Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23637 |
|---|---|
| ensemblid | ENSG00000011454.18 |
| hgncid | 17155 |
| symbol | RABGAP1 |
| name | RAB GTPase activating protein 1 |
| refseq_nuc | NM_012197.4 |
| refseq_prot | NP_036329.3 |
| ensembl_nuc | ENST00000373647.9 |
| ensembl_prot | ENSP00000362751.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 122941020 |
| end | 123104866 |
| strand | + |
| ver | v1.2 |
| region | chr9:122941020-123104866 |
| region5000 | chr9:122936020-123109866 |
| regionname0 | RABGAP1_chr9_122941020_123104866 |
| regionname5000 | RABGAP1_chr9_122936020_123109866 |
| 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 | 1069 | 251 | 72 | 52 | 100 | 10 | 15 | 72 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0002 | 0/0 | 1069 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0003 | 0/0 | 1069 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0004 | 0/0 | 1069 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| 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 | 3210 | 228 | 72 | 51 | 82 | 8 | 13 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| c0002 | 0/0 | 3210 | 21 | 0 | 1 | 16 | 2 | 2 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| c0003 | 0/0 | 3210 | 5 | 0 | 0 | 5 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| c0004 | 0/0 | 3210 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| c0005 | 0/0 | 3210 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| c0006 | 0/0 | 3210 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| c0007 | 0/0 | 3210 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| 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 | 0/0 | 1764 | 7 | 0 | 3 | 0 | 2 | 2 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0002 | 0/0 | 1778 | 7 | 0 | 0 | 7 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0003 | 0/0 | 1786 | 7 | 0 | 4 | 3 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0004 | 0/0 | 1782 | 7 | 1 | 1 | 5 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0005 | 0/0 | 1769 | 7 | 0 | 0 | 6 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0006 | 0/0 | 1768 | 6 | 0 | 1 | 4 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0007 | 0/0 | 1780 | 6 | 1 | 1 | 4 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0008 | 0/0 | 1748 | 5 | 4 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0009 | 0/0 | 1766 | 5 | 5 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0010 | 0/0 | 1746 | 4 | 1 | 2 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0011 | 0/0 | 1770 | 4 | 4 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0012 | 0/0 | 1766 | 4 | 1 | 2 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0013 | 0/0 | 1778 | 4 | 0 | 2 | 1 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0014 | 0/0 | 1784 | 4 | 0 | 4 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0015 | 0/0 | 1790 | 4 | 0 | 0 | 1 | 2 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0016 | 0/0 | 1792 | 4 | 0 | 4 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0017 | 0/0 | 1760 | 3 | 2 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0018 | 0/0 | 1764 | 3 | 2 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0019 | 0/0 | 1766 | 3 | 2 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0020 | 0/0 | 1760 | 3 | 1 | 2 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0021 | 0/0 | 1768 | 3 | 3 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0022 | 0/0 | 1764 | 3 | 0 | 0 | 3 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0023 | 0/0 | 1770 | 3 | 3 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0024 | 0/0 | 1770 | 3 | 0 | 0 | 3 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0025 | 0/0 | 1774 | 3 | 1 | 0 | 1 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0026 | 0/1 | 1772 | 3 | 0 | 1 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0027 | 0/0 | 1782 | 3 | 0 | 1 | 1 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0028 | 0/0 | 1778 | 3 | 3 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0029 | 1/0 | 1777 | 3 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0030 | 0/0 | 1788 | 3 | 0 | 1 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0031 | 0/0 | 1784 | 3 | 0 | 0 | 3 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0032 | 0/0 | 1800 | 3 | 0 | 0 | 3 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0033 | 0/0 | 1750 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0034 | 0/0 | 1768 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0035 | 0/0 | 1762 | 2 | 1 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0036 | 0/0 | 1772 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0037 | 0/0 | 1772 | 2 | 1 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0038 | 0/0 | 1770 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0039 | 0/0 | 1776 | 2 | 1 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0040 | 0/0 | 1772 | 2 | 0 | 1 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0041 | 0/0 | 1780 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0042 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0043 | 0/0 | 1784 | 2 | 0 | 2 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0044 | 0/0 | 1776 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0045 | 0/0 | 1786 | 2 | 1 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0046 | 0/0 | 1796 | 2 | 0 | 1 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0047 | 0/0 | 1800 | 2 | 0 | 1 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0048 | 0/0 | 1780 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0049 | 0/0 | 1773 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0050 | 0/0 | 1767 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0051 | 0/0 | 1777 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0052 | 0/0 | 1773 | 2 | 0 | 0 | 1 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0053 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0054 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0055 | 0/0 | 1796 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0056 | 0/0 | 1752 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0057 | 0/0 | 1754 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0058 | 0/0 | 1762 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0059 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0060 | 0/0 | 1762 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0061 | 0/0 | 1760 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0062 | 0/0 | 1762 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0063 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0064 | 0/0 | 1768 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0065 | 0/0 | 1772 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0066 | 0/0 | 1774 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0067 | 0/0 | 1769 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0068 | 0/0 | 1768 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0069 | 0/0 | 1764 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0070 | 0/0 | 1774 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0071 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0072 | 0/0 | 1768 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0073 | 0/0 | 1768 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0074 | 0/0 | 1770 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0075 | 0/0 | 1776 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0076 | 0/0 | 1782 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0077 | 0/0 | 1772 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0078 | 0/0 | 1776 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0079 | 0/0 | 1775 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0080 | 0/0 | 1778 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0081 | 0/0 | 1778 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0082 | 0/0 | 1777 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0083 | 0/0 | 1782 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0084 | 0/0 | 1780 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0085 | 0/0 | 1782 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0086 | 0/0 | 1781 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0087 | 0/0 | 1784 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0088 | 0/0 | 1786 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0089 | 0/0 | 1784 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0090 | 0/0 | 1794 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0091 | 0/0 | 1783 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0092 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0093 | 0/0 | 1790 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0094 | 0/0 | 1776 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0095 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0096 | 0/0 | 1790 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0097 | 0/0 | 1794 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0098 | 0/0 | 1790 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0099 | 0/0 | 1798 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0100 | 0/0 | 1789 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0101 | 0/0 | 1791 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0102 | 0/0 | 1792 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0103 | 0/0 | 1798 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0104 | 0/0 | 1798 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0105 | 0/0 | 1808 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0106 | 0/0 | 1790 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0107 | 0/0 | 1798 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0108 | 0/0 | 1800 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0109 | 0/0 | 1796 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0110 | 0/0 | 1802 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0111 | 0/0 | 1802 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0112 | 0/0 | 1798 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0113 | 0/0 | 1798 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0114 | 0/0 | 1806 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0115 | 0/0 | 1808 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0116 | 0/0 | 1802 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0117 | 0/0 | 1804 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0118 | 0/0 | 1806 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0119 | 0/0 | 1798 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0120 | 0/0 | 1738 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0121 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0122 | 0/0 | 1765 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0123 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0124 | 0/0 | 1763 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0125 | 0/0 | 1768 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0126 | 0/0 | 1771 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0127 | 0/0 | 1775 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0128 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0129 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0130 | 0/0 | 1784 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0131 | 0/0 | 1784 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0132 | 0/0 | 1776 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0133 | 0/0 | 1776 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0134 | 0/0 | 1778 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0135 | 0/0 | 1782 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0136 | 0/0 | 1784 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| t0137 | 0/0 | 1786 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| 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 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| 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 | 3210 | 228 | 72 | 51 | 82 | 8 | 13 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0002 | 0/0 | 3210 | 21 | 0 | 1 | 16 | 2 | 2 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0006 | 0/0 | 3210 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0007 | 0/0 | 3210 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0002c0003 | 0/0 | 3210 | 5 | 0 | 0 | 5 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0003c0004 | 0/0 | 3210 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0004c0005 | 0/0 | 3210 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4973 | 7 | 0 | 3 | 0 | 2 | 2 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0002 | 0/0 | 4987 | 7 | 0 | 0 | 7 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0003 | 0/0 | 4995 | 7 | 0 | 4 | 3 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0004 | 0/0 | 4991 | 7 | 1 | 1 | 5 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0006 | 0/0 | 4977 | 5 | 0 | 1 | 4 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0007 | 0/0 | 4989 | 6 | 1 | 1 | 4 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0008 | 0/0 | 4957 | 5 | 4 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0009 | 0/0 | 4975 | 5 | 5 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0010 | 0/0 | 4955 | 4 | 1 | 2 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0011 | 0/0 | 4979 | 4 | 4 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0012 | 0/0 | 4975 | 4 | 1 | 2 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0013 | 0/0 | 4987 | 4 | 0 | 2 | 1 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0014 | 0/0 | 4993 | 4 | 0 | 4 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0015 | 0/0 | 4999 | 4 | 0 | 0 | 1 | 2 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0016 | 0/0 | 5001 | 4 | 0 | 4 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0017 | 0/0 | 4969 | 3 | 2 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0018 | 0/0 | 4973 | 3 | 2 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0019 | 0/0 | 4975 | 3 | 2 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0020 | 0/0 | 4969 | 3 | 1 | 2 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0021 | 0/0 | 4977 | 3 | 3 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0022 | 0/0 | 4973 | 3 | 0 | 0 | 3 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0023 | 0/0 | 4979 | 3 | 3 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0025 | 0/0 | 4983 | 3 | 1 | 0 | 1 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0026 | 0/1 | 4981 | 3 | 0 | 1 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0027 | 0/0 | 4991 | 3 | 0 | 1 | 1 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0028 | 0/0 | 4987 | 3 | 3 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0029 | 1/0 | 4986 | 3 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0030 | 0/0 | 4997 | 3 | 0 | 1 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0031 | 0/0 | 4993 | 3 | 0 | 0 | 3 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0032 | 0/0 | 5009 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0033 | 0/0 | 4959 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0034 | 0/0 | 4977 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0035 | 0/0 | 4971 | 2 | 1 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0036 | 0/0 | 4981 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0037 | 0/0 | 4981 | 2 | 1 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0038 | 0/0 | 4979 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0039 | 0/0 | 4985 | 2 | 1 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0040 | 0/0 | 4981 | 2 | 0 | 1 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0041 | 0/0 | 4989 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0042 | 0/0 | 4982 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0043 | 0/0 | 4993 | 2 | 0 | 2 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0044 | 0/0 | 4985 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0045 | 0/0 | 4995 | 2 | 1 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0046 | 0/0 | 5005 | 2 | 0 | 1 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0047 | 0/0 | 5009 | 2 | 0 | 1 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0048 | 0/0 | 4989 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0051 | 0/0 | 4986 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0053 | 0/0 | 4979 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0054 | 0/0 | 4979 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0055 | 0/0 | 5005 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0056 | 0/0 | 4961 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0057 | 0/0 | 4963 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0058 | 0/0 | 4971 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0059 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0060 | 0/0 | 4971 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0061 | 0/0 | 4969 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0062 | 0/0 | 4971 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0063 | 0/0 | 4979 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0064 | 0/0 | 4977 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0065 | 0/0 | 4981 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0066 | 0/0 | 4983 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0067 | 0/0 | 4978 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0068 | 0/0 | 4977 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0069 | 0/0 | 4973 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0070 | 0/0 | 4983 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0071 | 0/0 | 4967 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0073 | 0/0 | 4977 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0074 | 0/0 | 4979 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0075 | 0/0 | 4985 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0076 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0078 | 0/0 | 4985 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0079 | 0/0 | 4984 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0080 | 0/0 | 4987 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0081 | 0/0 | 4987 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0082 | 0/0 | 4986 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0083 | 0/0 | 4991 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0084 | 0/0 | 4989 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0085 | 0/0 | 4991 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0086 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0087 | 0/0 | 4993 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0088 | 0/0 | 4995 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0089 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0090 | 0/0 | 5003 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0091 | 0/0 | 4992 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0092 | 0/0 | 4997 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0093 | 0/0 | 4999 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0094 | 0/0 | 4985 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0095 | 0/0 | 4997 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0096 | 0/0 | 4999 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0097 | 0/0 | 5003 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0098 | 0/0 | 4999 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0099 | 0/0 | 5007 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0100 | 0/0 | 4998 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0101 | 0/0 | 5000 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0102 | 0/0 | 5001 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0103 | 0/0 | 5007 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0104 | 0/0 | 5007 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0105 | 0/0 | 5017 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0107 | 0/0 | 5007 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0108 | 0/0 | 5009 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0109 | 0/0 | 5005 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0110 | 0/0 | 5011 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0111 | 0/0 | 5011 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0112 | 0/0 | 5007 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0113 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0114 | 0/0 | 5015 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0115 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0116 | 0/0 | 5011 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0117 | 0/0 | 5013 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0118 | 0/0 | 5015 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0119 | 0/0 | 5007 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0120 | 0/0 | 4947 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0121 | 0/0 | 4982 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0128 | 0/0 | 4988 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0132 | 0/0 | 4985 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0133 | 0/0 | 4985 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0134 | 0/0 | 4987 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0135 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0136 | 0/0 | 4993 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0001t0137 | 0/0 | 4995 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0002t0005 | 0/0 | 4978 | 7 | 0 | 0 | 6 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0002t0049 | 0/0 | 4982 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0002t0050 | 0/0 | 4976 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0002t0052 | 0/0 | 4982 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0002t0122 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0002t0123 | 0/0 | 4976 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0002t0124 | 0/0 | 4972 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0002t0125 | 0/0 | 4977 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0002t0126 | 0/0 | 4980 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0002t0127 | 0/0 | 4984 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0002t0129 | 0/0 | 4988 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0002t0130 | 0/0 | 4993 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0002t0131 | 0/0 | 4993 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0006t0032 | 0/0 | 5009 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0001c0007t0052 | 0/0 | 4982 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0002c0003t0024 | 0/0 | 4979 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0002c0003t0072 | 0/0 | 4977 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0002c0003t0077 | 0/0 | 4981 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0002c0003t0106 | 0/0 | 4999 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0003c0004t0024 | 0/0 | 4979 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| a0004c0005t0006 | 0/0 | 4977 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | copy fasta | chr9 | 122936020 | 123109866 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0008g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0008g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0009g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0010g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0010g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0010g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0010g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0011g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0011g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0011g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0012g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0012g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0012g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0012g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0013g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0013g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0013g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0013g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0014g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0014g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0014g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0014g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0015g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0015g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0015g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0015g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0016g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0016g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0016g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0016g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0017g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0017g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0017g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0018g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0018g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0018g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0019g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0019g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0019g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0020g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0020g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0020g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0021g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0021g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0021g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0022g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0022g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0022g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0023g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0023g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0023g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0025g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0025g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0025g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0026g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0026g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0026g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0027g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0027g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0027g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0028g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0028g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0028g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0029g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0029g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0029g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0030g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0030g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0030g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0031g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0031g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0031g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0032g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0032g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0033g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0034g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0034g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0035g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0035g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0036g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0036g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0037g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0037g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0038g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0038g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0039g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0039g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0040g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0040g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0041g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0041g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0042g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0042g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0043g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0043g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0044g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0044g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0045g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0045g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0046g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0046g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0047g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0047g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0048g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0048g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0051g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0051g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0053g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0054g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0055g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0056g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0057g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0058g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0059g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0060g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0061g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0062g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0063g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0064g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0065g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0066g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0067g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0068g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0069g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0070g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0071g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0073g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0074g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0075g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0076g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0078g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0079g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0080g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0081g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0082g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0083g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0084g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0085g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0086g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0087g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0088g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0089g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0090g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0091g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0092g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0093g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0094g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0095g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0096g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0097g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0098g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0099g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0100g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0101g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0102g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0103g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0104g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0105g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0107g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0108g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0109g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0110g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0111g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0112g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0113g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0114g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0115g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0116g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0117g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0118g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0119g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0120g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0121g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0128g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0132g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0133g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0134g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0135g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0136g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0137g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0005g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0049g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0049g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0050g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0050g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0052g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0122g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0123g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0124g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0125g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0126g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0127g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0129g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0130g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0131g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0006t0032g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0007t0052g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0002c0003t0024g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0002c0003t0024g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0002c0003t0072g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0002c0003t0077g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0002c0003t0106g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0003c0004t0024g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0004c0005t0006g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0120 | g0199 | EUR | GBR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00099 | hp2 | a0001 | c0001 | t0015 | g0220 | EUR | GBR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00280 | hp1 | a0001 | c0002 | t0130 | g0043 | EUR | FIN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00280 | hp2 | a0001 | c0001 | t0085 | g0189 | EUR | FIN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00323 | hp1 | a0001 | c0001 | t0010 | g0081 | EUR | FIN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00323 | hp2 | a0001 | c0002 | t0052 | g0038 | EUR | FIN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00544 | hp1 | a0002 | c0003 | t0072 | g0062 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00544 | hp2 | a0001 | c0001 | t0046 | g0175 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00558 | hp1 | a0001 | c0001 | t0030 | g0169 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00558 | hp2 | a0001 | c0001 | t0118 | g0116 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00597 | hp2 | a0001 | c0001 | t0041 | g0254 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00621 | hp1 | a0001 | c0001 | t0080 | g0133 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00621 | hp2 | a0001 | c0001 | t0064 | g0212 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00639 | hp1 | a0001 | c0001 | t0105 | g0234 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00639 | hp2 | a0001 | c0001 | t0043 | g0203 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00642 | hp1 | a0001 | c0001 | t0075 | g0208 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00642 | hp2 | a0001 | c0001 | t0074 | g0219 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00673 | hp1 | a0001 | c0001 | t0030 | g0236 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00733 | hp1 | a0001 | c0001 | t0040 | g0151 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00733 | hp2 | a0001 | c0001 | t0012 | g0215 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00735 | hp1 | a0001 | c0001 | t0046 | g0168 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00735 | hp2 | a0001 | c0001 | t0043 | g0204 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00738 | hp1 | a0001 | c0001 | t0039 | g0171 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0060 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00741 | hp1 | a0001 | c0001 | t0014 | g0232 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00741 | hp2 | a0001 | c0002 | t0131 | g0045 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01069 | hp1 | a0001 | c0001 | t0012 | g0217 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01069 | hp2 | a0001 | c0001 | t0067 | g0013 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01070 | hp2 | a0001 | c0001 | t0137 | g0198 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01081 | hp1 | a0001 | c0001 | t0112 | g0136 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01099 | hp1 | a0001 | c0001 | t0119 | g0190 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01099 | hp2 | a0001 | c0001 | t0018 | g0073 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01106 | hp2 | a0001 | c0001 | t0047 | g0139 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01109 | hp1 | a0001 | c0001 | t0061 | g0241 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01109 | hp2 | a0001 | c0001 | t0020 | g0088 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01167 | hp1 | a0001 | c0001 | t0037 | g0022 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01167 | hp2 | a0001 | c0001 | t0090 | g0228 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0080 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01243 | hp1 | a0001 | c0001 | t0017 | g0251 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01243 | hp2 | a0001 | c0001 | t0020 | g0089 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01256 | hp2 | a0001 | c0001 | t0101 | g0135 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01258 | hp1 | a0001 | c0001 | t0014 | g0224 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01258 | hp2 | a0001 | c0001 | t0016 | g0138 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01361 | hp1 | a0001 | c0001 | t0007 | g0137 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01361 | hp2 | a0001 | c0001 | t0014 | g0235 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0069 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | IBS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01515 | hp2 | a0001 | c0001 | t0015 | g0225 | EUR | IBS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01884 | hp1 | a0001 | c0001 | t0044 | g0090 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01884 | hp2 | a0001 | c0001 | t0034 | g0056 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01934 | hp2 | a0001 | c0001 | t0030 | g0166 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01943 | hp1 | a0001 | c0001 | t0016 | g0140 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01943 | hp2 | a0001 | c0001 | t0027 | g0165 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01952 | hp1 | a0001 | c0001 | t0016 | g0257 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01952 | hp2 | a0001 | c0001 | t0013 | g0172 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01981 | hp1 | a0001 | c0001 | t0013 | g0195 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0125 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01993 | hp1 | a0001 | c0001 | t0069 | g0210 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0149 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02004 | hp1 | a0001 | c0001 | t0026 | g0214 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02004 | hp2 | a0001 | c0001 | t0016 | g0141 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02027 | hp1 | a0001 | c0001 | t0087 | g0084 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02027 | hp2 | a0001 | c0001 | t0015 | g0196 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02040 | hp1 | a0001 | c0001 | t0098 | g0160 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02040 | hp2 | a0001 | c0001 | t0057 | g0126 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02055 | hp1 | a0001 | c0001 | t0065 | g0058 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02055 | hp2 | a0001 | c0001 | t0113 | g0247 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02056 | hp1 | a0001 | c0001 | t0135 | g0205 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02056 | hp2 | a0001 | c0001 | t0078 | g0253 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02071 | hp1 | a0001 | c0001 | t0088 | g0130 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02071 | hp2 | a0001 | c0001 | t0093 | g0170 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02129 | hp1 | a0001 | c0001 | t0099 | g0003 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02132 | hp1 | a0001 | c0001 | t0031 | g0237 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02132 | hp2 | a0001 | c0007 | t0052 | g0035 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02135 | hp1 | a0001 | c0001 | t0055 | g0188 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02135 | hp2 | a0001 | c0001 | t0025 | g0148 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02145 | hp1 | a0001 | c0001 | t0023 | g0010 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02145 | hp2 | a0001 | c0001 | t0029 | g0082 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02155 | hp1 | a0002 | c0003 | t0024 | g0079 | EAS | CDX | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02155 | hp2 | a0001 | c0001 | t0071 | g0114 | EAS | CDX | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02165 | hp1 | a0001 | c0001 | t0094 | g0113 | EAS | CDX | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02165 | hp2 | a0001 | c0002 | t0049 | g0049 | EAS | CDX | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02257 | hp1 | a0001 | c0001 | t0037 | g0027 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0061 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02258 | hp1 | a0001 | c0001 | t0033 | g0001 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02280 | hp1 | a0001 | c0001 | t0011 | g0014 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02280 | hp2 | a0001 | c0001 | t0019 | g0186 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02300 | hp1 | a0001 | c0001 | t0019 | g0111 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02300 | hp2 | a0001 | c0001 | t0014 | g0161 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02572 | hp1 | a0001 | c0001 | t0025 | g0144 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02572 | hp2 | a0001 | c0001 | t0036 | g0029 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02717 | hp1 | a0001 | c0001 | t0017 | g0249 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0021 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02723 | hp1 | a0001 | c0001 | t0062 | g0023 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02723 | hp2 | a0001 | c0001 | t0121 | g0233 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02735 | hp1 | a0001 | c0002 | t0127 | g0042 | SAS | PJL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02735 | hp2 | a0001 | c0001 | t0108 | g0163 | SAS | PJL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02738 | hp2 | a0004 | c0005 | t0006 | g0156 | SAS | PJL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02809 | hp1 | a0001 | c0001 | t0017 | g0026 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02809 | hp2 | a0001 | c0001 | t0029 | g0099 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02818 | hp1 | a0001 | c0001 | t0028 | g0244 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02818 | hp2 | a0001 | c0001 | t0018 | g0071 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02886 | hp1 | a0001 | c0001 | t0084 | g0245 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02886 | hp2 | a0001 | c0001 | t0066 | g0055 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0030 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02895 | hp2 | a0001 | c0001 | t0044 | g0068 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02896 | hp1 | a0001 | c0001 | t0092 | g0239 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02896 | hp2 | a0001 | c0001 | t0011 | g0019 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02897 | hp1 | a0001 | c0001 | t0096 | g0248 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0024 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02965 | hp1 | a0001 | c0001 | t0079 | g0094 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02965 | hp2 | a0001 | c0001 | t0021 | g0016 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02970 | hp1 | a0001 | c0001 | t0128 | g0065 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02970 | hp2 | a0001 | c0001 | t0023 | g0028 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02976 | hp1 | a0001 | c0001 | t0021 | g0018 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02976 | hp2 | a0001 | c0001 | t0100 | g0096 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03098 | hp1 | a0001 | c0001 | t0045 | g0064 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0015 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03130 | hp2 | a0001 | c0001 | t0019 | g0185 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03139 | hp1 | a0001 | c0001 | t0028 | g0240 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03139 | hp2 | a0001 | c0001 | t0095 | g0077 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03195 | hp1 | a0001 | c0001 | t0051 | g0067 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03195 | hp2 | a0001 | c0001 | t0042 | g0095 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03225 | hp1 | a0001 | c0001 | t0021 | g0100 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03225 | hp2 | a0001 | c0001 | t0034 | g0025 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03239 | hp2 | a0001 | c0001 | t0027 | g0223 | SAS | PJL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03453 | hp1 | a0001 | c0001 | t0082 | g0093 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03486 | hp1 | a0001 | c0001 | t0109 | g0242 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0059 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0072 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03579 | hp1 | a0001 | c0001 | t0089 | g0243 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03579 | hp2 | a0001 | c0001 | t0059 | g0256 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03831 | hp1 | a0001 | c0001 | t0026 | g0181 | SAS | BEB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03831 | hp2 | a0001 | c0001 | t0013 | g0207 | SAS | BEB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03834 | hp1 | a0001 | c0001 | t0083 | g0150 | SAS | BEB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03834 | hp2 | a0001 | c0002 | t0005 | g0052 | SAS | BEB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03942 | hp1 | a0001 | c0001 | t0058 | g0180 | SAS | BEB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03942 | hp2 | a0001 | c0001 | t0012 | g0162 | SAS | BEB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG04115 | hp1 | a0001 | c0001 | t0015 | g0178 | SAS | STU | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG04115 | hp2 | a0001 | c0001 | t0025 | g0153 | SAS | STU | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG04199 | hp1 | a0001 | c0001 | t0073 | g0222 | SAS | STU | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG04199 | hp2 | a0001 | c0001 | t0136 | g0226 | SAS | STU | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18522 | hp1 | a0001 | c0001 | t0028 | g0246 | AFR | YRI | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18522 | hp2 | a0001 | c0001 | t0042 | g0098 | AFR | YRI | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18747 | hp1 | a0001 | c0001 | t0022 | g0102 | EAS | CHB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18747 | hp2 | a0001 | c0001 | t0103 | g0184 | EAS | CHB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18906 | hp1 | a0001 | c0001 | t0086 | g0097 | AFR | YRI | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0009 | AFR | YRI | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18939 | hp1 | a0001 | c0001 | t0111 | g0187 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18939 | hp2 | a0001 | c0001 | t0054 | g0252 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18944 | hp1 | a0001 | c0001 | t0102 | g0108 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18944 | hp2 | a0002 | c0003 | t0024 | g0078 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18945 | hp1 | a0003 | c0004 | t0024 | g0076 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18945 | hp2 | a0001 | c0002 | t0129 | g0047 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18949 | hp1 | a0001 | c0002 | t0050 | g0044 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18951 | hp2 | a0001 | c0001 | t0060 | g0200 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18952 | hp1 | a0001 | c0001 | t0048 | g0105 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18952 | hp2 | a0001 | c0002 | t0005 | g0036 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18956 | hp1 | a0001 | c0001 | t0132 | g0174 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18956 | hp2 | a0001 | c0001 | t0038 | g0255 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18959 | hp1 | a0001 | c0001 | t0116 | g0120 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18959 | hp2 | a0001 | c0001 | t0107 | g0231 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18961 | hp1 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18961 | hp2 | a0001 | c0001 | t0134 | g0202 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18964 | hp1 | a0001 | c0001 | t0104 | g0197 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18964 | hp2 | a0001 | c0001 | t0006 | g0145 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18966 | hp1 | a0001 | c0001 | t0038 | g0157 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18966 | hp2 | a0001 | c0001 | t0031 | g0154 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18969 | hp1 | a0001 | c0001 | t0027 | g0194 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18969 | hp2 | a0001 | c0001 | t0081 | g0118 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18970 | hp2 | a0001 | c0001 | t0115 | g0004 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18973 | hp1 | a0001 | c0001 | t0022 | g0115 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18973 | hp2 | a0001 | c0001 | t0013 | g0192 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18975 | hp1 | a0001 | c0001 | t0040 | g0104 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18975 | hp2 | a0001 | c0001 | t0097 | g0227 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18979 | hp1 | a0001 | c0001 | t0007 | g0117 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18979 | hp2 | a0001 | c0006 | t0032 | g0008 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18983 | hp1 | a0001 | c0001 | t0068 | g0147 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18983 | hp2 | a0001 | c0001 | t0041 | g0193 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18984 | hp2 | a0001 | c0001 | t0032 | g0006 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18986 | hp1 | a0001 | c0001 | t0053 | g0158 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18986 | hp2 | a0001 | c0002 | t0123 | g0041 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18990 | hp1 | a0001 | c0001 | t0007 | g0124 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18990 | hp2 | a0001 | c0001 | t0110 | g0177 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18992 | hp1 | a0001 | c0002 | t0005 | g0051 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18992 | hp2 | a0001 | c0001 | t0117 | g0101 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19001 | hp1 | a0001 | c0002 | t0122 | g0031 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19001 | hp2 | a0001 | c0001 | t0056 | g0086 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19004 | hp1 | a0002 | c0003 | t0077 | g0075 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19004 | hp2 | a0001 | c0001 | t0047 | g0128 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19011 | hp2 | a0001 | c0002 | t0005 | g0034 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19043 | hp1 | a0001 | c0001 | t0036 | g0053 | AFR | LWK | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0070 | AFR | LWK | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19058 | hp1 | a0001 | c0001 | t0007 | g0238 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19058 | hp2 | a0001 | c0001 | t0133 | g0230 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19065 | hp1 | a0001 | c0001 | t0006 | g0146 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19065 | hp2 | a0001 | c0001 | t0076 | g0191 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19067 | hp2 | a0001 | c0002 | t0049 | g0046 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19068 | hp1 | a0001 | c0001 | t0006 | g0155 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19068 | hp2 | a0002 | c0003 | t0106 | g0074 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19072 | hp2 | a0001 | c0002 | t0126 | g0048 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19074 | hp1 | a0001 | c0001 | t0114 | g0005 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19074 | hp2 | a0001 | c0002 | t0005 | g0040 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19077 | hp1 | a0001 | c0001 | t0048 | g0127 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19077 | hp2 | a0001 | c0002 | t0124 | g0050 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19080 | hp1 | a0001 | c0002 | t0005 | g0032 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19080 | hp2 | a0001 | c0001 | t0031 | g0085 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19082 | hp1 | a0001 | c0001 | t0045 | g0107 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19082 | hp2 | a0001 | c0002 | t0050 | g0033 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19088 | hp1 | a0001 | c0001 | t0006 | g0152 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19088 | hp2 | a0001 | c0002 | t0005 | g0037 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19091 | hp1 | a0001 | c0001 | t0032 | g0007 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19091 | hp2 | a0001 | c0001 | t0022 | g0112 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | TSI | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA20752 | hp2 | a0001 | c0001 | t0035 | g0129 | EUR | TSI | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02109 | hp1 | a0001 | c0001 | t0033 | g0001 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02109 | hp2 | a0001 | c0001 | t0051 | g0066 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0142 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0221 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02559 | hp1 | a0001 | c0001 | t0020 | g0250 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02559 | hp2 | a0001 | c0001 | t0023 | g0011 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG06807 | hp1 | a0001 | c0001 | t0070 | g0012 | AFR | USA | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG06807 | hp2 | a0001 | c0001 | t0091 | g0092 | AFR | USA | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18955 | hp1 | a0001 | c0002 | t0125 | g0039 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA20300 | hp1 | a0001 | c0001 | t0035 | g0134 | AFR | USA | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA20300 | hp2 | a0001 | c0001 | t0063 | g0057 | AFR | USA | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA21309 | hp1 | a0001 | c0001 | t0018 | g0054 | AFR | LWK | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA21309 | hp2 | a0001 | c0001 | t0039 | g0209 | AFR | LWK | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0026 | g0183 | REF | REF | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0029 | g0091 | REF | REF | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122986335
|
G | A | 1 | a0003 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.506G>A | p.Arg169Lys | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/26 | 629/4986 | 506/3210 | 169/1069 | chr9 | 122986335 | ||
| chr9:123020458
|
A | G | 2 | a0002a0003 | 6 | HG00544.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.1793A>G | p.Lys598Arg | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/26 | 1916/4986 | 1793/3210 | 598/1069 | chr9 | 123020458 | ||
| chr9:123101585
|
A | G | 1 | a0004 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.2909A>G | p.Glu970Gly | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/26 | 3032/4986 | 2909/3210 | 970/1069 | chr9 | 123101585 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122986249
|
C | T | 1 | a0001c0007 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.420C>T | p.Ala140Ala | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/26 | 543/4986 | 420/3210 | 140/1069 | chr9 | 122986249 | ||
| chr9:123010485
|
A | G | 1 | a0001c0006 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.1506A>G | p.Gln502Gln | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/26 | 1629/4986 | 1506/3210 | 502/1069 | chr9 | 123010485 | ||
| chr9:123020384
|
A | G | 2 | a0001c0002a0001c0007 | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
synonymous_variant | LOW | c.1719A>G | p.Gly573Gly | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/26 | 1842/4986 | 1719/3210 | 573/1069 | chr9 | 123020384 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122941023
|
T | G | 1 | a0001c0001t0053 | 1 | NA18986.hp1 | 5_prime_UTR_variant | MODIFIER | c.-120T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/26 | 16037 | chr9 | 122941023 | |||||
| chr9:123103357
|
C | T | 6 | a0001c0001t0132a0001c0001t0133a0001c0001t0134others(3): Show | 6 | HG01070.hp2 HG02056.hp1 HG04199.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*144C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 144 | chr9 | 123103357 | |||||
| chr9:123103581
|
T | A | 1 | a0001c0001t0054 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*368T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 368 | chr9 | 123103581 | |||||
| chr9:123103582
|
A | T | 17 | a0001c0001t0051a0001c0001t0121a0001c0001t0128others(14): Show | 26 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*369A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 369 | chr9 | 123103582 | |||||
| chr9:123103582
|
AATATACA others(29): Show |
A | 1 | a0001c0001t0120 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*375_*410delCATATA others(30): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 375 | INFO_REALIGN_3_PRIME | chr9 | 123103582 | ||||
| chr9:123103583
|
ATATACAT others(4): Show |
A | 1 | a0001c0002t0129 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371_*381delTATACA others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 371 | chr9 | 123103583 | |||||
| chr9:123103583
|
ATATACAT others(6): Show |
A | 3 | a0001c0001t0128a0001c0002t0052a0001c0007t0052 | 3 | HG00323.hp2 HG02132.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*371_*383delTATACA others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 371 | chr9 | 123103583 | |||||
| chr9:123103583
|
ATATACAT others(8): Show |
A | 4 | a0001c0001t0051a0001c0002t0050a0001c0002t0126others(1): Show | 6 | HG02109.hp2 HG02735.hp1 HG03195.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*371_*385delTATACA others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 371 | chr9 | 123103583 | |||||
| chr9:123103583
|
ATATACAT others(10): Show |
A | 4 | a0001c0002t0005a0001c0002t0049a0001c0002t0124others(1): Show | 11 | HG02165.hp2 HG03834.hp2 NA18952.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*371_*387delTATACA others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 371 | chr9 | 123103583 | |||||
| chr9:123103583
|
ATATACAT others(12): Show |
A | 2 | a0001c0002t0122a0001c0002t0123 | 2 | NA18986.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*371_*389delTATACA others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 371 | chr9 | 123103583 | |||||
| chr9:123103583
|
ATATACAT others(18): Show |
A | 1 | a0001c0001t0121 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371_*395delTATACA others(19): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 371 | chr9 | 123103583 | |||||
| chr9:123103588
|
C | CAT | 5 | a0001c0001t0003a0001c0001t0004a0001c0001t0084others(2): Show | 17 | HG00280.hp2 HG00597.hp1 HG00673.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*423_*424dupTA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
C | CATAT | 5 | a0001c0001t0030a0001c0001t0031a0001c0001t0086others(2): Show | 9 | HG00558.hp1 HG00673.hp1 HG01934.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*421_*424dupTATA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
C | CATATACA others(5): Show |
1 | a0001c0001t0055 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*380_*381insCATATA others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 381 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
C | CATATAT | 5 | a0001c0001t0015a0001c0001t0045a0001c0001t0089others(2): Show | 9 | HG00099.hp2 HG01167.hp2 HG01515.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*419_*424dupTATATA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
C | CATATATA others(3): Show |
4 | a0001c0001t0092a0001c0001t0093a0001c0001t0094others(1): Show | 4 | HG02071.hp2 HG02165.hp1 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*415_*424dupTATATA others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
C | CATATATA others(5): Show |
9 | a0001c0001t0016a0001c0001t0046a0001c0001t0096others(6): Show | 13 | HG00544.hp2 HG00735.hp1 HG01256.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*413_*424dupTATATA others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
C | CATATATA others(7): Show |
6 | a0001c0001t0032a0001c0001t0103a0001c0001t0104others(3): Show | 7 | HG00639.hp1 NA18747.hp2 NA18964.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*411_*424dupTATATA others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
C | CATATATA others(9): Show |
2 | a0001c0001t0107a0001c0001t0108 | 2 | HG02735.hp2 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*409_*424dupTATATA others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
C | CATATATA others(11): Show |
4 | a0001c0001t0109a0001c0001t0110a0001c0001t0111others(1): Show | 4 | HG01081.hp1 HG03486.hp1 NA18939.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*407_*424dupTATATA others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
C | CATATATA others(13): Show |
3 | a0001c0001t0047a0001c0001t0113a0001c0001t0114 | 4 | HG01106.hp2 HG02055.hp2 NA19004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*405_*424dupTATATA others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
C | CATATATA others(15): Show |
2 | a0001c0001t0115a0001c0001t0116 | 2 | NA18959.hp1 NA18970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*403_*424dupTATATA others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
C | CATATATA others(17): Show |
1 | a0001c0001t0117 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*401_*424dupTATATA others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
C | CATATATA others(19): Show |
1 | a0001c0001t0118 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*399_*424dupTATATA others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
C | T | 1 | a0001c0001t0048 | 2 | NA18952.hp1 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*375C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 375 | chr9 | 123103588 | |||||
| chr9:123103588
|
CAT | C | 9 | a0001c0001t0002a0001c0001t0026a0001c0001t0027others(6): Show | 21 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*423_*424delTA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 423 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
CATAT | C | 7 | a0001c0001t0041a0001c0001t0042a0001c0001t0074others(4): Show | 9 | HG00597.hp2 HG00642.hp1 HG00642.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*421_*424delTATA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 421 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
CATATAT | C | 6 | a0001c0001t0013a0001c0001t0025a0001c0001t0073others(3): Show | 12 | HG01952.hp2 HG01981.hp1 HG02135.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*419_*424delTATATA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 419 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
CATATATA others(1): Show |
C | 6 | a0001c0001t0012a0001c0001t0039a0001c0001t0040others(3): Show | 11 | HG00544.hp1 HG00733.hp1 HG00733.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*417_*424delTATATA others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 417 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
CATATATA others(3): Show |
C | 7 | a0001c0001t0001a0001c0001t0038a0001c0001t0053others(4): Show | 14 | HG01070.hp1 HG01081.hp2 HG01106.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*415_*424delTATATA others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 415 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
CATATATA others(5): Show |
C | 4 | a0001c0001t0006a0001c0001t0037a0001c0001t0068others(1): Show | 9 | HG01167.hp1 HG01993.hp2 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*413_*424delTATATA others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 413 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
CATATATA others(7): Show |
C | 3 | a0001c0001t0023a0001c0001t0036a0001c0001t0067 | 6 | HG01069.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*411_*424delTATATA others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 411 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
CATATATA others(9): Show |
C | 6 | a0001c0001t0011a0001c0001t0021a0001c0001t0022others(3): Show | 13 | HG00621.hp2 HG02055.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*409_*424delTATATA others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 409 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
CATATATA others(11): Show |
C | 9 | a0001c0001t0009a0001c0001t0018a0001c0001t0019others(6): Show | 21 | HG01099.hp2 HG01109.hp1 HG01109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*407_*424delTATATA others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 407 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
CATATATA others(15): Show |
C | 3 | a0001c0001t0058a0001c0001t0059a0001c0001t0060 | 3 | HG03579.hp2 HG03942.hp1 NA18951.hp2 |
3_prime_UTR_variant | MODIFIER | c.*403_*424delTATATA others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 403 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
CATATATA others(19): Show |
C | 1 | a0001c0001t0057 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*399_*424delTATATA others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 399 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
CATATATA others(21): Show |
C | 2 | a0001c0001t0017a0001c0001t0056 | 4 | HG01243.hp1 HG02717.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*397_*424delTATATA others(22): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 397 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103588
|
CATATATA others(25): Show |
C | 3 | a0001c0001t0008a0001c0001t0010a0001c0001t0033 | 11 | HG00323.hp1 HG00738.hp2 HG01175.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*393_*424delTATATA others(26): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 393 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | ||||
| chr9:123103596
|
T | C | 1 | a0001c0002t0130 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*383T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 383 | chr9 | 123103596 | |||||
| chr9:123103598
|
T | C | 1 | a0001c0002t0131 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*385T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 385 | chr9 | 123103598 | |||||
| chr9:123103600
|
T | C | 1 | a0001c0002t0129 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*387T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 387 | chr9 | 123103600 | |||||
| chr9:123103602
|
T | C | 3 | a0001c0001t0128a0001c0002t0052a0001c0007t0052 | 3 | HG00323.hp2 HG02132.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*389T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 389 | chr9 | 123103602 | |||||
| chr9:123103604
|
T | C | 4 | a0001c0001t0051a0001c0002t0050a0001c0002t0126others(1): Show | 6 | HG02109.hp2 HG02735.hp1 HG03195.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*391T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 391 | chr9 | 123103604 | |||||
| chr9:123103606
|
T | C | 4 | a0001c0002t0005a0001c0002t0049a0001c0002t0124others(1): Show | 11 | HG02165.hp2 HG03834.hp2 NA18952.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*393T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 393 | chr9 | 123103606 | |||||
| chr9:123103608
|
T | C | 2 | a0001c0002t0122a0001c0002t0123 | 2 | NA18986.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*395T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 395 | chr9 | 123103608 | |||||
| chr9:123103614
|
T | C | 1 | a0001c0001t0121 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*401T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 401 | chr9 | 123103614 | |||||
| chr9:123103623
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0119 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421_*422insGTATAT others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 422 | INFO_REALIGN_3_PRIME | chr9 | 123103623 | ||||
| chr9:123103791
|
G | C | 88 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(85): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*578G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 578 | chr9 | 123103791 | |||||
| chr9:123103825
|
C | T | 6 | a0001c0001t0081a0001c0001t0087a0001c0001t0088others(3): Show | 6 | HG00558.hp2 HG02027.hp1 HG02071.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*612C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 612 | chr9 | 123103825 | |||||
| chr9:123103861
|
C | A | 1 | a0001c0001t0069 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*648C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 648 | chr9 | 123103861 | |||||
| chr9:123103933
|
C | G | 4 | a0001c0001t0051a0001c0001t0105a0001c0001t0121others(1): Show | 5 | HG00639.hp1 HG02109.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*720C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 720 | chr9 | 123103933 | |||||
| chr9:123103963
|
T | TTG | 35 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(32): Show | 77 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*782_*783dupGT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 784 | INFO_REALIGN_3_PRIME | chr9 | 123103963 | ||||
| chr9:123103963
|
T | TTGTG | 3 | a0001c0001t0018a0001c0001t0083a0001c0001t0088 | 5 | HG01099.hp2 HG02071.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*780_*783dupGTGT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 784 | INFO_REALIGN_3_PRIME | chr9 | 123103963 | ||||
| chr9:123103963
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0063 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*774_*783dupGTGTGT others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 784 | INFO_REALIGN_3_PRIME | chr9 | 123103963 | ||||
| chr9:123103963
|
TTG | T | 5 | a0002c0003t0024a0002c0003t0072a0002c0003t0077others(2): Show | 6 | HG00544.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*782_*783delGT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 782 | INFO_REALIGN_3_PRIME | chr9 | 123103963 | ||||
| chr9:123103963
|
TTGTGTGT others(5): Show |
T | 2 | a0001c0001t0071a0001c0001t0094 | 2 | HG02155.hp2 HG02165.hp1 |
3_prime_UTR_variant | MODIFIER | c.*772_*783delGTGTGT others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 772 | INFO_REALIGN_3_PRIME | chr9 | 123103963 | ||||
| chr9:123103991
|
G | A | 7 | a0001c0001t0001a0001c0001t0012a0001c0001t0026others(4): Show | 18 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*778G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 778 | chr9 | 123103991 | |||||
| chr9:123103993
|
G | GTGTGTGT others(1): Show |
2 | a0001c0001t0043a0001c0001t0076 | 3 | HG00639.hp2 HG00735.hp2 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*783_*784insGTGTAT others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 784 | INFO_REALIGN_3_PRIME | chr9 | 123103993 | ||||
| chr9:123103993
|
G | GTGTGTGT others(5): Show |
1 | a0001c0002t0127 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*783_*784insGTGTGT others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 784 | INFO_REALIGN_3_PRIME | chr9 | 123103993 | ||||
| chr9:123103993
|
GTGTA | G | 7 | a0001c0001t0001a0001c0001t0012a0001c0001t0026others(4): Show | 18 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*786_*789delGTAT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 786 | INFO_REALIGN_3_PRIME | chr9 | 123103993 | ||||
| chr9:123103995
|
G | A | 8 | a0001c0001t0028a0001c0001t0061a0001c0001t0084others(5): Show | 10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*782G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 782 | chr9 | 123103995 | |||||
| chr9:123103997
|
A | G | 69 | a0001c0001t0003a0001c0001t0009a0001c0001t0011others(66): Show | 120 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*784A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 784 | chr9 | 123103997 | |||||
| chr9:123103999
|
G | A | 18 | a0001c0001t0001a0001c0001t0012a0001c0001t0026others(15): Show | 32 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*786G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 786 | chr9 | 123103999 | |||||
| chr9:123103999
|
G | GTA | 9 | a0001c0001t0033a0001c0001t0062a0001c0001t0075others(6): Show | 11 | HG00280.hp2 HG00642.hp1 HG02071.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*799_*800dupTA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 801 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | ||||
| chr9:123103999
|
G | GTATGTA | 30 | a0001c0001t0003a0001c0001t0009a0001c0001t0013others(27): Show | 63 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*789_*790insGTATAT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 790 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | ||||
| chr9:123103999
|
G | GTGTATGT others(1): Show |
17 | a0001c0001t0011a0001c0001t0032a0001c0001t0034others(14): Show | 29 | HG00323.hp2 HG01099.hp1 HG01884.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*787_*788insGTATGT others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 788 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | ||||
| chr9:123103999
|
G | GTGTGTA | 3 | a0001c0001t0060a0001c0001t0104a0001c0001t0111 | 3 | NA18939.hp1 NA18951.hp2 NA18964.hp1 |
3_prime_UTR_variant | MODIFIER | c.*787_*788insGTGTAT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 788 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | ||||
| chr9:123103999
|
G | GTGTGTAT others(3): Show |
3 | a0001c0001t0017a0001c0001t0065a0001c0001t0090 | 5 | HG01167.hp2 HG01243.hp1 HG02055.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*787_*788insGTGTAT others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 788 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | ||||
| chr9:123103999
|
G | GTGTGTGT others(5): Show |
5 | a0001c0001t0051a0001c0001t0066a0001c0001t0128others(2): Show | 7 | HG02109.hp2 HG02165.hp2 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*787_*788insGTGTGT others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 788 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | ||||
| chr9:123103999
|
G | GTGTGTGT others(9): Show |
1 | a0001c0001t0105 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*787_*788insGTGTGT others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 788 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | ||||
| chr9:123103999
|
G | GTGTGTGT others(13): Show |
1 | a0001c0001t0121 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*787_*788insGTGTGT others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 788 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | ||||
| chr9:123104081
|
T | A | 1 | a0001c0001t0017 | 3 | HG01243.hp1 HG02717.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*868T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 868 | chr9 | 123104081 | |||||
| chr9:123104132
|
T | A | 2 | a0001c0001t0105a0001c0001t0121 | 2 | HG00639.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*919T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 919 | chr9 | 123104132 | |||||
| chr9:123104288
|
T | TCC | 2 | a0001c0001t0051a0001c0001t0128 | 3 | HG02109.hp2 HG02970.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1076_*1077dupCC | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 1078 | INFO_REALIGN_3_PRIME | chr9 | 123104288 | ||||
| chr9:123104417
|
T | TA | 131 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(128): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*1218dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 1219 | INFO_REALIGN_3_PRIME | chr9 | 123104417 | ||||
| chr9:123104481
|
T | C | 1 | a0001c0001t0080 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1268T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 1268 | chr9 | 123104481 | |||||
| chr9:123104493
|
C | G | 48 | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(45): Show | 85 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1280C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 1280 | chr9 | 123104493 | |||||
| chr9:123104517
|
G | A | 1 | a0001c0001t0082 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1304G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 1304 | chr9 | 123104517 | |||||
| chr9:123104646
|
C | T | 1 | a0001c0001t0073 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1433C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 1433 | chr9 | 123104646 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122941126
|
C | G | 1 | a0001c0001t0016g0257 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-50+33C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941126 | ||||||
| chr9:122941183
|
T | C | 1 | a0001c0001t0008g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-50+90T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941183 | ||||||
| chr9:122941241
|
C | T | 1 | a0001c0001t0059g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-50+148C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941241 | ||||||
| chr9:122941348
|
C | G | 1 | a0001c0001t0038g0255 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-50+255C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941348 | ||||||
| chr9:122941536
|
C | T | 1 | a0001c0001t0041g0254 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-50+443C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941536 | ||||||
| chr9:122941711
|
G | C | 6 | a0001c0001t0032g0006a0001c0001t0032g0007a0001c0001t0099g0003others(3): Show | 6 | HG02129.hp1 NA18970.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+618G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941711 | ||||||
| chr9:122941756
|
A | G | 1 | a0001c0001t0078g0253 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-50+663A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941756 | ||||||
