038G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271188 | ||||||
| chr9:119271276
|
G | C | 203 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.219-22126C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271276 | ||||||
| chr9:119271324
|
C | CA | 180 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.219-22175dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271324 | ||||||
| chr9:119271324
|
C | CAA | 17 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0081others(14): Show | 17 | HG00423.hp1 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.219-22176_219-2217 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271324 | ||||||
| chr9:119271388
|
A | G | 5 | a0001c0001t0002g0231a0001c0003t0001g0193a0001c0003t0001g0211others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-22238T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271388 | ||||||
| chr9:119271541
|
C | A | 5 | a0001c0001t0002g0231a0001c0003t0001g0193a0001c0003t0001g0211others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-22391G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271541 | ||||||
| chr9:119271695
|
G | A | 5 | a0001c0001t0002g0231a0001c0003t0001g0193a0001c0003t0001g0211others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-22545C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271695 | ||||||
| chr9:119271728
|
G | A | 150 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0037others(147): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.219-22578C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271728 | ||||||
| chr9:119271989
|
G | T | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-22839C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271989 | ||||||
| chr9:119271993
|
C | G | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-22843G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119271993 | ||||||
| chr9:119272049
|
G | A | 155 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0037others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.219-22899C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272049 | ||||||
| chr9:119272052
|
A | G | 5 | a0001c0001t0002g0231a0001c0003t0001g0193a0001c0003t0001g0211others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-22902T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272052 | ||||||
| chr9:119272091
|
C | CA | 6 | a0001c0001t0002g0235a0001c0003t0001g0060a0001c0003t0001g0073others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-22942dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272091 | ||||||
| chr9:119272091
|
CA | C | 154 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.219-22942delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272091 | ||||||
| chr9:119272091
|
CAA | C | 25 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(22): Show | 25 | HG01109.hp2 HG01123.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.219-22943_219-2294 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272091 | ||||||
| chr9:119272091
|
CAAA | C | 9 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-22944_219-2294 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272091 | ||||||
| chr9:119272142
|
G | T | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-22992C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272142 | ||||||
| chr9:119272165
|
G | A | 9 | a0001c0001t0001g0044a0001c0003t0001g0180a0001c0003t0001g0183others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-23015C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272165 | ||||||
| chr9:119272206
|
G | GA | 5 | a0001c0001t0002g0231a0001c0003t0001g0193a0001c0003t0001g0211others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-23057dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272206 | ||||||
| chr9:119272378
|
C | T | 6 | a0001c0001t0001g0065a0001c0001t0002g0235a0001c0002t0001g0168others(3): Show | 6 | HG01943.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-23228G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272378 | ||||||
| chr9:119272411
|
T | C | 150 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0037others(147): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.219-23261A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272411 | ||||||
| chr9:119272448
|
A | G | 5 | a0001c0001t0002g0231a0001c0003t0001g0193a0001c0003t0001g0211others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-23298T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272448 | ||||||
| chr9:119272563
|
C | G | 5 | a0001c0001t0002g0231a0001c0003t0001g0193a0001c0003t0001g0211others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-23413G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272563 | ||||||
| chr9:119272575
|
C | A | 152 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0037others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.219-23425G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272575 | ||||||
| chr9:119272760
|
C | T | 147 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0037others(144): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.219-23610G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272760 | ||||||
| chr9:119272795
|
C | T | 151 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0037others(148): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.219-23645G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272795 | ||||||
| chr9:119272816
|
C | G | 1 | a0001c0001t0001g0156 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.219-23666G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272816 | ||||||
| chr9:119272954
|
T | C | 11 | a0001c0001t0002g0231a0001c0003t0001g0189a0001c0003t0001g0193others(8): Show | 11 | HG01109.hp1 HG02109.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.219-23804A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119272954 | ||||||
| chr9:119273096
|
A | G | 11 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(8): Show | 11 | HG00639.hp2 HG00735.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.219-23946T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273096 | ||||||
| chr9:119273178
|
A | C | 1 | a0001c0002t0001g0154 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.219-24028T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273178 | ||||||
| chr9:119273322
|
T | C | 3 | a0001c0003t0001g0040a0001c0003t0001g0041a0001c0003t0001g0187 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219-24172A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273322 | ||||||
| chr9:119273421
|
G | C | 8 | a0001c0001t0001g0044a0001c0001t0001g0212a0001c0003t0001g0107others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-24271C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273421 | ||||||
| chr9:119273601
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.219-24451T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273601 | ||||||
| chr9:119273693
|
T | C | 10 | a0001c0001t0001g0044a0001c0001t0001g0212a0001c0003t0001g0107others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-24543A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273693 | ||||||
| chr9:119273714
|
A | G | 70 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0065others(67): Show | 70 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.219-24564T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273714 | ||||||
| chr9:119273857
|
A | G | 83 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.219-24707T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119273857 | ||||||
| chr9:119274100
|
T | C | 12 | a0001c0001t0001g0200a0001c0003t0001g0040a0001c0003t0001g0041others(9): Show | 12 | HG00639.hp2 HG00735.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-24950A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119274100 | ||||||
| chr9:119274179
|
T | G | 14 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(11): Show | 14 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-25029A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119274179 | ||||||
| chr9:119274180
|
C | A | 3 | a0001c0001t0002g0235a0001c0003t0001g0060a0001c0003t0001g0073 | 3 | HG02258.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.219-25030G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119274180 | ||||||
| chr9:119274396
|
G | C | 24 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0204others(21): Show | 24 | HG00639.hp2 HG00735.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.219-25246C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119274396 | ||||||
| chr9:119274715
|
C | T | 44 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0056others(41): Show | 44 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.219-25565G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119274715 | ||||||
| chr9:119274809
|
G | C | 1 | a0001c0001t0003g0009 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.219-25659C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119274809 | ||||||
| chr9:119274848
|
G | T | 44 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0056others(41): Show | 44 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.219-25698C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119274848 | ||||||
| chr9:119275018
|
C | T | 44 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0056others(41): Show | 44 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.219-25868G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275018 | ||||||
| chr9:119275073
|
C | T | 3 | a0001c0001t0001g0124a0001c0002t0001g0095a0001c0002t0001g0104 | 3 | HG02074.hp1 NA18946.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.219-25923G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275073 | ||||||
| chr9:119275148
|
T | C | 2 | a0001c0001t0001g0172a0001c0003t0002g0226 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.219-25998A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275148 | ||||||
| chr9:119275188
|
A | G | 2 | a0001c0005t0001g0199a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.219-26038T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275188 | ||||||
| chr9:119275266
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.219-26116A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275266 | ||||||
| chr9:119275390
|
G | A | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.219-26240C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275390 | ||||||
| chr9:119275400
|
C | G | 44 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0056others(41): Show | 44 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.219-26250G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275400 | ||||||
| chr9:119275569
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.219-26419G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275569 | ||||||
| chr9:119275607
|
A | G | 1 | a0001c0001t0002g0231 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.219-26457T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275607 | ||||||
| chr9:119275679
|
G | C | 9 | a0001c0001t0001g0044a0001c0001t0001g0212a0001c0003t0001g0107others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-26529C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275679 | ||||||
| chr9:119275807
|
C | T | 2 | a0001c0002t0001g0110a0001c0002t0001g0131 | 2 | NA18994.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.219-26657G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275807 | ||||||
| chr9:119275856
|
C | T | 2 | a0001c0003t0001g0193a0001c0003t0001g0213 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.219-26706G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275856 | ||||||
| chr9:119275897
|
G | A | 5 | a0001c0003t0001g0022a0001c0006t0001g0017a0001c0006t0001g0018others(2): Show | 5 | HG01123.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-26747C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275897 | ||||||
| chr9:119275899
|
G | A | 42 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0056others(39): Show | 42 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.219-26749C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275899 | ||||||
| chr9:119275945
|
C | A | 2 | a0001c0001t0001g0065a0001c0002t0001g0168 | 2 | HG01943.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.219-26795G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119275945 | ||||||
| chr9:119276216
|
A | G | 66 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(63): Show | 66 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.219-27066T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119276216 | ||||||
| chr9:119276229
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0158 | 2 | HG01069.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.219-27079A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119276229 | ||||||
| chr9:119276272
|
C | T | 6 | a0001c0001t0001g0195a0001c0001t0001g0204a0001c0003t0001g0085others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-27122G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119276272 | ||||||
| chr9:119276582
|
G | A | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.219-27432C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119276582 | ||||||
| chr9:119276691
|
G | A | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-27541C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119276691 | ||||||
| chr9:119276801
|
G | A | 33 | a0001c0001t0001g0044a0001c0001t0001g0195a0001c0001t0001g0200others(30): Show | 33 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.219-27651C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119276801 | ||||||
| chr9:119277119
|
G | A | 43 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0056others(40): Show | 43 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.219-27969C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277119 | ||||||
| chr9:119277229
|
G | C | 63 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(60): Show | 63 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.219-28079C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277229 | ||||||
| chr9:119277286
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.219-28136C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277286 | ||||||
| chr9:119277291
|
A | G | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-28141T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277291 | ||||||
| chr9:119277298
|
G | A | 140 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.219-28148C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277298 | ||||||
| chr9:119277322
|
G | A | 12 | a0001c0001t0001g0200a0001c0003t0001g0040a0001c0003t0001g0041others(9): Show | 12 | HG00639.hp2 HG00735.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-28172C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277322 | ||||||
| chr9:119277369
|
G | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0084a0001c0001t0001g0184others(3): Show | 6 | HG01261.hp1 HG02572.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-28219C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277369 | ||||||
| chr9:119277426
|
A | G | 63 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(60): Show | 63 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.219-28276T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277426 | ||||||
| chr9:119277495
|
G | T | 33 | a0001c0001t0001g0044a0001c0001t0001g0195a0001c0001t0001g0200others(30): Show | 33 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.219-28345C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277495 | ||||||
| chr9:119277556
|
C | A | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.219-28406G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277556 | ||||||
| chr9:119277584
|
G | A | 43 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0056others(40): Show | 43 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.219-28434C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277584 | ||||||
| chr9:119277688
|
T | C | 1 | a0001c0004t0002g0232 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.219-28538A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277688 | ||||||
| chr9:119277826
|
G | A | 1 | a0001c0002t0001g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.219-28676C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277826 | ||||||
| chr9:119277969
|
T | A | 1 | a0001c0002t0001g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.219-28819A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119277969 | ||||||
| chr9:119278310
|
C | CA | 7 | a0001c0001t0001g0044a0001c0001t0001g0212a0001c0003t0001g0107others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-29161_219-2916 others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119278310 | ||||||
| chr9:119278342
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.219-29192G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119278342 | ||||||
| chr9:119278611
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0204 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.219-29461A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119278611 | ||||||
| chr9:119278616
|
G | A | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-29466C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119278616 | ||||||
| chr9:119278626
|
G | A | 43 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0056others(40): Show | 43 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.219-29476C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119278626 | ||||||
| chr9:119278628
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.219-29478C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119278628 | ||||||
| chr9:119278974
|
C | G | 1 | a0001c0001t0002g0231 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.219-29824G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119278974 | ||||||
| chr9:119279079
|
A | G | 4 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(1): Show | 4 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-29929T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279079 | ||||||
| chr9:119279182
|
C | T | 133 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.219-30032G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279182 | ||||||
| chr9:119279298
|
C | T | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.219-30148G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279298 | ||||||
| chr9:119279356
|
C | G | 1 | a0001c0001t0001g0080 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.219-30206G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279356 | ||||||
| chr9:119279363
|
C | T | 127 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.219-30213G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279363 | ||||||
| chr9:119279419
|
C | T | 1 | a0001c0002t0001g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.219-30269G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279419 | ||||||
| chr9:119279888
|
G | C | 1 | a0001c0001t0001g0216 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.219-30738C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279888 | ||||||
| chr9:119279892
|
C | A | 1 | a0001c0003t0001g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.219-30742G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119279892 | ||||||
| chr9:119280028
|
G | GA | 6 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-30879dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280028 | ||||||
| chr9:119280233
|
G | C | 39 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.219-31083C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280233 | ||||||
| chr9:119280246
|
C | CT | 109 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0046others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.219-31097dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280246 | ||||||
| chr9:119280260
|
T | A | 125 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.219-31110A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280260 | ||||||
| chr9:119280301
|
C | T | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-31151G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280301 | ||||||
| chr9:119280302
|
G | A | 19 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-31152C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280302 | ||||||
| chr9:119280342
|
C | A | 1 | a0001c0003t0001g0073 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.219-31192G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280342 | ||||||
| chr9:119280404
|
A | AT | 5 | a0001c0001t0001g0137a0001c0001t0001g0170a0001c0003t0001g0178others(2): Show | 5 | HG00544.hp2 HG02698.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-31255dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280404 | ||||||
| chr9:119280404
|
A | ATT | 66 | a0001c0001t0001g0044a0001c0001t0001g0053a0001c0001t0001g0056others(63): Show | 66 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.219-31256_219-3125 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280404 | ||||||
| chr9:119280404
|
A | T | 1 | a0001c0002t0001g0168 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.219-31254T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280404 | ||||||
| chr9:119280445
|
C | T | 14 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(11): Show | 14 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-31295G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280445 | ||||||
| chr9:119280486
|
C | T | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-31336G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280486 | ||||||
| chr9:119280531
|
A | G | 2 | a0001c0003t0001g0213a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.219-31381T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280531 | ||||||
| chr9:119280650
|
C | T | 14 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(11): Show | 14 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-31500G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280650 | ||||||
| chr9:119280705
|
G | A | 1 | a0001c0004t0001g0188 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.219-31555C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280705 | ||||||
| chr9:119280718
|
T | G | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.219-31568A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280718 | ||||||
| chr9:119280842
|
TTTATTTA others(8): Show |
T | 1 | a0001c0001t0001g0101 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.219-31707_219-3169 others(19): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280842 | ||||||
| chr9:119280906
|
C | T | 14 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(11): Show | 14 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-31756G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280906 | ||||||
| chr9:119280942
|
G | A | 18 | a0001c0001t0001g0184a0001c0001t0002g0231a0001c0002t0001g0202others(15): Show | 18 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.219-31792C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119280942 | ||||||
| chr9:119281222
|
T | C | 1 | a0001c0002t0001g0142 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.218+31916A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281222 | ||||||
| chr9:119281268
|
C | A | 4 | a0001c0001t0001g0184a0001c0001t0002g0231a0001c0003t0001g0211others(1): Show | 4 | HG02976.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+31870G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281268 | ||||||
| chr9:119281278
|
T | C | 37 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.218+31860A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281278 | ||||||
| chr9:119281317
|