| chr9:122941785
|
C | G | 1 | a0001c0001t0054g0252 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-50+692C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941785 | ||||||
| chr9:122941907
|
A | C | 3 | a0001c0001t0017g0249a0001c0001t0017g0251a0001c0001t0020g0250 | 3 | HG01243.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-50+814A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941907 | ||||||
| chr9:122941946
|
G | A | 22 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(19): Show | 22 | HG01069.hp2 HG01167.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50+853G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941946 | ||||||
| chr9:122942322
|
A | G | 10 | a0001c0001t0028g0240a0001c0001t0028g0244a0001c0001t0028g0246others(7): Show | 10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-50+1229A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122942322 | ||||||
| chr9:122942499
|
G | T | 3 | a0001c0001t0007g0238a0001c0001t0031g0237a0001c0001t0078g0253 | 3 | HG02056.hp2 HG02132.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-50+1406G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122942499 | ||||||
| chr9:122942563
|
G | C | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-50+1470G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122942563 | ||||||
| chr9:122942664
|
C | T | 107 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.-50+1571C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122942664 | ||||||
| chr9:122942669
|
C | CA | 27 | a0001c0001t0002g0083a0001c0001t0004g0087a0001c0001t0008g0002others(24): Show | 28 | HG00323.hp1 HG00673.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.-50+1595dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | |||||
| chr9:122942669
|
C | CAA | 8 | a0001c0001t0002g0063a0001c0001t0008g0059a0001c0001t0010g0060others(5): Show | 8 | HG00544.hp1 HG00639.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+1594_-50+1595d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | |||||
| chr9:122942669
|
C | CAAA | 17 | a0001c0001t0009g0030a0001c0002t0005g0036a0001c0002t0005g0037others(14): Show | 17 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-50+1593_-50+1595d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | |||||
| chr9:122942669
|
C | CAAAA | 29 | a0001c0001t0009g0015a0001c0001t0009g0017a0001c0001t0009g0024others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-50+1592_-50+1595d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | |||||
| chr9:122942669
|
C | CAAAAA | 19 | a0001c0001t0001g0229a0001c0001t0009g0009a0001c0001t0014g0224others(16): Show | 19 | HG00741.hp1 HG01167.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+1591_-50+1595d others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | |||||
| chr9:122942669
|
C | CAAAAAA | 40 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0001g0216others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.-50+1590_-50+1595d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | |||||
| chr9:122942669
|
C | CAAAAAAA | 26 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0003g0159others(23): Show | 26 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.-50+1589_-50+1595d others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | |||||
| chr9:122942669
|
CA | C | 20 | a0001c0001t0004g0143a0001c0001t0006g0145a0001c0001t0006g0146others(17): Show | 20 | HG00733.hp1 HG01993.hp2 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.-50+1595delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | |||||
| chr9:122943023
|
TAAAAA | T | 8 | a0001c0001t0007g0137a0001c0001t0016g0138a0001c0001t0016g0140others(5): Show | 8 | HG01081.hp1 HG01106.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+1933_-50+1937d others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943023 | |||||
| chr9:122943034
|
CA | C | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-50+1947delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943034 | |||||
| chr9:122943050
|
T | TAGTC | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-50+1959_-50+1962d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943050 | |||||
| chr9:122943061
|
T | A | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-50+1968T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943061 | ||||||
| chr9:122943072
|
CTTT | C | 18 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(15): Show | 18 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50+2006_-50+2008d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | |||||
| chr9:122943072
|
CTTTTT | C | 39 | a0001c0001t0002g0063a0001c0001t0002g0131a0001c0001t0004g0132others(36): Show | 39 | HG00621.hp1 HG01069.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.-50+2004_-50+2008d others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | |||||
| chr9:122943072
|
CTTTTTT | C | 73 | a0001c0001t0002g0083a0001c0001t0002g0103a0001c0001t0002g0110others(70): Show | 74 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-50+2003_-50+2008d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | |||||
| chr9:122943072
|
CTTTTTTT | C | 16 | a0001c0001t0020g0088a0001c0001t0020g0089a0001c0001t0020g0250others(13): Show | 16 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.-50+2002_-50+2008d others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | |||||
| chr9:122943072
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0023g0011a0001c0001t0070g0012 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-50+1997_-50+2008d others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | |||||
| chr9:122943072
|
CTTTTTTT others(6): Show |
C | 19 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(16): Show | 19 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.-50+1996_-50+2008d others(15): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | |||||
| chr9:122943072
|
CTTTTTTT others(7): Show |
C | 64 | a0001c0001t0001g0229a0001c0001t0003g0159a0001c0001t0003g0164others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-50+1995_-50+2008d others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | |||||
| chr9:122943072
|
CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0022g0102a0001c0001t0117g0101 | 2 | NA18747.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-50+1993_-50+2008d others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | |||||
| chr9:122943072
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0017g0249 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-50+1991_-50+2008d others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | |||||
| chr9:122943196
|
A | C | 1 | a0001c0001t0047g0128 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-50+2103A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943196 | ||||||
| chr9:122943199
|
T | C | 107 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.-50+2106T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943199 | ||||||
| chr9:122943256
|
A | C | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-50+2163A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943256 | ||||||
| chr9:122943477
|
A | G | 1 | a0001c0001t0035g0134 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-50+2384A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943477 | ||||||
| chr9:122943669
|
G | A | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+2576G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943669 | ||||||
| chr9:122943733
|
A | G | 1 | a0001c0001t0009g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-50+2640A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943733 | ||||||
| chr9:122943794
|
A | T | 1 | a0001c0001t0039g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-50+2701A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943794 | ||||||
| chr9:122943862
|
A | G | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-50+2769A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943862 | ||||||
| chr9:122943877
|
C | T | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-50+2784C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943877 | ||||||
| chr9:122943952
|
C | CA | 52 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(49): Show | 52 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.-50+2869dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943952 | |||||
| chr9:122943972
|
G | T | 1 | a0001c0001t0073g0222 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-50+2879G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943972 | ||||||
| chr9:122944229
|
CT | C | 8 | a0001c0001t0002g0103a0001c0001t0003g0159a0001c0001t0036g0053others(5): Show | 8 | HG01069.hp2 HG01496.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+3150delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122944229 | |||||
| chr9:122944243
|
T | A | 10 | a0001c0001t0028g0240a0001c0001t0028g0244a0001c0001t0028g0246others(7): Show | 10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-50+3150T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122944243 | ||||||
| chr9:122944566
|
G | A | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-50+3473G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122944566 | ||||||
| chr9:122944664
|
G | A | 2 | a0001c0001t0004g0143a0001c0001t0007g0142 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-50+3571G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122944664 | ||||||
| chr9:122944737
|
A | AT | 12 | a0001c0001t0009g0009a0001c0001t0009g0024a0001c0001t0009g0030others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-50+3657dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122944737 | |||||
| chr9:122944744
|
T | C | 1 | a0001c0001t0121g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-50+3651T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122944744 | ||||||
| chr9:122944751
|
A | T | 1 | a0001c0001t0121g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-50+3658A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122944751 | ||||||
| chr9:122944872
|
C | T | 2 | a0001c0001t0010g0080a0001c0001t0010g0081 | 2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-50+3779C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122944872 | ||||||
| chr9:122945068
|
C | G | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.-50+3975C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122945068 | ||||||
| chr9:122945147
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-50+4061_-50+4070d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | |||||
| chr9:122945147
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0018g0054a0001c0002t0052g0038a0001c0002t0125g0039 | 3 | HG00323.hp2 NA18955.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-50+4058_-50+4070d others(15): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | |||||
| chr9:122945147
|
C | CTTTTTTT others(7): Show |
32 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(29): Show | 32 | HG00280.hp1 HG01884.hp2 HG02132.hp2 others(29): Show |
intron_variant | MODIFIER | c.-50+4057_-50+4070d others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | |||||
| chr9:122945147
|
C | CTTTTTTT others(8): Show |
14 | a0001c0001t0011g0019a0001c0001t0011g0020a0001c0001t0011g0021others(11): Show | 14 | HG00741.hp2 HG01069.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50+4056_-50+4070d others(17): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | |||||
| chr9:122945147
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0036g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-50+4055_-50+4070d others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | |||||
| chr9:122945147
|
C | CTTTTTTT others(10): Show |
3 | a0001c0001t0019g0185a0001c0001t0019g0186a0001c0001t0098g0160 | 3 | HG02040.hp1 HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-50+4070_-50+4071i others(19): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | |||||
| chr9:122945147
|
C | CTTTTTTT others(11): Show |
23 | a0001c0001t0003g0159a0001c0001t0003g0164a0001c0001t0012g0162others(20): Show | 23 | HG00280.hp2 HG01099.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.-50+4070_-50+4071i others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | |||||
| chr9:122945147
|
C | CTTTTTTT others(12): Show |
28 | a0001c0001t0001g0211a0001c0001t0003g0167a0001c0001t0003g0201others(25): Show | 28 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.-50+4070_-50+4071i others(21): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | |||||
| chr9:122945147
|
C | CTTTTTTT others(13): Show |
20 | a0001c0001t0001g0179a0001c0001t0001g0213a0001c0001t0001g0216others(17): Show | 20 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+4070_-50+4071i others(22): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | |||||
| chr9:122945147
|
C | CTTTTTTT others(14): Show |
5 | a0001c0001t0001g0182a0001c0001t0001g0218a0001c0001t0014g0232others(2): Show | 5 | HG00099.hp2 HG00642.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+4070_-50+4071i others(23): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | |||||
| chr9:122945147
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0026g0183 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-50+4070_-50+4071i others(24): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | |||||
| chr9:122945147
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0012g0221a0001c0001t0073g0222 | 2 | HG02486.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-50+4070_-50+4071i others(25): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | |||||
| chr9:122945147
|
CT | C | 96 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(93): Show | 97 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-50+4070delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | |||||
| chr9:122945372
|
G | A | 2 | a0001c0001t0048g0105a0001c0001t0048g0127 | 2 | NA18952.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-50+4279G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122945372 | ||||||
| chr9:122945534
|
T | G | 1 | a0001c0001t0099g0003 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-50+4441T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122945534 | ||||||
| chr9:122945615
|
T | C | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-50+4522T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122945615 | ||||||
| chr9:122945934
|
T | C | 107 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(104): Show | 108 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.-50+4841T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122945934 | ||||||
| chr9:122946036
|
A | C | 2 | a0001c0001t0003g0164a0001c0001t0013g0195 | 2 | HG01175.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-50+4943A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122946036 | ||||||
| chr9:122946070
|
A | T | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-50+4977A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122946070 | ||||||
| chr9:122946193
|
A | C | 1 | a0001c0001t0004g0132 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-50+5100A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122946193 | ||||||
| chr9:122946265
|
G | C | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-50+5172G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122946265 | ||||||
| chr9:122946661
|
A | G | 1 | a0001c0001t0009g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-50+5568A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122946661 | ||||||
| chr9:122946809
|
A | G | 1 | a0001c0001t0012g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-50+5716A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122946809 | ||||||
| chr9:122946995
|
C | T | 1 | a0001c0001t0053g0158 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-50+5902C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122946995 | ||||||
| chr9:122947044
|
A | G | 63 | a0001c0001t0003g0159a0001c0001t0003g0164a0001c0001t0003g0167others(60): Show | 63 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-50+5951A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947044 | ||||||
| chr9:122947135
|
C | T | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.-50+6042C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947135 | ||||||
| chr9:122947236
|
T | C | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-50+6143T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947236 | ||||||
| chr9:122947292
|
A | G | 32 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(29): Show | 32 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.-50+6199A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947292 | ||||||
| chr9:122947328
|
G | T | 1 | a0001c0001t0099g0003 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-50+6235G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947328 | ||||||
| chr9:122947456
|
C | G | 1 | a0001c0001t0038g0157 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-50+6363C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947456 | ||||||
| chr9:122947480
|
T | A | 2 | a0001c0001t0010g0080a0001c0001t0010g0081 | 2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-50+6387T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947480 | ||||||
| chr9:122947586
|
T | C | 2 | a0001c0001t0092g0239a0001c0001t0096g0248 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-50+6493T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947586 | ||||||
| chr9:122947601
|
A | C | 1 | a0001c0001t0010g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-50+6508A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947601 | ||||||
| chr9:122947652
|
C | T | 1 | a0001c0001t0135g0205 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-50+6559C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947652 | ||||||
| chr9:122947676
|
G | A | 7 | a0001c0001t0003g0167a0001c0001t0003g0173a0001c0001t0014g0161others(4): Show | 7 | HG01361.hp2 HG01934.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+6583G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947676 | ||||||
| chr9:122947693
|
T | C | 1 | a0001c0002t0005g0040 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-50+6600T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947693 | ||||||
| chr9:122948042
|
A | AAC | 63 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(60): Show | 63 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-50+6989_-50+6990d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | |||||
| chr9:122948042
|
A | AACAC | 19 | a0001c0001t0002g0131a0001c0001t0004g0123a0001c0001t0004g0125others(16): Show | 19 | HG00738.hp2 HG01884.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+6987_-50+6990d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | |||||
| chr9:122948042
|
A | AACACAC | 17 | a0001c0001t0007g0238a0001c0001t0022g0102a0001c0001t0028g0246others(14): Show | 17 | HG00544.hp1 HG00639.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.-50+6985_-50+6990d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | |||||
| chr9:122948042
|
A | AACACACA others(3): Show |
1 | a0002c0003t0024g0079 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-50+6981_-50+6990d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | |||||
| chr9:122948042
|
AAC | A | 16 | a0001c0001t0006g0155a0001c0001t0007g0106a0001c0001t0010g0061others(13): Show | 16 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50+6989_-50+6990d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | |||||
| chr9:122948042
|
AACACAC | A | 21 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-50+6985_-50+6990d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | |||||
| chr9:122948042
|
AACACACA others(3): Show |
A | 8 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0003g0164others(5): Show | 8 | HG01070.hp1 HG01175.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.-50+6981_-50+6990d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | |||||
| chr9:122948042
|
AACACACA others(5): Show |
A | 77 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0213others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.-50+6979_-50+6990d others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | |||||
| chr9:122948213
|
T | G | 2 | a0001c0001t0023g0011a0001c0001t0070g0012 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-50+7120T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122948213 | ||||||
| chr9:122948358
|
A | G | 7 | a0001c0001t0095g0077a0002c0003t0024g0078a0002c0003t0024g0079others(4): Show | 7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+7265A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122948358 | ||||||
| chr9:122948574
|
T | C | 2 | a0001c0001t0104g0197a0001c0001t0111g0187 | 2 | NA18939.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-50+7481T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122948574 | ||||||
| chr9:122948611
|
T | G | 1 | a0001c0001t0133g0230 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-50+7518T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122948611 | ||||||
| chr9:122948915
|
T | C | 1 | a0001c0001t0003g0159 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-50+7822T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122948915 | ||||||
| chr9:122948998
|
G | A | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.-50+7905G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122948998 | ||||||
| chr9:122949073
|
C | T | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-49-7938C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122949073 | ||||||
| chr9:122949323
|
G | A | 1 | a0001c0001t0006g0145 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-49-7688G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122949323 | ||||||
| chr9:122949324
|
C | A | 81 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.-49-7687C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122949324 | ||||||
| chr9:122949438
|
T | G | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-7573T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122949438 | ||||||
| chr9:122949594
|
C | G | 5 | a0001c0001t0028g0244a0001c0001t0089g0243a0001c0001t0092g0239others(2): Show | 5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-7417C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122949594 | ||||||
| chr9:122949693
|
C | CA | 16 | a0001c0001t0001g0218a0001c0001t0001g0229a0001c0001t0002g0110others(13): Show | 16 | HG00639.hp1 HG01081.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-7300dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122949693 | |||||
| chr9:122949693
|
C | CAA | 7 | a0001c0001t0036g0053a0001c0001t0095g0077a0002c0003t0024g0078others(4): Show | 7 | HG02155.hp1 HG03139.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-7301_-49-7300d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122949693 | |||||
| chr9:122949693
|
C | CAAA | 28 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(25): Show | 28 | HG00544.hp1 HG01069.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-49-7302_-49-7300d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122949693 | |||||
| chr9:122949693
|
CAA | C | 21 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-49-7301_-49-7300d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122949693 | |||||
| chr9:122949713
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-49-7298G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122949713 | ||||||
| chr9:122949817
|
T | A | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-49-7194T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122949817 | ||||||
| chr9:122950198
|
T | G | 1 | a0001c0001t0137g0198 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-49-6813T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122950198 | ||||||
| chr9:122950377
|
C | CT | 115 | a0001c0001t0001g0179a0001c0001t0001g0213a0001c0001t0001g0216others(112): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-49-6612dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122950377 | |||||
| chr9:122950377
|
C | CTT | 61 | a0001c0001t0001g0182a0001c0001t0001g0211a0001c0001t0003g0176others(58): Show | 61 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-49-6613_-49-6612d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122950377 | |||||
| chr9:122950377
|
C | CTTT | 58 | a0001c0001t0002g0063a0001c0001t0002g0103a0001c0001t0002g0110others(55): Show | 58 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-49-6614_-49-6612d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122950377 | |||||
| chr9:122950465
|
C | T | 1 | a0001c0001t0014g0232 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-49-6546C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122950465 | ||||||
| chr9:122950628
|
A | G | 1 | a0001c0001t0061g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-49-6383A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122950628 | ||||||
| chr9:122950986
|
G | A | 1 | a0001c0001t0006g0146 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-49-6025G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122950986 | ||||||
| chr9:122951115
|
T | C | 1 | a0001c0001t0103g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-49-5896T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951115 | ||||||
| chr9:122951247
|
T | G | 81 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.-49-5764T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951247 | ||||||
| chr9:122951272
|
T | A | 1 | a0001c0001t0058g0180 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-49-5739T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951272 | ||||||
| chr9:122951308
|
G | A | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49-5703G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951308 | ||||||
| chr9:122951446
|
G | A | 1 | a0001c0001t0051g0066 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-49-5565G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951446 | ||||||
| chr9:122951623
|
C | T | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49-5388C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951623 | ||||||
| chr9:122951951
|
G | A | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49-5060G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951951 | ||||||
| chr9:122951995
|
T | A | 2 | a0001c0001t0015g0225a0001c0001t0046g0168 | 2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-49-5016T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951995 | ||||||
| chr9:122952069
|
T | A | 1 | a0001c0001t0047g0128 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-49-4942T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952069 | ||||||
| chr9:122952193
|
C | T | 1 | a0001c0001t0036g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-49-4818C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952193 | ||||||
| chr9:122952492
|
T | G | 7 | a0001c0001t0006g0145a0001c0001t0006g0146a0001c0001t0006g0149others(4): Show | 7 | HG01993.hp2 HG02135.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-4519T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952492 | ||||||
| chr9:122952519
|
C | T | 1 | a0001c0002t0049g0046 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-49-4492C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952519 | ||||||
| chr9:122952562
|
C | G | 7 | a0001c0001t0006g0145a0001c0001t0006g0146a0001c0001t0006g0149others(4): Show | 7 | HG01993.hp2 HG02135.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-4449C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952562 | ||||||
| chr9:122952687
|
G | C | 1 | a0001c0001t0003g0164 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-49-4324G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952687 | ||||||
| chr9:122952839
|
A | G | 2 | a0001c0001t0104g0197a0001c0001t0111g0187 | 2 | NA18939.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-49-4172A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952839 | ||||||
| chr9:122952851
|
T | C | 1 | a0001c0001t0059g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-49-4160T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952851 | ||||||
| chr9:122952906
|
C | A | 2 | a0001c0001t0017g0249a0001c0001t0017g0251 | 2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-49-4105C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952906 | ||||||
| chr9:122953064
|
A | G | 1 | a0001c0001t0004g0123 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-49-3947A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953064 | ||||||
| chr9:122953097
|
C | T | 1 | a0001c0001t0054g0252 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-49-3914C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953097 | ||||||
| chr9:122953252
|
C | T | 1 | a0001c0001t0055g0188 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-49-3759C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953252 | ||||||
| chr9:122953405
|
C | CT | 14 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(11): Show | 15 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.-49-3591dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122953405 | |||||
| chr9:122953466
|
A | G | 1 | a0001c0001t0044g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-49-3545A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953466 | ||||||
| chr9:122953506
|
A | T | 3 | a0001c0001t0002g0122a0001c0001t0002g0131a0001c0001t0004g0087 | 3 | HG00673.hp2 NA18951.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-49-3505A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953506 | ||||||
| chr9:122953621
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-49-3390G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953621 | ||||||
| chr9:122953666
|
T | A | 2 | a0001c0001t0003g0206a0001c0001t0120g0199 | 2 | HG00099.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-49-3345T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953666 | ||||||
| chr9:122953679
|
G | A | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-49-3332G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953679 | ||||||
| chr9:122953722
|
A | T | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.-49-3289A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953722 | ||||||
| chr9:122953987
|
A | G | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-49-3024A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953987 | ||||||
| chr9:122954038
|
T | C | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.-49-2973T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954038 | ||||||
| chr9:122954180
|
G | T | 1 | a0001c0001t0037g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-49-2831G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954180 | ||||||
| chr9:122954292
|
C | T | 4 | a0001c0001t0012g0215a0001c0001t0012g0221a0001c0001t0015g0220others(1): Show | 4 | HG00099.hp2 HG00733.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-2719C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954292 | ||||||
| chr9:122954487
|
G | C | 1 | a0001c0001t0103g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-49-2524G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954487 | ||||||
| chr9:122954488
|
C | T | 1 | a0002c0003t0024g0079 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-49-2523C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954488 | ||||||
| chr9:122954595
|
C | T | 1 | a0001c0001t0088g0130 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-49-2416C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954595 | ||||||
| chr9:122954633
|
A | G | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-49-2378A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954633 | ||||||
| chr9:122954784
|
G | A | 12 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(9): Show | 13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.-49-2227G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954784 | ||||||
| chr9:122954856
|
C | T | 4 | a0001c0001t0010g0060a0001c0001t0010g0061a0001c0001t0010g0080others(1): Show | 4 | HG00323.hp1 HG00738.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-2155C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954856 | ||||||
| chr9:122955130
|
G | A | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.-49-1881G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955130 | ||||||
| chr9:122955194
|
G | A | 3 | a0001c0001t0014g0224a0001c0001t0014g0232a0001c0001t0027g0223 | 3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-49-1817G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955194 | ||||||
| chr9:122955270
|
G | A | 15 | a0001c0001t0006g0145a0001c0001t0006g0146a0001c0001t0006g0149others(12): Show | 15 | HG00733.hp1 HG01993.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.-49-1741G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955270 | ||||||
| chr9:122955364
|
A | G | 1 | a0001c0001t0061g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-49-1647A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955364 | ||||||
| chr9:122955365
|
A | G | 1 | a0001c0001t0006g0149 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-49-1646A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955365 | ||||||
| chr9:122955455
|
A | C | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-49-1556A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955455 | ||||||
| chr9:122955949
|
G | C | 5 | a0001c0001t0028g0244a0001c0001t0089g0243a0001c0001t0092g0239others(2): Show | 5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-1062G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955949 | ||||||
| chr9:122955961
|
A | G | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49-1050A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955961 | ||||||
| chr9:122956104
|
A | G | 1 | a0001c0001t0076g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-49-907A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956104 | ||||||
| chr9:122956297
|
CATGTTAA others(129): Show |
C | 1 | a0001c0001t0011g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-49-712_-49-577del | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122956297 | |||||
| chr9:122956366
|
G | A | 1 | a0001c0001t0078g0253 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-49-645G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956366 | ||||||
| chr9:122956375
|
A | G | 1 | a0001c0001t0018g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-49-636A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956375 | ||||||
| chr9:122956409
|
G | T | 7 | a0001c0001t0095g0077a0002c0003t0024g0078a0002c0003t0024g0079others(4): Show | 7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-602G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956409 | ||||||
| chr9:122956416
|
C | T | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-49-595C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956416 | ||||||
| chr9:122956425
|
C | T | 2 | a0001c0001t0043g0203a0001c0001t0043g0204 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-49-586C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956425 | ||||||
| chr9:122956433
|
G | T | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-49-578G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956433 | ||||||
| chr9:122956450
|
A | G | 2 | a0001c0001t0043g0203a0001c0001t0043g0204 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-49-561A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956450 | ||||||
| chr9:122956598
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-49-413C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956598 | ||||||
| chr9:122956649
|
C | CA | 186 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-49-344dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122956649 | |||||
| chr9:122956649
|
C | CAA | 57 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(54): Show | 57 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.-49-345_-49-344dup others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122956649 | |||||
| chr9:122956690
|
C | T | 2 | a0001c0001t0002g0103a0001c0001t0002g0121 | 2 | HG02129.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-49-321C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956690 | ||||||
| chr9:122956783
|
T | C | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49-228T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956783 | ||||||
| chr9:122957314
|
G | A | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.150+105G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122957314 | ||||||
| chr9:122957502
|
C | G | 10 | a0001c0001t0028g0240a0001c0001t0028g0244a0001c0001t0028g0246others(7): Show | 10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.150+293C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122957502 | ||||||
| chr9:122957512
|
T | TGGGGGGG others(132): Show |
1 | a0001c0001t0011g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.150+303_150+304ins others(139): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122957512 | ||||||
| chr9:122957513
|
T | G | 1 | a0001c0001t0011g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.150+304T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122957513 | ||||||
| chr9:122957644
|
C | G | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.150+435C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122957644 | ||||||
| chr9:122957720
|
T | C | 1 | a0001c0001t0061g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150+511T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122957720 | ||||||
| chr9:122957735
|
G | A | 1 | a0001c0001t0019g0185 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.150+526G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122957735 | ||||||
| chr9:122957884
|
C | CT | 22 | a0001c0001t0076g0191a0001c0002t0005g0032a0001c0002t0005g0034others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+690dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122957884 | |||||
| chr9:122957884
|
CT | C | 108 | a0001c0001t0002g0063a0001c0001t0002g0103a0001c0001t0002g0110others(105): Show | 109 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.150+690delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122957884 | |||||
| chr9:122958102
|
C | T | 12 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(9): Show | 13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.150+893C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958102 | ||||||
| chr9:122958151
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+942G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958151 | ||||||
| chr9:122958155
|
A | G | 1 | a0001c0001t0014g0161 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.150+946A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958155 | ||||||
| chr9:122958196
|
A | G | 1 | a0001c0001t0080g0133 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.150+987A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958196 | ||||||
| chr9:122958348
|
A | G | 2 | a0001c0001t0003g0206a0001c0001t0120g0199 | 2 | HG00099.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.150+1139A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958348 | ||||||
| chr9:122958365
|
T | C | 3 | a0001c0001t0001g0211a0001c0001t0026g0181a0001c0001t0069g0210 | 3 | HG01070.hp1 HG01993.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.150+1156T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958365 | ||||||
| chr9:122958475
|
A | G | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.150+1266A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958475 | ||||||
| chr9:122958565
|
A | T | 1 | a0001c0001t0066g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.150+1356A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958565 | ||||||
| chr9:122958670
|
A | G | 1 | a0001c0002t0005g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.150+1461A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958670 | ||||||
| chr9:122958694
|
T | A | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.150+1485T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958694 | ||||||
| chr9:122958709
|