A | G | 4 | a0001c0003t0001g0178a0001c0004t0001g0015a0001c0004t0001g0177others(1): Show | 4 | HG02965.hp2 HG03453.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+31821T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281317 | ||||||
| chr9:119281542
|
A | G | 126 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.218+31596T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281542 | ||||||
| chr9:119281594
|
G | A | 1 | a0001c0002t0003g0002 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.218+31544C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281594 | ||||||
| chr9:119281677
|
TATATAA | T | 130 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.218+31455_218+3146 others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281677 | ||||||
| chr9:119281743
|
ATGATG | A | 2 | a0001c0003t0009g0214a0001c0005t0001g0201 | 2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.218+31390_218+3139 others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281743 | ||||||
| chr9:119281806
|
T | G | 1 | a0001c0002t0001g0105 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.218+31332A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281806 | ||||||
| chr9:119281915
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.218+31223G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119281915 | ||||||
| chr9:119282115
|
T | G | 2 | a0001c0002t0001g0089a0001c0002t0001g0092 | 2 | NA18977.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.218+31023A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282115 | ||||||
| chr9:119282143
|
T | C | 47 | a0001c0001t0001g0044a0001c0001t0001g0053a0001c0001t0001g0056others(44): Show | 47 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.218+30995A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282143 | ||||||
| chr9:119282183
|
C | T | 127 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.218+30955G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282183 | ||||||
| chr9:119282296
|
C | G | 2 | a0001c0003t0009g0214a0001c0005t0001g0201 | 2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.218+30842G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282296 | ||||||
| chr9:119282356
|
G | A | 3 | a0001c0003t0001g0181a0001c0003t0001g0182a0001c0005t0001g0199 | 3 | HG00639.hp2 HG00735.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.218+30782C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282356 | ||||||
| chr9:119282365
|
C | T | 42 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0065others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.218+30773G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282365 | ||||||
| chr9:119282383
|
G | A | 3 | a0001c0003t0001g0181a0001c0003t0001g0182a0001c0005t0001g0199 | 3 | HG00639.hp2 HG00735.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.218+30755C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282383 | ||||||
| chr9:119282709
|
A | G | 2 | a0001c0001t0003g0008a0001c0010t0001g0098 | 2 | HG02523.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.218+30429T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282709 | ||||||
| chr9:119282872
|
T | G | 7 | a0001c0001t0001g0212a0001c0003t0001g0107a0001c0003t0001g0139others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+30266A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282872 | ||||||
| chr9:119282885
|
G | A | 1 | a0001c0001t0001g0080 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.218+30253C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282885 | ||||||
| chr9:119282951
|
A | G | 110 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.218+30187T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119282951 | ||||||
| chr9:119283085
|
G | C | 3 | a0001c0001t0002g0231a0001c0003t0001g0175a0001c0003t0001g0207 | 3 | HG01496.hp1 HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.218+30053C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283085 | ||||||
| chr9:119283121
|
G | A | 136 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.218+30017C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283121 | ||||||
| chr9:119283237
|
A | AGCCTCAG others(2): Show |
38 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(35): Show | 38 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.218+29900_218+2990 others(13): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283237 | ||||||
| chr9:119283240
|
T | C | 42 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(39): Show | 42 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.218+29898A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283240 | ||||||
| chr9:119283462
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0153a0001c0002t0001g0116 | 3 | HG00544.hp1 NA18977.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.218+29676T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283462 | ||||||
| chr9:119283491
|
T | C | 37 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.218+29647A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283491 | ||||||
| chr9:119283548
|
T | C | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+29590A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283548 | ||||||
| chr9:119283827
|
C | T | 57 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.218+29311G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283827 | ||||||
| chr9:119283832
|
C | A | 1 | a0001c0001t0001g0090 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.218+29306G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283832 | ||||||
| chr9:119283878
|
T | A | 1 | a0001c0001t0002g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.218+29260A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283878 | ||||||
| chr9:119283915
|
T | A | 107 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0046others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.218+29223A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283915 | ||||||
| chr9:119283949
|
C | T | 3 | a0001c0001t0001g0084a0001c0003t0001g0085a0001c0004t0001g0188 | 3 | HG01261.hp1 HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.218+29189G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119283949 | ||||||
| chr9:119284159
|
C | T | 3 | a0001c0001t0002g0231a0001c0003t0001g0175a0001c0003t0001g0207 | 3 | HG01496.hp1 HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.218+28979G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119284159 | ||||||
| chr9:119284271
|
T | A | 206 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.218+28867A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119284271 | ||||||
| chr9:119284597
|
C | G | 131 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.218+28541G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119284597 | ||||||
| chr9:119284806
|
A | G | 2 | a0001c0003t0001g0186a0001c0003t0001g0198 | 2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218+28332T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119284806 | ||||||
| chr9:119284818
|
T | C | 3 | a0001c0001t0001g0212a0001c0003t0001g0178a0001c0004t0001g0177 | 3 | HG02258.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.218+28320A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119284818 | ||||||
| chr9:119284850
|
G | A | 1 | a0001c0015t0001g0133 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.218+28288C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119284850 | ||||||
| chr9:119285021
|
C | T | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+28117G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285021 | ||||||
| chr9:119285069
|
C | G | 1 | a0001c0001t0001g0101 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218+28069G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285069 | ||||||
| chr9:119285070
|
G | C | 1 | a0001c0001t0001g0101 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218+28068C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285070 | ||||||
| chr9:119285103
|
G | A | 57 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.218+28035C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285103 | ||||||
| chr9:119285169
|
C | T | 61 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.218+27969G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285169 | ||||||
| chr9:119285174
|
G | A | 1 | a0001c0002t0001g0077 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.218+27964C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285174 | ||||||
| chr9:119285201
|
C | CA | 25 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0163others(22): Show | 25 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.218+27936dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285201 | ||||||
| chr9:119285201
|
CA | C | 34 | a0001c0001t0001g0039a0001c0001t0001g0065a0001c0001t0001g0090others(31): Show | 34 | HG00280.hp1 HG00741.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.218+27936delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285201 | ||||||
| chr9:119285201
|
CAA | C | 19 | a0001c0001t0001g0109a0001c0001t0001g0117a0001c0001t0001g0121others(16): Show | 19 | HG00423.hp2 HG01256.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.218+27935_218+2793 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285201 | ||||||
| chr9:119285201
|
CAAA | C | 12 | a0001c0001t0001g0037a0001c0001t0001g0103a0001c0001t0001g0200others(9): Show | 12 | HG01891.hp2 HG02615.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+27934_218+2793 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285201 | ||||||
| chr9:119285201
|
CAAAAAAA | C | 61 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.218+27930_218+2793 others(11): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285201 | ||||||
| chr9:119285219
|
A | T | 1 | a0001c0001t0001g0101 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218+27919T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285219 | ||||||
| chr9:119285395
|
C | G | 62 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.218+27743G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285395 | ||||||
| chr9:119285402
|
T | C | 5 | a0001c0003t0002g0223a0001c0003t0002g0228a0001c0003t0002g0233others(2): Show | 5 | HG01109.hp1 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+27736A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285402 | ||||||
| chr9:119285672
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+27466A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285672 | ||||||
| chr9:119285697
|
C | A | 1 | a0001c0004t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.218+27441G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285697 | ||||||
| chr9:119285698
|
G | A | 81 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.218+27440C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285698 | ||||||
| chr9:119285767
|
C | T | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.218+27371G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285767 | ||||||
| chr9:119285771
|
G | T | 1 | a0001c0002t0001g0024 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.218+27367C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285771 | ||||||
| chr9:119285819
|
A | G | 4 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0005t0001g0192others(1): Show | 4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+27319T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285819 | ||||||
| chr9:119285831
|
G | A | 6 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+27307C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285831 | ||||||
| chr9:119285894
|
A | G | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+27244T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285894 | ||||||
| chr9:119285908
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+27230G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285908 | ||||||
| chr9:119285954
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.218+27184G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285954 | ||||||
| chr9:119285973
|
C | G | 1 | a0001c0003t0002g0224 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.218+27165G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119285973 | ||||||
| chr9:119286179
|
A | T | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.218+26959T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286179 | ||||||
| chr9:119286211
|
G | A | 4 | a0001c0001t0001g0212a0001c0001t0002g0231a0001c0003t0001g0178others(1): Show | 4 | HG02258.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+26927C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286211 | ||||||
| chr9:119286238
|
C | CT | 100 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.218+26899dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286238 | ||||||
| chr9:119286343
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218+26795G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286343 | ||||||
| chr9:119286344
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218+26794A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286344 | ||||||
| chr9:119286345
|
C | G | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+26793G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286345 | ||||||
| chr9:119286389
|
C | T | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+26749G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286389 | ||||||
| chr9:119286428
|
G | A | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+26710C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286428 | ||||||
| chr9:119286476
|
C | T | 3 | a0001c0001t0001g0058a0001c0003t0001g0020a0001c0005t0001g0199 | 3 | HG02572.hp1 HG03239.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.218+26662G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286476 | ||||||
| chr9:119286492
|
C | A | 1 | a0001c0001t0001g0101 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218+26646G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286492 | ||||||
| chr9:119286523
|
T | C | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+26615A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286523 | ||||||
| chr9:119286529
|
C | T | 1 | a0001c0003t0008g0185 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.218+26609G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286529 | ||||||
| chr9:119286785
|
A | T | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+26353T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286785 | ||||||
| chr9:119286831
|
C | T | 2 | a0001c0001t0001g0176a0001c0002t0001g0165 | 2 | HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.218+26307G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286831 | ||||||
| chr9:119286846
|
A | T | 1 | a0001c0001t0001g0101 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218+26292T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286846 | ||||||
| chr9:119286849
|
C | T | 3 | a0001c0001t0001g0084a0001c0003t0001g0085a0001c0004t0001g0188 | 3 | HG01261.hp1 HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.218+26289G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119286849 | ||||||
| chr9:119287044
|
T | A | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+26094A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287044 | ||||||
| chr9:119287060
|
GA | G | 27 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0101others(24): Show | 27 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.218+26077delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287060 | ||||||
| chr9:119287188
|
T | A | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+25950A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287188 | ||||||
| chr9:119287226
|
C | T | 63 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0055others(60): Show | 63 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.218+25912G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287226 | ||||||
| chr9:119287377
|
T | C | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+25761A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287377 | ||||||
| chr9:119287391
|
T | C | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+25747A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287391 | ||||||
| chr9:119287536
|
G | A | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+25602C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287536 | ||||||
| chr9:119287586
|
A | C | 1 | a0001c0003t0001g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218+25552T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119287586 | ||||||
| chr9:119288003
|
G | A | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+25135C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288003 | ||||||
| chr9:119288140
|
T | A | 2 | a0001c0007t0001g0082a0001c0007t0001g0083 | 2 | HG01099.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.218+24998A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288140 | ||||||
| chr9:119288328
|
G | C | 1 | a0001c0001t0002g0229 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218+24810C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288328 | ||||||
| chr9:119288350
|
A | AT | 60 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(57): Show | 60 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.218+24787dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288350 | ||||||
| chr9:119288417
|
T | C | 1 | a0001c0001t0002g0229 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218+24721A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288417 | ||||||
| chr9:119288497
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.218+24641C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288497 | ||||||
| chr9:119288538
|
CT | C | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24599delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288538 | ||||||
| chr9:119288644
|
G | A | 1 | a0001c0004t0002g0232 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.218+24494C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288644 | ||||||
| chr9:119288769
|
G | T | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24369C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288769 | ||||||
| chr9:119288798
|
G | GT | 5 | a0001c0001t0001g0212a0001c0001t0002g0231a0001c0003t0001g0178others(2): Show | 5 | HG02258.hp1 NA18522.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+24339dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288798 | ||||||
| chr9:119288803
|
T | G | 78 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.218+24335A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288803 | ||||||
| chr9:119288821
|
C | T | 2 | a0001c0001t0001g0134a0004c0011t0001g0125 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.218+24317G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288821 | ||||||
| chr9:119288823
|
C | T | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24315G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288823 | ||||||
| chr9:119288846
|
T | C | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24292A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288846 | ||||||
| chr9:119288901
|
T | A | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24237A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288901 | ||||||
| chr9:119288903
|
C | T | 2 | a0001c0003t0002g0223a0001c0004t0001g0016 | 2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.218+24235G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288903 | ||||||
| chr9:119288952
|
C | T | 2 | a0001c0001t0003g0008a0001c0010t0001g0098 | 2 | HG02523.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.218+24186G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119288952 | ||||||
| chr9:119289017
|
C | T | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24121G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289017 | ||||||
| chr9:119289061
|
A | C | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24077T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289061 | ||||||
| chr9:119289080
|
G | A | 3 | a0001c0002t0001g0071a0001c0002t0001g0141a0001c0002t0001g0155 | 3 | HG01123.hp2 HG01257.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.218+24058C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289080 | ||||||
| chr9:119289095
|
C | T | 10 | a0001c0001t0001g0055a0001c0001t0001g0160a0001c0002t0001g0027others(7): Show | 10 | HG01123.hp2 HG01169.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.218+24043G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289095 | ||||||
| chr9:119289114
|
C | T | 63 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0055others(60): Show | 63 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.218+24024G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289114 | ||||||
| chr9:119289132
|
G | C | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+24006C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289132 | ||||||
| chr9:119289151
|
C | T | 18 | a0001c0001t0001g0037a0001c0001t0001g0090a0001c0001t0001g0103others(15): Show | 18 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218+23987G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289151 | ||||||
| chr9:119289275
|
G | T | 2 | a0001c0003t0001g0213a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+23863C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289275 | ||||||
| chr9:119289419
|
T | C | 4 | a0001c0001t0001g0212a0001c0001t0002g0231a0001c0003t0001g0178others(1): Show | 4 | HG02258.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+23719A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289419 | ||||||
| chr9:119289428
|
T | A | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+23710A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289428 | ||||||
| chr9:119289429
|
C | A | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+23709G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289429 | ||||||
| chr9:119289474
|
A | T | 1 | a0001c0003t0001g0031 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.218+23664T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289474 | ||||||
| chr9:119289709
|
C | T | 1 | a0001c0002t0001g0024 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.218+23429G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289709 | ||||||
| chr9:119289713
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+23425A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289713 | ||||||
| chr9:119289826
|
A | C | 1 | a0001c0002t0001g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.218+23312T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289826 | ||||||
| chr9:119289870
|
G | A | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+23268C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289870 | ||||||
| chr9:119289874
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+23264C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289874 | ||||||
| chr9:119289899
|
T | A | 72 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.218+23239A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119289899 | ||||||
| chr9:119290090
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.218+23048G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119290090 | ||||||
| chr9:119290236
|
C | T | 16 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0003t0001g0022others(13): Show | 16 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.218+22902G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119290236 | ||||||
| chr9:119290246
|
A | G | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+22892T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119290246 | ||||||
| chr9:119290519
|
C | G | 135 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.218+22619G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119290519 | ||||||
| chr9:119290858
|
C | T | 1 | a0001c0003t0001g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.218+22280G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119290858 | ||||||
| chr9:119290889
|
G | A | 18 | a0001c0001t0001g0037a0001c0001t0001g0090a0001c0001t0001g0103others(15): Show | 18 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218+22249C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119290889 | ||||||
| chr9:119291041
|
T | A | 2 | a0001c0003t0001g0197a0001c0009t0001g0191 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.218+22097A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291041 | ||||||
| chr9:119291058
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.218+22080C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291058 | ||||||
| chr9:119291122
|
C | CA | 53 | a0001c0001t0001g0037a0001c0001t0001g0084a0001c0001t0001g0090others(50): Show | 53 | HG00423.hp2 HG00639.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.218+22015dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291122 | ||||||
| chr9:119291122
|
CA | C | 59 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0053others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.218+22015delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291122 | ||||||
| chr9:119291258
|
G | C | 135 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.218+21880C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291258 | ||||||
| chr9:119291924
|
T | G | 2 | a0001c0003t0001g0213a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+21214A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291924 | ||||||
| chr9:119291977
|
A | C | 1 | a0001c0003t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.218+21161T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291977 | ||||||
| chr9:119291993
|
A | G | 1 | a0001c0002t0001g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.218+21145T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119291993 | ||||||
| chr9:119292526
|
G | A | 2 | a0001c0003t0001g0213a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+20612C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119292526 | ||||||
| chr9:119292588
|
T | C | 8 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(5): Show | 8 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+20550A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119292588 | ||||||
| chr9:119292601
|
C | G | 8 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(5): Show | 8 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+20537G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119292601 | ||||||
| chr9:119292870
|
A | G | 58 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+20268T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119292870 | ||||||
| chr9:119292993
|
T | C | 1 | a0001c0002t0001g0092 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.218+20145A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119292993 | ||||||
| chr9:119293010
|
T | C | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+20128A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119293010 | ||||||
| chr9:119293412
|
G | A | 1 | a0001c0006t0002g0225 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.218+19726C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119293412 | ||||||
| chr9:119293697
|
T | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0204 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.218+19441A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119293697 | ||||||
| chr9:119293922
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.218+19216A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119293922 | ||||||
| chr9:119294156
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.218+18982G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294156 | ||||||
| chr9:119294157
|
C | T | 1 | a0001c0003t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.218+18981G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294157 | ||||||
| chr9:119294182
|
T | C | 3 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190 | 3 | HG01243.hp1 HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.218+18956A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294182 | ||||||
| chr9:119294285
|
C | T | 1 | a0001c0004t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+18853G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294285 | ||||||
| chr9:119294297
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.218+18841C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294297 | ||||||
| chr9:119294378
|
C | T | 64 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.218+18760G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294378 | ||||||
| chr9:119294695
|
A | G | 1 | a0001c0002t0001g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.218+18443T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294695 | ||||||
| chr9:119294704
|
A | G | 1 | a0001c0002t0001g0116 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.218+18434T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294704 | ||||||
| chr9:119294817
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+18321G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294817 | ||||||
| chr9:119294850
|
C | T | 72 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.218+18288G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294850 | ||||||
| chr9:119294853
|
T | TA | 21 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0003t0001g0022others(18): Show | 21 | HG01123.hp1 HG01884.hp1 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.218+18284dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294853 | ||||||
| chr9:119294853
|
T | TAAAAAA | 5 | a0001c0001t0001g0061a0001c0001t0001g0137a0001c0002t0001g0116others(2): Show | 5 | HG00738.hp2 HG01243.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+18279_218+1828 others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294853 | ||||||
| chr9:119294853
|
T | TAAAAAAA | 55 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.218+18278_218+1828 others(11): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294853 | ||||||
| chr9:119294853
|
TA | T | 6 | a0001c0001t0002g0234a0001c0002t0001g0127a0001c0002t0001g0142others(3): Show | 6 | HG01496.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+18284delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294853 | ||||||
| chr9:119294974
|
C | CA | 134 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.218+18163dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119294974 | ||||||
| chr9:119295063
|
T | A | 5 | a0001c0003t0002g0223a0001c0003t0002g0228a0001c0003t0002g0233others(2): Show | 5 | HG01109.hp1 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+18075A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295063 | ||||||
| chr9:119295077
|
C | T | 64 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.218+18061G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295077 | ||||||
| chr9:119295085
|
T | A | 4 | a0001c0001t0001g0200a0001c0003t0001g0040a0001c0003t0001g0041others(1): Show | 4 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+18053A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295085 | ||||||
| chr9:119295160
|
AT | A | 32 | a0001c0001t0001g0037a0001c0001t0001g0090a0001c0001t0001g0103others(29): Show | 32 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.218+17977delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295160 | ||||||
| chr9:119295393
|
A | T | 2 | a0001c0003t0001g0213a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+17745T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295393 | ||||||
| chr9:119295498
|
T | C | 6 | a0001c0003t0001g0139a0001c0003t0002g0223a0001c0003t0002g0228others(3): Show | 6 | HG01109.hp1 HG02886.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+17640A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295498 | ||||||
| chr9:119295523
|
A | C | 2 | a0001c0003t0001g0213a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+17615T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295523 | ||||||
| chr9:119295580
|
A | C | 134 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.218+17558T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295580 | ||||||
| chr9:119295664
|
A | AGTAT | 62 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.218+17470_218+1747 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295664 | ||||||
| chr9:119295784
|
G | T | 11 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0003t0001g0022others(8): Show | 11 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+17354C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295784 | ||||||
| chr9:119295786
|
G | A | 2 | a0001c0003t0001g0213a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+17352C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295786 | ||||||
| chr9:119295868
|
G | C | 134 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.218+17270C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295868 | ||||||
| chr9:119295895
|
G | A | 2 | a0001c0003t0001g0213a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+17243C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119295895 | ||||||
| chr9:119296354
|
G | C | 62 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.218+16784C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296354 | ||||||
| chr9:119296550
|
G | C | 1 | a0001c0002t0001g0149 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.218+16588C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296550 | ||||||
| chr9:119296679
|
A | G | 62 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.218+16459T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296679 | ||||||
| chr9:119296757
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.218+16381C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296757 | ||||||
| chr9:119296892
|
TACGA | T | 62 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.218+16242_218+1624 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296892 | ||||||
| chr9:119296901
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+16237T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296901 | ||||||
| chr9:119296963
|
T | A | 1 | a0001c0003t0001g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.218+16175A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296963 | ||||||
| chr9:119296964
|
A | T | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | HG00099.hp1 HG01099.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+16174T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119296964 | ||||||
| chr9:119297037
|
G | A | 134 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.218+16101C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297037 | ||||||
| chr9:119297121
|
A | G | 62 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.218+16017T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297121 | ||||||
| chr9:119297266
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.218+15872A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297266 | ||||||
| chr9:119297431
|
T | C | 134 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.218+15707A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297431 | ||||||
| chr9:119297503
|
G | A | 16 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0003t0001g0022others(13): Show | 16 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.218+15635C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297503 | ||||||
| chr9:119297689
|
G | A | 2 | a0001c0003t0001g0213a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+15449C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297689 | ||||||
| chr9:119297746
|
T | A | 62 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.218+15392A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297746 | ||||||
| chr9:119297836
|
A | ATAAT | 61 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.218+15301_218+1530 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297836 | ||||||
| chr9:119297836
|
A | ATAATAAT | 3 | a0001c0001t0001g0173a0001c0003t0001g0213a0001c0005t0001g0210 | 3 | HG02622.hp2 HG03017.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+15301_218+1530 others(11): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297836 | ||||||
| chr9:119297842
|
T | C | 2 | a0001c0003t0001g0213a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+15296A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119297842 | ||||||
| chr9:119298079
|
C | T | 26 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 26 | HG00099.hp1 HG00544.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.218+15059G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119298079 | ||||||
| chr9:119298232
|
C | A | 1 | a0001c0003t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.218+14906G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119298232 | ||||||
| chr9:119298474
|
C | A | 2 | a0001c0002t0001g0110a0001c0002t0001g0131 | 2 | NA18994.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.218+14664G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119298474 | ||||||
| chr9:119298596
|
T | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0219 | 2 | HG02129.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.218+14542A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119298596 | ||||||
| chr9:119298781
|
A | C | 1 | a0001c0004t0002g0232 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.218+14357T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119298781 | ||||||
| chr9:119298909
|
CAATACTT others(21): Show |
C | 1 | a0001c0001t0005g0217 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.218+14201_218+1422 others(32): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119298909 | ||||||
| chr9:119299015
|
T | C | 1 | a0001c0004t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+14123A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299015 | ||||||
| chr9:119299036
|
T | C | 62 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.218+14102A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299036 | ||||||
| chr9:119299157
|
T | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0106a0001c0001t0001g0150others(1): Show | 4 | HG00423.hp1 HG00438.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+13981A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299157 | ||||||
| chr9:119299228
|
C | G | 1 | a0001c0015t0001g0133 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.218+13910G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299228 | ||||||
| chr9:119299306
|
T | A | 131 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.218+13832A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299306 | ||||||
| chr9:119299315
|
A | G | 1 | a0001c0002t0002g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.218+13823T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299315 | ||||||
| chr9:119299342
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.218+13796C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299342 | ||||||
| chr9:119299443
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+13695C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299443 | ||||||
| chr9:119299612
|
C | CA | 5 | a0001c0001t0001g0204a0001c0002t0001g0049a0001c0002t0001g0110others(2): Show | 5 | HG01175.hp2 HG02145.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+13525dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299612 | ||||||
| chr9:119299621
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0153 | 2 | HG00544.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.218+13517T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299621 | ||||||
| chr9:119299670
|
C | T | 132 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.218+13468G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299670 | ||||||
| chr9:119299946
|
T | C | 17 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0003t0001g0022others(14): Show | 17 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.218+13192A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119299946 | ||||||
| chr9:119300046
|
T | G | 2 | a0001c0002t0001g0110a0001c0002t0001g0131 | 2 | NA18994.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.218+13092A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300046 | ||||||
| chr9:119300047
|
T | G | 2 | a0001c0002t0001g0110a0001c0002t0001g0131 | 2 | NA18994.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.218+13091A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300047 | ||||||
| chr9:119300049
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+13089C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300049 | ||||||
| chr9:119300050
|
T | G | 2 | a0001c0002t0001g0110a0001c0002t0001g0131 | 2 | NA18994.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.218+13088A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300050 | ||||||
| chr9:119300051
|
T | TAC | 2 | a0001c0002t0001g0110a0001c0002t0001g0131 | 2 | NA18994.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.218+13086_218+1308 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300051 | ||||||
| chr9:119300365
|
T | C | 2 | a0001c0002t0003g0012a0001c0007t0001g0038 | 2 | HG00140.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.218+12773A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300365 | ||||||
| chr9:119300536
|
A | T | 13 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0003t0001g0022others(10): Show | 13 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+12602T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300536 | ||||||
| chr9:119300662
|
C | T | 2 | a0001c0003t0001g0213a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+12476G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300662 | ||||||
| chr9:119300848
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.218+12290C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300848 | ||||||
| chr9:119300882
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.218+12256A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119300882 | ||||||
| chr9:119301252
|
A | G | 18 | a0001c0001t0001g0037a0001c0001t0001g0090a0001c0001t0001g0103others(15): Show | 18 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218+11886T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119301252 | ||||||
| chr9:119301875
|
C | T | 11 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0003t0001g0022others(8): Show | 11 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+11263G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119301875 | ||||||
| chr9:119302132
|
A | C | 59 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.218+11006T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302132 | ||||||
| chr9:119302220
|
T | G | 2 | a0001c0003t0001g0213a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.218+10918A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302220 | ||||||
| chr9:119302388
|
T | A | 1 | a0001c0001t0005g0217 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.218+10750A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302388 | ||||||
| chr9:119302401
|
T | TAGCCACT others(16): Show |
1 | a0001c0001t0005g0217 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.218+10714_218+1073 others(27): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302401 | ||||||
| chr9:119302487
|
TG | T | 7 | a0001c0003t0001g0022a0001c0003t0001g0122a0001c0004t0001g0074others(4): Show | 7 | HG01123.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+10650delC | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302487 | ||||||
| chr9:119302540
|
T | C | 1 | a0001c0002t0001g0119 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.218+10598A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302540 | ||||||
| chr9:119302595
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.218+10543A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302595 | ||||||
| chr9:119302828
|
C | T | 8 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(5): Show | 8 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+10310G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302828 | ||||||
| chr9:119302959
|
C | A | 39 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0090others(36): Show | 39 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.218+10179G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119302959 | ||||||
| chr9:119303052
|
GGGAGACT others(6): Show |
G | 1 | a0001c0001t0001g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.218+10073_218+1008 others(17): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303052 | ||||||
| chr9:119303191
|
C | T | 1 | a0001c0003t0008g0185 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.218+9947G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303191 | ||||||
| chr9:119303232
|
C | T | 59 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.218+9906G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303232 | ||||||
| chr9:119303264
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+9874T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303264 | ||||||
| chr9:119303291
|
G | GAC | 68 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0053others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.218+9845_218+9846d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303291 | ||||||
| chr9:119303291
|
G | GACAC | 17 | a0001c0001t0001g0035a0001c0001t0001g0046a0001c0001t0001g0101others(14): Show | 17 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.218+9843_218+9846d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303291 | ||||||
| chr9:119303291
|
G | GACACAC | 11 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0212others(8): Show | 11 | HG02109.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.218+9841_218+9846d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303291 | ||||||
| chr9:119303291
|
G | GACACACA others(1): Show |
4 | a0001c0002t0001g0202a0001c0003t0001g0180a0001c0003t0001g0183others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+9839_218+9846d others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303291 | ||||||
| chr9:119303291
|
G | GACACACA others(3): Show |
5 | a0001c0002t0001g0203a0001c0002t0001g0205a0001c0002t0001g0206others(2): Show | 5 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+9837_218+9846d others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303291 | ||||||
| chr9:119303291
|
GAC | G | 6 | a0001c0002t0001g0162a0001c0003t0001g0042a0001c0003t0001g0186others(3): Show | 6 | HG01891.hp2 HG01934.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+9845_218+9846d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303291 | ||||||
| chr9:119303291
|
GACAC | G | 2 | a0001c0003t0001g0139a0001c0004t0001g0016 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.218+9843_218+9846d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303291 | ||||||
| chr9:119303303
|
C | G | 1 | a0001c0003t0009g0214 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.218+9835G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303303 | ||||||
| chr9:119303425
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+9713C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303425 | ||||||
| chr9:119303427
|
C | T | 59 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.218+9711G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303427 | ||||||
| chr9:119303520
|
G | A | 2 | a0001c0003t0002g0223a0001c0004t0001g0016 | 2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.218+9618C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303520 | ||||||
| chr9:119303523
|