G | C | 1 | a0001c0001t0107g0231 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.150+1500G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958709 | ||||||
| chr9:122958789
|
A | G | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.150+1580A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958789 | ||||||
| chr9:122959095
|
A | T | 3 | a0001c0001t0034g0056a0001c0001t0065g0058a0001c0001t0066g0055 | 3 | HG01884.hp2 HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.150+1886A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959095 | ||||||
| chr9:122959336
|
G | A | 3 | a0001c0001t0008g0069a0001c0001t0008g0070a0001c0001t0033g0001 | 4 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+2127G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959336 | ||||||
| chr9:122959364
|
C | CA | 196 | a0001c0001t0001g0179a0001c0001t0001g0211a0001c0001t0001g0213others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.150+2175dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122959364 | |||||
| chr9:122959364
|
C | CAA | 40 | a0001c0001t0001g0182a0001c0001t0002g0063a0001c0001t0003g0201others(37): Show | 41 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.150+2174_150+2175d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122959364 | |||||
| chr9:122959407
|
T | C | 1 | a0001c0001t0016g0257 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.150+2198T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959407 | ||||||
| chr9:122959543
|
T | C | 10 | a0001c0001t0028g0240a0001c0001t0028g0244a0001c0001t0028g0246others(7): Show | 10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.150+2334T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959543 | ||||||
| chr9:122959604
|
A | T | 1 | a0001c0001t0021g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.150+2395A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959604 | ||||||
| chr9:122959688
|
T | C | 2 | a0001c0001t0014g0235a0001c0001t0027g0165 | 2 | HG01361.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.150+2479T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959688 | ||||||
| chr9:122959719
|
G | T | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.150+2510G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959719 | ||||||
| chr9:122959726
|
A | G | 1 | a0001c0001t0062g0023 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150+2517A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959726 | ||||||
| chr9:122959781
|
C | T | 1 | a0001c0001t0002g0121 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.150+2572C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959781 | ||||||
| chr9:122959886
|
G | A | 8 | a0001c0001t0007g0137a0001c0001t0016g0138a0001c0001t0016g0140others(5): Show | 8 | HG01081.hp1 HG01106.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.150+2677G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959886 | ||||||
| chr9:122959946
|
G | C | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.150+2737G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959946 | ||||||
| chr9:122960161
|
G | C | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.150+2952G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122960161 | ||||||
| chr9:122960657
|
C | T | 4 | a0001c0001t0010g0060a0001c0001t0010g0061a0001c0001t0010g0080others(1): Show | 4 | HG00323.hp1 HG00738.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+3448C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122960657 | ||||||
| chr9:122960860
|
G | A | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.150+3651G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122960860 | ||||||
| chr9:122960922
|
A | G | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.150+3713A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122960922 | ||||||
| chr9:122960948
|
T | A | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.150+3739T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122960948 | ||||||
| chr9:122961182
|
T | A | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.150+3973T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961182 | ||||||
| chr9:122961208
|
C | T | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.150+3999C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961208 | ||||||
| chr9:122961226
|
TGATAAA | T | 6 | a0001c0001t0017g0249a0001c0001t0017g0251a0001c0001t0020g0088others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.150+4021_150+4026d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122961226 | |||||
| chr9:122961303
|
A | G | 1 | a0002c0003t0024g0078 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.150+4094A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961303 | ||||||
| chr9:122961311
|
A | G | 2 | a0001c0001t0097g0227a0001c0001t0107g0231 | 2 | NA18959.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.150+4102A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961311 | ||||||
| chr9:122961404
|
C | T | 1 | a0001c0001t0095g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.150+4195C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961404 | ||||||
| chr9:122961441
|
C | T | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.150+4232C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961441 | ||||||
| chr9:122961489
|
T | C | 7 | a0001c0001t0095g0077a0002c0003t0024g0078a0002c0003t0024g0079others(4): Show | 7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.150+4280T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961489 | ||||||
| chr9:122961522
|
C | G | 1 | a0001c0001t0064g0212 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.150+4313C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961522 | ||||||
| chr9:122961535
|
T | C | 1 | a0001c0001t0006g0145 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.150+4326T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961535 | ||||||
| chr9:122961550
|
A | G | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+4341A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961550 | ||||||
| chr9:122961661
|
G | A | 1 | a0001c0001t0006g0146 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.150+4452G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961661 | ||||||
| chr9:122961775
|
A | G | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.150+4566A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961775 | ||||||
| chr9:122961818
|
T | C | 249 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(246): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.150+4609T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961818 | ||||||
| chr9:122961863
|
T | C | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+4654T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961863 | ||||||
| chr9:122962248
|
T | A | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.150+5039T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122962248 | ||||||
| chr9:122962403
|
G | GA | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.150+5196dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122962403 | |||||
| chr9:122962420
|
C | G | 1 | a0001c0001t0008g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.150+5211C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122962420 | ||||||
| chr9:122962452
|
T | C | 6 | a0001c0001t0013g0192a0001c0001t0027g0194a0001c0001t0041g0193others(3): Show | 6 | HG00597.hp2 HG00621.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.150+5243T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122962452 | ||||||
| chr9:122962529
|
A | T | 63 | a0001c0001t0003g0159a0001c0001t0003g0164a0001c0001t0003g0167others(60): Show | 63 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.150+5320A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122962529 | ||||||
| chr9:122962729
|
C | T | 1 | a0001c0001t0046g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.150+5520C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122962729 | ||||||
| chr9:122962863
|
A | G | 11 | a0001c0001t0009g0009a0001c0001t0009g0024a0001c0001t0009g0030others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+5654A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122962863 | ||||||
| chr9:122963366
|
C | G | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+6157C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963366 | ||||||
| chr9:122963467
|
A | C | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.150+6258A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963467 | ||||||
| chr9:122963507
|
A | G | 3 | a0001c0001t0004g0119a0001c0001t0040g0104a0001c0001t0057g0126 | 3 | HG00597.hp1 HG02040.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.150+6298A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963507 | ||||||
| chr9:122963606
|
G | A | 1 | a0001c0001t0067g0013 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.150+6397G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963606 | ||||||
| chr9:122963624
|
C | A | 1 | a0001c0001t0019g0111 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.150+6415C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963624 | ||||||
| chr9:122963694
|
G | C | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.150+6485G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963694 | ||||||
| chr9:122963736
|
A | T | 1 | a0001c0001t0056g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.150+6527A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963736 | ||||||
| chr9:122963742
|
C | T | 7 | a0001c0001t0095g0077a0002c0003t0024g0078a0002c0003t0024g0079others(4): Show | 7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.150+6533C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963742 | ||||||
| chr9:122963759
|
A | AAAG | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.150+6553_150+6555d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122963759 | |||||
| chr9:122963935
|
C | T | 5 | a0001c0001t0011g0014a0001c0001t0011g0019a0001c0001t0011g0020others(2): Show | 5 | HG02280.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.150+6726C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963935 | ||||||
| chr9:122964015
|
A | T | 1 | a0001c0001t0018g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.150+6806A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964015 | ||||||
| chr9:122964208
|
C | T | 1 | a0001c0001t0081g0118 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.150+6999C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964208 | ||||||
| chr9:122964274
|
C | T | 2 | a0001c0001t0007g0106a0001c0001t0031g0154 | 2 | NA18961.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.150+7065C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964274 | ||||||
| chr9:122964616
|
A | T | 1 | a0001c0001t0016g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.150+7407A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964616 | ||||||
| chr9:122964771
|
A | G | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.150+7562A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964771 | ||||||
| chr9:122964811
|
G | A | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.150+7602G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964811 | ||||||
| chr9:122964852
|
C | T | 2 | a0001c0001t0017g0249a0001c0001t0017g0251 | 2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.150+7643C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964852 | ||||||
| chr9:122964993
|
T | C | 15 | a0001c0001t0006g0145a0001c0001t0006g0146a0001c0001t0006g0149others(12): Show | 15 | HG00733.hp1 HG01993.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.150+7784T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964993 | ||||||
| chr9:122965286
|
A | G | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+8077A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965286 | ||||||
| chr9:122965396
|
A | T | 4 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144others(1): Show | 4 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+8187A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965396 | ||||||
| chr9:122965444
|
C | T | 1 | a0001c0001t0110g0177 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.150+8235C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965444 | ||||||
| chr9:122965487
|
G | A | 6 | a0001c0001t0017g0249a0001c0001t0017g0251a0001c0001t0020g0088others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.150+8278G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965487 | ||||||
| chr9:122965603
|
C | T | 1 | a0002c0003t0024g0078 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.150+8394C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965603 | ||||||
| chr9:122965739
|
G | A | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.150+8530G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965739 | ||||||
| chr9:122965769
|
A | C | 13 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(10): Show | 14 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.150+8560A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965769 | ||||||
| chr9:122965967
|
A | T | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.150+8758A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965967 | ||||||
| chr9:122966098
|
T | C | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.150+8889T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122966098 | ||||||
| chr9:122966253
|
A | G | 1 | a0001c0002t0049g0049 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.150+9044A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122966253 | ||||||
| chr9:122966694
|
A | T | 1 | a0001c0001t0083g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.150+9485A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122966694 | ||||||
| chr9:122966707
|
C | T | 2 | a0001c0001t0097g0227a0001c0001t0107g0231 | 2 | NA18959.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.150+9498C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122966707 | ||||||
| chr9:122966856
|
G | A | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+9647G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122966856 | ||||||
| chr9:122966868
|
C | T | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.150+9659C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122966868 | ||||||
| chr9:122967091
|
G | A | 12 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(9): Show | 13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.150+9882G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122967091 | ||||||
| chr9:122967387
|
A | C | 107 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(104): Show | 108 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.150+10178A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122967387 | ||||||
| chr9:122967728
|
C | CT | 255 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.150+10526dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122967728 | |||||
| chr9:122967782
|
G | A | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.150+10573G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122967782 | ||||||
| chr9:122967843
|
C | G | 1 | a0001c0001t0025g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.150+10634C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122967843 | ||||||
| chr9:122967902
|
A | G | 1 | a0001c0001t0083g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.150+10693A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122967902 | ||||||
| chr9:122968089
|
TGTA | T | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+10881_150+1088 others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122968089 | ||||||
| chr9:122968094
|
AT | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+10886delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122968094 | ||||||
| chr9:122968220
|
C | CT | 21 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0213others(18): Show | 21 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.150+11031dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122968220 | |||||
| chr9:122968220
|
CT | C | 6 | a0001c0001t0037g0022a0001c0001t0045g0064a0001c0001t0051g0066others(3): Show | 6 | HG01167.hp1 HG02109.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.150+11031delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122968220 | |||||
| chr9:122968491
|
A | T | 1 | a0001c0001t0040g0151 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.150+11282A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122968491 | ||||||
| chr9:122968659
|
C | G | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.150+11450C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122968659 | ||||||
| chr9:122969161
|
A | C | 1 | a0001c0001t0074g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.150+11952A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122969161 | ||||||
| chr9:122969211
|
CT | C | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.150+12003delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122969211 | ||||||
| chr9:122969264
|
A | G | 1 | a0001c0001t0004g0087 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.150+12055A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122969264 | ||||||
| chr9:122969522
|
C | T | 1 | a0001c0001t0008g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.150+12313C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122969522 | ||||||
| chr9:122969576
|
G | A | 30 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(27): Show | 30 | HG01069.hp2 HG01109.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.150+12367G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122969576 | ||||||
| chr9:122969736
|
C | CATTTT | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.150+12533_150+1253 others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122969736 | |||||
| chr9:122969753
|
A | G | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.150+12544A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122969753 | ||||||
| chr9:122969857
|
C | T | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.150+12648C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122969857 | ||||||
| chr9:122970074
|
A | AT | 80 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.150+12881dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122970074 | |||||
| chr9:122970453
|
A | C | 1 | a0001c0001t0007g0117 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.150+13244A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122970453 | ||||||
| chr9:122970522
|
A | G | 1 | a0001c0001t0006g0145 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.150+13313A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122970522 | ||||||
| chr9:122970906
|
T | G | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.151-13579T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122970906 | ||||||
| chr9:122971275
|
T | G | 1 | a0001c0002t0127g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.151-13210T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122971275 | ||||||
| chr9:122971454
|
G | T | 1 | a0001c0001t0013g0192 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.151-13031G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122971454 | ||||||
| chr9:122971849
|
A | G | 1 | a0001c0001t0048g0127 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.151-12636A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122971849 | ||||||
| chr9:122972051
|
G | C | 2 | a0001c0002t0130g0043a0001c0002t0131g0045 | 2 | HG00280.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.151-12434G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122972051 | ||||||
| chr9:122972730
|
A | C | 21 | a0001c0001t0003g0159a0001c0001t0003g0164a0001c0001t0003g0167others(18): Show | 21 | HG00544.hp2 HG00673.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.151-11755A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122972730 | ||||||
| chr9:122972736
|
A | T | 1 | a0001c0001t0090g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.151-11749A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122972736 | ||||||
| chr9:122972978
|
T | TA | 110 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(107): Show | 111 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.151-11495dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122972978 | |||||
| chr9:122972978
|
T | TAA | 30 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(27): Show | 30 | HG00639.hp1 HG01069.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.151-11496_151-1149 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122972978 | |||||
| chr9:122972978
|
T | TAAA | 104 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.151-11497_151-1149 others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122972978 | |||||
| chr9:122973048
|
C | T | 1 | a0001c0001t0062g0023 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.151-11437C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973048 | ||||||
| chr9:122973052
|
A | G | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.151-11433A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973052 | ||||||
| chr9:122973250
|
G | T | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.151-11235G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973250 | ||||||
| chr9:122973356
|
G | T | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151-11129G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973356 | ||||||
| chr9:122973362
|
C | G | 2 | a0001c0001t0043g0203a0001c0001t0043g0204 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.151-11123C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973362 | ||||||
| chr9:122973393
|
T | C | 4 | a0001c0001t0004g0109a0001c0001t0004g0119a0001c0001t0022g0102others(1): Show | 4 | HG00597.hp1 NA18747.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-11092T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973393 | ||||||
| chr9:122973397
|
C | T | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.151-11088C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973397 | ||||||
| chr9:122973426
|
T | C | 1 | a0001c0001t0002g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.151-11059T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973426 | ||||||
| chr9:122973430
|
G | C | 1 | a0001c0001t0046g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.151-11055G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973430 | ||||||
| chr9:122973484
|
C | T | 52 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(49): Show | 52 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.151-11001C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973484 | ||||||
| chr9:122973690
|
T | C | 82 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.151-10795T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973690 | ||||||
| chr9:122973735
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.151-10750C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973735 | ||||||
| chr9:122973893
|
C | T | 2 | a0001c0001t0020g0088a0001c0001t0020g0089 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.151-10592C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973893 | ||||||
| chr9:122974009
|
C | CA | 15 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0213others(12): Show | 15 | HG00642.hp2 HG00733.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.151-10476_151-1047 others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974009 | ||||||
| chr9:122974010
|
C | A | 245 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.151-10475C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974010 | ||||||
| chr9:122974056
|
A | G | 4 | a0001c0002t0122g0031a0001c0002t0123g0041a0001c0002t0124g0050others(1): Show | 4 | NA18955.hp1 NA18986.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-10429A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974056 | ||||||
| chr9:122974067
|
T | C | 1 | a0001c0001t0068g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.151-10418T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974067 | ||||||
| chr9:122974247
|
T | C | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-10238T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974247 | ||||||
| chr9:122974311
|
G | C | 6 | a0001c0001t0013g0172a0001c0001t0039g0171a0001c0001t0043g0203others(3): Show | 6 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-10174G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974311 | ||||||
| chr9:122974415
|
C | CT | 71 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(68): Show | 72 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.151-10044dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122974415 | |||||
| chr9:122974415
|
C | CTT | 33 | a0001c0001t0004g0143a0001c0001t0006g0145a0001c0001t0006g0146others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.151-10045_151-1004 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122974415 | |||||
| chr9:122974415
|
CT | C | 45 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(42): Show | 45 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.151-10044delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122974415 | |||||
| chr9:122974415
|
CTT | C | 82 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.151-10045_151-1004 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122974415 | |||||
| chr9:122974443
|
G | A | 1 | a0001c0001t0099g0003 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.151-10042G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974443 | ||||||
| chr9:122974478
|
C | T | 1 | a0001c0001t0037g0022 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.151-10007C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974478 | ||||||
| chr9:122974696
|
G | A | 3 | a0001c0001t0014g0224a0001c0001t0014g0232a0001c0001t0027g0223 | 3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.151-9789G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974696 | ||||||
| chr9:122975077
|
C | T | 21 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.151-9408C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122975077 | ||||||
| chr9:122975162
|
C | A | 1 | a0001c0002t0049g0049 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.151-9323C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122975162 | ||||||
| chr9:122975244
|
T | C | 84 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.151-9241T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122975244 | ||||||
| chr9:122975417
|
G | T | 1 | a0001c0001t0074g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.151-9068G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122975417 | ||||||
| chr9:122975691
|
C | T | 21 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.151-8794C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122975691 | ||||||
| chr9:122976046
|
T | C | 2 | a0001c0001t0018g0071a0001c0001t0018g0073 | 2 | HG01099.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.151-8439T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122976046 | ||||||
| chr9:122976191
|
TA | T | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.151-8291delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122976191 | |||||
| chr9:122976399
|
G | T | 1 | a0001c0001t0025g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.151-8086G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122976399 | ||||||
| chr9:122976610
|
G | T | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.151-7875G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122976610 | ||||||
| chr9:122976926
|
T | C | 1 | a0001c0001t0010g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.151-7559T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122976926 | ||||||
| chr9:122976979
|
G | T | 1 | a0001c0001t0051g0066 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151-7506G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122976979 | ||||||
| chr9:122977013
|
A | G | 1 | a0001c0001t0040g0151 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.151-7472A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122977013 | ||||||
| chr9:122977434
|
G | A | 2 | a0001c0001t0086g0097a0001c0001t0100g0096 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.151-7051G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122977434 | ||||||
| chr9:122977513
|
C | G | 1 | a0001c0001t0014g0161 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151-6972C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122977513 | ||||||
| chr9:122977574
|
C | T | 1 | a0001c0001t0136g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.151-6911C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122977574 | ||||||
| chr9:122977575
|
G | A | 1 | a0001c0001t0022g0112 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.151-6910G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122977575 | ||||||
| chr9:122977687
|
G | A | 1 | a0001c0001t0099g0003 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.151-6798G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122977687 | ||||||
| chr9:122978055
|
A | G | 13 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(10): Show | 14 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.151-6430A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978055 | ||||||
| chr9:122978131
|
A | AT | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.151-6353dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122978131 | |||||
| chr9:122978256
|
A | G | 1 | a0001c0001t0095g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.151-6229A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978256 | ||||||
| chr9:122978461
|
A | G | 1 | a0001c0001t0081g0118 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.151-6024A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978461 | ||||||
| chr9:122978709
|
G | C | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.151-5776G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978709 | ||||||
| chr9:122978792
|
A | T | 1 | a0001c0001t0010g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.151-5693A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978792 | ||||||
| chr9:122978819
|
C | T | 135 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.151-5666C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978819 | ||||||
| chr9:122978834
|
C | A | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-5651C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978834 | ||||||
| chr9:122978877
|
CATTTT | C | 134 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.151-5586_151-5582d others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122978877 | |||||
| chr9:122978877
|
CATTTTAT others(3): Show |
C | 1 | a0001c0001t0025g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.151-5591_151-5582d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122978877 | |||||
| chr9:122978932
|
C | T | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.151-5553C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978932 | ||||||
| chr9:122978963
|
G | T | 1 | a0001c0001t0080g0133 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.151-5522G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978963 | ||||||
| chr9:122979141
|
A | C | 2 | a0001c0001t0042g0095a0001c0001t0042g0098 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.151-5344A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122979141 | ||||||
| chr9:122979212
|
T | C | 5 | a0001c0001t0011g0014a0001c0001t0011g0019a0001c0001t0011g0020others(2): Show | 5 | HG02280.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-5273T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122979212 | ||||||
| chr9:122979422
|
G | A | 2 | a0001c0001t0003g0201a0001c0001t0137g0198 | 2 | HG01070.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.151-5063G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122979422 | ||||||
| chr9:122979535
|
A | G | 5 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(2): Show | 5 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-4950A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122979535 | ||||||
| chr9:122979590
|
T | G | 1 | a0001c0001t0013g0207 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.151-4895T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122979590 | ||||||
| chr9:122980293
|
A | T | 21 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.151-4192A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122980293 | ||||||
| chr9:122980294
|
C | G | 1 | a0001c0001t0020g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.151-4191C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122980294 | ||||||
| chr9:122980835
|
T | C | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151-3650T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122980835 | ||||||
| chr9:122980853
|
G | A | 1 | a0001c0001t0091g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.151-3632G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122980853 | ||||||
| chr9:122981024
|
T | TTTGTTG | 3 | a0001c0001t0017g0249a0001c0001t0017g0251a0001c0001t0020g0250 | 3 | HG01243.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.151-3440_151-3435d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122981024 | |||||
| chr9:122981236
|
G | A | 1 | a0001c0001t0056g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.151-3249G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122981236 | ||||||
| chr9:122981388
|
A | G | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.151-3097A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122981388 | ||||||
| chr9:122981398
|
C | T | 1 | a0001c0001t0051g0066 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151-3087C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122981398 | ||||||
| chr9:122981585
|
T | C | 6 | a0001c0002t0122g0031a0001c0002t0123g0041a0001c0002t0124g0050others(3): Show | 6 | NA18945.hp2 NA18955.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.151-2900T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122981585 | ||||||
| chr9:122981604
|
G | A | 2 | a0001c0001t0020g0088a0001c0001t0020g0089 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.151-2881G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122981604 | ||||||
| chr9:122981880
|
C | A | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.151-2605C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122981880 | ||||||
| chr9:122982048
|
C | CA | 7 | a0001c0001t0002g0110a0001c0001t0003g0176a0001c0001t0014g0232others(4): Show | 7 | HG00741.hp1 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.151-2420dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122982048 | |||||
| chr9:122982403
|
C | T | 1 | a0001c0001t0013g0172 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.151-2082C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122982403 | ||||||
| chr9:122982621
|
A | C | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151-1864A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122982621 | ||||||
| chr9:122982763
|
G | A | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.151-1722G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122982763 | ||||||
| chr9:122982778
|
G | A | 3 | a0001c0001t0017g0249a0001c0001t0017g0251a0001c0001t0020g0250 | 3 | HG01243.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.151-1707G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122982778 | ||||||
| chr9:122982826
|
A | G | 1 | a0001c0001t0014g0235 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.151-1659A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122982826 | ||||||
| chr9:122982862
|
G | A | 1 | a0001c0001t0074g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.151-1623G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122982862 | ||||||
| chr9:122982950
|
G | T | 2 | a0001c0002t0126g0048a0001c0002t0129g0047 | 2 | NA18945.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.151-1535G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122982950 | ||||||
| chr9:122983166
|
C | CA | 14 | a0001c0001t0002g0083a0001c0001t0002g0110a0001c0001t0003g0201others(11): Show | 14 | HG00597.hp1 HG01175.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-1305dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122983166 | |||||
| chr9:122983176
|
A | C | 21 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.151-1309A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122983176 | ||||||
| chr9:122983181
|
C | A | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.151-1304C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122983181 | ||||||
| chr9:122983273
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0024a0001c0001t0009g0030 | 3 | HG02895.hp1 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.151-1212C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122983273 | ||||||
| chr9:122983330
|
A | G | 3 | a0001c0001t0028g0240a0001c0001t0028g0246a0001c0001t0084g0245 | 3 | HG02886.hp1 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.151-1155A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122983330 | ||||||
| chr9:122984001
|
A | G | 1 | a0001c0001t0044g0068 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.151-484A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122984001 | ||||||
| chr9:122984272
|
A | G | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.151-213A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122984272 | ||||||
| chr9:122984333
|
A | T | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.151-152A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122984333 | ||||||
| chr9:122984354
|
A | T | 1 | a0001c0001t0088g0130 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.151-131A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122984354 | ||||||
| chr9:122984759
|
G | T | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.385+40G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122984759 | ||||||
| chr9:122984877
|
T | C | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.385+158T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122984877 | ||||||
| chr9:122984991
|
C | T | 1 | a0001c0001t0056g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.385+272C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122984991 | ||||||
| chr9:122984997
|
A | C | 1 | a0001c0001t0056g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.385+278A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122984997 | ||||||
| chr9:122984997
|
AG | A | 245 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.385+280delG | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr9 | 122984997 | |||||
| chr9:122984998
|
G | A | 1 | a0001c0001t0056g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.385+279G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122984998 | ||||||
| chr9:122985229
|
A | G | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.385+510A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122985229 | ||||||
| chr9:122985430
|
G | A | 134 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.385+711G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122985430 | ||||||
| chr9:122985611
|
C | CA | 86 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.386-583dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr9 | 122985611 | |||||
| chr9:122985611
|
C | CAA | 27 | a0001c0001t0009g0015a0001c0001t0013g0192a0001c0001t0015g0196others(24): Show | 27 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.386-584_386-583dup others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr9 | 122985611 | |||||
| chr9:122985611
|
C | CAAA | 5 | a0001c0001t0032g0006a0001c0001t0099g0003a0001c0001t0114g0005others(2): Show | 5 | HG02129.hp1 NA18970.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.386-585_386-583dup others(3): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr9 | 122985611 | |||||
| chr9:122985611
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0021g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.386-593_386-583del others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr9 | 122985611 | |||||
| chr9:122985680
|
A | G | 3 | a0001c0001t0001g0182a0001c0001t0003g0201a0001c0001t0137g0198 | 3 | HG01070.hp2 HG01106.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.386-535A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122985680 | ||||||