G | A | 8 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(5): Show | 8 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+9615C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303523 | ||||||
| chr9:119303572
|
G | C | 2 | a0001c0003t0001g0175a0001c0003t0001g0207 | 2 | HG01496.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.218+9566C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303572 | ||||||
| chr9:119303875
|
CT | C | 130 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.218+9262delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303875 | ||||||
| chr9:119303950
|
G | T | 1 | a0001c0003t0001g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.218+9188C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119303950 | ||||||
| chr9:119304069
|
G | T | 1 | a0001c0001t0002g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.218+9069C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304069 | ||||||
| chr9:119304094
|
G | A | 18 | a0001c0001t0001g0037a0001c0001t0001g0090a0001c0001t0001g0103others(15): Show | 18 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218+9044C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304094 | ||||||
| chr9:119304175
|
C | T | 1 | a0001c0003t0002g0230 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.218+8963G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304175 | ||||||
| chr9:119304191
|
T | C | 17 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0003t0001g0022others(14): Show | 17 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.218+8947A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304191 | ||||||
| chr9:119304192
|
C | T | 1 | a0001c0003t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218+8946G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304192 | ||||||
| chr9:119304287
|
C | T | 6 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+8851G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304287 | ||||||
| chr9:119304941
|
A | C | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.218+8197T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304941 | ||||||
| chr9:119304957
|
A | G | 4 | a0001c0001t0001g0132a0001c0002t0001g0049a0001c0002t0001g0079others(1): Show | 4 | HG00741.hp2 HG03942.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+8181T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304957 | ||||||
| chr9:119304963
|
T | C | 59 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.218+8175A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119304963 | ||||||
| chr9:119305071
|
G | A | 1 | a0001c0002t0001g0114 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.218+8067C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305071 | ||||||
| chr9:119305089
|
G | A | 8 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(5): Show | 8 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+8049C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305089 | ||||||
| chr9:119305092
|
T | C | 4 | a0001c0001t0001g0086a0001c0001t0001g0106a0001c0001t0001g0150others(1): Show | 4 | HG00423.hp1 HG00438.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+8046A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305092 | ||||||
| chr9:119305193
|
G | C | 1 | a0001c0002t0001g0142 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.218+7945C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305193 | ||||||
| chr9:119305245
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.218+7893C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305245 | ||||||
| chr9:119305257
|
G | C | 4 | a0001c0002t0001g0071a0001c0002t0001g0141a0001c0002t0001g0155others(1): Show | 4 | HG01123.hp2 HG01257.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+7881C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305257 | ||||||
| chr9:119305401
|
C | T | 59 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.218+7737G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305401 | ||||||
| chr9:119305509
|
A | G | 16 | a0001c0001t0001g0037a0001c0001t0001g0090a0001c0001t0001g0103others(13): Show | 16 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.218+7629T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305509 | ||||||
| chr9:119305684
|
G | A | 37 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0090others(34): Show | 37 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.218+7454C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305684 | ||||||
| chr9:119305810
|
T | C | 27 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0002t0001g0202others(24): Show | 27 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.218+7328A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305810 | ||||||
| chr9:119305916
|
A | G | 1 | a0001c0003t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.218+7222T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119305916 | ||||||
| chr9:119306029
|
C | T | 1 | a0001c0003t0008g0185 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.218+7109G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306029 | ||||||
| chr9:119306230
|
C | T | 129 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.218+6908G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306230 | ||||||
| chr9:119306557
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.218+6581C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306557 | ||||||
| chr9:119306603
|
C | T | 37 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0090others(34): Show | 37 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.218+6535G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306603 | ||||||
| chr9:119306604
|
G | A | 1 | a0001c0003t0002g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.218+6534C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306604 | ||||||
| chr9:119306625
|
T | C | 27 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0002t0001g0202others(24): Show | 27 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.218+6513A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306625 | ||||||
| chr9:119306749
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.218+6389A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306749 | ||||||
| chr9:119306804
|
A | T | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+6334T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119306804 | ||||||
| chr9:119307113
|
G | A | 8 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(5): Show | 8 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+6025C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307113 | ||||||
| chr9:119307186
|
A | G | 132 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.218+5952T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307186 | ||||||
| chr9:119307374
|
T | C | 132 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.218+5764A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307374 | ||||||
| chr9:119307557
|
T | G | 34 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0002t0001g0202others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.218+5581A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307557 | ||||||
| chr9:119307629
|
C | A | 4 | a0001c0001t0001g0212a0001c0001t0002g0231a0001c0003t0001g0178others(1): Show | 4 | HG02258.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+5509G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307629 | ||||||
| chr9:119307701
|
T | G | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.218+5437A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307701 | ||||||
| chr9:119307706
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.218+5432G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307706 | ||||||
| chr9:119307980
|
G | A | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+5158C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119307980 | ||||||
| chr9:119308170
|
G | T | 1 | a0001c0002t0001g0143 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.218+4968C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119308170 | ||||||
| chr9:119308551
|
C | T | 30 | a0001c0001t0001g0037a0001c0001t0001g0090a0001c0001t0001g0103others(27): Show | 30 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.218+4587G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119308551 | ||||||
| chr9:119308827
|
G | A | 132 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.218+4311C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119308827 | ||||||
| chr9:119308918
|
C | A | 1 | a0001c0002t0001g0024 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.218+4220G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119308918 | ||||||
| chr9:119308973
|
G | GA | 10 | a0001c0002t0001g0095a0001c0002t0006g0013a0001c0003t0001g0166others(7): Show | 10 | HG01109.hp1 HG01515.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.218+4164dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119308973 | ||||||
| chr9:119308973
|
G | GAA | 29 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0002t0001g0202others(26): Show | 29 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.218+4163_218+4164d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119308973 | ||||||
| chr9:119308973
|
GA | G | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.218+4164delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119308973 | ||||||
| chr9:119309116
|
C | T | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.218+4022G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119309116 | ||||||
| chr9:119309361
|
T | C | 37 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0090others(34): Show | 37 | HG00423.hp2 HG01256.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.218+3777A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119309361 | ||||||
| chr9:119309478
|
C | T | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.218+3660G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119309478 | ||||||
| chr9:119309735
|
T | C | 1 | a0001c0002t0001g0135 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.218+3403A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119309735 | ||||||
| chr9:119309736
|
C | A | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.218+3402G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119309736 | ||||||
| chr9:119309841
|
G | A | 4 | a0001c0003t0001g0180a0001c0003t0001g0183a0001c0003t0001g0190others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+3297C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119309841 | ||||||
| chr9:119309867
|
C | T | 1 | a0001c0003t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218+3271G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119309867 | ||||||
| chr9:119310063
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.218+3075A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119310063 | ||||||
| chr9:119310250
|
G | A | 4 | a0001c0001t0001g0023a0001c0002t0001g0029a0001c0004t0001g0026others(1): Show | 4 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+2888C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119310250 | ||||||
| chr9:119310403
|
G | A | 14 | a0001c0001t0001g0037a0001c0001t0001g0090a0001c0001t0001g0103others(11): Show | 14 | HG00423.hp2 HG01256.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+2735C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119310403 | ||||||
| chr9:119310648
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.218+2490C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119310648 | ||||||
| chr9:119310739
|
A | C | 1 | a0001c0001t0001g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.218+2399T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119310739 | ||||||
| chr9:119310776
|
A | G | 2 | a0001c0001t0001g0134a0004c0011t0001g0125 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.218+2362T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119310776 | ||||||
| chr9:119310929
|
G | C | 98 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.218+2209C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119310929 | ||||||
| chr9:119311147
|
T | C | 1 | a0001c0003t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.218+1991A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119311147 | ||||||
| chr9:119311189
|
T | C | 1 | a0001c0001t0002g0235 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.218+1949A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119311189 | ||||||
| chr9:119311396
|
A | C | 13 | a0001c0001t0001g0200a0001c0003t0001g0040a0001c0003t0001g0041others(10): Show | 13 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+1742T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119311396 | ||||||
| chr9:119311621
|
C | T | 115 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.218+1517G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119311621 | ||||||
| chr9:119311761
|
T | C | 53 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(50): Show | 53 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.218+1377A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119311761 | ||||||
| chr9:119311781
|
G | A | 11 | a0001c0003t0001g0022a0001c0003t0001g0094a0001c0003t0001g0181others(8): Show | 11 | HG00639.hp2 HG00735.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+1357C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119311781 | ||||||
| chr9:119312035
|
T | G | 1 | a0001c0010t0001g0098 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.218+1103A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119312035 | ||||||
| chr9:119312446
|
G | C | 1 | a0001c0002t0001g0116 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.218+692C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119312446 | ||||||
| chr9:119312576
|
G | A | 4 | a0001c0001t0001g0184a0001c0003t0001g0180a0001c0003t0001g0183others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+562C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119312576 | ||||||
| chr9:119312996
|
A | T | 119 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.218+142T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 2/7 | chr9 | 119312996 | ||||||
| chr9:119313433
|
A | G | 1 | a0001c0003t0002g0230 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-50-28T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119313433 | ||||||
| chr9:119313700
|
T | C | 97 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-50-295A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119313700 | ||||||
| chr9:119313734
|
G | C | 7 | a0001c0001t0001g0184a0001c0003t0001g0180a0001c0003t0001g0183others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-329C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119313734 | ||||||
| chr9:119314100
|
A | G | 4 | a0001c0003t0001g0107a0001c0003t0001g0139a0001c0003t0001g0208others(1): Show | 4 | HG01884.hp2 HG02717.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-695T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314100 | ||||||
| chr9:119314296
|
A | T | 224 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-50-891T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314296 | ||||||
| chr9:119314352
|
A | G | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-947T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314352 | ||||||
| chr9:119314357
|
C | T | 97 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-50-952G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314357 | ||||||
| chr9:119314388
|
C | T | 97 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-50-983G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314388 | ||||||
| chr9:119314425
|
G | A | 97 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-50-1020C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314425 | ||||||
| chr9:119314801
|
T | C | 53 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(50): Show | 53 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.-50-1396A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314801 | ||||||
| chr9:119314836
|
C | T | 53 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(50): Show | 53 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.-50-1431G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314836 | ||||||
| chr9:119314888
|
T | G | 97 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-50-1483A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314888 | ||||||
| chr9:119314941
|
A | G | 1 | a0001c0002t0001g0025 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-50-1536T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119314941 | ||||||
| chr9:119315274
|
G | A | 97 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-50-1869C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119315274 | ||||||
| chr9:119315286
|
T | C | 97 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-50-1881A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119315286 | ||||||
| chr9:119315336
|
T | A | 15 | a0001c0001t0002g0231a0001c0003t0001g0022a0001c0003t0001g0181others(12): Show | 15 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50-1931A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119315336 | ||||||
| chr9:119315345
|
T | C | 1 | a0001c0004t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-50-1940A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119315345 | ||||||
| chr9:119315346
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-50-1941C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119315346 | ||||||
| chr9:119315454
|
C | G | 112 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-50-2049G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119315454 | ||||||
| chr9:119315928
|
G | A | 22 | a0001c0001t0001g0184a0001c0001t0002g0231a0001c0003t0001g0022others(19): Show | 22 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-2523C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119315928 | ||||||
| chr9:119316115
|
C | G | 22 | a0001c0001t0001g0184a0001c0001t0002g0231a0001c0003t0001g0022others(19): Show | 22 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-2710G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316115 | ||||||
| chr9:119316119
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-50-2714G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316119 | ||||||
| chr9:119316126
|
G | A | 1 | a0001c0003t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-50-2721C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316126 | ||||||
| chr9:119316136
|
G | A | 1 | a0001c0002t0001g0196 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-50-2731C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316136 | ||||||
| chr9:119316254
|
T | G | 1 | a0001c0003t0001g0107 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-50-2849A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316254 | ||||||
| chr9:119316355
|
T | C | 3 | a0001c0003t0001g0042a0001c0003t0008g0185a0001c0004t0001g0177 | 3 | HG01891.hp2 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-50-2950A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316355 | ||||||
| chr9:119316445
|
T | C | 44 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(41): Show | 44 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-50-3040A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316445 | ||||||
| chr9:119316448
|
T | C | 7 | a0001c0001t0001g0184a0001c0003t0001g0180a0001c0003t0001g0183others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-3043A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316448 | ||||||
| chr9:119316504
|
G | A | 3 | a0001c0001t0001g0046a0001c0003t0001g0045a0001c0003t0001g0047 | 3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-50-3099C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316504 | ||||||
| chr9:119316614
|
A | G | 1 | a0001c0002t0001g0075 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-50-3209T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316614 | ||||||
| chr9:119316877
|
G | A | 1 | a0001c0002t0004g0030 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-50-3472C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316877 | ||||||
| chr9:119316892
|
ACTATCCT others(259): Show |
A | 7 | a0001c0001t0001g0184a0001c0003t0001g0180a0001c0003t0001g0183others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-3753_-50-3488d others(2): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316892 | ||||||
| chr9:119316920
|
G | T | 53 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(50): Show | 53 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.-50-3515C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119316920 | ||||||
| chr9:119317048
|
A | G | 112 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-50-3643T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119317048 | ||||||
| chr9:119317071
|
C | T | 3 | a0001c0001t0003g0001a0001c0002t0003g0005a0002c0013t0003g0006 | 3 | HG01074.hp1 HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-50-3666G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119317071 | ||||||
| chr9:119317781
|
A | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-50-4376T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119317781 | ||||||
| chr9:119317902
|
T | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-50-4497A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119317902 | ||||||
| chr9:119317948
|
G | A | 1 | a0001c0003t0001g0190 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-50-4543C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119317948 | ||||||
| chr9:119318145
|
C | G | 3 | a0001c0001t0001g0156a0001c0001t0001g0170a0001c0002t0001g0088 | 3 | HG00544.hp2 HG02165.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.-50-4740G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318145 | ||||||
| chr9:119318253
|
C | T | 1 | a0001c0004t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-50-4848G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318253 | ||||||
| chr9:119318290
|
G | T | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-4885C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318290 | ||||||
| chr9:119318547
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-50-5142G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318547 | ||||||
| chr9:119318734
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0003g0009 | 2 | HG00741.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-50-5329C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318734 | ||||||
| chr9:119318841
|
T | TG | 6 | a0001c0001t0001g0117a0001c0002t0001g0196a0001c0003t0001g0042others(3): Show | 6 | HG00639.hp1 HG02809.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50-5437dupC | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318841 | ||||||
| chr9:119318841
|
T | TGG | 45 | a0001c0001t0001g0053a0001c0001t0001g0061a0001c0001t0001g0067others(42): Show | 45 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.-50-5438_-50-5437d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318841 | ||||||
| chr9:119318843
|
G | T | 1 | a0001c0003t0002g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-50-5438C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318843 | ||||||
| chr9:119318844
|
G | GGGGGT | 15 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(12): Show | 15 | HG00099.hp1 HG01099.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50-5440_-50-5439i others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | ||||||
| chr9:119318844
|
G | GGGGT | 8 | a0001c0001t0001g0056a0001c0001t0001g0102a0001c0001t0001g0106others(5): Show | 8 | HG00735.hp1 HG01934.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.-50-5440_-50-5439i others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | ||||||
| chr9:119318844
|
G | GGGTGT | 4 | a0001c0001t0001g0078a0001c0001t0001g0090a0001c0003t0001g0208others(1): Show | 4 | HG01261.hp2 HG01884.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-5440_-50-5439i others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | ||||||
| chr9:119318844
|
G | GGT | 24 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0001g0064others(21): Show | 24 | HG01074.hp2 HG01109.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.-50-5441_-50-5440d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | ||||||
| chr9:119318844
|
G | GGTGT | 7 | a0001c0001t0003g0008a0001c0003t0001g0180a0001c0003t0001g0181others(4): Show | 7 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50-5443_-50-5440d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | ||||||
| chr9:119318844
|
G | GT | 2 | a0001c0002t0001g0036a0001c0002t0001g0062 | 2 | HG01358.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-50-5440_-50-5439i others(3): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | ||||||
| chr9:119318844
|
G | T | 1 | a0001c0007t0001g0038 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-50-5439C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | ||||||
| chr9:119318844
|
GGT | G | 7 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0002t0001g0049others(4): Show | 7 | HG02572.hp1 HG02698.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50-5441_-50-5440d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | ||||||
| chr9:119318844
|
GGTGT | G | 28 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0055others(25): Show | 28 | HG01099.hp2 HG01123.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.-50-5443_-50-5440d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | ||||||
| chr9:119318844
|
GGTGTGT | G | 28 | a0001c0001t0001g0108a0001c0001t0001g0111a0001c0001t0001g0123others(25): Show | 28 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.-50-5445_-50-5440d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318844 | ||||||
| chr9:119318846
|
T | G | 17 | a0001c0001t0001g0117a0001c0001t0001g0147a0001c0001t0001g0194others(14): Show | 17 | HG01891.hp1 HG02071.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.-50-5441A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318846 | ||||||
| chr9:119318848
|
T | G | 12 | a0001c0001t0001g0058a0001c0001t0001g0200a0001c0003t0001g0040others(9): Show | 12 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50-5443A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318848 | ||||||
| chr9:119318850
|
T | G | 5 | a0001c0001t0001g0039a0001c0003t0001g0189a0001c0003t0001g0197others(2): Show | 5 | HG01346.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50-5445A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318850 | ||||||
| chr9:119318852
|
T | G | 2 | a0001c0002t0001g0169a0001c0009t0001g0191 | 2 | HG03195.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-50-5447A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318852 | ||||||
| chr9:119318966
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-50-5561G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318966 | ||||||
| chr9:119318984
|
C | G | 1 | a0001c0002t0001g0154 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-50-5579G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119318984 | ||||||
| chr9:119319161
|
T | A | 5 | a0001c0001t0001g0081a0001c0001t0001g0132a0001c0002t0001g0049others(2): Show | 5 | HG00741.hp2 HG03669.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50-5756A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319161 | ||||||
| chr9:119319255
|
T | C | 1 | a0001c0003t0001g0122 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-50-5850A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319255 | ||||||
| chr9:119319391
|
G | A | 4 | a0001c0001t0001g0184a0001c0003t0001g0180a0001c0003t0001g0183others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-5986C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319391 | ||||||
| chr9:119319400
|
C | T | 1 | a0003c0008t0001g0174 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-50-5995G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319400 | ||||||
| chr9:119319540
|
A | G | 44 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(41): Show | 44 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-50-6135T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319540 | ||||||
| chr9:119319597
|
T | C | 104 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-50-6192A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319597 | ||||||
| chr9:119319746
|
G | A | 2 | a0001c0002t0001g0050a0001c0002t0001g0051 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-50-6341C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319746 | ||||||
| chr9:119319762
|
A | G | 1 | a0001c0002t0001g0157 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-50-6357T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319762 | ||||||
| chr9:119319766
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0204 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-50-6361G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319766 | ||||||
| chr9:119319854
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0148a0001c0001t0001g0152 | 3 | HG01346.hp1 HG01975.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-50-6449G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119319854 | ||||||
| chr9:119320074
|
G | GT | 5 | a0001c0001t0002g0231a0001c0003t0002g0223a0001c0003t0002g0228others(2): Show | 5 | HG01109.hp1 HG02886.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50-6670_-50-6669i others(3): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119320074 | ||||||
| chr9:119320075
|
A | C | 5 | a0001c0001t0002g0231a0001c0003t0002g0223a0001c0003t0002g0228others(2): Show | 5 | HG01109.hp1 HG02886.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50-6670T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119320075 | ||||||
| chr9:119320250
|
G | A | 1 | a0001c0002t0003g0002 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-50-6845C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119320250 | ||||||
| chr9:119320281
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-50-6876G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119320281 | ||||||
| chr9:119320446
|
C | G | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-7041G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119320446 | ||||||
| chr9:119320991
|
C | T | 2 | a0001c0003t0001g0213a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-50-7586G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119320991 | ||||||
| chr9:119321062
|
C | T | 1 | a0001c0002t0001g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-50-7657G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321062 | ||||||
| chr9:119321133
|
G | A | 14 | a0001c0001t0001g0200a0001c0003t0001g0040a0001c0003t0001g0041others(11): Show | 14 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50-7728C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321133 | ||||||
| chr9:119321223
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-50-7818T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321223 | ||||||
| chr9:119321226
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-50-7821G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321226 | ||||||
| chr9:119321274
|
T | C | 1 | a0003c0008t0001g0174 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-50-7869A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321274 | ||||||
| chr9:119321342
|
T | C | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0002t0001g0059others(1): Show | 4 | HG01943.hp1 HG01943.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50-7937A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321342 | ||||||
| chr9:119321496
|
A | G | 49 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(46): Show | 49 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.-50-8091T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321496 | ||||||
| chr9:119321500
|
T | A | 1 | a0001c0001t0001g0067 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-50-8095A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321500 | ||||||
| chr9:119321700
|
C | T | 18 | a0001c0001t0001g0200a0001c0003t0001g0040a0001c0003t0001g0041others(15): Show | 18 | HG00639.hp2 HG00735.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.-50-8295G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321700 | ||||||
| chr9:119321757
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-50-8352A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321757 | ||||||
| chr9:119321861
|
C | G | 1 | a0001c0004t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-50-8456G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321861 | ||||||
| chr9:119321977
|
A | G | 12 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(9): Show | 12 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50-8572T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119321977 | ||||||
| chr9:119322166
|
C | G | 4 | a0001c0001t0001g0055a0001c0001t0001g0160a0001c0002t0001g0057others(1): Show | 4 | HG01169.hp2 HG01517.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50-8761G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119322166 | ||||||
| chr9:119322375
|
C | T | 4 | a0001c0001t0001g0184a0001c0003t0001g0180a0001c0003t0001g0183others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-8970G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119322375 | ||||||
| chr9:119322578
|
T | C | 53 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-50-9173A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119322578 | ||||||
| chr9:119323660
|
A | C | 52 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(49): Show | 52 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-50-10255T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119323660 | ||||||
| chr9:119323919
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-50-10514G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119323919 | ||||||
| chr9:119323948
|
AC | A | 52 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(49): Show | 52 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-50-10544delG | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119323948 | ||||||
| chr9:119324027
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50-10622C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119324027 | ||||||
| chr9:119324225
|
C | A | 1 | a0001c0003t0001g0207 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-50-10820G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119324225 | ||||||
| chr9:119324357
|
G | T | 1 | a0001c0002t0001g0142 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-50-10952C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119324357 | ||||||
| chr9:119324869
|
G | A | 1 | a0001c0002t0001g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-50-11464C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119324869 | ||||||
| chr9:119325335
|
T | A | 1 | a0001c0003t0001g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-50-11930A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119325335 | ||||||
| chr9:119325379
|
T | C | 52 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(49): Show | 52 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-50-11974A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119325379 | ||||||
| chr9:119325555
|
C | T | 1 | a0001c0003t0002g0224 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-50-12150G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119325555 | ||||||
| chr9:119325863
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-50-12458C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119325863 | ||||||
| chr9:119326253
|
G | C | 52 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(49): Show | 52 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-50-12848C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119326253 | ||||||
| chr9:119326254
|
G | T | 1 | a0001c0001t0002g0235 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50-12849C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119326254 | ||||||
| chr9:119326913
|
A | C | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-50-13508T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119326913 | ||||||
| chr9:119327269
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-50-13864G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119327269 | ||||||
| chr9:119327476
|
A | T | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-14071T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119327476 | ||||||
| chr9:119327555
|
A | G | 1 | a0001c0002t0001g0027 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-50-14150T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119327555 | ||||||
| chr9:119327676
|
ATTAGCAA others(3): Show |
A | 1 | a0001c0007t0001g0083 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-50-14281_-50-1427 others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119327676 | ||||||
| chr9:119328026
|
A | T | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG00099.hp1 HG00423.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-14621T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119328026 | ||||||
| chr9:119328117
|
C | T | 1 | a0001c0001t0002g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-50-14712G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119328117 | ||||||
| chr9:119328190
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-50-14785C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119328190 | ||||||
| chr9:119328192
|
T | C | 53 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-50-14787A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119328192 | ||||||
| chr9:119328208
|
C | T | 1 | a0001c0003t0009g0214 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-50-14803G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119328208 | ||||||
| chr9:119328737
|
A | G | 19 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(16): Show | 19 | HG00099.hp1 HG00423.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50-15332T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119328737 | ||||||
| chr9:119328843
|
A | C | 4 | a0001c0001t0001g0054a0001c0002t0001g0119a0001c0002t0001g0143others(1): Show | 4 | HG01074.hp2 HG01175.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-15438T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119328843 | ||||||
| chr9:119329187
|
A | C | 2 | a0001c0003t0001g0060a0001c0004t0001g0074 | 2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-50-15782T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119329187 | ||||||
| chr9:119329193
|
T | C | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG00099.hp1 HG00423.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-15788A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119329193 | ||||||
| chr9:119329203
|
A | G | 7 | a0001c0001t0001g0184a0001c0003t0001g0180a0001c0003t0001g0183others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-15798T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119329203 | ||||||
| chr9:119329453
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-50-16048C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119329453 | ||||||
| chr9:119329513
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-50-16108A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119329513 | ||||||
| chr9:119329735
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-50-16330T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119329735 | ||||||
| chr9:119330141
|
T | G | 2 | a0001c0001t0002g0220a0001c0001t0002g0229 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-50-16736A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330141 | ||||||
| chr9:119330206
|
C | T | 1 | a0001c0003t0001g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-50-16801G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330206 | ||||||
| chr9:119330482
|
C | T | 5 | a0001c0001t0001g0081a0001c0001t0001g0132a0001c0002t0001g0049others(2): Show | 5 | HG00741.hp2 HG03669.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50-17077G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330482 | ||||||
| chr9:119330557
|
T | A | 1 | a0001c0015t0001g0133 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-50-17152A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330557 | ||||||
| chr9:119330651
|
C | T | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-17246G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330651 | ||||||
| chr9:119330798
|
CG | C | 7 | a0001c0001t0001g0184a0001c0003t0001g0180a0001c0003t0001g0183others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-17394delC | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330798 | ||||||
| chr9:119330970
|
C | T | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-50-17565G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330970 | ||||||
| chr9:119330983
|
T | C | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-17578A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119330983 | ||||||
| chr9:119331086
|
T | C | 1 | a0001c0002t0001g0029 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-50-17681A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331086 | ||||||
| chr9:119331193
|
A | T | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG00099.hp1 HG00423.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-17788T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331193 | ||||||
| chr9:119331460
|
G | C | 1 | a0001c0003t0001g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-50-18055C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331460 | ||||||
| chr9:119331513
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-50-18108G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331513 | ||||||
| chr9:119331874
|
G | A | 47 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(44): Show | 47 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.-50-18469C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331874 | ||||||
| chr9:119331895
|
A | G | 14 | a0001c0001t0003g0001a0001c0002t0001g0070a0001c0002t0001g0071others(11): Show | 14 | HG00140.hp1 HG00738.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.-50-18490T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331895 | ||||||
| chr9:119331936
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-50-18531C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331936 | ||||||
| chr9:119331970
|
T | G | 9 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0002t0001g0202others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-50-18565A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119331970 | ||||||
| chr9:119332524
|
T | C | 15 | a0001c0001t0001g0200a0001c0003t0001g0040a0001c0003t0001g0041others(12): Show | 15 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50-19119A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119332524 | ||||||
| chr9:119332694
|
G | A | 1 | a0001c0004t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-50-19289C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119332694 | ||||||
| chr9:119333010
|
A | T | 1 | a0001c0002t0001g0114 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-50-19605T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333010 | ||||||
| chr9:119333336
|
G | A | 1 | a0001c0003t0001g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-50-19931C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333336 | ||||||
| chr9:119333456
|
T | C | 114 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.-50-20051A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333456 | ||||||
| chr9:119333462
|
C | CA | 8 | a0001c0001t0001g0053a0001c0001t0001g0069a0001c0001t0001g0081others(5): Show | 8 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50-20058dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333462 | ||||||
| chr9:119333462
|
CA | C | 43 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(40): Show | 43 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.-50-20058delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333462 | ||||||
| chr9:119333462
|
CAA | C | 13 | a0001c0001t0001g0200a0001c0003t0001g0040a0001c0003t0001g0041others(10): Show | 13 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-20059_-50-2005 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333462 | ||||||
| chr9:119333555
|
T | C | 59 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(56): Show | 59 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.-50-20150A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333555 | ||||||
| chr9:119333667
|
G | A | 1 | a0001c0003t0001g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-50-20262C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333667 | ||||||
| chr9:119333878
|
T | G | 1 | a0001c0002t0001g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-50-20473A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333878 | ||||||
| chr9:119333925
|
A | C | 1 | a0001c0003t0002g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-50-20520T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119333925 | ||||||
| chr9:119334141
|
G | C | 1 | a0001c0003t0001g0031 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-50-20736C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334141 | ||||||
| chr9:119334254
|
C | A | 57 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0055others(54): Show | 57 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.-50-20849G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334254 | ||||||
| chr9:119334308
|
G | T | 2 | a0001c0003t0001g0094a0001c0003t0001g0151 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-50-20903C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334308 | ||||||
| chr9:119334343
|
T | C | 2 | a0001c0001t0001g0115a0001c0002t0001g0159 | 2 | HG02015.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.-50-20938A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334343 | ||||||
| chr9:119334355
|
C | T | 7 | a0001c0001t0001g0184a0001c0003t0001g0180a0001c0003t0001g0183others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-20950G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334355 | ||||||
| chr9:119334461
|
C | A | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-50-21056G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334461 | ||||||
| chr9:119334493
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-50-21088T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334493 | ||||||
| chr9:119334795
|
T | C | 1 | a0001c0002t0001g0062 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-50-21390A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334795 | ||||||
| chr9:119334861
|
A | G | 3 | a0001c0001t0001g0046a0001c0003t0001g0045a0001c0003t0001g0047 | 3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-50-21456T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334861 | ||||||
| chr9:119334981
|
A | C | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-21576T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119334981 | ||||||
| chr9:119335038
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-50-21633C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119335038 | ||||||
| chr9:119335080
|
G | A | 7 | a0001c0001t0001g0184a0001c0003t0001g0180a0001c0003t0001g0183others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-21675C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119335080 | ||||||
| chr9:119335126
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-50-21721T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119335126 | ||||||
| chr9:119335927
|
T | C | 29 | a0001c0001t0001g0023a0001c0001t0001g0054a0001c0001t0001g0064others(26): Show | 29 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.-50-22522A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119335927 | ||||||