| chr9:122985965
|
T | G | 1 | a0001c0001t0004g0087 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.386-250T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122985965 | ||||||
| chr9:122986025
|
T | C | 1 | a0001c0001t0016g0257 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.386-190T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122986025 | ||||||
| chr9:122986449
|
A | G | 1 | a0002c0003t0106g0074 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.590+30A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122986449 | ||||||
| chr9:122986588
|
G | C | 84 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.590+169G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122986588 | ||||||
| chr9:122986624
|
G | A | 23 | a0001c0001t0017g0249a0001c0001t0017g0251a0001c0001t0020g0088others(20): Show | 23 | HG00544.hp1 HG01109.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.590+205G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122986624 | ||||||
| chr9:122986817
|
C | T | 2 | a0001c0001t0020g0088a0001c0001t0020g0089 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.590+398C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122986817 | ||||||
| chr9:122987098
|
C | T | 1 | a0001c0001t0045g0064 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.590+679C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122987098 | ||||||
| chr9:122987221
|
T | C | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.590+802T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122987221 | ||||||
| chr9:122987434
|
G | C | 1 | a0001c0001t0083g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.590+1015G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122987434 | ||||||
| chr9:122987460
|
A | G | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.590+1041A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122987460 | ||||||
| chr9:122987908
|
T | C | 1 | a0001c0001t0023g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.591-1389T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122987908 | ||||||
| chr9:122987929
|
A | G | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.591-1368A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122987929 | ||||||
| chr9:122987986
|
T | C | 1 | a0001c0001t0036g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.591-1311T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122987986 | ||||||
| chr9:122988257
|
C | T | 1 | a0001c0001t0119g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.591-1040C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122988257 | ||||||
| chr9:122988499
|
A | AT | 55 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(52): Show | 55 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.591-785dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr9 | 122988499 | |||||
| chr9:122988499
|
A | ATT | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.591-786_591-785dup others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr9 | 122988499 | |||||
| chr9:122988851
|
G | C | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.591-446G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122988851 | ||||||
| chr9:122988883
|
C | T | 2 | a0001c0001t0021g0016a0001c0001t0021g0018 | 2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.591-414C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122988883 | ||||||
| chr9:122988899
|
C | T | 2 | a0001c0001t0014g0161a0001c0001t0030g0166 | 2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.591-398C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122988899 | ||||||
| chr9:122988942
|
C | CA | 10 | a0001c0001t0009g0015a0001c0001t0015g0178a0001c0001t0026g0181others(7): Show | 10 | HG00544.hp2 HG00621.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.591-337dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr9 | 122988942 | |||||
| chr9:122989083
|
A | G | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.591-214A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122989083 | ||||||
| chr9:122989084
|
A | ACATGATA others(91): Show |
2 | a0001c0001t0015g0225a0001c0001t0046g0168 | 2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.591-209_591-112dup others(98): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr9 | 122989084 | |||||
| chr9:122989121
|
G | A | 1 | a0001c0001t0095g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.591-176G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122989121 | ||||||
| chr9:122989183
|
C | T | 21 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.591-114C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122989183 | ||||||
| chr9:122989731
|
C | T | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.765+260C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 5/25 | chr9 | 122989731 | ||||||
| chr9:122990325
|
A | T | 1 | a0001c0001t0037g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.923+112A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990325 | ||||||
| chr9:122990334
|
C | G | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.923+121C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990334 | ||||||
| chr9:122990354
|
AATACATA others(8): Show |
A | 1 | a0001c0001t0021g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.923+143_923+157del others(15): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990354 | |||||
| chr9:122990431
|
C | T | 1 | a0001c0001t0113g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.923+218C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990431 | ||||||
| chr9:122990690
|
A | T | 3 | a0001c0001t0008g0069a0001c0001t0008g0070a0001c0001t0033g0001 | 4 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.923+477A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990690 | ||||||
| chr9:122990711
|
G | A | 5 | a0001c0001t0028g0244a0001c0001t0089g0243a0001c0001t0092g0239others(2): Show | 5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.923+498G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990711 | ||||||
| chr9:122990764
|
C | T | 11 | a0001c0001t0009g0015a0001c0001t0028g0240a0001c0001t0028g0244others(8): Show | 11 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.923+551C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990764 | ||||||
| chr9:122990769
|
C | CAA | 6 | a0001c0001t0008g0002a0001c0001t0008g0069a0001c0001t0008g0070others(3): Show | 7 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.923+583_923+584dup others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | |||||
| chr9:122990769
|
CAAA | C | 5 | a0001c0001t0015g0178a0001c0001t0027g0223a0001c0001t0030g0166others(2): Show | 5 | HG00673.hp1 HG01099.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+582_923+584del others(3): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | |||||
| chr9:122990769
|
CAAAAA | C | 8 | a0001c0001t0003g0167a0001c0001t0003g0173a0001c0001t0014g0161others(5): Show | 8 | HG00544.hp2 HG01361.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.923+580_923+584del others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | |||||
| chr9:122990769
|
CAAAAAA | C | 6 | a0001c0001t0003g0164a0001c0001t0003g0201a0001c0001t0032g0006others(3): Show | 6 | HG00597.hp2 HG01175.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+579_923+584del others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | |||||
| chr9:122990769
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0013g0195a0001c0001t0030g0169a0001c0001t0090g0228others(3): Show | 6 | HG00558.hp1 HG01167.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+577_923+584del others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | |||||
| chr9:122990769
|
CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0001g0179a0001c0001t0001g0229a0001c0001t0003g0176others(4): Show | 7 | HG00741.hp1 HG01258.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.923+576_923+584del others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | |||||
| chr9:122990769
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0046g0168a0001c0001t0060g0200a0001c0001t0076g0191others(2): Show | 5 | HG00735.hp1 HG02040.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+575_923+584del others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | |||||
| chr9:122990769
|
CAAAAAAA others(4): Show |
C | 7 | a0001c0001t0003g0206a0001c0001t0013g0172a0001c0001t0013g0207others(4): Show | 7 | HG00639.hp2 HG00735.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.923+574_923+584del others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | |||||
| chr9:122990769
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0015g0225 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.923+573_923+584del others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | |||||
| chr9:122990786
|
A | AATATATA others(3): Show |
1 | a0001c0001t0108g0163 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.923+574_923+575ins others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990786 | |||||
| chr9:122990786
|
AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0097g0227a0001c0001t0107g0231 | 2 | NA18959.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.923+575_923+586del others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990786 | |||||
| chr9:122990786
|
AAAAAAAA others(25): Show |
A | 1 | a0001c0001t0093g0170 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.923+575_923+606del others(32): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990786 | |||||
| chr9:122990787
|
AAAAAAAA others(4): Show |
A | 3 | a0001c0001t0012g0221a0001c0001t0039g0171a0001c0001t0085g0189 | 3 | HG00280.hp2 HG00738.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.923+576_923+586del others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990787 | |||||
| chr9:122990787
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0027g0194 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.923+576_923+588del others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990787 | |||||
| chr9:122990788
|
A | T | 4 | a0001c0001t0015g0196a0001c0001t0015g0220a0001c0001t0055g0188others(1): Show | 4 | HG00099.hp2 HG02027.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.923+575A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990788 | ||||||
| chr9:122990788
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0064g0212 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.923+577_923+586del others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990788 | |||||
| chr9:122990788
|
AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0026g0183a0001c0001t0041g0193 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.923+577_923+588del others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990788 | |||||
| chr9:122990788
|
AAAAAAAA others(27): Show |
A | 1 | a0001c0001t0058g0180 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.923+577_923+610del others(34): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990788 | |||||
| chr9:122990789
|
AAAAAAAA others(4): Show |
A | 5 | a0001c0001t0001g0182a0001c0001t0026g0181a0001c0001t0075g0208others(2): Show | 5 | HG00099.hp1 HG00642.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+578_923+588del others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990789 | |||||
| chr9:122990789
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0012g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.923+578_923+590del others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990789 | |||||
| chr9:122990790
|
A | T | 8 | a0001c0001t0015g0196a0001c0001t0015g0220a0001c0001t0027g0223others(5): Show | 8 | HG00099.hp2 HG00673.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.923+577A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990790 | ||||||
| chr9:122990790
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.923+579_923+590del others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990790 | |||||
| chr9:122990791
|
AAAAAAAT others(4): Show |
A | 1 | a0001c0001t0001g0216 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.923+580_923+590del others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990791 | |||||
| chr9:122990792
|
A | T | 15 | a0001c0001t0003g0167a0001c0001t0003g0173a0001c0001t0012g0162others(12): Show | 15 | HG00099.hp2 HG00673.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+579A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990792 | ||||||
| chr9:122990792
|
AAAAAATA others(5): Show |
A | 1 | a0001c0001t0023g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.923+581_923+592del others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990792 | |||||
| chr9:122990794
|
A | T | 24 | a0001c0001t0003g0159a0001c0001t0003g0167a0001c0001t0003g0173others(21): Show | 24 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.923+581A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990794 | ||||||
| chr9:122990794
|
AAAATATA others(9): Show |
A | 2 | a0001c0001t0017g0249a0001c0001t0017g0251 | 2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.923+583_923+598del others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990794 | |||||
| chr9:122990796
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0020g0088 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.923+584_923+585ins others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0044g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.923+584_923+585ins others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0020g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.923+584_923+585ins others(19): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0113g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.923+584_923+585ins others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
A | AAAAAAAT others(12): Show |
1 | a0001c0001t0020g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.923+584_923+585ins others(19): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0010g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.923+584_923+585ins others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
A | AAAATATA others(5): Show |
1 | a0001c0001t0028g0244 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.923+584_923+585ins others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
A | AAATATAT others(4): Show |
1 | a0001c0001t0084g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.923+584_923+585ins others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
A | AAATATAT others(6): Show |
1 | a0001c0001t0105g0234 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.923+584_923+585ins others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
A | AATATATA others(3): Show |
1 | a0001c0001t0121g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.923+614_923+623dup others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
A | T | 42 | a0001c0001t0003g0159a0001c0001t0003g0164a0001c0001t0003g0167others(39): Show | 42 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.923+583A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990796 | ||||||
| chr9:122990796
|
AAT | A | 6 | a0001c0001t0002g0063a0001c0001t0022g0112a0001c0001t0056g0086others(3): Show | 6 | HG02896.hp1 HG02897.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+622_923+623del others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
AATAT | A | 7 | a0001c0001t0007g0106a0001c0001t0023g0010a0001c0001t0047g0128others(4): Show | 7 | HG02055.hp1 HG02145.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.923+620_923+623del others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
AATATAT | A | 23 | a0001c0001t0002g0083a0001c0001t0004g0119a0001c0001t0006g0145others(20): Show | 23 | HG00597.hp1 HG01081.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.923+618_923+623del others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
AATATATA others(1): Show |
A | 6 | a0001c0001t0004g0109a0001c0001t0017g0026a0001c0001t0040g0151others(3): Show | 6 | HG00733.hp1 HG02056.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+616_923+623del others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
AATATATA others(11): Show |
A | 3 | a0001c0002t0005g0034a0001c0002t0005g0051a0001c0002t0050g0033 | 3 | NA18992.hp1 NA19011.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.923+606_923+623del others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990796
|
AATATATA others(13): Show |
A | 11 | a0001c0001t0007g0142a0001c0002t0005g0036a0001c0002t0005g0037others(8): Show | 11 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.923+604_923+623del others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | |||||
| chr9:122990797
|
AT | A | 8 | a0001c0001t0010g0080a0001c0001t0029g0099a0001c0001t0079g0094others(5): Show | 8 | HG01175.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.923+585delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | ||||||
| chr9:122990797
|
ATAT | A | 5 | a0001c0001t0018g0071a0001c0001t0018g0073a0001c0001t0022g0115others(2): Show | 5 | HG00544.hp1 HG01099.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+585_923+587del others(3): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | ||||||
| chr9:122990797
|
ATATAT | A | 15 | a0001c0001t0006g0146a0001c0001t0009g0015a0001c0001t0016g0257others(12): Show | 15 | HG00621.hp1 HG01884.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+585_923+589del others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | ||||||
| chr9:122990797
|
ATATATAT | A | 35 | a0001c0001t0002g0103a0001c0001t0002g0110a0001c0001t0002g0121others(32): Show | 35 | HG00558.hp2 HG00673.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.923+585_923+591del others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | ||||||
| chr9:122990797
|
ATATATAT others(4): Show |
A | 2 | a0001c0001t0028g0240a0001c0001t0028g0246 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.923+585_923+595del others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | ||||||
| chr9:122990797
|
ATATATAT others(10): Show |
A | 1 | a0001c0002t0005g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.923+585_923+601del others(17): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | ||||||
| chr9:122990797
|
ATATATAT others(12): Show |
A | 6 | a0001c0002t0005g0032a0001c0002t0049g0046a0001c0002t0050g0044others(3): Show | 6 | NA18945.hp2 NA18949.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+585_923+603del others(19): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | ||||||
| chr9:122990797
|
ATATATAT others(14): Show |
A | 3 | a0001c0001t0004g0143a0001c0001t0025g0144a0001c0002t0123g0041 | 3 | HG02258.hp2 HG02572.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.923+585_923+605del others(21): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | ||||||
| chr9:122990797
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0042g0095 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.923+585_923+607del others(23): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | ||||||
| chr9:122990798
|
T | A | 10 | a0001c0001t0008g0002a0001c0001t0008g0069a0001c0001t0008g0072others(7): Show | 11 | HG00323.hp1 HG01496.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.923+585T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990798 | ||||||
| chr9:122990800
|
T | A | 17 | a0001c0001t0002g0063a0001c0001t0008g0002a0001c0001t0010g0080others(14): Show | 17 | HG00323.hp1 HG01175.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.923+587T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990800 | ||||||
| chr9:122990802
|
T | A | 19 | a0001c0001t0002g0063a0001c0001t0018g0071a0001c0001t0018g0073others(16): Show | 19 | HG01099.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.923+589T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990802 | ||||||
| chr9:122990804
|
T | A | 43 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0004g0119others(40): Show | 43 | HG00597.hp1 HG00621.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.923+591T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990804 | ||||||
| chr9:122990806
|
T | A | 69 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(66): Show | 69 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.923+593T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990806 | ||||||
| chr9:122990808
|
T | A | 56 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(53): Show | 56 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.923+595T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990808 | ||||||
| chr9:122990810
|
T | A | 26 | a0001c0001t0002g0063a0001c0001t0002g0103a0001c0001t0002g0110others(23): Show | 26 | HG00733.hp1 HG01361.hp1 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.923+597T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990810 | ||||||
| chr9:122990816
|
T | A | 4 | a0001c0002t0005g0034a0001c0002t0005g0051a0001c0002t0005g0052others(1): Show | 4 | HG03834.hp2 NA18992.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+603T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990816 | ||||||
| chr9:122990818
|
T | A | 21 | a0001c0001t0007g0142a0001c0002t0005g0032a0001c0002t0005g0034others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.923+605T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990818 | ||||||
| chr9:122990820
|
T | A | 21 | a0001c0001t0025g0144a0001c0002t0005g0032a0001c0002t0005g0034others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.923+607T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990820 | ||||||
| chr9:122990822
|
T | A | 13 | a0001c0002t0005g0032a0001c0002t0005g0036a0001c0002t0005g0037others(10): Show | 13 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.923+609T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990822 | ||||||
| chr9:122990824
|
T | A | 1 | a0001c0002t0124g0050 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.923+611T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990824 | ||||||
| chr9:122990886
|
G | T | 1 | a0001c0001t0018g0073 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.923+673G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990886 | ||||||
| chr9:122990929
|
C | T | 1 | a0001c0007t0052g0035 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.923+716C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990929 | ||||||
| chr9:122990942
|
G | A | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.923+729G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990942 | ||||||
| chr9:122991133
|
A | G | 1 | a0001c0001t0015g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.923+920A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991133 | ||||||
| chr9:122991157
|
A | G | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.923+944A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991157 | ||||||
| chr9:122991335
|
G | C | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.923+1122G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991335 | ||||||
| chr9:122991543
|
G | A | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.923+1330G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991543 | ||||||
| chr9:122991556
|
CATT | C | 21 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.923+1344_923+1346d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991556 | ||||||
| chr9:122991605
|
C | CT | 34 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(31): Show | 34 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.923+1408dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122991605 | |||||
| chr9:122991605
|
CT | C | 7 | a0001c0001t0001g0218a0001c0001t0003g0159a0001c0001t0004g0109others(4): Show | 7 | HG00099.hp2 HG00323.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.923+1408delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122991605 | |||||
| chr9:122991607
|
T | C | 66 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(63): Show | 66 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.923+1394T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991607 | ||||||
| chr9:122991608
|
T | C | 1 | a0001c0001t0004g0109 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.923+1395T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991608 | ||||||
| chr9:122991875
|
A | G | 84 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.923+1662A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991875 | ||||||
| chr9:122991984
|
T | A | 1 | a0001c0001t0058g0180 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.923+1771T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991984 | ||||||
| chr9:122992150
|
C | T | 1 | a0001c0001t0017g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.923+1937C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992150 | ||||||
| chr9:122992256
|
C | T | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.923+2043C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992256 | ||||||
| chr9:122992280
|
C | G | 3 | a0001c0001t0001g0211a0001c0001t0026g0181a0001c0001t0069g0210 | 3 | HG01070.hp1 HG01993.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.923+2067C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992280 | ||||||
| chr9:122992347
|
T | C | 2 | a0001c0001t0009g0024a0001c0001t0009g0030 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.923+2134T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992347 | ||||||
| chr9:122992442
|
C | G | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.923+2229C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992442 | ||||||
| chr9:122992620
|
A | T | 1 | a0001c0001t0002g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.923+2407A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992620 | ||||||
| chr9:122992622
|
A | G | 21 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.923+2409A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992622 | ||||||
| chr9:122992749
|
T | C | 1 | a0001c0001t0017g0251 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.923+2536T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992749 | ||||||
| chr9:122992909
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.923+2696A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992909 | ||||||
| chr9:122992917
|
C | T | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.923+2704C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992917 | ||||||
| chr9:122993265
|
T | A | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.924-2776T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993265 | ||||||
| chr9:122993292
|
C | T | 101 | a0001c0001t0001g0211a0001c0001t0002g0063a0001c0001t0002g0083others(98): Show | 102 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.924-2749C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993292 | ||||||
| chr9:122993365
|
G | A | 1 | a0001c0001t0035g0134 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.924-2676G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993365 | ||||||
| chr9:122993424
|
G | A | 27 | a0001c0001t0013g0192a0001c0001t0015g0225a0001c0001t0027g0194others(24): Show | 27 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.924-2617G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993424 | ||||||
| chr9:122993428
|
C | T | 4 | a0001c0001t0020g0088a0001c0001t0020g0089a0001c0001t0044g0068others(1): Show | 4 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.924-2613C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993428 | ||||||
| chr9:122993460
|
C | T | 1 | a0001c0001t0006g0146 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.924-2581C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993460 | ||||||
| chr9:122993559
|
A | G | 18 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(15): Show | 18 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.924-2482A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993559 | ||||||
| chr9:122993645
|
G | T | 1 | a0001c0001t0003g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.924-2396G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993645 | ||||||
| chr9:122993715
|
G | A | 2 | a0001c0001t0028g0240a0001c0001t0028g0246 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.924-2326G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993715 | ||||||
| chr9:122993824
|
C | T | 1 | a0001c0001t0009g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.924-2217C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993824 | ||||||
| chr9:122994240
|
A | C | 2 | a0001c0001t0023g0028a0001c0001t0034g0025 | 2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.924-1801A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122994240 | ||||||
| chr9:122994952
|
C | T | 1 | a0001c0001t0099g0003 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.924-1089C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122994952 | ||||||
| chr9:122994975
|
G | A | 1 | a0001c0001t0037g0022 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.924-1066G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122994975 | ||||||
| chr9:122995298
|
C | T | 1 | a0001c0001t0047g0128 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.924-743C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122995298 | ||||||
| chr9:122995348
|
A | G | 107 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(104): Show | 108 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.924-693A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122995348 | ||||||
| chr9:122995566
|
A | AT | 139 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(136): Show | 140 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.924-455dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122995566 | |||||
| chr9:122995566
|
A | ATT | 102 | a0001c0001t0001g0182a0001c0001t0001g0211a0001c0001t0001g0213others(99): Show | 102 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.924-456_924-455dup others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122995566 | |||||
| chr9:122995600
|
G | T | 1 | a0001c0001t0110g0177 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.924-441G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122995600 | ||||||
| chr9:122996332
|
T | TA | 6 | a0001c0001t0032g0006a0001c0001t0032g0007a0001c0001t0099g0003others(3): Show | 6 | HG02129.hp1 NA18970.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.1034+182dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 122996332 | |||||
| chr9:122996334
|
C | T | 1 | a0001c0001t0017g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1034+183C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 7/25 | chr9 | 122996334 | ||||||
| chr9:122997162
|
A | G | 1 | a0001c0001t0076g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1102-97A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 8/25 | chr9 | 122997162 | ||||||
| chr9:122997213
|
T | C | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1102-46T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 8/25 | chr9 | 122997213 | ||||||
| chr9:122997219
|
C | T | 1 | a0001c0001t0008g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1102-40C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 8/25 | chr9 | 122997219 | ||||||
| chr9:122997428
|
C | A | 1 | a0001c0001t0031g0237 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1204+67C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122997428 | ||||||
| chr9:122997582
|
TTTTC | T | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1204+231_1204+234d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 122997582 | |||||
| chr9:122997613
|
C | G | 1 | a0001c0001t0134g0202 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1204+252C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122997613 | ||||||
| chr9:122997743
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1204+382G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122997743 | ||||||
| chr9:122997787
|
G | A | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204+426G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122997787 | ||||||
| chr9:122997873
|
A | G | 4 | a0001c0001t0020g0088a0001c0001t0020g0089a0001c0001t0044g0068others(1): Show | 4 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204+512A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122997873 | ||||||
| chr9:122997989
|
A | G | 28 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(25): Show | 28 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1205-608A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122997989 | ||||||
| chr9:122998235
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1205-362G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122998235 | ||||||
| chr9:122998432
|
C | T | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1205-165C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122998432 | ||||||
| chr9:122998584
|
T | C | 81 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1205-13T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122998584 | ||||||
| chr9:122998772
|
G | A | 81 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
splice_region_variant&intron_variant | LOW | c.1374+6G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122998772 | ||||||
| chr9:122998772
|
G | C | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
splice_region_variant&intron_variant | LOW | c.1374+6G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122998772 | ||||||
| chr9:122998780
|
C | T | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1374+14C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122998780 | ||||||
| chr9:122998795
|
G | A | 2 | a0001c0001t0048g0105a0001c0001t0048g0127 | 2 | NA18952.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1374+29G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122998795 | ||||||
| chr9:122998913
|
C | T | 1 | a0001c0001t0059g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1374+147C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122998913 | ||||||
| chr9:122999124
|
T | G | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1374+358T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999124 | ||||||
| chr9:122999209
|
C | T | 1 | a0001c0001t0015g0220 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1374+443C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999209 | ||||||
| chr9:122999245
|
G | A | 1 | a0001c0001t0094g0113 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1374+479G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999245 | ||||||
| chr9:122999270
|
G | A | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1374+504G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999270 | ||||||
| chr9:122999323
|
A | AC | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1374+557_1374+558i others(3): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999323 | ||||||
| chr9:122999406
|
G | A | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1374+640G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999406 | ||||||
| chr9:122999780
|
C | T | 1 | a0001c0001t0066g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1374+1014C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999780 | ||||||
| chr9:122999933
|
A | C | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1374+1167A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999933 | ||||||
| chr9:123000126
|
A | G | 1 | a0001c0001t0015g0225 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1374+1360A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123000126 | ||||||
| chr9:123000228
|
C | G | 1 | a0001c0001t0020g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1374+1462C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123000228 | ||||||
| chr9:123000314
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1374+1548G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123000314 | ||||||
| chr9:123000350
|
C | T | 1 | a0001c0001t0007g0106 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1374+1584C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123000350 | ||||||
| chr9:123000428
|
T | C | 110 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(107): Show | 111 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1374+1662T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123000428 | ||||||
| chr9:123000433
|
A | G | 2 | a0001c0001t0023g0010a0001c0001t0037g0027 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1374+1667A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123000433 | ||||||
| chr9:123000819
|
A | T | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1374+2053A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123000819 | ||||||
| chr9:123001138
|
G | A | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1374+2372G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001138 | ||||||
| chr9:123001147
|
C | T | 1 | a0001c0001t0110g0177 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1374+2381C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001147 | ||||||
| chr9:123001242
|
C | T | 1 | a0001c0001t0070g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1374+2476C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001242 | ||||||
| chr9:123001625
|
A | T | 3 | a0001c0001t0004g0109a0001c0001t0022g0102a0001c0001t0117g0101 | 3 | NA18747.hp1 NA18984.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1374+2859A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001625 | ||||||
| chr9:123001829
|
G | A | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1374+3063G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001829 | ||||||
| chr9:123001859
|
A | G | 1 | a0001c0001t0068g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1374+3093A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001859 | ||||||
| chr9:123001934
|
G | A | 2 | a0001c0001t0075g0208a0001c0001t0085g0189 | 2 | HG00280.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.1374+3168G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001934 | ||||||
| chr9:123001958
|
G | A | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1374+3192G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001958 | ||||||
| chr9:123002122
|
A | T | 1 | a0001c0001t0001g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1374+3356A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002122 | ||||||
| chr9:123002346
|
T | C | 2 | a0001c0001t0010g0080a0001c0001t0010g0081 | 2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1374+3580T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002346 | ||||||
| chr9:123002356
|
T | TTA | 30 | a0001c0001t0010g0060a0001c0001t0013g0192a0001c0001t0015g0225others(27): Show | 30 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1374+3602_1374+360 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123002356 | |||||
| chr9:123002368
|
A | AT | 49 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(46): Show | 50 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1374+3612dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123002368 | |||||
| chr9:123002369
|
T | TA | 163 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(160): Show | 163 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1374+3603_1374+360 others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002369 | ||||||
| chr9:123002370
|
T | A | 10 | a0001c0001t0029g0082a0001c0001t0029g0099a0001c0001t0036g0053others(7): Show | 10 | HG02145.hp2 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1374+3604T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002370 | ||||||
| chr9:123002371
|
T | A | 70 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(67): Show | 70 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1374+3605T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002371 | ||||||
| chr9:123002373
|
T | A | 1 | a0001c0001t0007g0124 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1374+3607T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002373 | ||||||
| chr9:123002473
|
A | G | 1 | a0001c0001t0014g0224 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1374+3707A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002473 | ||||||
| chr9:123002522
|
C | T | 32 | a0001c0001t0003g0176a0001c0001t0009g0009a0001c0001t0009g0015others(29): Show | 32 | HG00544.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1374+3756C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002522 | ||||||
| chr9:123002704
|
AATATT | A | 81 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1374+3941_1374+394 others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123002704 | |||||
| chr9:123002728
|
C | G | 3 | a0001c0001t0045g0064a0001c0001t0051g0067a0001c0001t0128g0065 | 3 | HG02970.hp1 HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1374+3962C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002728 | ||||||
| chr9:123002748
|
A | G | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1374+3982A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002748 | ||||||
| chr9:123002822
|
A | G | 1 | a0001c0001t0010g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1374+4056A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002822 | ||||||
| chr9:123002883
|
G | T | 1 | a0001c0001t0063g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1374+4117G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002883 | ||||||
| chr9:123002888
|
C | G | 52 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(49): Show | 52 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1374+4122C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002888 | ||||||
| chr9:123003226
|
G | T | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1374+4460G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123003226 | ||||||
| chr9:123003284
|
A | G | 1 | a0001c0001t0007g0124 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1374+4518A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123003284 | ||||||
| chr9:123003835
|
G | A | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1374+5069G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123003835 | ||||||
| chr9:123004167
|
T | G | 13 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(10): Show | 14 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.1374+5401T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123004167 | ||||||
| chr9:123004252
|
G | T | 5 | a0001c0001t0028g0244a0001c0001t0089g0243a0001c0001t0092g0239others(2): Show | 5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1374+5486G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123004252 | ||||||
| chr9:123004266
|
A | G | 134 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1374+5500A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123004266 | ||||||
| chr9:123004361
|
C | G | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1374+5595C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123004361 | ||||||
| chr9:123004593
|
T | A | 2 | a0001c0001t0079g0094a0001c0001t0091g0092 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1375-5761T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123004593 | ||||||
| chr9:123004970
|
C | T | 1 | a0001c0001t0006g0152 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1375-5384C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123004970 | ||||||
| chr9:123005010
|
C | G | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1375-5344C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005010 | ||||||
| chr9:123005012
|
C | T | 12 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(9): Show | 13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1375-5342C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005012 | ||||||
| chr9:123005056
|
C | CA | 91 | a0001c0001t0002g0083a0001c0001t0002g0103a0001c0001t0002g0110others(88): Show | 92 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1375-5277dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123005056 | |||||
| chr9:123005056
|
C | CAA | 10 | a0001c0001t0002g0063a0001c0001t0002g0122a0001c0001t0004g0119others(7): Show | 10 | HG00597.hp1 HG00621.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1375-5278_1375-527 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123005056 | |||||
| chr9:123005056
|
CA | C | 8 | a0001c0001t0001g0216a0001c0001t0003g0176a0001c0001t0004g0143others(5): Show | 8 | HG00741.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-5277delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123005056 | |||||
| chr9:123005056
|
CAA | C | 130 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1375-5278_1375-527 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123005056 | |||||
| chr9:123005261
|
C | G | 107 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(104): Show | 108 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1375-5093C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005261 | ||||||
| chr9:123005288
|
AT | A | 133 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(130): Show | 133 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1375-5055delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123005288 | |||||
| chr9:123005299
|
T | C | 1 | a0001c0001t0030g0166 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1375-5055T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005299 | ||||||
| chr9:123005301
|
C | T | 1 | a0001c0001t0030g0166 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1375-5053C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005301 | ||||||
| chr9:123005707
|
A | G | 1 | a0001c0001t0015g0220 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1375-4647A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005707 | ||||||
| chr9:123005800
|
A | T | 2 | a0001c0001t0017g0249a0001c0001t0017g0251 | 2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1375-4554A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005800 | ||||||
| chr9:123005808
|
C | T | 1 | a0001c0002t0052g0038 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1375-4546C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005808 | ||||||
| chr9:123006152
|
T | A | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1375-4202T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123006152 | ||||||
| chr9:123006171
|
G | A | 1 | a0001c0001t0006g0152 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1375-4183G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123006171 | ||||||
| chr9:123006401
|
T | G | 107 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(104): Show | 108 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1375-3953T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123006401 | ||||||
| chr9:123006428
|
T | C | 1 | a0001c0001t0020g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1375-3926T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123006428 | ||||||
| chr9:123006590
|
T | C | 110 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(107): Show | 111 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1375-3764T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123006590 | ||||||
| chr9:123007089
|
A | AT | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1375-3259dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123007089 | |||||
| chr9:123007369
|
C | T | 1 | a0001c0001t0036g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1375-2985C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123007369 | ||||||
| chr9:123007373
|
C | CT | 11 | a0001c0001t0001g0179a0001c0001t0001g0216a0001c0001t0003g0176others(8): Show | 11 | HG00597.hp2 HG00741.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1375-2961dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123007373 | |||||
| chr9:123007373
|
CT | C | 97 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(94): Show | 98 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1375-2961delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123007373 | |||||
| chr9:123007470
|
C | T | 81 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1375-2884C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123007470 | ||||||
| chr9:123007553
|
A | AT | 114 | a0001c0001t0001g0182a0001c0001t0001g0211a0001c0001t0001g0213others(111): Show | 114 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1375-2779dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123007553 | |||||
| chr9:123007553
|
A | ATT | 13 | a0001c0001t0001g0179a0001c0001t0003g0201a0001c0001t0013g0172others(10): Show | 13 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.1375-2780_1375-277 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123007553 | |||||
| chr9:123007553
|
AT | A | 13 | a0001c0001t0002g0083a0001c0001t0002g0103a0001c0001t0004g0143others(10): Show | 13 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1375-2779delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123007553 | |||||
| chr9:123007629
|
G | A | 1 | a0001c0001t0132g0174 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1375-2725G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123007629 | ||||||
| chr9:123007669
|
A | G | 1 | a0001c0001t0121g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1375-2685A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123007669 | ||||||
| chr9:123007723
|
A | T | 3 | a0001c0001t0045g0064a0001c0001t0051g0067a0001c0001t0128g0065 | 3 | HG02970.hp1 HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1375-2631A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123007723 | ||||||
| chr9:123008413
|
C | T | 1 | a0001c0001t0119g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1375-1941C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123008413 | ||||||
| chr9:123008544
|
C | CA | 12 | a0001c0001t0014g0161a0001c0001t0017g0249a0001c0001t0017g0251others(9): Show | 12 | HG00558.hp1 HG01243.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1375-1792dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123008544 | |||||
| chr9:123008560
|
AAAG | A | 23 | a0001c0001t0003g0176a0001c0002t0005g0032a0001c0002t0005g0034others(20): Show | 23 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1375-1792_1375-179 others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123008560 | |||||
| chr9:123008775
|
C | CT | 23 | a0001c0001t0003g0176a0001c0002t0005g0032a0001c0002t0005g0034others(20): Show | 23 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1375-1578dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123008775 | |||||
| chr9:123009206
|
T | C | 3 | a0001c0001t0001g0211a0001c0001t0026g0181a0001c0001t0069g0210 | 3 | HG01070.hp1 HG01993.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1375-1148T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123009206 | ||||||
| chr9:123009316
|
C | T | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1375-1038C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123009316 | ||||||
| chr9:123009806
|
T | TC | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1375-546dupC | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123009806 | |||||
| chr9:123009835
|
A | T | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1375-519A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123009835 | ||||||
| chr9:123010046
|
G | A | 1 | a0001c0001t0021g0018 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1375-308G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123010046 | ||||||
| chr9:123010196
|
T | TA | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1375-157dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123010196 | |||||
| chr9:123010592
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1549+64G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123010592 | ||||||
| chr9:123010970
|
C | T | 1 | a0001c0001t0006g0149 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1549+442C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123010970 | ||||||
| chr9:123011475
|
ACTTT | A | 3 | a0001c0001t0017g0249a0001c0001t0017g0251a0001c0001t0020g0250 | 3 | HG01243.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1549+951_1549+954d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123011475 | |||||
| chr9:123011738
|
T | G | 18 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(15): Show | 18 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1549+1210T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123011738 | ||||||
| chr9:123011798
|
CA | C | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1549+1277delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123011798 | |||||
| chr9:123011955
|
T | TCAA | 3 | a0001c0001t0025g0153a0001c0001t0040g0151a0004c0005t0006g0156 | 3 | HG00733.hp1 HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1549+1449_1549+145 others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123011955 | |||||
| chr9:123012824
|
A | G | 13 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(10): Show | 14 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.1549+2296A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123012824 | ||||||
| chr9:123012870
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1549+2342G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123012870 | ||||||
| chr9:123013040
|
A | G | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1550-2503A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123013040 | ||||||
| chr9:123013086
|
A | G | 1 | a0001c0001t0036g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1550-2457A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123013086 | ||||||
| chr9:123013148
|
T | C | 1 | a0001c0001t0026g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1550-2395T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123013148 | ||||||
| chr9:123013338
|
C | CT | 81 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1550-2194dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123013338 | |||||
| chr9:123013556
|
C | T | 1 | a0001c0001t0034g0056 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1550-1987C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123013556 | ||||||
| chr9:123013581
|
C | T | 21 | a0001c0001t0003g0159a0001c0001t0003g0164a0001c0001t0003g0167others(18): Show | 21 | HG00544.hp2 HG00673.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1550-1962C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123013581 | ||||||
| chr9:123013601
|
G | A | 1 | a0001c0001t0084g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1550-1942G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123013601 | ||||||
| chr9:123013867
|
A | T | 2 | a0001c0001t0065g0058a0001c0001t0066g0055 | 2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1550-1676A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123013867 | ||||||
| chr9:123014011
|
G | A | 1 | a0001c0001t0025g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1550-1532G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123014011 | ||||||
| chr9:123014051
|
A | C | 6 | a0002c0003t0024g0078a0002c0003t0024g0079a0002c0003t0072g0062others(3): Show | 6 | HG00544.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1550-1492A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123014051 | ||||||
| chr9:123014149
|
G | A | 81 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1550-1394G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123014149 | ||||||
| chr9:123014175
|
C | T | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1550-1368C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123014175 | ||||||
| chr9:123014345
|
A | G | 1 | a0001c0001t0080g0133 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1550-1198A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123014345 | ||||||
| chr9:123014573
|
G | A | 3 | a0001c0001t0025g0153a0001c0001t0040g0151a0004c0005t0006g0156 | 3 | HG00733.hp1 HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1550-970G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123014573 | ||||||
| chr9:123014658
|
AT | A | 151 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(148): Show | 152 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1550-864delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123014658 | |||||
| chr9:123014658
|
ATT | A | 91 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1550-865_1550-864d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123014658 | |||||
| chr9:123014999
|
A | T | 6 | a0001c0002t0122g0031a0001c0002t0123g0041a0001c0002t0124g0050others(3): Show | 6 | NA18945.hp2 NA18955.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.1550-544A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123014999 | ||||||
| chr9:123015029
|
C | T | 1 | a0001c0001t0066g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1550-514C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123015029 | ||||||
| chr9:123015289
|
C | CT | 45 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0216others(42): Show | 45 | HG00099.hp1 HG00544.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1550-235dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123015289 | |||||
| chr9:123015289
|
C | CTT | 32 | a0001c0001t0003g0167a0001c0001t0003g0173a0001c0001t0012g0217others(29): Show | 32 | HG00280.hp1 HG00741.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.1550-236_1550-235d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123015289 | |||||
| chr9:123015289
|
CT | C | 42 | a0001c0001t0003g0206a0001c0001t0004g0087a0001c0001t0004g0109others(39): Show | 42 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.1550-235delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123015289 | |||||
| chr9:123015289
|
CTT | C | 10 | a0001c0001t0008g0059a0001c0001t0008g0072a0001c0001t0018g0071others(7): Show | 11 | HG01099.hp2 HG02040.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1550-236_1550-235d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123015289 | |||||
| chr9:123015289
|
CTTT | C | 9 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0008g0002others(6): Show | 9 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1550-237_1550-235d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123015289 | |||||
| chr9:123015368
|
A | G | 1 | a0001c0001t0004g0109 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1550-175A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123015368 | ||||||
| chr9:123015425
|
G | T | 1 | a0001c0001t0004g0125 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1550-118G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123015425 | ||||||
| chr9:123015512
|
T | C | 1 | a0001c0001t0014g0224 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1550-31T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123015512 | ||||||
| chr9:123015648
|
T | C | 5 | a0001c0001t0001g0179a0001c0001t0001g0213a0001c0001t0001g0218others(2): Show | 5 | HG01081.hp2 HG01515.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1643+12T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123015648 | ||||||
| chr9:123015663
|
T | A | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1643+27T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123015663 | ||||||
| chr9:123015711
|
C | G | 1 | a0001c0001t0019g0111 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1643+75C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123015711 | ||||||
| chr9:123015774
|
A | T | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1643+138A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123015774 | ||||||
| chr9:123015909
|
G | A | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1643+273G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123015909 | ||||||
| chr9:123016001
|
C | T | 5 | a0001c0001t0028g0244a0001c0001t0089g0243a0001c0001t0092g0239others(2): Show | 5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1643+365C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123016001 | ||||||
| chr9:123016215
|
A | G | 5 | a0001c0001t0028g0244a0001c0001t0089g0243a0001c0001t0092g0239others(2): Show | 5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1643+579A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123016215 | ||||||
| chr9:123016366
|
G | A | 1 | a0001c0001t0128g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1643+730G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123016366 | ||||||
| chr9:123016368
|
G | A | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1643+732G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123016368 | ||||||
| chr9:123016477
|
A | G | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1643+841A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123016477 | ||||||
| chr9:123016562
|
T | TTTA | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1643+927_1643+929d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr9 | 123016562 | |||||
| chr9:123016646
|
A | G | 2 | a0001c0001t0097g0227a0001c0001t0107g0231 | 2 | NA18959.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1643+1010A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123016646 | ||||||
| chr9:123016685
|
C | A | 1 | a0001c0001t0055g0188 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1643+1049C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123016685 | ||||||
| chr9:123017014
|
G | C | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1643+1378G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123017014 | ||||||
| chr9:123017224
|
A | G | 1 | a0001c0001t0034g0056 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1643+1588A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123017224 | ||||||
| chr9:123017261
|
TA | T | 5 | a0001c0001t0028g0244a0001c0001t0089g0243a0001c0001t0092g0239others(2): Show | 5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1643+1626delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123017261 | ||||||
| chr9:123017312
|
C | T | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1643+1676C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123017312 | ||||||
| chr9:123017529
|
T | C | 1 | a0001c0001t0015g0196 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1643+1893T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123017529 | ||||||
| chr9:123017905
|
C | T | 1 | a0001c0001t0028g0246 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1643+2269C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123017905 | ||||||
| chr9:123018033
|
G | T | 12 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(9): Show | 13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1644-2276G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018033 | ||||||
| chr9:123018196
|
G | A | 2 | a0001c0001t0027g0194a0001c0001t0041g0193 | 2 | NA18969.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1644-2113G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018196 | ||||||
| chr9:123018360
|
T | C | 1 | a0001c0001t0132g0174 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1644-1949T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018360 | ||||||
| chr9:123018420
|
A | G | 2 | a0001c0001t0035g0129a0001c0001t0035g0134 | 2 | NA20300.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1644-1889A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018420 | ||||||
| chr9:123018435
|
A | G | 11 | a0001c0001t0009g0009a0001c0001t0009g0024a0001c0001t0009g0030others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1644-1874A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018435 | ||||||
| chr9:123018578
|
T | C | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1644-1731T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018578 | ||||||
| chr9:123018653
|
A | C | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1644-1656A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018653 | ||||||
| chr9:123018978
|
C | T | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1644-1331C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018978 | ||||||
| chr9:123019012
|
G | C | 12 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(9): Show | 13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1644-1297G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019012 | ||||||
| chr9:123019043
|
C | T | 2 | a0001c0002t0050g0033a0001c0002t0050g0044 | 2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1644-1266C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019043 | ||||||
| chr9:123019064
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1644-1245G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019064 | ||||||
| chr9:123019450
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1644-859G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019450 | ||||||
| chr9:123019473
|
G | A | 1 | a0001c0001t0060g0200 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1644-836G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019473 | ||||||
| chr9:123019542
|
T | G | 1 | a0001c0001t0004g0132 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1644-767T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019542 | ||||||
| chr9:123019623
|
G | A | 245 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(242): Show | 246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1644-686G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019623 | ||||||
| chr9:123019686
|
T | TTTTG | 134 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1644-603_1644-600d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr9 | 123019686 | |||||
| chr9:123019847
|
G | C | 2 | a0002c0003t0077g0075a0003c0004t0024g0076 | 2 | NA18945.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1644-462G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019847 | ||||||
| chr9:123019935
|
C | T | 1 | a0001c0001t0030g0166 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1644-374C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019935 | ||||||
| chr9:123019954
|
G | A | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1644-355G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019954 | ||||||
| chr9:123020038
|
C | T | 1 | a0001c0001t0132g0174 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1644-271C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020038 | ||||||
| chr9:123020043
|
T | G | 1 | a0001c0001t0132g0174 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1644-266T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020043 | ||||||
| chr9:123020044
|
T | G | 176 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1644-265T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020044 | ||||||
| chr9:123020050
|
T | G | 1 | a0001c0001t0120g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1644-259T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020050 | ||||||
| chr9:123020051
|
T | C | 1 | a0001c0001t0090g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1644-258T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020051 | ||||||
| chr9:123020120
|
A | G | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1644-189A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020120 | ||||||
| chr9:123020133
|
C | T | 1 | a0001c0001t0007g0124 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1644-176C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020133 | ||||||
| chr9:123020161
|
C | G | 1 | a0001c0001t0083g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1644-148C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020161 | ||||||
| chr9:123020706
|
G | T | 1 | a0001c0001t0020g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1794+247G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123020706 | ||||||
| chr9:123021051
|
C | T | 2 | a0001c0001t0027g0194a0001c0001t0041g0193 | 2 | NA18969.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1794+592C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021051 | ||||||
| chr9:123021091
|
A | G | 1 | a0001c0001t0004g0109 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1794+632A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021091 | ||||||
| chr9:123021203
|
A | G | 11 | a0001c0001t0009g0009a0001c0001t0009g0024a0001c0001t0009g0030others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1794+744A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021203 | ||||||
| chr9:123021291
|
T | C | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1794+832T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021291 | ||||||
| chr9:123021293
|
TA | T | 41 | a0001c0001t0007g0117a0001c0001t0008g0002a0001c0001t0008g0059others(38): Show | 42 | HG00323.hp1 HG00544.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.1794+850delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123021293 | |||||
| chr9:123021311
|
C | T | 81 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1794+852C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021311 | ||||||
| chr9:123021317
|
A | T | 18 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(15): Show | 18 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1794+858A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021317 | ||||||
| chr9:123021330
|
C | CT | 36 | a0001c0001t0002g0131a0001c0001t0003g0176a0001c0001t0004g0119others(33): Show | 36 | HG00597.hp1 HG01069.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1794+890dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123021330 | |||||
| chr9:123021416
|
C | T | 1 | a0001c0001t0067g0013 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1794+957C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021416 | ||||||
| chr9:123021470
|
C | T | 1 | a0001c0001t0014g0224 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1794+1011C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021470 | ||||||
| chr9:123021495
|
A | T | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1794+1036A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021495 | ||||||
| chr9:123021560
|
A | G | 4 | a0001c0001t0020g0088a0001c0001t0020g0089a0001c0001t0044g0068others(1): Show | 4 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794+1101A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021560 | ||||||
| chr9:123021701
|
C | T | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1794+1242C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021701 | ||||||
| chr9:123021809
|
C | A | 1 | a0001c0001t0088g0130 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1794+1350C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021809 | ||||||
| chr9:123021986
|
T | C | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1794+1527T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021986 | ||||||
| chr9:123022086
|
T | G | 1 | a0001c0001t0120g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1794+1627T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022086 | ||||||
| chr9:123022315
|
A | G | 1 | a0001c0001t0034g0056 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1794+1856A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022315 | ||||||
| chr9:123022634
|
T | C | 12 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(9): Show | 13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1794+2175T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022634 | ||||||
| chr9:123022660
|
C | T | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794+2201C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022660 | ||||||
| chr9:123022695
|
G | A | 1 | a0001c0001t0002g0110 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1794+2236G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022695 | ||||||
| chr9:123022696
|
C | T | 81 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1794+2237C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022696 | ||||||
| chr9:123022724
|
T | C | 110 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(107): Show | 111 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1794+2265T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022724 | ||||||
| chr9:123022746
|
G | T | 2 | a0001c0002t0124g0050a0001c0002t0125g0039 | 2 | NA18955.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1794+2287G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022746 | ||||||
| chr9:123022748
|
A | G | 2 | a0001c0002t0124g0050a0001c0002t0125g0039 | 2 | NA18955.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1794+2289A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022748 | ||||||
| chr9:123022764
|
G | T | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794+2305G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022764 | ||||||
| chr9:123023138
|
A | G | 84 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1794+2679A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023138 | ||||||
| chr9:123023139
|
T | C | 1 | a0001c0002t0127g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1794+2680T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023139 | ||||||
| chr9:123023141
|
A | T | 1 | a0001c0002t0127g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1794+2682A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023141 | ||||||
| chr9:123023301
|
C | T | 2 | a0001c0001t0015g0225a0001c0001t0046g0168 | 2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1794+2842C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023301 | ||||||
| chr9:123023373
|
G | A | 1 | a0001c0001t0121g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1794+2914G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023373 | ||||||
| chr9:123023656
|
G | A | 1 | a0001c0001t0017g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1794+3197G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023656 | ||||||
| chr9:123023698
|
G | A | 2 | a0001c0001t0013g0172a0001c0001t0013g0207 | 2 | HG01952.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1794+3239G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023698 | ||||||
| chr9:123023943
|
G | T | 1 | a0001c0001t0015g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1794+3484G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023943 | ||||||
| chr9:123024289
|
C | T | 1 | a0001c0001t0007g0124 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1794+3830C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123024289 | ||||||
| chr9:123024370
|
A | G | 1 | a0001c0001t0018g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1794+3911A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123024370 | ||||||
| chr9:123024460
|
G | A | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1794+4001G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123024460 | ||||||
| chr9:123024699
|
A | G | 1 | a0001c0001t0019g0111 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1794+4240A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123024699 | ||||||
| chr9:123024708
|
G | A | 1 | a0001c0001t0004g0119 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1794+4249G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123024708 | ||||||
| chr9:123024960
|
A | T | 2 | a0001c0001t0097g0227a0001c0001t0107g0231 | 2 | NA18959.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1794+4501A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123024960 | ||||||
| chr9:123025112
|
C | G | 2 | a0001c0001t0044g0068a0001c0001t0044g0090 | 2 | HG01884.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1794+4653C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123025112 | ||||||
| chr9:123025117
|
C | T | 2 | a0001c0001t0116g0120a0001c0001t0118g0116 | 2 | HG00558.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1794+4658C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123025117 | ||||||
| chr9:123025471
|
A | G | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794+5012A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123025471 | ||||||
| chr9:123025543
|
C | CTTTTTTT | 73 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(70): Show | 73 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1794+5095_1794+510 others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123025543 | |||||
| chr9:123025543
|
C | CTTTTTTT others(1): Show |
56 | a0001c0001t0001g0216a0001c0001t0003g0159a0001c0001t0003g0173others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1794+5094_1794+510 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123025543 | |||||
| chr9:123025543
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0009g0009a0001c0001t0009g0024a0001c0001t0009g0030others(3): Show | 6 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1794+5093_1794+510 others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123025543 | |||||
| chr9:123025543
|
CT | C | 17 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0008g0002others(14): Show | 18 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.1794+5101delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123025543 | |||||
| chr9:123025637
|
G | A | 1 | a0001c0002t0122g0031 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1794+5178G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123025637 | ||||||
| chr9:123025663
|
T | C | 1 | a0002c0003t0072g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1794+5204T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123025663 | ||||||
| chr9:123025781
|
G | A | 1 | a0001c0001t0098g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1794+5322G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123025781 | ||||||
| chr9:123026005
|
C | CT | 73 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(70): Show | 73 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.1794+5564dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123026005 | |||||
| chr9:123026005
|
C | CTT | 19 | a0001c0001t0006g0145a0001c0001t0006g0146a0001c0001t0006g0149others(16): Show | 19 | HG00733.hp1 HG01109.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.1794+5563_1794+556 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123026005 | |||||
| chr9:123026005
|
CT | C | 133 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1794+5564delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123026005 | |||||
| chr9:123026536
|
A | G | 3 | a0001c0001t0014g0224a0001c0001t0014g0232a0001c0001t0027g0223 | 3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1794+6077A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123026536 | ||||||
| chr9:123026876
|
A | C | 2 | a0001c0001t0042g0095a0001c0001t0042g0098 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1794+6417A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123026876 | ||||||
| chr9:123026881
|
A | G | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1794+6422A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123026881 | ||||||
| chr9:123027066
|
G | A | 1 | a0001c0001t0004g0125 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1794+6607G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123027066 | ||||||
| chr9:123027108
|
C | CT | 7 | a0001c0001t0007g0106a0001c0001t0040g0104a0001c0001t0042g0098others(4): Show | 7 | HG01884.hp1 HG02895.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1794+6668dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123027108 | |||||
| chr9:123027108
|
CT | C | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1794+6668delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123027108 | |||||
| chr9:123027112
|
T | C | 1 | a0001c0001t0112g0136 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1794+6653T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123027112 | ||||||
| chr9:123027203
|
G | A | 2 | a0001c0001t0014g0161a0001c0001t0030g0166 | 2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1794+6744G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123027203 | ||||||
| chr9:123027472
|
G | T | 107 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(104): Show | 108 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1794+7013G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123027472 | ||||||
| chr9:123027628
|
G | A | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1794+7169G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123027628 | ||||||
| chr9:123027690
|
C | T | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794+7231C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123027690 | ||||||
| chr9:123027848
|
G | T | 1 | a0001c0001t0095g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1794+7389G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123027848 | ||||||
| chr9:123028575
|
G | A | 1 | a0001c0001t0105g0234 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1794+8116G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123028575 | ||||||