| chr9:119335942
|
A | G | 7 | a0001c0001t0001g0184a0001c0003t0001g0180a0001c0003t0001g0183others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-22537T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119335942 | ||||||
| chr9:119336273
|
A | C | 1 | a0001c0004t0002g0232 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-50-22868T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119336273 | ||||||
| chr9:119336494
|
A | G | 111 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-50-23089T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119336494 | ||||||
| chr9:119336567
|
A | T | 14 | a0001c0001t0001g0200a0001c0003t0001g0040a0001c0003t0001g0041others(11): Show | 14 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50-23162T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119336567 | ||||||
| chr9:119337196
|
C | T | 2 | a0001c0001t0003g0008a0001c0010t0001g0098 | 2 | HG02523.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-50-23791G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119337196 | ||||||
| chr9:119337207
|
C | A | 48 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(45): Show | 48 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.-50-23802G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119337207 | ||||||
| chr9:119337252
|
C | T | 7 | a0001c0001t0001g0184a0001c0003t0001g0180a0001c0003t0001g0183others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-23847G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119337252 | ||||||
| chr9:119337351
|
T | C | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-23946A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119337351 | ||||||
| chr9:119337639
|
T | G | 48 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(45): Show | 48 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.-50-24234A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119337639 | ||||||
| chr9:119337687
|
G | A | 53 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-50-24282C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119337687 | ||||||
| chr9:119337790
|
G | A | 1 | a0003c0008t0001g0174 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-50-24385C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119337790 | ||||||
| chr9:119338246
|
C | CT | 48 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(45): Show | 48 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.-50-24842dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338246 | ||||||
| chr9:119338246
|
CT | C | 173 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(170): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.-50-24842delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338246 | ||||||
| chr9:119338261
|
T | A | 1 | a0001c0003t0001g0122 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-50-24856A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338261 | ||||||
| chr9:119338469
|
G | A | 2 | a0001c0002t0001g0097a0001c0002t0001g0168 | 2 | NA18953.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-50-25064C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338469 | ||||||
| chr9:119338716
|
C | CA | 49 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(46): Show | 49 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.-50-25312dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338716 | ||||||
| chr9:119338716
|
C | CAAA | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-25314_-50-2531 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338716 | ||||||
| chr9:119338810
|
A | G | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-25405T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338810 | ||||||
| chr9:119338840
|
A | ACAC | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-25438_-50-2543 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338840 | ||||||
| chr9:119338847
|
C | T | 14 | a0001c0001t0001g0200a0001c0003t0001g0040a0001c0003t0001g0041others(11): Show | 14 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50-25442G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338847 | ||||||
| chr9:119338900
|
CA | C | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-25496delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119338900 | ||||||
| chr9:119339201
|
T | G | 4 | a0001c0003t0001g0189a0001c0003t0001g0197a0001c0005t0001g0192others(1): Show | 4 | HG02809.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50-25796A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119339201 | ||||||
| chr9:119339341
|
C | T | 176 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-50-25936G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119339341 | ||||||
| chr9:119339368
|
T | TA | 48 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(45): Show | 48 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.-50-25964dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119339368 | ||||||
| chr9:119339389
|
A | G | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-25984T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119339389 | ||||||
| chr9:119339465
|
G | C | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-26060C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119339465 | ||||||
| chr9:119339906
|
A | G | 7 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0004t0002g0232others(4): Show | 7 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50-26501T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119339906 | ||||||
| chr9:119340096
|
T | C | 9 | a0001c0001t0001g0037a0001c0001t0001g0090a0001c0001t0001g0103others(6): Show | 9 | HG02135.hp1 NA18940.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.-50-26691A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340096 | ||||||
| chr9:119340264
|
C | T | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-26859G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340264 | ||||||
| chr9:119340310
|
A | T | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-26905T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340310 | ||||||
| chr9:119340375
|
A | C | 1 | a0001c0003t0001g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-50-26970T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340375 | ||||||
| chr9:119340413
|
G | GA | 7 | a0001c0003t0001g0022a0001c0003t0001g0213a0001c0003t0002g0230others(4): Show | 7 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50-27009dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340413 | ||||||
| chr9:119340612
|
T | C | 1 | a0001c0002t0004g0118 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-50-27207A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340612 | ||||||
| chr9:119340679
|
G | A | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-27274C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340679 | ||||||
| chr9:119340728
|
C | T | 1 | a0001c0001t0003g0008 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-50-27323G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340728 | ||||||
| chr9:119340965
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-50-27560G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119340965 | ||||||
| chr9:119341035
|
C | T | 1 | a0001c0002t0001g0057 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-50-27630G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341035 | ||||||
| chr9:119341404
|
A | G | 3 | a0001c0001t0001g0106a0001c0001t0005g0215a0001c0001t0005g0217 | 3 | NA18993.hp1 NA18993.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-51+27652T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341404 | ||||||
| chr9:119341408
|
G | A | 56 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(53): Show | 56 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.-51+27648C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341408 | ||||||
| chr9:119341452
|
G | C | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+27604C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341452 | ||||||
| chr9:119341762
|
GTAT | G | 6 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0001g0121others(3): Show | 6 | NA18940.hp1 NA18948.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51+27291_-51+2729 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341762 | ||||||
| chr9:119341786
|
C | T | 1 | a0001c0003t0001g0122 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-51+27270G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341786 | ||||||
| chr9:119341866
|
C | T | 2 | a0001c0001t0001g0061a0001c0002t0001g0062 | 2 | HG00738.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-51+27190G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341866 | ||||||
| chr9:119341912
|
C | T | 9 | a0001c0001t0001g0084a0001c0003t0001g0022a0001c0003t0001g0085others(6): Show | 9 | HG01123.hp1 HG01261.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+27144G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119341912 | ||||||
| chr9:119342100
|
T | TAAAGATC others(316): Show |
6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+26955_-51+2695 others(327): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119342100 | ||||||
| chr9:119342250
|
T | C | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+26806A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119342250 | ||||||
| chr9:119342356
|
G | A | 2 | a0001c0001t0001g0172a0001c0003t0002g0226 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-51+26700C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119342356 | ||||||
| chr9:119342849
|
G | C | 1 | a0001c0003t0001g0122 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-51+26207C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119342849 | ||||||
| chr9:119342883
|
C | T | 12 | a0001c0001t0001g0054a0001c0001t0001g0064a0001c0001t0001g0065others(9): Show | 12 | HG01074.hp2 HG01175.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+26173G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119342883 | ||||||
| chr9:119343152
|
A | G | 48 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(45): Show | 48 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.-51+25904T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119343152 | ||||||
| chr9:119343427
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-51+25629C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119343427 | ||||||
| chr9:119343520
|
A | G | 10 | a0001c0001t0001g0184a0001c0003t0001g0022a0001c0003t0001g0180others(7): Show | 10 | HG01123.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51+25536T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119343520 | ||||||
| chr9:119343680
|
T | G | 10 | a0001c0001t0001g0184a0001c0003t0001g0022a0001c0003t0001g0180others(7): Show | 10 | HG01123.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51+25376A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119343680 | ||||||
| chr9:119343837
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-51+25219T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119343837 | ||||||
| chr9:119344001
|
C | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0219 | 2 | HG02129.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.-51+25055G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119344001 | ||||||
| chr9:119344025
|
G | T | 1 | a0001c0003t0001g0122 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-51+25031C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119344025 | ||||||
| chr9:119344199
|
A | G | 58 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(55): Show | 58 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-51+24857T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119344199 | ||||||
| chr9:119344429
|
A | T | 1 | a0001c0007t0001g0083 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-51+24627T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119344429 | ||||||
| chr9:119344917
|
T | C | 1 | a0001c0007t0001g0083 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-51+24139A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119344917 | ||||||
| chr9:119344998
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-51+24058A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119344998 | ||||||
| chr9:119345083
|
C | T | 46 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(43): Show | 46 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-51+23973G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119345083 | ||||||
| chr9:119345109
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-51+23947G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119345109 | ||||||
| chr9:119345607
|
C | T | 1 | a0001c0003t0001g0122 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-51+23449G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119345607 | ||||||
| chr9:119345766
|
C | T | 53 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-51+23290G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119345766 | ||||||
| chr9:119346179
|
A | C | 48 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(45): Show | 48 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.-51+22877T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119346179 | ||||||
| chr9:119346568
|
C | T | 1 | a0001c0002t0001g0154 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-51+22488G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119346568 | ||||||
| chr9:119347260
|
T | C | 10 | a0001c0001t0001g0184a0001c0003t0001g0022a0001c0003t0001g0180others(7): Show | 10 | HG01123.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51+21796A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119347260 | ||||||
| chr9:119347344
|
G | A | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-51+21712C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119347344 | ||||||
| chr9:119347614
|
C | T | 1 | a0001c0003t0001g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-51+21442G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119347614 | ||||||
| chr9:119347809
|
T | C | 1 | a0001c0004t0001g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-51+21247A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119347809 | ||||||
| chr9:119347871
|
T | C | 4 | a0001c0001t0001g0023a0001c0002t0001g0029a0001c0004t0001g0026others(1): Show | 4 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+21185A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119347871 | ||||||
| chr9:119348314
|
G | C | 1 | a0001c0002t0003g0012 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-51+20742C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119348314 | ||||||
| chr9:119348513
|
T | G | 2 | a0001c0001t0001g0123a0001c0002t0001g0179 | 2 | HG03669.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-51+20543A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119348513 | ||||||
| chr9:119348528
|
C | T | 1 | a0001c0003t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-51+20528G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119348528 | ||||||
| chr9:119348616
|
C | G | 1 | a0001c0003t0001g0122 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-51+20440G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119348616 | ||||||
| chr9:119348968
|
T | C | 3 | a0001c0001t0001g0046a0001c0003t0001g0045a0001c0003t0001g0047 | 3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-51+20088A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119348968 | ||||||
| chr9:119349144
|
C | T | 3 | a0001c0001t0001g0046a0001c0003t0001g0045a0001c0003t0001g0047 | 3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-51+19912G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119349144 | ||||||
| chr9:119349178
|
C | A | 46 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(43): Show | 46 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-51+19878G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119349178 | ||||||
| chr9:119349481
|
A | C | 2 | a0001c0001t0001g0048a0001c0001t0003g0009 | 2 | HG00741.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-51+19575T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119349481 | ||||||
| chr9:119349495
|
T | A | 111 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-51+19561A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119349495 | ||||||
| chr9:119349737
|
T | C | 1 | a0001c0003t0001g0197 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-51+19319A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119349737 | ||||||
| chr9:119349790
|
G | GGGGAAAA others(9): Show |
1 | a0001c0002t0001g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-51+19250_-51+1926 others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119349790 | ||||||
| chr9:119350115
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-51+18941A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119350115 | ||||||
| chr9:119350285
|
C | T | 47 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(44): Show | 47 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.-51+18771G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119350285 | ||||||
| chr9:119350901
|
T | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-51+18155A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119350901 | ||||||
| chr9:119350902
|
C | CT | 53 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-51+18153dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119350902 | ||||||
| chr9:119351399
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-51+17657G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351399 | ||||||
| chr9:119351545
|
G | A | 28 | a0001c0001t0001g0023a0001c0001t0001g0054a0001c0001t0001g0064others(25): Show | 28 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-51+17511C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351545 | ||||||
| chr9:119351624
|
T | G | 48 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(45): Show | 48 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.-51+17432A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351624 | ||||||
| chr9:119351686
|
G | T | 1 | a0001c0002t0003g0005 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-51+17370C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351686 | ||||||
| chr9:119351818
|
A | T | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+17238T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351818 | ||||||
| chr9:119351818
|
AT | A | 103 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-51+17237delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351818 | ||||||
| chr9:119351819
|
T | A | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+17237A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351819 | ||||||
| chr9:119351865
|
G | A | 6 | a0001c0003t0001g0022a0001c0003t0002g0230a0001c0006t0001g0017others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+17191C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351865 | ||||||
| chr9:119351886
|
G | C | 5 | a0001c0001t0001g0081a0001c0001t0001g0132a0001c0002t0001g0049others(2): Show | 5 | HG00741.hp2 HG03669.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51+17170C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351886 | ||||||
| chr9:119351982
|
G | C | 3 | a0001c0001t0001g0046a0001c0003t0001g0045a0001c0003t0001g0047 | 3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-51+17074C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119351982 | ||||||
| chr9:119352018
|
G | A | 1 | a0001c0015t0001g0133 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-51+17038C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119352018 | ||||||
| chr9:119352052
|
C | T | 1 | a0001c0002t0001g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-51+17004G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119352052 | ||||||
| chr9:119352201
|
G | A | 2 | a0001c0001t0001g0037a0001c0002t0001g0032 | 2 | NA18946.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-51+16855C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119352201 | ||||||
| chr9:119352801
|
T | C | 1 | a0001c0002t0001g0169 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-51+16255A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119352801 | ||||||
| chr9:119352821
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-51+16235G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119352821 | ||||||
| chr9:119353020
|
C | A | 47 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0058others(44): Show | 47 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.-51+16036G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353020 | ||||||
| chr9:119353061
|
GCTCCAAT others(3): Show |
G | 1 | a0001c0001t0001g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-51+15985_-51+1599 others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353061 | ||||||
| chr9:119353368
|
T | A | 1 | a0001c0001t0003g0009 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-51+15688A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353368 | ||||||
| chr9:119353411
|
G | C | 115 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.-51+15645C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353411 | ||||||
| chr9:119353479
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-51+15577G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353479 | ||||||
| chr9:119353511
|
C | T | 108 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-51+15545G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353511 | ||||||
| chr9:119353781
|
T | G | 1 | a0001c0002t0001g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-51+15275A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353781 | ||||||
| chr9:119353822
|
C | CT | 9 | a0001c0001t0001g0023a0001c0001t0001g0064a0001c0001t0001g0170others(6): Show | 9 | HG00544.hp2 HG00741.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51+15233dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353822 | ||||||
| chr9:119353822
|
CT | C | 64 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0044others(61): Show | 64 | HG00140.hp1 HG00438.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.-51+15233delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353822 | ||||||
| chr9:119353822
|
CTT | C | 24 | a0001c0001t0001g0058a0001c0001t0001g0106a0001c0001t0001g0113others(21): Show | 24 | HG00438.hp2 HG00544.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.-51+15232_-51+1523 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353822 | ||||||
| chr9:119353822
|
CTTT | C | 38 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0067others(35): Show | 38 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.-51+15231_-51+1523 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353822 | ||||||
| chr9:119353822
|
CTTTT | C | 26 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 26 | HG00099.hp1 HG01070.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.-51+15230_-51+1523 others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353822 | ||||||
| chr9:119353822
|
CTTTTT | C | 13 | a0001c0001t0001g0200a0001c0003t0001g0040a0001c0003t0001g0041others(10): Show | 13 | HG01891.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+15229_-51+1523 others(9): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353822 | ||||||
| chr9:119353880
|
T | C | 1 | a0001c0003t0001g0151 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-51+15176A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119353880 | ||||||
| chr9:119354685
|
A | C | 111 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-51+14371T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354685 | ||||||
| chr9:119354686
|
C | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0152 | 2 | HG01346.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-51+14370G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354686 | ||||||
| chr9:119354695
|
TA | T | 108 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-51+14360delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354695 | ||||||
| chr9:119354703
|
A | G | 3 | a0001c0003t0001g0107a0001c0003t0001g0208a0001c0003t0001g0209 | 3 | HG01884.hp2 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-51+14353T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354703 | ||||||
| chr9:119354704
|
A | T | 3 | a0001c0001t0001g0046a0001c0003t0001g0045a0001c0003t0001g0047 | 3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-51+14352T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354704 | ||||||
| chr9:119354789
|
A | G | 1 | a0001c0003t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-51+14267T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354789 | ||||||
| chr9:119354837
|
C | G | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-51+14219G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354837 | ||||||
| chr9:119354909
|
G | A | 1 | a0001c0004t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-51+14147C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354909 | ||||||
| chr9:119354928
|
T | C | 3 | a0001c0001t0001g0046a0001c0003t0001g0045a0001c0003t0001g0047 | 3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-51+14128A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354928 | ||||||
| chr9:119354996
|
A | G | 9 | a0001c0001t0001g0204a0001c0001t0002g0235a0001c0002t0001g0202others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51+14060T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119354996 | ||||||
| chr9:119355137
|
T | C | 3 | a0001c0001t0001g0195a0001c0003t0002g0224a0001c0004t0001g0016 | 3 | HG02486.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-51+13919A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355137 | ||||||
| chr9:119355258
|
C | A | 1 | a0001c0001t0004g0096 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-51+13798G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355258 | ||||||
| chr9:119355373
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-51+13683G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355373 | ||||||
| chr9:119355446
|
C | T | 5 | a0001c0001t0001g0176a0001c0001t0001g0212a0001c0003t0001g0193others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+13610G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355446 | ||||||
| chr9:119355447
|
G | A | 1 | a0001c0002t0001g0168 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-51+13609C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355447 | ||||||
| chr9:119355451
|
G | A | 2 | a0001c0003t0001g0208a0001c0003t0001g0209 | 2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-51+13605C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355451 | ||||||
| chr9:119355455
|
A | G | 37 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0056others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.-51+13601T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355455 | ||||||
| chr9:119355456
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-51+13600G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355456 | ||||||
| chr9:119355467
|
G | A | 3 | a0001c0003t0001g0193a0001c0003t0001g0211a0001c0005t0001g0210 | 3 | HG02109.hp2 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-51+13589C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355467 | ||||||
| chr9:119355485
|
T | C | 13 | a0001c0001t0001g0048a0001c0001t0001g0076a0001c0001t0001g0081others(10): Show | 13 | HG00741.hp2 HG01074.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51+13571A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355485 | ||||||
| chr9:119355524
|
T | C | 12 | a0001c0001t0001g0048a0001c0001t0001g0076a0001c0001t0001g0080others(9): Show | 12 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.-51+13532A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355524 | ||||||
| chr9:119355556
|
A | G | 1 | a0001c0005t0001g0199 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-51+13500T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355556 | ||||||
| chr9:119355558
|
C | G | 2 | a0001c0001t0001g0037a0001c0002t0001g0032 | 2 | NA18946.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-51+13498G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355558 | ||||||
| chr9:119355589
|
C | A | 1 | a0001c0003t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-51+13467G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355589 | ||||||
| chr9:119355601
|
T | C | 1 | a0001c0001t0004g0096 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-51+13455A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355601 | ||||||
| chr9:119355642
|
T | C | 35 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(32): Show | 35 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-51+13414A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355642 | ||||||
| chr9:119355665
|
C | G | 1 | a0001c0003t0002g0226 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-51+13391G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355665 | ||||||
| chr9:119355723
|
C | T | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-51+13333G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355723 | ||||||
| chr9:119355728
|
C | CA | 45 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0035others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.-51+13327dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355728 | ||||||
| chr9:119355836
|
C | T | 136 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0048others(133): Show | 136 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-51+13220G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355836 | ||||||
| chr9:119355883
|
T | C | 8 | a0001c0001t0001g0194a0001c0001t0001g0200a0001c0002t0001g0196others(5): Show | 8 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-51+13173A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119355883 | ||||||
| chr9:119356033
|
G | A | 3 | a0001c0003t0001g0181a0001c0003t0001g0182a0001c0003t0001g0207 | 3 | HG00639.hp2 HG00735.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-51+13023C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356033 | ||||||
| chr9:119356130
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-51+12926T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356130 | ||||||
| chr9:119356253
|
C | G | 4 | a0001c0001t0001g0212a0001c0003t0001g0211a0001c0003t0001g0213others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+12803G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356253 | ||||||
| chr9:119356343
|
C | G | 12 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+12713G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356343 | ||||||
| chr9:119356423
|
T | C | 1 | a0001c0003t0001g0073 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-51+12633A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356423 | ||||||
| chr9:119356676
|
G | A | 1 | a0001c0003t0001g0207 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-51+12380C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356676 | ||||||
| chr9:119356800
|
G | A | 29 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-51+12256C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356800 | ||||||
| chr9:119356804
|
C | CA | 97 | a0001c0001t0001g0048a0001c0001t0001g0076a0001c0001t0001g0086others(94): Show | 97 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-51+12251dupT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356804 | ||||||
| chr9:119356923
|
T | C | 2 | a0001c0001t0001g0109a0001c0003t0001g0166 | 2 | HG01256.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-51+12133A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119356923 | ||||||
| chr9:119357029
|
T | A | 175 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-51+12027A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357029 | ||||||
| chr9:119357053
|
C | T | 2 | a0001c0003t0001g0060a0001c0004t0001g0074 | 2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-51+12003G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357053 | ||||||
| chr9:119357123
|
A | G | 2 | a0001c0001t0001g0084a0001c0003t0001g0085 | 2 | HG01261.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-51+11933T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357123 | ||||||
| chr9:119357168
|
G | A | 2 | a0001c0003t0001g0060a0001c0004t0001g0074 | 2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-51+11888C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357168 | ||||||
| chr9:119357243
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-51+11813C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357243 | ||||||
| chr9:119357254
|
C | CAT | 2 | a0001c0001t0001g0109a0001c0003t0001g0166 | 2 | HG01256.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-51+11800_-51+1180 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357254 | ||||||
| chr9:119357385
|
T | C | 1 | a0001c0004t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-51+11671A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357385 | ||||||
| chr9:119357411
|
C | T | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-51+11645G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357411 | ||||||
| chr9:119357433
|
CT | C | 7 | a0001c0001t0001g0084a0001c0001t0001g0176a0001c0002t0001g0179others(4): Show | 7 | HG01261.hp1 HG01884.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51+11622delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357433 | ||||||
| chr9:119357660
|
C | T | 235 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-51+11396G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357660 | ||||||
| chr9:119357736
|
G | C | 12 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+11320C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357736 | ||||||
| chr9:119357748
|
A | G | 3 | a0001c0001t0001g0046a0001c0003t0001g0045a0001c0003t0001g0047 | 3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-51+11308T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357748 | ||||||
| chr9:119357831
|
T | G | 180 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(177): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-51+11225A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357831 | ||||||
| chr9:119357838
|
A | G | 1 | a0001c0002t0001g0025 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-51+11218T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357838 | ||||||
| chr9:119357919
|
T | G | 180 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(177): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-51+11137A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119357919 | ||||||
| chr9:119358277
|
C | A | 155 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(152): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-51+10779G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358277 | ||||||
| chr9:119358331
|
G | A | 12 | a0001c0001t0001g0084a0001c0001t0001g0176a0001c0002t0001g0179others(9): Show | 12 | HG01123.hp1 HG01261.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-51+10725C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358331 | ||||||
| chr9:119358384
|
T | C | 3 | a0001c0002t0001g0093a0001c0003t0001g0107a0001c0003t0001g0139 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-51+10672A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358384 | ||||||
| chr9:119358387
|
TA | T | 43 | a0001c0001t0001g0090a0001c0001t0001g0102a0001c0001t0001g0103others(40): Show | 43 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-51+10668delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358387 | ||||||
| chr9:119358387
|
TAA | T | 122 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(119): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.-51+10667_-51+1066 others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358387 | ||||||
| chr9:119358387
|
TAAA | T | 15 | a0001c0001t0001g0172a0001c0001t0003g0001a0001c0001t0003g0008others(12): Show | 15 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-51+10666_-51+1066 others(7): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358387 | ||||||
| chr9:119358416
|
A | G | 222 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.-51+10640T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358416 | ||||||
| chr9:119358464
|
T | C | 212 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-51+10592A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358464 | ||||||
| chr9:119358481
|
G | A | 32 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0056others(29): Show | 32 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.-51+10575C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358481 | ||||||
| chr9:119358537
|
A | G | 97 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0076others(94): Show | 97 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.-51+10519T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358537 | ||||||
| chr9:119358550
|
C | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0002g0220others(4): Show | 7 | HG02886.hp1 HG02976.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51+10506G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358550 | ||||||
| chr9:119358551
|
G | T | 1 | a0003c0008t0001g0174 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-51+10505C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358551 | ||||||
| chr9:119358559
|
C | T | 2 | a0001c0001t0001g0126a0001c0002t0001g0169 | 2 | HG01346.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-51+10497G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358559 | ||||||
| chr9:119358560
|
G | T | 12 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+10496C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358560 | ||||||
| chr9:119358563
|
G | A | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-51+10493C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358563 | ||||||
| chr9:119358714
|
A | G | 97 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0076others(94): Show | 97 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.-51+10342T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358714 | ||||||
| chr9:119358730
|
C | G | 21 | a0001c0001t0001g0084a0001c0001t0001g0109a0001c0001t0001g0176others(18): Show | 21 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-51+10326G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358730 | ||||||
| chr9:119358811
|
C | T | 1 | a0001c0006t0002g0225 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-51+10245G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358811 | ||||||
| chr9:119358861
|
G | A | 5 | a0001c0001t0001g0084a0001c0001t0001g0176a0001c0002t0001g0179others(2): Show | 5 | HG01261.hp1 HG02965.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+10195C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358861 | ||||||
| chr9:119358871
|
G | A | 12 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+10185C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358871 | ||||||
| chr9:119358878
|
T | C | 21 | a0001c0001t0001g0084a0001c0001t0001g0109a0001c0001t0001g0176others(18): Show | 21 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-51+10178A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119358878 | ||||||
| chr9:119359852
|
G | A | 5 | a0001c0001t0001g0084a0001c0001t0001g0176a0001c0002t0001g0179others(2): Show | 5 | HG01261.hp1 HG02965.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+9204C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119359852 | ||||||
| chr9:119359906
|
A | G | 1 | a0001c0003t0001g0175 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51+9150T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119359906 | ||||||
| chr9:119359998
|
G | C | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-51+9058C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119359998 | ||||||
| chr9:119360006
|
G | C | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-51+9050C>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360006 | ||||||
| chr9:119360009
|
C | T | 5 | a0001c0001t0001g0084a0001c0001t0001g0176a0001c0002t0001g0179others(2): Show | 5 | HG01261.hp1 HG02965.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+9047G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360009 | ||||||
| chr9:119360063
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0076a0001c0002t0001g0075 | 3 | HG01106.hp2 HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-51+8993C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360063 | ||||||
| chr9:119360488
|
C | G | 1 | a0001c0002t0001g0159 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-51+8568G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360488 | ||||||
| chr9:119360518
|
G | A | 1 | a0001c0002t0001g0079 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-51+8538C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360518 | ||||||
| chr9:119360527
|
G | GAC | 96 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0087others(93): Show | 96 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.-51+8527_-51+8528d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360527 | ||||||
| chr9:119360636
|
T | C | 9 | a0001c0001t0001g0194a0001c0001t0001g0200a0001c0002t0001g0196others(6): Show | 9 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+8420A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360636 | ||||||
| chr9:119360946
|
G | T | 1 | a0001c0004t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-51+8110C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119360946 | ||||||
| chr9:119361013
|
C | T | 177 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-51+8043G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119361013 | ||||||
| chr9:119361087
|
G | A | 7 | a0001c0001t0001g0084a0001c0001t0001g0176a0001c0002t0001g0179others(4): Show | 7 | HG01261.hp1 HG01884.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51+7969C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119361087 | ||||||
| chr9:119361515
|
C | G | 177 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-51+7541G>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119361515 | ||||||
| chr9:119361608
|
ATTC | A | 46 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(43): Show | 46 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.-51+7445_-51+7447d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119361608 | ||||||
| chr9:119361797
|
A | AT | 31 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0055others(28): Show | 31 | HG00639.hp1 HG01069.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.-51+7258dupA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119361797 | ||||||
| chr9:119361797
|
AT | A | 106 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0044others(103): Show | 106 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-51+7258delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119361797 | ||||||
| chr9:119362047
|
A | AC | 10 | a0001c0001t0001g0048a0001c0001t0001g0078a0001c0001t0003g0001others(7): Show | 10 | HG00423.hp1 HG00741.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51+7008dupG | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362047 | ||||||
| chr9:119362098
|
G | T | 1 | a0001c0002t0006g0013 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-51+6958C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362098 | ||||||
| chr9:119362223
|
T | C | 1 | a0001c0002t0001g0196 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-51+6833A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362223 | ||||||
| chr9:119362342
|
T | C | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-51+6714A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362342 | ||||||
| chr9:119362372
|
T | A | 4 | a0001c0001t0001g0108a0001c0002t0001g0097a0001c0002t0001g0116others(1): Show | 4 | HG02071.hp1 NA18747.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+6684A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362372 | ||||||
| chr9:119362509
|
T | C | 12 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+6547A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362509 | ||||||
| chr9:119362511
|
G | A | 93 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0090others(90): Show | 93 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.-51+6545C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362511 | ||||||
| chr9:119362542
|
T | C | 3 | a0001c0001t0001g0212a0001c0003t0001g0211a0001c0003t0001g0213 | 3 | HG02258.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51+6514A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362542 | ||||||
| chr9:119362576
|
C | T | 1 | a0001c0004t0002g0232 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-51+6480G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362576 | ||||||
| chr9:119362624
|
G | T | 9 | a0001c0001t0001g0194a0001c0001t0001g0200a0001c0002t0001g0196others(6): Show | 9 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+6432C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362624 | ||||||
| chr9:119362705
|
C | A | 35 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0055others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.-51+6351G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119362705 | ||||||
| chr9:119363066
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-51+5990C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363066 | ||||||
| chr9:119363076
|
G | A | 19 | a0001c0001t0001g0084a0001c0001t0001g0176a0001c0001t0003g0001others(16): Show | 19 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-51+5980C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363076 | ||||||
| chr9:119363263
|
T | A | 12 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+5793A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363263 | ||||||
| chr9:119363323
|
A | G | 44 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.-51+5733T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363323 | ||||||
| chr9:119363326
|
A | G | 3 | a0001c0002t0001g0093a0001c0003t0001g0107a0001c0003t0001g0139 | 3 | HG03041.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-51+5730T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363326 | ||||||
| chr9:119363335
|
C | T | 5 | a0001c0001t0001g0084a0001c0001t0001g0176a0001c0002t0001g0179others(2): Show | 5 | HG01261.hp1 HG02965.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+5721G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363335 | ||||||
| chr9:119363341
|
A | T | 2 | a0001c0001t0001g0084a0001c0003t0001g0085 | 2 | HG01261.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-51+5715T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363341 | ||||||
| chr9:119363398
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-51+5658C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363398 | ||||||
| chr9:119363881
|
G | A | 1 | a0001c0003t0001g0175 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51+5175C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363881 | ||||||
| chr9:119363935
|
G | A | 2 | a0001c0003t0001g0181a0001c0003t0001g0182 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-51+5121C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363935 | ||||||
| chr9:119363974
|
A | G | 12 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+5082T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119363974 | ||||||
| chr9:119364018
|
CT | C | 18 | a0001c0001t0001g0043a0001c0001t0003g0001a0001c0001t0003g0008others(15): Show | 18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-51+5037delA | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364018 | ||||||