| chr9:123028736
|
A | G | 1 | a0001c0001t0059g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1794+8277A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123028736 | ||||||
| chr9:123028962
|
T | C | 2 | a0001c0002t0130g0043a0001c0002t0131g0045 | 2 | HG00280.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1794+8503T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123028962 | ||||||
| chr9:123029060
|
A | C | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1794+8601A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123029060 | ||||||
| chr9:123029259
|
A | G | 2 | a0001c0001t0039g0171a0001c0001t0069g0210 | 2 | HG00738.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1794+8800A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123029259 | ||||||
| chr9:123029544
|
C | G | 111 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(108): Show | 112 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.1794+9085C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123029544 | ||||||
| chr9:123029725
|
G | C | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1794+9266G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123029725 | ||||||
| chr9:123029872
|
T | C | 1 | a0004c0005t0006g0156 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1794+9413T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123029872 | ||||||
| chr9:123029982
|
C | G | 1 | a0001c0001t0118g0116 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1794+9523C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123029982 | ||||||
| chr9:123029995
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1794+9536G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123029995 | ||||||
| chr9:123030018
|
G | A | 1 | a0001c0001t0095g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1794+9559G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030018 | ||||||
| chr9:123030026
|
G | C | 2 | a0001c0001t0065g0058a0001c0001t0066g0055 | 2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1794+9567G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030026 | ||||||
| chr9:123030125
|
A | G | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794+9666A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030125 | ||||||
| chr9:123030191
|
A | G | 3 | a0001c0001t0006g0145a0001c0001t0006g0152a0001c0002t0126g0048 | 3 | NA18964.hp2 NA19072.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1794+9732A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030191 | ||||||
| chr9:123030216
|
AT | A | 27 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(24): Show | 27 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1794+9759delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123030216 | |||||
| chr9:123030520
|
G | A | 1 | a0001c0001t0073g0222 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1794+10061G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030520 | ||||||
| chr9:123030590
|
A | C | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1794+10131A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030590 | ||||||
| chr9:123030675
|
T | C | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1794+10216T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030675 | ||||||
| chr9:123030784
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1794+10325A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030784 | ||||||
| chr9:123031357
|
G | A | 2 | a0001c0001t0022g0112a0001c0001t0022g0115 | 2 | NA18973.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1794+10898G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123031357 | ||||||
| chr9:123031441
|
G | A | 1 | a0001c0001t0021g0018 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1794+10982G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123031441 | ||||||
| chr9:123031708
|
G | T | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1794+11249G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123031708 | ||||||
| chr9:123031720
|
A | G | 1 | a0001c0001t0030g0166 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1794+11261A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123031720 | ||||||
| chr9:123032069
|
A | G | 4 | a0001c0001t0016g0138a0001c0001t0047g0139a0001c0001t0101g0135others(1): Show | 4 | HG01081.hp1 HG01106.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1794+11610A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123032069 | ||||||
| chr9:123032367
|
A | G | 1 | a0001c0001t0015g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1794+11908A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123032367 | ||||||
| chr9:123032431
|
A | G | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1794+11972A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123032431 | ||||||
| chr9:123032442
|
G | A | 1 | a0001c0001t0020g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1794+11983G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123032442 | ||||||
| chr9:123032475
|
C | T | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1794+12016C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123032475 | ||||||
| chr9:123032882
|
T | C | 1 | a0001c0001t0048g0127 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1794+12423T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123032882 | ||||||
| chr9:123033063
|
T | A | 10 | a0001c0001t0028g0240a0001c0001t0028g0244a0001c0001t0028g0246others(7): Show | 10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1794+12604T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123033063 | ||||||
| chr9:123033138
|
C | G | 1 | a0001c0001t0039g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1794+12679C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123033138 | ||||||
| chr9:123034064
|
C | T | 2 | a0001c0002t0050g0033a0001c0002t0050g0044 | 2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1794+13605C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123034064 | ||||||
| chr9:123034110
|
G | A | 8 | a0001c0001t0008g0059a0001c0001t0008g0069a0001c0001t0008g0070others(5): Show | 9 | HG01099.hp2 HG01496.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1794+13651G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123034110 | ||||||
| chr9:123034267
|
G | A | 1 | a0001c0001t0068g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1794+13808G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123034267 | ||||||
| chr9:123034589
|
A | G | 1 | a0001c0001t0019g0185 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1794+14130A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123034589 | ||||||
| chr9:123034962
|
T | C | 1 | a0001c0001t0120g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1794+14503T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123034962 | ||||||
| chr9:123035005
|
C | T | 1 | a0001c0001t0008g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1794+14546C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123035005 | ||||||
| chr9:123035200
|
T | G | 3 | a0001c0001t0018g0071a0001c0001t0018g0073a0001c0001t0044g0068 | 3 | HG01099.hp2 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1794+14741T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123035200 | ||||||
| chr9:123035214
|
C | T | 1 | a0001c0001t0039g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1794+14755C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123035214 | ||||||
| chr9:123035245
|
G | A | 1 | a0001c0001t0022g0102 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1794+14786G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123035245 | ||||||
| chr9:123035639
|
CGT | C | 4 | a0001c0001t0010g0061a0001c0001t0100g0096a0001c0002t0005g0036others(1): Show | 4 | HG02257.hp2 HG02976.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1794+15223_1794+15 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | |||||
| chr9:123035639
|
CGTGT | C | 5 | a0001c0001t0051g0066a0001c0001t0128g0065a0001c0002t0005g0037others(2): Show | 5 | HG02109.hp2 HG02165.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1794+15221_1794+15 others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | |||||
| chr9:123035639
|
CGTGTGT | C | 28 | a0001c0001t0006g0145a0001c0001t0006g0152a0001c0001t0006g0155others(25): Show | 28 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1794+15219_1794+15 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | |||||
| chr9:123035639
|
CGTGTGTG others(1): Show |
C | 42 | a0001c0001t0001g0229a0001c0001t0006g0146a0001c0001t0006g0149others(39): Show | 43 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1794+15217_1794+15 others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | |||||
| chr9:123035639
|
CGTGTGTG others(3): Show |
C | 91 | a0001c0001t0001g0179a0001c0001t0001g0213a0001c0001t0001g0216others(88): Show | 91 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.1794+15215_1794+15 others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | |||||
| chr9:123035639
|
CGTGTGTG others(5): Show |
C | 44 | a0001c0001t0001g0182a0001c0001t0001g0211a0001c0001t0003g0164others(41): Show | 44 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.1794+15213_1794+15 others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | |||||
| chr9:123035639
|
CGTGTGTG others(7): Show |
C | 28 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0024others(25): Show | 28 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1794+15211_1794+15 others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | |||||
| chr9:123035639
|
CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0003g0159 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1794+15209_1794+15 others(22): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | |||||
| chr9:123035639
|
CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0044g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1794+15207_1794+15 others(24): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | |||||
| chr9:123035802
|
A | G | 1 | a0001c0001t0044g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1794+15343A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123035802 | ||||||
| chr9:123035896
|
G | C | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1794+15437G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123035896 | ||||||
| chr9:123036856
|
G | T | 11 | a0001c0001t0009g0009a0001c0001t0009g0024a0001c0001t0009g0030others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1794+16397G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123036856 | ||||||
| chr9:123037248
|
T | C | 1 | a0001c0001t0088g0130 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1794+16789T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123037248 | ||||||
| chr9:123037588
|
T | C | 7 | a0001c0001t0095g0077a0002c0003t0024g0078a0002c0003t0024g0079others(4): Show | 7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1794+17129T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123037588 | ||||||
| chr9:123037648
|
T | C | 70 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(67): Show | 70 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1794+17189T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123037648 | ||||||
| chr9:123037725
|
T | TTG | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1794+17274_1794+17 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123037725 | |||||
| chr9:123037735
|
A | G | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1794+17276A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123037735 | ||||||
| chr9:123037735
|
A | T | 2 | a0001c0002t0050g0033a0001c0002t0050g0044 | 2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1794+17276A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123037735 | ||||||
| chr9:123037852
|
A | G | 1 | a0001c0001t0045g0107 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1794+17393A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123037852 | ||||||
| chr9:123037866
|
A | G | 2 | a0001c0001t0086g0097a0001c0001t0100g0096 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1794+17407A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123037866 | ||||||
| chr9:123038226
|
A | G | 10 | a0001c0001t0028g0240a0001c0001t0028g0244a0001c0001t0028g0246others(7): Show | 10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1794+17767A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123038226 | ||||||
| chr9:123038440
|
G | A | 1 | a0001c0001t0004g0123 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1794+17981G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123038440 | ||||||
| chr9:123038517
|
C | CT | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1794+18060dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123038517 | |||||
| chr9:123038819
|
G | A | 1 | a0001c0002t0129g0047 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1794+18360G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123038819 | ||||||
| chr9:123039467
|
C | T | 2 | a0001c0001t0071g0114a0001c0001t0094g0113 | 2 | HG02155.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1794+19008C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123039467 | ||||||
| chr9:123039607
|
T | C | 1 | a0001c0001t0038g0157 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1794+19148T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123039607 | ||||||
| chr9:123039886
|
T | A | 1 | a0001c0001t0020g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1794+19427T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123039886 | ||||||
| chr9:123039899
|
TC | T | 27 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(24): Show | 27 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1794+19442delC | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123039899 | |||||
| chr9:123039978
|
T | C | 1 | a0001c0001t0026g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1794+19519T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123039978 | ||||||
| chr9:123040148
|
A | G | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1794+19689A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123040148 | ||||||
| chr9:123040191
|
A | G | 134 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1794+19732A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123040191 | ||||||
| chr9:123040241
|
C | G | 1 | a0001c0001t0137g0198 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1794+19782C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123040241 | ||||||
| chr9:123040351
|
A | G | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1794+19892A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123040351 | ||||||
| chr9:123040391
|
G | A | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1794+19932G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123040391 | ||||||
| chr9:123040553
|
C | G | 1 | a0001c0001t0008g0072 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1794+20094C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123040553 | ||||||
| chr9:123041101
|
G | A | 2 | a0001c0002t0050g0033a0001c0002t0050g0044 | 2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1794+20642G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123041101 | ||||||
| chr9:123041418
|
T | C | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1794+20959T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123041418 | ||||||
| chr9:123041566
|
T | C | 1 | a0001c0001t0070g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1794+21107T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123041566 | ||||||
| chr9:123041787
|
A | G | 2 | a0001c0001t0104g0197a0001c0001t0111g0187 | 2 | NA18939.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1794+21328A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123041787 | ||||||
| chr9:123042068
|
G | A | 1 | a0001c0001t0054g0252 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1794+21609G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123042068 | ||||||
| chr9:123042767
|
A | T | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1794+22308A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123042767 | ||||||
| chr9:123042822
|
A | T | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1794+22363A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123042822 | ||||||
| chr9:123043083
|
T | C | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1795-22265T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043083 | ||||||
| chr9:123043092
|
A | G | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1795-22256A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043092 | ||||||
| chr9:123043304
|
G | A | 10 | a0001c0001t0028g0240a0001c0001t0028g0244a0001c0001t0028g0246others(7): Show | 10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1795-22044G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043304 | ||||||
| chr9:123043384
|
G | A | 1 | a0001c0001t0002g0110 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1795-21964G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043384 | ||||||
| chr9:123043504
|
T | C | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1795-21844T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043504 | ||||||
| chr9:123043634
|
G | C | 63 | a0001c0001t0003g0159a0001c0001t0003g0164a0001c0001t0003g0167others(60): Show | 63 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.1795-21714G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043634 | ||||||
| chr9:123043900
|
C | CT | 24 | a0001c0001t0002g0121a0001c0001t0004g0143a0001c0001t0006g0149others(21): Show | 25 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1795-21430dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123043900 | |||||
| chr9:123043900
|
CT | C | 9 | a0001c0001t0027g0165a0001c0001t0095g0077a0001c0001t0096g0248others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1795-21430delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123043900 | |||||
| chr9:123043986
|
C | T | 1 | a0001c0001t0020g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1795-21362C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043986 | ||||||
| chr9:123043987
|
G | A | 1 | a0001c0001t0006g0155 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1795-21361G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043987 | ||||||
| chr9:123044112
|
C | T | 3 | a0001c0001t0011g0014a0001c0001t0011g0019a0001c0001t0011g0020 | 3 | HG02280.hp1 HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1795-21236C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123044112 | ||||||
| chr9:123044138
|
C | T | 1 | a0001c0001t0045g0064 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1795-21210C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123044138 | ||||||
| chr9:123044461
|
T | G | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1795-20887T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123044461 | ||||||
| chr9:123044497
|
A | G | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1795-20851A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123044497 | ||||||
| chr9:123044626
|
C | CGT | 42 | a0001c0001t0002g0122a0001c0001t0002g0131a0001c0001t0004g0087others(39): Show | 42 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1795-20695_1795-20 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | |||||
| chr9:123044626
|
C | CGTGTGT | 23 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(20): Show | 23 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1795-20699_1795-20 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | |||||
| chr9:123044626
|
C | CGTGTGTG others(1): Show |
3 | a0001c0001t0023g0028a0001c0001t0034g0025a0001c0001t0062g0023 | 3 | HG02723.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1795-20701_1795-20 others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | |||||
| chr9:123044626
|
C | CGTGTGTG others(5): Show |
2 | a0001c0001t0021g0016a0001c0001t0021g0018 | 2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1795-20705_1795-20 others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | |||||
| chr9:123044626
|
CGT | C | 78 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1795-20695_1795-20 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | |||||
| chr9:123044626
|
CGTGT | C | 5 | a0001c0001t0043g0203a0001c0001t0043g0204a0001c0001t0076g0191others(2): Show | 5 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1795-20697_1795-20 others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | |||||
| chr9:123044626
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0002t0049g0049 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1795-20703_1795-20 others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | |||||
| chr9:123044626
|
CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0036g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1795-20711_1795-20 others(24): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | |||||
| chr9:123044741
|
C | T | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1795-20607C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123044741 | ||||||
| chr9:123044743
|
T | C | 1 | a0001c0001t0021g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1795-20605T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123044743 | ||||||
| chr9:123045017
|
C | T | 12 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(9): Show | 13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1795-20331C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045017 | ||||||
| chr9:123045140
|
TTCTG | T | 3 | a0001c0001t0002g0122a0001c0001t0002g0131a0001c0001t0004g0087 | 3 | HG00673.hp2 NA18951.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1795-20204_1795-20 others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123045140 | |||||
| chr9:123045266
|
G | A | 7 | a0001c0001t0095g0077a0002c0003t0024g0078a0002c0003t0024g0079others(4): Show | 7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1795-20082G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045266 | ||||||
| chr9:123045393
|
C | T | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-19955C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045393 | ||||||
| chr9:123045417
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-19931G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045417 | ||||||
| chr9:123045452
|
C | T | 3 | a0001c0001t0014g0224a0001c0001t0014g0232a0001c0001t0027g0223 | 3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1795-19896C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045452 | ||||||
| chr9:123045502
|
G | A | 2 | a0001c0001t0020g0088a0001c0001t0020g0089 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1795-19846G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045502 | ||||||
| chr9:123045608
|
G | A | 1 | a0001c0001t0060g0200 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1795-19740G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045608 | ||||||
| chr9:123045655
|
T | A | 2 | a0001c0001t0086g0097a0001c0001t0100g0096 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1795-19693T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045655 | ||||||
| chr9:123045664
|
A | T | 1 | a0001c0001t0110g0177 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1795-19684A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045664 | ||||||
| chr9:123045889
|
A | G | 120 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(117): Show | 121 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1795-19459A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045889 | ||||||
| chr9:123046197
|
A | G | 2 | a0001c0001t0044g0068a0001c0001t0044g0090 | 2 | HG01884.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1795-19151A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123046197 | ||||||
| chr9:123046221
|
G | T | 1 | a0001c0001t0083g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1795-19127G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123046221 | ||||||
| chr9:123046582
|
C | A | 120 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(117): Show | 121 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1795-18766C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123046582 | ||||||
| chr9:123046617
|
A | G | 1 | a0001c0001t0121g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1795-18731A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123046617 | ||||||
| chr9:123046815
|
T | C | 1 | a0001c0001t0033g0001 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1795-18533T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123046815 | ||||||
| chr9:123046866
|
C | A | 120 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(117): Show | 121 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1795-18482C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123046866 | ||||||
| chr9:123047012
|
A | T | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-18336A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123047012 | ||||||
| chr9:123047919
|
G | GT | 28 | a0001c0001t0001g0211a0001c0001t0001g0229a0001c0001t0012g0217others(25): Show | 28 | HG00558.hp1 HG00597.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1795-17393dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | |||||
| chr9:123047919
|
G | GTT | 13 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0003g0201others(10): Show | 13 | HG00544.hp2 HG00621.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1795-17394_1795-17 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | |||||
| chr9:123047919
|
G | GTTT | 6 | a0001c0001t0003g0164a0001c0001t0013g0195a0001c0001t0015g0196others(3): Show | 6 | HG01175.hp1 HG01981.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.1795-17395_1795-17 others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | |||||
| chr9:123047919
|
G | GTTTTTTT others(10): Show |
1 | a0001c0001t0119g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1795-17409_1795-17 others(23): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | |||||
| chr9:123047919
|
GTTTTTT | G | 17 | a0001c0001t0009g0015a0001c0001t0011g0014a0001c0001t0011g0019others(14): Show | 17 | HG00323.hp2 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1795-17398_1795-17 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | |||||
| chr9:123047919
|
GTTTTTTT | G | 32 | a0001c0001t0009g0009a0001c0001t0009g0017a0001c0001t0009g0024others(29): Show | 32 | HG00280.hp1 HG00639.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1795-17399_1795-17 others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | |||||
| chr9:123047919
|
GTTTTTTT others(1): Show |
G | 5 | a0001c0001t0019g0185a0001c0001t0121g0233a0001c0002t0005g0051others(2): Show | 5 | HG02723.hp2 HG03130.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795-17400_1795-17 others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | |||||
| chr9:123047919
|
GTTTTTTT others(8): Show |
G | 19 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0010g0080others(16): Show | 19 | HG00544.hp1 HG00621.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1795-17407_1795-17 others(21): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | |||||
| chr9:123047919
|
GTTTTTTT others(9): Show |
G | 87 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(84): Show | 88 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1795-17408_1795-17 others(22): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | |||||
| chr9:123047919
|
GTTTTTTT others(10): Show |
G | 12 | a0001c0001t0004g0109a0001c0001t0016g0140a0001c0001t0021g0100others(9): Show | 12 | HG01943.hp1 HG02040.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1795-17409_1795-17 others(23): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | |||||
| chr9:123047919
|
GTTTTTTT others(11): Show |
G | 2 | a0001c0001t0079g0094a0001c0001t0091g0092 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1795-17410_1795-17 others(24): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | |||||
| chr9:123048260
|
C | G | 1 | a0001c0001t0021g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1795-17088C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123048260 | ||||||
| chr9:123048365
|
C | G | 1 | a0001c0001t0136g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1795-16983C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123048365 | ||||||
| chr9:123048564
|
C | A | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-16784C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123048564 | ||||||
| chr9:123048710
|
T | C | 1 | a0001c0001t0017g0251 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1795-16638T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123048710 | ||||||
| chr9:123048843
|
A | G | 107 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(104): Show | 108 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1795-16505A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123048843 | ||||||
| chr9:123048877
|
G | A | 2 | a0001c0001t0007g0106a0001c0001t0031g0154 | 2 | NA18961.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1795-16471G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123048877 | ||||||
| chr9:123049114
|
T | C | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1795-16234T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123049114 | ||||||
| chr9:123049189
|
T | TGTTAAA | 119 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(116): Show | 120 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.1795-16157_1795-16 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123049189 | |||||
| chr9:123049290
|
T | TTTG | 5 | a0001c0001t0011g0014a0001c0001t0011g0019a0001c0001t0011g0020others(2): Show | 5 | HG02280.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1795-16037_1795-16 others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123049290 | |||||
| chr9:123049290
|
T | TTTGTTG | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-16040_1795-16 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123049290 | |||||
| chr9:123049364
|
A | C | 1 | a0001c0001t0037g0022 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1795-15984A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123049364 | ||||||
| chr9:123050182
|
CTG | C | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1795-15161_1795-15 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123050182 | |||||
| chr9:123051049
|
A | G | 1 | a0001c0001t0113g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1795-14299A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051049 | ||||||
| chr9:123051124
|
T | A | 1 | a0002c0003t0072g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1795-14224T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051124 | ||||||
| chr9:123051216
|
G | GTTTTTTT others(9): Show |
1 | a0001c0001t0074g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1795-14099_1795-14 others(22): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTT | G | 5 | a0001c0001t0012g0162a0001c0001t0012g0215a0001c0001t0012g0217others(2): Show | 5 | HG00733.hp2 HG01069.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1795-14085_1795-14 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTT | G | 6 | a0001c0001t0013g0172a0001c0001t0013g0207a0001c0001t0019g0185others(3): Show | 6 | HG00558.hp1 HG01952.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1795-14089_1795-14 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT | G | 23 | a0001c0001t0003g0164a0001c0001t0003g0173a0001c0001t0014g0161others(20): Show | 23 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1795-14090_1795-14 others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(1): Show |
G | 21 | a0001c0001t0003g0167a0001c0001t0003g0176a0001c0001t0013g0192others(18): Show | 21 | HG00673.hp1 HG00738.hp1 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.1795-14091_1795-14 others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(2): Show |
G | 16 | a0001c0001t0003g0159a0001c0001t0003g0201a0001c0001t0009g0024others(13): Show | 16 | HG00280.hp2 HG00544.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1795-14092_1795-14 others(15): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(3): Show |
G | 6 | a0001c0001t0009g0015a0001c0001t0011g0014a0001c0001t0011g0019others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1795-14093_1795-14 others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(4): Show |
G | 13 | a0001c0001t0009g0017a0001c0001t0011g0021a0001c0001t0018g0054others(10): Show | 13 | HG01069.hp2 HG01167.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1795-14094_1795-14 others(17): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(5): Show |
G | 38 | a0001c0001t0002g0121a0001c0001t0004g0087a0001c0001t0006g0145others(35): Show | 38 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.1795-14095_1795-14 others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(6): Show |
G | 72 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(69): Show | 73 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.1795-14096_1795-14 others(19): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(7): Show |
G | 8 | a0001c0001t0001g0182a0001c0001t0010g0060a0002c0003t0024g0078others(5): Show | 8 | HG00544.hp1 HG00738.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1795-14097_1795-14 others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0073g0222 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1795-14100_1795-14 others(23): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(16): Show |
G | 1 | a0001c0001t0135g0205 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1795-14106_1795-14 others(29): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(17): Show |
G | 2 | a0001c0001t0037g0027a0001c0001t0107g0231 | 2 | HG02257.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1795-14107_1795-14 others(30): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(18): Show |
G | 1 | a0001c0001t0097g0227 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1795-14108_1795-14 others(31): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(20): Show |
G | 3 | a0001c0002t0005g0040a0001c0002t0124g0050a0001c0002t0125g0039 | 3 | NA18955.hp1 NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1795-14110_1795-14 others(33): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(21): Show |
G | 19 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(16): Show | 19 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1795-14111_1795-14 others(34): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(23): Show |
G | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-14113_1795-14 others(36): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(27): Show |
G | 2 | a0001c0001t0003g0206a0001c0001t0030g0166 | 2 | HG01934.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1795-14117_1795-14 others(40): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051216
|
GTTTTTTT others(28): Show |
G | 1 | a0001c0001t0015g0220 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1795-14118_1795-14 others(41): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | |||||
| chr9:123051237
|
T | G | 4 | a0001c0001t0020g0089a0001c0001t0037g0022a0001c0001t0038g0255others(1): Show | 4 | HG01167.hp1 HG01243.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1795-14111T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051237 | ||||||
| chr9:123051238
|
T | G | 41 | a0001c0001t0002g0121a0001c0001t0004g0087a0001c0001t0006g0145others(38): Show | 41 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.1795-14110T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051238 | ||||||
| chr9:123051239
|
T | G | 110 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(107): Show | 111 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.1795-14109T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051239 | ||||||
| chr9:123051240
|
T | G | 80 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(77): Show | 81 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1795-14108T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051240 | ||||||
| chr9:123051241
|
T | G | 7 | a0001c0001t0010g0060a0002c0003t0024g0078a0002c0003t0024g0079others(4): Show | 7 | HG00544.hp1 HG00738.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1795-14107T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051241 | ||||||
| chr9:123051297
|
G | C | 1 | a0002c0003t0024g0078 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1795-14051G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051297 | ||||||
| chr9:123051406
|
G | C | 173 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(170): Show | 174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1795-13942G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051406 | ||||||
| chr9:123051409
|
G | C | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795-13939G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051409 | ||||||
| chr9:123051449
|
G | A | 2 | a0001c0001t0003g0167a0001c0001t0003g0173 | 2 | NA19060.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1795-13899G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051449 | ||||||
| chr9:123051548
|
C | T | 1 | a0001c0001t0007g0142 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1795-13800C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051548 | ||||||
| chr9:123051720
|
A | C | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-13628A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051720 | ||||||
| chr9:123051742
|
CTATTT | C | 118 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0003g0159others(115): Show | 118 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.1795-13556_1795-13 others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051742 | |||||
| chr9:123051742
|
CTATTTTA others(3): Show |
C | 112 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(109): Show | 113 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1795-13561_1795-13 others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051742 | |||||
| chr9:123051742
|
CTATTTTA others(8): Show |
C | 1 | a0001c0001t0017g0249 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1795-13566_1795-13 others(21): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051742 | |||||
| chr9:123051742
|
CTATTTTA others(13): Show |
C | 6 | a0001c0001t0028g0244a0001c0001t0038g0157a0001c0001t0089g0243others(3): Show | 6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1795-13571_1795-13 others(26): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051742 | |||||
| chr9:123051779
|
ATTTTATT others(5): Show |
A | 1 | a0001c0001t0018g0071 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1795-13566_1795-13 others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051779 | |||||
| chr9:123051815
|
G | A | 40 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(37): Show | 41 | HG00323.hp1 HG00544.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1795-13533G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051815 | ||||||
| chr9:123051958
|
A | AT | 11 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0012g0162others(8): Show | 11 | HG00597.hp2 HG00621.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1795-13370dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051958 | |||||
| chr9:123051958
|
AT | A | 17 | a0001c0001t0006g0155a0001c0001t0008g0002a0001c0001t0008g0059others(14): Show | 18 | HG00323.hp1 HG00558.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1795-13370delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051958 | |||||
| chr9:123051958
|
ATT | A | 10 | a0001c0001t0021g0100a0001c0001t0029g0082a0001c0001t0029g0099others(7): Show | 10 | HG02145.hp2 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1795-13371_1795-13 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051958 | |||||
| chr9:123051958
|
ATTTTTTT | A | 30 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(27): Show | 30 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1795-13376_1795-13 others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051958 | |||||
| chr9:123051987
|
C | T | 1 | a0001c0001t0021g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1795-13361C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051987 | ||||||