| chr9:119364018
|
CTT | C | 100 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0001g0090others(97): Show | 100 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.-51+5036_-51+5037d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364018 | ||||||
| chr9:119364018
|
CTTT | C | 60 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.-51+5035_-51+5037d others(5): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364018 | ||||||
| chr9:119364048
|
G | A | 95 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0090others(92): Show | 95 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.-51+5008C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364048 | ||||||
| chr9:119364200
|
A | G | 176 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(173): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-51+4856T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364200 | ||||||
| chr9:119364387
|
C | T | 3 | a0001c0001t0001g0212a0001c0003t0001g0211a0001c0003t0001g0213 | 3 | HG02258.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51+4669G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364387 | ||||||
| chr9:119364416
|
C | T | 1 | a0001c0005t0001g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-51+4640G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364416 | ||||||
| chr9:119364445
|
C | T | 176 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(173): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-51+4611G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364445 | ||||||
| chr9:119364655
|
G | A | 3 | a0001c0001t0001g0134a0001c0002t0001g0135a0004c0011t0001g0125 | 3 | HG01256.hp1 HG01258.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-51+4401C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364655 | ||||||
| chr9:119364893
|
C | T | 1 | a0001c0003t0001g0207 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-51+4163G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364893 | ||||||
| chr9:119364917
|
A | G | 1 | a0001c0003t0001g0175 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51+4139T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364917 | ||||||
| chr9:119364964
|
T | A | 1 | a0001c0003t0001g0175 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51+4092A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119364964 | ||||||
| chr9:119365098
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-51+3958A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365098 | ||||||
| chr9:119365210
|
G | A | 2 | a0001c0003t0001g0208a0001c0003t0001g0209 | 2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-51+3846C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365210 | ||||||
| chr9:119365284
|
G | T | 7 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0117others(4): Show | 7 | HG00423.hp2 HG00438.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51+3772C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365284 | ||||||
| chr9:119365330
|
GA | G | 3 | a0001c0001t0001g0212a0001c0003t0001g0211a0001c0003t0001g0213 | 3 | HG02258.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51+3725delT | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365330 | ||||||
| chr9:119365468
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0121 | 2 | NA18940.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-51+3588C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365468 | ||||||
| chr9:119365752
|
C | A | 1 | a0001c0001t0002g0235 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-51+3304G>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365752 | ||||||
| chr9:119365816
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-51+3240G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365816 | ||||||
| chr9:119365996
|
C | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0076a0001c0002t0001g0075 | 3 | HG01106.hp2 HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-51+3060G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119365996 | ||||||
| chr9:119366052
|
C | T | 9 | a0001c0001t0001g0194a0001c0001t0001g0200a0001c0002t0001g0196others(6): Show | 9 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+3004G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366052 | ||||||
| chr9:119366336
|
C | T | 12 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+2720G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366336 | ||||||
| chr9:119366498
|
A | G | 223 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.-51+2558T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366498 | ||||||
| chr9:119366503
|
C | CGT | 2 | a0001c0001t0001g0204a0001c0007t0001g0082 | 2 | HG01169.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-51+2551_-51+2552d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | ||||||
| chr9:119366503
|
C | CGTGT | 2 | a0001c0002t0001g0202a0001c0002t0001g0203 | 2 | HG01109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+2549_-51+2552d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | ||||||
| chr9:119366503
|
CGT | C | 9 | a0001c0001t0001g0086a0001c0002t0001g0025a0001c0002t0001g0027others(6): Show | 9 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+2551_-51+2552d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | ||||||
| chr9:119366503
|
CGTGT | C | 12 | a0001c0001t0001g0053a0001c0001t0001g0167a0001c0001t0003g0008others(9): Show | 12 | HG00280.hp2 HG00738.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.-51+2549_-51+2552d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | ||||||
| chr9:119366503
|
CGTGTGT | C | 25 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(22): Show | 25 | HG00099.hp1 HG00735.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.-51+2547_-51+2552d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | ||||||
| chr9:119366503
|
CGTGTGTG others(1): Show |
C | 47 | a0001c0001t0001g0046a0001c0001t0001g0058a0001c0001t0001g0099others(44): Show | 47 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.-51+2545_-51+2552d others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | ||||||
| chr9:119366503
|
CGTGTGTG others(3): Show |
C | 104 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0043others(101): Show | 104 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.-51+2543_-51+2552d others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | ||||||
| chr9:119366503
|
CGTGTGTG others(5): Show |
C | 15 | a0001c0001t0001g0076a0001c0001t0001g0146a0001c0001t0001g0163others(12): Show | 15 | HG00639.hp1 HG01106.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.-51+2541_-51+2552d others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | ||||||
| chr9:119366503
|
CGTGTGTG others(7): Show |
C | 5 | a0001c0001t0001g0078a0001c0001t0001g0158a0001c0001t0001g0195others(2): Show | 5 | HG01261.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51+2539_-51+2552d others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | ||||||
| chr9:119366503
|
CGTGTGTG others(9): Show |
C | 2 | a0001c0003t0001g0189a0001c0003t0001g0211 | 2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-51+2537_-51+2552d others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | ||||||
| chr9:119366503
|
CGTGTGTG others(11): Show |
C | 2 | a0001c0001t0001g0212a0001c0005t0002g0236 | 2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-51+2535_-51+2552d others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | ||||||
| chr9:119366503
|
CGTGTGTG others(13): Show |
C | 2 | a0001c0003t0001g0213a0001c0005t0001g0210 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51+2533_-51+2552d others(22): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | ||||||
| chr9:119366503
|
CGTGTGTG others(21): Show |
C | 3 | a0001c0002t0001g0089a0001c0002t0001g0092a0001c0003t0001g0175 | 3 | HG02145.hp2 NA18977.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-51+2525_-51+2552d others(30): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366503 | ||||||
| chr9:119366504
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-51+2552C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366504 | ||||||
| chr9:119366506
|
G | A | 2 | a0001c0001t0001g0086a0001c0003t0001g0151 | 2 | HG06807.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-51+2550C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366506 | ||||||
| chr9:119366508
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-51+2548C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366508 | ||||||
| chr9:119366510
|
G | A | 6 | a0001c0001t0001g0106a0001c0001t0001g0148a0001c0001t0001g0152others(3): Show | 6 | HG01257.hp1 HG01952.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+2546C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366510 | ||||||
| chr9:119366512
|
G | A | 16 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG00423.hp2 HG00438.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.-51+2544C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366512 | ||||||
| chr9:119366514
|
G | A | 61 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0102others(58): Show | 61 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.-51+2542C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366514 | ||||||
| chr9:119366516
|
G | A | 4 | a0001c0001t0001g0146a0001c0001t0001g0163a0001c0002t0001g0143others(1): Show | 4 | HG01169.hp2 HG01175.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+2540C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366516 | ||||||
| chr9:119366518
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-51+2538C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366518 | ||||||
| chr9:119366532
|
G | A | 2 | a0001c0002t0001g0089a0001c0002t0001g0092 | 2 | NA18977.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-51+2524C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366532 | ||||||
| chr9:119366741
|
T | C | 176 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(173): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-51+2315A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366741 | ||||||
| chr9:119366833
|
A | G | 12 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+2223T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119366833 | ||||||
| chr9:119367094
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-51+1962C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367094 | ||||||
| chr9:119367097
|
T | C | 4 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0002t0001g0049others(1): Show | 4 | HG03669.hp2 HG03942.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+1959A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367097 | ||||||
| chr9:119367177
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-51+1879G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367177 | ||||||
| chr9:119367193
|
A | ATG | 11 | a0001c0001t0001g0084a0001c0001t0001g0176a0001c0002t0001g0179others(8): Show | 11 | HG00639.hp2 HG00735.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.-51+1861_-51+1862d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367193 | ||||||
| chr9:119367193
|
A | ATGTG | 32 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(29): Show | 32 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-51+1859_-51+1862d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367193 | ||||||
| chr9:119367194
|
T | C | 1 | a0001c0003t0001g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-51+1862A>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367194 | ||||||
| chr9:119367215
|
G | GAT | 2 | a0001c0007t0001g0082a0001c0007t0001g0083 | 2 | HG01099.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-51+1840_-51+1841i others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367215 | ||||||
| chr9:119367217
|
G | GTGTGATA others(1): Show |
2 | a0001c0002t0003g0011a0001c0002t0003g0012 | 2 | HG00140.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGATA others(5): Show |
3 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0002t0003g0010 | 3 | HG00741.hp1 HG02683.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGATA others(7): Show |
4 | a0001c0002t0003g0005a0001c0002t0003g0007a0001c0014t0003g0004others(1): Show | 4 | HG00738.hp1 HG01074.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGATA others(9): Show |
5 | a0001c0001t0001g0200a0001c0002t0003g0002a0001c0002t0003g0003others(2): Show | 5 | HG01070.hp2 HG01106.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGATA others(11): Show |
2 | a0001c0001t0003g0001a0001c0002t0001g0196 | 2 | HG00639.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGATA others(13): Show |
1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(22): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGATA others(15): Show |
1 | a0001c0003t0001g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(24): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGATA others(17): Show |
2 | a0001c0003t0001g0186a0001c0003t0008g0185 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(26): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGATA others(23): Show |
1 | a0001c0003t0001g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(32): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGATT others(17): Show |
3 | a0001c0003t0001g0190a0001c0005t0001g0192a0001c0009t0001g0191 | 3 | HG03041.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(26): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGATT others(21): Show |
3 | a0001c0001t0001g0184a0001c0003t0001g0183a0001c0004t0001g0015 | 3 | HG01243.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(30): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGATT others(23): Show |
1 | a0001c0003t0001g0180 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(32): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGATT others(27): Show |
1 | a0001c0004t0001g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(36): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGATT others(29): Show |
1 | a0001c0003t0001g0175 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(38): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGATT others(41): Show |
1 | a0003c0008t0001g0174 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(50): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGTGA others(17): Show |
1 | a0001c0001t0001g0195 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-51+1838_-51+1839i others(26): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
G | GTGTGTGA others(19): Show |
2 | a0001c0003t0001g0189a0001c0004t0001g0188 | 2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-51+1838_-51+1839i others(28): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367217
|
GAT | G | 3 | a0001c0001t0001g0172a0001c0003t0001g0208a0001c0003t0001g0209 | 3 | HG01884.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-51+1837_-51+1838d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367217 | ||||||
| chr9:119367220
|
T | A | 36 | a0001c0001t0001g0184a0001c0001t0001g0194a0001c0001t0001g0195others(33): Show | 36 | HG00140.hp1 HG00639.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-51+1836A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367220 | ||||||
| chr9:119367221
|
G | GAT | 24 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-51+1833_-51+1834d others(4): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATAT | 34 | a0001c0001t0001g0023a0001c0001t0001g0053a0001c0001t0001g0054others(31): Show | 34 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-51+1831_-51+1834d others(6): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATAT | 3 | a0001c0001t0001g0048a0001c0001t0001g0170a0001c0002t0001g0049 | 3 | HG00544.hp2 HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-51+1829_-51+1834d others(8): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(1): Show |
10 | a0001c0001t0001g0084a0001c0001t0001g0204a0001c0002t0001g0169others(7): Show | 10 | HG01109.hp2 HG01261.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.-51+1827_-51+1834d others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(3): Show |
3 | a0001c0001t0001g0046a0001c0003t0001g0045a0001c0003t0001g0047 | 3 | HG02451.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-51+1825_-51+1834d others(12): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(5): Show |
3 | a0001c0001t0001g0167a0001c0002t0001g0168a0001c0005t0001g0201 | 3 | HG02683.hp1 HG03579.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.-51+1823_-51+1834d others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(7): Show |
3 | a0001c0002t0001g0165a0001c0003t0001g0166a0001c0003t0009g0214 | 3 | HG01515.hp1 HG01884.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-51+1821_-51+1834d others(16): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(9): Show |
5 | a0001c0001t0001g0163a0001c0002t0001g0161a0001c0002t0001g0162others(2): Show | 5 | HG00438.hp1 HG01169.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+1819_-51+1834d others(18): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(11): Show |
2 | a0001c0001t0001g0160a0001c0002t0001g0159 | 2 | HG01517.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.-51+1817_-51+1834d others(20): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(13): Show |
5 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0002t0001g0155others(2): Show | 5 | HG01952.hp2 HG02109.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+1815_-51+1834d others(22): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(15): Show |
5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0002t0001g0154others(2): Show | 5 | HG01978.hp1 HG02074.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51+1813_-51+1834d others(24): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(17): Show |
9 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0150others(6): Show | 9 | HG00438.hp2 HG01975.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(26): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(19): Show |
4 | a0001c0001t0001g0146a0001c0002t0001g0145a0001c0003t0001g0181others(1): Show | 4 | HG00639.hp2 HG00735.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(28): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(21): Show |
9 | a0001c0001t0001g0044a0001c0001t0001g0138a0001c0001t0001g0140others(6): Show | 9 | HG00423.hp2 HG00741.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(30): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(23): Show |
17 | a0001c0001t0001g0043a0001c0001t0001g0123a0001c0001t0001g0124others(14): Show | 17 | HG01256.hp1 HG01258.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(32): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(25): Show |
6 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0176others(3): Show | 6 | HG00423.hp1 HG03130.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(34): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(27): Show |
13 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0109others(10): Show | 13 | HG00544.hp1 HG01256.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(36): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(29): Show |
9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(38): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(31): Show |
5 | a0001c0001t0004g0096a0001c0002t0001g0093a0001c0002t0001g0095others(2): Show | 5 | HG02074.hp1 HG02523.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(40): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(33): Show |
4 | a0001c0001t0001g0090a0001c0002t0001g0092a0001c0002t0006g0013others(1): Show | 4 | HG02135.hp1 NA18747.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(42): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | GATATATA others(35): Show |
4 | a0001c0001t0001g0087a0001c0001t0002g0220a0001c0002t0001g0088others(1): Show | 4 | HG02165.hp1 HG02886.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+1834_-51+1835i others(44): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
G | T | 36 | a0001c0001t0001g0184a0001c0001t0001g0194a0001c0001t0001g0195others(33): Show | 36 | HG00140.hp1 HG00639.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-51+1835C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367221
|
GATATATA others(5): Show |
G | 4 | a0001c0001t0001g0212a0001c0003t0001g0211a0001c0003t0001g0213others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+1823_-51+1834d others(14): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367221 | ||||||
| chr9:119367224
|
A | T | 3 | a0001c0001t0001g0172a0001c0003t0001g0208a0001c0003t0001g0209 | 3 | HG01884.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-51+1832T>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367224 | ||||||
| chr9:119367225
|
T | G | 3 | a0001c0001t0001g0172a0001c0003t0001g0208a0001c0003t0001g0209 | 3 | HG01884.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-51+1831A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367225 | ||||||
| chr9:119367238
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0086 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-51+1817_-51+1818i others(31): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367238 | ||||||
| chr9:119367245
|
T | A | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-51+1811A>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367245 | ||||||
| chr9:119367297
|
C | T | 94 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0090others(91): Show | 94 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.-51+1759G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367297 | ||||||
| chr9:119367318
|
G | T | 2 | a0001c0001t0001g0084a0001c0003t0001g0085 | 2 | HG01261.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-51+1738C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367318 | ||||||
| chr9:119367359
|
G | A | 3 | a0001c0001t0001g0212a0001c0003t0001g0211a0001c0003t0001g0213 | 3 | HG02258.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51+1697C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367359 | ||||||
| chr9:119367605
|
T | G | 1 | a0001c0003t0009g0214 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-51+1451A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367605 | ||||||
| chr9:119367815
|
ACTCTCTC others(1): Show |
A | 4 | a0001c0001t0001g0216a0001c0001t0005g0215a0001c0001t0005g0217others(1): Show | 4 | NA18966.hp1 NA18970.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+1233_-51+1240d others(10): Show |
BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367815 | ||||||
| chr9:119367933
|
G | A | 176 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(173): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-51+1123C>T | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119367933 | ||||||
| chr9:119368004
|
A | C | 12 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+1052T>G | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119368004 | ||||||
| chr9:119368410
|
T | G | 1 | a0001c0002t0001g0219 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-51+646A>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119368410 | ||||||
| chr9:119368459
|
A | G | 7 | a0001c0003t0001g0020a0001c0003t0001g0022a0001c0004t0001g0016others(4): Show | 7 | HG01123.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51+597T>C | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119368459 | ||||||
| chr9:119368886
|
C | T | 26 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(23): Show | 26 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.-51+170G>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119368886 | ||||||
| chr9:119368925
|
G | T | 1 | a0001c0004t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-51+131C>A | BRINP1 | ENSG00000078725.13 | transcript | ENST00000265922.8 | protein_coding | 1/7 | chr9 | 119368925 |