| chr9:123052345
|
A | G | 10 | a0001c0001t0021g0100a0001c0001t0029g0082a0001c0001t0029g0099others(7): Show | 10 | HG02145.hp2 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1795-13003A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123052345 | ||||||
| chr9:123052437
|
C | G | 1 | a0001c0001t0012g0162 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1795-12911C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123052437 | ||||||
| chr9:123052614
|
G | T | 173 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(170): Show | 174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1795-12734G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123052614 | ||||||
| chr9:123052667
|
C | T | 1 | a0001c0001t0008g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1795-12681C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123052667 | ||||||
| chr9:123052727
|
C | T | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-12621C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123052727 | ||||||
| chr9:123053064
|
T | C | 1 | a0001c0001t0066g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1795-12284T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123053064 | ||||||
| chr9:123053156
|
T | G | 5 | a0001c0001t0008g0059a0001c0001t0008g0069a0001c0001t0008g0070others(2): Show | 6 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1795-12192T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123053156 | ||||||
| chr9:123053216
|
A | G | 2 | a0001c0001t0017g0249a0001c0001t0017g0251 | 2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1795-12132A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123053216 | ||||||
| chr9:123053529
|
T | G | 3 | a0001c0001t0025g0153a0001c0001t0040g0151a0004c0005t0006g0156 | 3 | HG00733.hp1 HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1795-11819T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123053529 | ||||||
| chr9:123053539
|
C | G | 10 | a0001c0001t0021g0100a0001c0001t0029g0082a0001c0001t0029g0099others(7): Show | 10 | HG02145.hp2 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1795-11809C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123053539 | ||||||
| chr9:123053756
|
G | A | 256 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(253): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1795-11592G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123053756 | ||||||
| chr9:123054100
|
G | A | 6 | a0002c0003t0024g0078a0002c0003t0024g0079a0002c0003t0072g0062others(3): Show | 6 | HG00544.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1795-11248G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123054100 | ||||||
| chr9:123054181
|
C | T | 1 | a0001c0001t0025g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1795-11167C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123054181 | ||||||
| chr9:123054421
|
C | T | 2 | a0001c0001t0020g0088a0001c0001t0020g0089 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1795-10927C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123054421 | ||||||
| chr9:123054890
|
T | G | 173 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(170): Show | 174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1795-10458T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123054890 | ||||||
| chr9:123054907
|
G | C | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1795-10441G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123054907 | ||||||
| chr9:123055129
|
C | T | 1 | a0001c0001t0110g0177 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1795-10219C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055129 | ||||||
| chr9:123055254
|
C | G | 1 | a0001c0001t0025g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1795-10094C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055254 | ||||||
| chr9:123055364
|
G | A | 10 | a0001c0001t0021g0100a0001c0001t0029g0082a0001c0001t0029g0099others(7): Show | 10 | HG02145.hp2 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1795-9984G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055364 | ||||||
| chr9:123055389
|
G | A | 3 | a0001c0001t0020g0088a0001c0001t0020g0089a0001c0001t0044g0090 | 3 | HG01109.hp2 HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1795-9959G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055389 | ||||||
| chr9:123055432
|
G | A | 1 | a0001c0001t0016g0140 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1795-9916G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055432 | ||||||
| chr9:123055440
|
C | T | 1 | a0001c0001t0015g0225 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1795-9908C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055440 | ||||||
| chr9:123055514
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-9834G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055514 | ||||||
| chr9:123055546
|
C | CT | 15 | a0001c0001t0007g0106a0001c0001t0007g0117a0001c0001t0011g0014others(12): Show | 15 | HG00639.hp1 HG01069.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.1795-9782dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123055546 | |||||
| chr9:123055546
|
CT | C | 17 | a0001c0001t0001g0229a0001c0001t0009g0030a0001c0001t0012g0217others(14): Show | 17 | HG00099.hp1 HG00544.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1795-9782delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123055546 | |||||
| chr9:123055549
|
T | C | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-9799T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055549 | ||||||
| chr9:123055588
|
C | T | 3 | a0001c0001t0034g0056a0001c0001t0065g0058a0001c0001t0066g0055 | 3 | HG01884.hp2 HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1795-9760C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055588 | ||||||
| chr9:123055706
|
C | T | 1 | a0001c0001t0007g0238 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1795-9642C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055706 | ||||||
| chr9:123055769
|
C | T | 120 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(117): Show | 121 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1795-9579C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055769 | ||||||
| chr9:123055905
|
T | G | 1 | a0001c0001t0020g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1795-9443T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055905 | ||||||
| chr9:123056177
|
G | C | 120 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(117): Show | 121 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1795-9171G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056177 | ||||||
| chr9:123056245
|
T | C | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-9103T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056245 | ||||||
| chr9:123056278
|
T | C | 7 | a0001c0001t0095g0077a0002c0003t0024g0078a0002c0003t0024g0079others(4): Show | 7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1795-9070T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056278 | ||||||
| chr9:123056323
|
A | C | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1795-9025A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056323 | ||||||
| chr9:123056481
|
CT | C | 9 | a0001c0001t0001g0211a0001c0001t0016g0140a0001c0001t0030g0169others(6): Show | 9 | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1795-8850delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123056481 | |||||
| chr9:123056484
|
T | C | 1 | a0001c0001t0059g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1795-8864T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056484 | ||||||
| chr9:123056485
|
T | C | 12 | a0001c0002t0005g0032a0001c0002t0005g0052a0001c0002t0049g0046others(9): Show | 12 | HG00323.hp2 HG02132.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.1795-8863T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056485 | ||||||
| chr9:123056486
|
T | C | 1 | a0001c0001t0095g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1795-8862T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056486 | ||||||
| chr9:123056487
|
T | C | 3 | a0001c0001t0003g0173a0001c0001t0043g0203a0001c0001t0043g0204 | 3 | HG00639.hp2 HG00735.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1795-8861T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056487 | ||||||
| chr9:123056523
|
T | C | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1795-8825T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056523 | ||||||
| chr9:123056530
|
T | G | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1795-8818T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056530 | ||||||
| chr9:123056549
|
G | A | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1795-8799G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056549 | ||||||
| chr9:123056638
|
T | C | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1795-8710T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056638 | ||||||
| chr9:123056687
|
C | T | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-8661C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056687 | ||||||
| chr9:123056735
|
G | A | 2 | a0001c0001t0044g0068a0001c0001t0044g0090 | 2 | HG01884.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1795-8613G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056735 | ||||||
| chr9:123056746
|
A | G | 1 | a0001c0001t0060g0200 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1795-8602A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056746 | ||||||
| chr9:123056911
|
A | G | 1 | a0001c0001t0095g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1795-8437A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056911 | ||||||
| chr9:123056937
|
C | G | 4 | a0001c0002t0005g0040a0001c0002t0049g0046a0001c0002t0052g0038others(1): Show | 4 | HG00323.hp2 HG02132.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1795-8411C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056937 | ||||||
| chr9:123057072
|
C | T | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-8276C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057072 | ||||||
| chr9:123057098
|
C | T | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1795-8250C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057098 | ||||||
| chr9:123057110
|
CCCCCCAC others(39): Show |
C | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-8217_1795-817 others(50): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123057110 | |||||
| chr9:123057126
|
C | T | 2 | a0001c0001t0020g0088a0001c0001t0020g0089 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1795-8222C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057126 | ||||||
| chr9:123057127
|
G | A | 1 | a0001c0001t0023g0028 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1795-8221G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057127 | ||||||
| chr9:123057136
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-8212G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057136 | ||||||
| chr9:123057144
|
T | G | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795-8204T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057144 | ||||||
| chr9:123057228
|
C | T | 1 | a0001c0001t0031g0154 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1795-8120C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057228 | ||||||
| chr9:123057458
|
G | A | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1795-7890G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057458 | ||||||
| chr9:123057471
|
T | C | 1 | a0001c0001t0119g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1795-7877T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057471 | ||||||
| chr9:123057473
|
C | T | 4 | a0001c0002t0005g0040a0001c0002t0049g0046a0001c0002t0052g0038others(1): Show | 4 | HG00323.hp2 HG02132.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1795-7875C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057473 | ||||||
| chr9:123057537
|
C | T | 2 | a0001c0001t0028g0240a0001c0001t0028g0246 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1795-7811C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057537 | ||||||
| chr9:123057551
|
C | T | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795-7797C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057551 | ||||||
| chr9:123057618
|
A | T | 3 | a0001c0001t0003g0176a0001c0001t0030g0236a0001c0001t0046g0175 | 3 | HG00544.hp2 HG00673.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1795-7730A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057618 | ||||||
| chr9:123057658
|
G | A | 1 | a0001c0001t0012g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1795-7690G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057658 | ||||||
| chr9:123057710
|
G | T | 1 | a0001c0002t0050g0033 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1795-7638G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057710 | ||||||
| chr9:123057746
|
A | T | 18 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(15): Show | 18 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1795-7602A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057746 | ||||||
| chr9:123057801
|
A | G | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1795-7547A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057801 | ||||||
| chr9:123057808
|
C | T | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-7540C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057808 | ||||||
| chr9:123057827
|
G | A | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1795-7521G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057827 | ||||||
| chr9:123057921
|
C | T | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-7427C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057921 | ||||||
| chr9:123057925
|
C | G | 1 | a0001c0002t0125g0039 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1795-7423C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057925 | ||||||
| chr9:123058050
|
A | AGGGGAGA others(1): Show |
240 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1795-7283_1795-727 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123058050 | |||||
| chr9:123058050
|
A | AGGGGAGA others(9): Show |
1 | a0001c0001t0076g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1795-7291_1795-727 others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123058050 | |||||
| chr9:123058050
|
A | AGGGGAGA others(17): Show |
1 | a0001c0001t0119g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1795-7276_1795-727 others(28): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123058050 | |||||
| chr9:123058313
|
A | G | 1 | a0001c0001t0008g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1795-7035A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123058313 | ||||||
| chr9:123058394
|
G | T | 1 | a0001c0001t0110g0177 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1795-6954G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123058394 | ||||||
| chr9:123058545
|
A | AT | 26 | a0001c0001t0002g0110a0001c0001t0017g0249a0001c0001t0017g0251others(23): Show | 26 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1795-6791dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123058545 | |||||
| chr9:123058545
|
AT | A | 115 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1795-6791delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123058545 | |||||
| chr9:123058552
|
T | G | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1795-6796T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123058552 | ||||||
| chr9:123058702
|
T | C | 1 | a0001c0001t0099g0003 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1795-6646T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123058702 | ||||||
| chr9:123059336
|
C | T | 1 | a0001c0002t0049g0046 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1795-6012C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123059336 | ||||||
| chr9:123059337
|
G | A | 1 | a0001c0001t0132g0174 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1795-6011G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123059337 | ||||||
| chr9:123059423
|
C | G | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-5925C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123059423 | ||||||
| chr9:123059480
|
G | C | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-5868G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123059480 | ||||||
| chr9:123059795
|
T | C | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1795-5553T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123059795 | ||||||
| chr9:123059796
|
T | A | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1795-5552T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123059796 | ||||||
| chr9:123060033
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-5315G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123060033 | ||||||
| chr9:123060044
|
C | T | 1 | a0001c0001t0002g0083 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1795-5304C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123060044 | ||||||
| chr9:123060176
|
C | G | 1 | a0001c0001t0007g0106 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1795-5172C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123060176 | ||||||
| chr9:123060258
|
T | C | 110 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(107): Show | 111 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1795-5090T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123060258 | ||||||
| chr9:123060628
|
A | T | 1 | a0001c0001t0058g0180 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1795-4720A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123060628 | ||||||
| chr9:123060852
|
T | G | 1 | a0001c0001t0104g0197 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1795-4496T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123060852 | ||||||
| chr9:123061017
|
C | A | 1 | a0001c0001t0002g0083 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1795-4331C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061017 | ||||||
| chr9:123061018
|
A | C | 1 | a0001c0001t0002g0083 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1795-4330A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061018 | ||||||
| chr9:123061108
|
A | G | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-4240A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061108 | ||||||
| chr9:123061372
|
C | T | 1 | a0001c0001t0004g0125 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1795-3976C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061372 | ||||||
| chr9:123061416
|
G | A | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-3932G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061416 | ||||||
| chr9:123061417
|
C | T | 2 | a0001c0002t0005g0036a0001c0002t0005g0037 | 2 | NA18952.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1795-3931C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061417 | ||||||
| chr9:123061421
|
T | A | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-3927T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061421 | ||||||
| chr9:123061677
|
T | A | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-3671T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061677 | ||||||
| chr9:123061776
|
G | A | 114 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1795-3572G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061776 | ||||||
| chr9:123061849
|
A | T | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1795-3499A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061849 | ||||||
| chr9:123061892
|
G | C | 3 | a0001c0002t0005g0040a0001c0002t0049g0046a0001c0002t0052g0038 | 3 | HG00323.hp2 NA19067.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1795-3456G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061892 | ||||||
| chr9:123062097
|
G | A | 1 | a0001c0002t0129g0047 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1795-3251G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062097 | ||||||
| chr9:123062132
|
G | A | 1 | a0001c0001t0132g0174 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1795-3216G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062132 | ||||||
| chr9:123062154
|
G | A | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-3194G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062154 | ||||||
| chr9:123062194
|
G | A | 1 | a0001c0001t0059g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1795-3154G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062194 | ||||||
| chr9:123062199
|
C | T | 114 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1795-3149C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062199 | ||||||
| chr9:123062203
|
G | T | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-3145G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062203 | ||||||
| chr9:123062294
|
G | C | 1 | a0001c0001t0007g0117 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1795-3054G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062294 | ||||||
| chr9:123062845
|
G | T | 3 | a0001c0001t0014g0224a0001c0001t0014g0232a0001c0001t0027g0223 | 3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1795-2503G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062845 | ||||||
| chr9:123063897
|
C | T | 1 | a0001c0001t0066g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1795-1451C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123063897 | ||||||
| chr9:123063957
|
A | G | 2 | a0001c0001t0015g0225a0001c0001t0046g0168 | 2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1795-1391A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123063957 | ||||||
| chr9:123064095
|
G | C | 1 | a0001c0001t0015g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1795-1253G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123064095 | ||||||
| chr9:123064627
|
T | C | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-721T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123064627 | ||||||
| chr9:123064723
|
T | C | 2 | a0001c0002t0005g0040a0001c0002t0052g0038 | 2 | HG00323.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1795-625T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123064723 | ||||||
| chr9:123064996
|
C | T | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-352C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123064996 | ||||||
| chr9:123064999
|
C | A | 3 | a0001c0001t0025g0153a0001c0001t0040g0151a0004c0005t0006g0156 | 3 | HG00733.hp1 HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1795-349C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123064999 | ||||||
| chr9:123065069
|
A | G | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-279A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123065069 | ||||||
| chr9:123065227
|
A | C | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-121A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123065227 | ||||||
| chr9:123065657
|
G | A | 1 | a0001c0001t0012g0221 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1908+196G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123065657 | ||||||
| chr9:123065800
|
G | C | 6 | a0002c0003t0024g0078a0002c0003t0024g0079a0002c0003t0072g0062others(3): Show | 6 | HG00544.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1908+339G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123065800 | ||||||
| chr9:123066148
|
G | A | 1 | a0001c0001t0076g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1908+687G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123066148 | ||||||
| chr9:123066165
|
A | G | 1 | a0001c0006t0032g0008 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1908+704A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123066165 | ||||||
| chr9:123066313
|
T | C | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1908+852T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123066313 | ||||||
| chr9:123066635
|
G | A | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1908+1174G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123066635 | ||||||
| chr9:123066723
|
T | C | 6 | a0002c0003t0024g0078a0002c0003t0024g0079a0002c0003t0072g0062others(3): Show | 6 | HG00544.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1908+1262T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123066723 | ||||||
| chr9:123066912
|
C | T | 1 | a0001c0001t0004g0087 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1908+1451C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123066912 | ||||||
| chr9:123067209
|
G | A | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1908+1748G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123067209 | ||||||
| chr9:123067476
|
C | T | 1 | a0001c0001t0037g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1908+2015C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123067476 | ||||||
| chr9:123067637
|
C | T | 1 | a0001c0001t0004g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1908+2176C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123067637 | ||||||
| chr9:123067820
|
A | T | 1 | a0003c0004t0024g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1908+2359A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123067820 | ||||||
| chr9:123067821
|
T | C | 1 | a0003c0004t0024g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1908+2360T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123067821 | ||||||
| chr9:123068171
|
G | A | 3 | a0001c0001t0008g0069a0001c0001t0008g0070a0001c0001t0033g0001 | 4 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909-2179G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123068171 | ||||||
| chr9:123068348
|
C | CA | 7 | a0001c0001t0003g0176a0001c0001t0020g0088a0001c0001t0020g0089others(4): Show | 7 | HG00558.hp2 HG01109.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1909-1984dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr9 | 123068348 | |||||
| chr9:123068348
|
CA | C | 27 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(24): Show | 27 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1909-1984delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr9 | 123068348 | |||||
| chr9:123068656
|
A | G | 2 | a0001c0001t0020g0088a0001c0001t0020g0089 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1909-1694A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123068656 | ||||||
| chr9:123068679
|
C | T | 1 | a0001c0001t0090g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1909-1671C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123068679 | ||||||
| chr9:123068695
|
C | CTG | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1909-1654_1909-165 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr9 | 123068695 | |||||
| chr9:123068738
|
C | T | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1909-1612C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123068738 | ||||||
| chr9:123068814
|
T | A | 23 | a0001c0001t0073g0222a0001c0002t0005g0032a0001c0002t0005g0034others(20): Show | 23 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1909-1536T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123068814 | ||||||
| chr9:123069575
|
TA | T | 114 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1909-761delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr9 | 123069575 | |||||
| chr9:123069589
|
A | G | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1909-761A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123069589 | ||||||
| chr9:123069714
|
T | G | 27 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(24): Show | 27 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1909-636T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123069714 | ||||||
| chr9:123069729
|
T | A | 1 | a0001c0001t0002g0121 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1909-621T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123069729 | ||||||
| chr9:123070247
|
G | A | 1 | a0001c0001t0078g0253 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1909-103G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123070247 | ||||||
| chr9:123070600
|
T | C | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1983+176T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123070600 | ||||||
| chr9:123071220
|
T | C | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1983+796T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071220 | ||||||
| chr9:123071296
|
A | T | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1983+872A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071296 | ||||||
| chr9:123071345
|
A | G | 27 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(24): Show | 27 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1983+921A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071345 | ||||||
| chr9:123071390
|
G | T | 81 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1983+966G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071390 | ||||||
| chr9:123071468
|
C | T | 1 | a0001c0002t0005g0036 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1983+1044C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071468 | ||||||
| chr9:123071475
|
T | A | 1 | a0001c0001t0021g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1983+1051T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071475 | ||||||
| chr9:123071583
|
A | G | 2 | a0001c0001t0017g0249a0001c0001t0017g0251 | 2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1983+1159A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071583 | ||||||
| chr9:123071975
|
C | G | 1 | a0001c0001t0120g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1983+1551C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071975 | ||||||
| chr9:123072056
|
C | G | 1 | a0001c0001t0040g0104 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1984-1496C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123072056 | ||||||
| chr9:123072606
|
C | T | 1 | a0001c0001t0015g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1984-946C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123072606 | ||||||
| chr9:123072874
|
A | G | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1984-678A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123072874 | ||||||
| chr9:123072963
|
T | G | 15 | a0001c0001t0006g0145a0001c0001t0006g0146a0001c0001t0006g0149others(12): Show | 15 | HG00733.hp1 HG01993.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.1984-589T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123072963 | ||||||
| chr9:123072984
|
G | A | 1 | a0001c0001t0046g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1984-568G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123072984 | ||||||
| chr9:123073788
|
T | A | 2 | a0001c0001t0017g0249a0001c0001t0017g0251 | 2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2109+111T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 16/25 | chr9 | 123073788 | ||||||
| chr9:123073797
|
G | A | 2 | a0001c0002t0050g0033a0001c0002t0050g0044 | 2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2109+120G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 16/25 | chr9 | 123073797 | ||||||
| chr9:123073799
|
T | A | 7 | a0001c0001t0095g0077a0002c0003t0024g0078a0002c0003t0024g0079others(4): Show | 7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2109+122T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 16/25 | chr9 | 123073799 | ||||||
| chr9:123074661
|
T | C | 1 | a0001c0001t0113g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2253+233T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 17/25 | chr9 | 123074661 | ||||||
| chr9:123074909
|
A | C | 1 | a0001c0001t0009g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2253+481A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 17/25 | chr9 | 123074909 | ||||||
| chr9:123075058
|
C | T | 4 | a0001c0001t0010g0060a0001c0001t0010g0061a0001c0001t0010g0080others(1): Show | 4 | HG00323.hp1 HG00738.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2253+630C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 17/25 | chr9 | 123075058 | ||||||
| chr9:123075630
|
C | A | 1 | a0001c0001t0017g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2254-615C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 17/25 | chr9 | 123075630 | ||||||
| chr9:123075680
|
A | G | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2254-565A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 17/25 | chr9 | 123075680 | ||||||
| chr9:123075686
|
T | G | 1 | a0001c0001t0012g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2254-559T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 17/25 | chr9 | 123075686 | ||||||
| chr9:123075824
|
T | G | 1 | a0001c0001t0059g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2254-421T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 17/25 | chr9 | 123075824 | ||||||
| chr9:123076430
|
GAAGAAAT others(81): Show |
G | 1 | a0001c0001t0014g0235 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2295+150_2296-111d others(90): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr9 | 123076430 | |||||
| chr9:123076595
|
C | G | 1 | a0001c0001t0076g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2296-39C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 18/25 | chr9 | 123076595 | ||||||
| chr9:123076960
|
A | C | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2424+198A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123076960 | ||||||
| chr9:123077026
|
A | AG | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.2424+265dupG | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077026 | |||||
| chr9:123077051
|
G | GA | 137 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.2424+290dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077051 | |||||
| chr9:123077163
|
TG | T | 27 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(24): Show | 27 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.2424+402delG | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077163 | ||||||
| chr9:123077164
|
G | T | 2 | a0001c0001t0023g0028a0001c0001t0037g0027 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2424+402G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077164 | ||||||
| chr9:123077164
|
GT | G | 87 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.2424+415delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077164 | |||||
| chr9:123077166
|
T | C | 2 | a0001c0002t0124g0050a0001c0002t0125g0039 | 2 | NA18955.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2424+404T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077166 | ||||||
| chr9:123077170
|
T | G | 66 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(63): Show | 66 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.2424+408T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077170 | ||||||
| chr9:123077462
|
A | G | 2 | a0001c0001t0015g0220a0001c0001t0030g0166 | 2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.2424+700A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077462 | ||||||
| chr9:123077508
|
T | C | 2 | a0001c0001t0020g0088a0001c0001t0020g0089 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2424+746T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077508 | ||||||
| chr9:123077610
|
C | CATTGT | 9 | a0001c0001t0003g0167a0001c0001t0006g0152a0001c0001t0010g0080others(6): Show | 9 | HG01070.hp2 HG01175.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.2424+927_2424+931d others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | |||||
| chr9:123077610
|
C | CATTGTAT others(3): Show |
6 | a0001c0001t0002g0122a0001c0001t0013g0207a0001c0001t0051g0066others(3): Show | 6 | HG00280.hp2 HG00642.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2424+922_2424+931d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | |||||
| chr9:123077610
|
C | CATTGTAT others(8): Show |
5 | a0001c0001t0010g0060a0001c0001t0010g0061a0001c0001t0010g0081others(2): Show | 5 | HG00323.hp1 HG00738.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2424+917_2424+931d others(17): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | |||||
| chr9:123077610
|
C | CATTGTAT others(13): Show |
2 | a0001c0001t0030g0169a0001c0001t0099g0003 | 2 | HG00558.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2424+912_2424+931d others(22): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | |||||
| chr9:123077610
|
C | CATTGTAT others(18): Show |
1 | a0001c0001t0039g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2424+907_2424+931d others(27): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | |||||
| chr9:123077610
|
C | CATTGTAT others(228): Show |
1 | a0001c0001t0090g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2424+931_2424+932i others(237): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | |||||
| chr9:123077610
|
CATTGT | C | 54 | a0001c0001t0001g0213a0001c0001t0002g0121a0001c0001t0002g0131others(51): Show | 54 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.2424+927_2424+931d others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | |||||
| chr9:123077610
|
CATTGTAT others(3): Show |
C | 75 | a0001c0001t0001g0182a0001c0001t0001g0211a0001c0001t0001g0216others(72): Show | 76 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.2424+922_2424+931d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | |||||
| chr9:123077610
|
CATTGTAT others(8): Show |
C | 34 | a0001c0001t0001g0179a0001c0001t0001g0218a0001c0001t0001g0229others(31): Show | 34 | HG00558.hp2 HG00639.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2424+917_2424+931d others(17): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | |||||
| chr9:123077610
|
CATTGTAT others(13): Show |
C | 13 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144others(10): Show | 13 | HG01934.hp2 HG02258.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2424+912_2424+931d others(22): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | |||||
| chr9:123077610
|
CATTGTAT others(18): Show |
C | 17 | a0001c0001t0009g0015a0001c0001t0086g0097a0001c0001t0100g0096others(14): Show | 17 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.2424+907_2424+931d others(27): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | |||||
| chr9:123077640
|
T | C | 1 | a0004c0005t0006g0156 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2424+878T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077640 | ||||||
| chr9:123077691
|
A | G | 1 | a0001c0001t0002g0121 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2424+929A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077691 | ||||||
| chr9:123077809
|
G | A | 1 | a0001c0001t0051g0066 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2424+1047G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077809 | ||||||
| chr9:123077835
|
A | T | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2424+1073A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077835 | ||||||
| chr9:123077874
|
T | C | 1 | a0001c0001t0090g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2424+1112T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077874 | ||||||
| chr9:123077875
|
A | T | 1 | a0001c0001t0090g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2424+1113A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077875 | ||||||
| chr9:123077898
|
C | T | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2424+1136C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077898 | ||||||
| chr9:123077933
|
A | G | 14 | a0001c0001t0003g0201a0001c0001t0013g0172a0001c0001t0013g0207others(11): Show | 14 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.2424+1171A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077933 | ||||||
| chr9:123078159
|
T | C | 1 | a0001c0001t0068g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2424+1397T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123078159 | ||||||
| chr9:123078439
|
T | C | 67 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.2424+1677T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123078439 | ||||||
| chr9:123078483
|
T | G | 1 | a0001c0001t0004g0087 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2424+1721T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123078483 | ||||||
| chr9:123078684
|
C | A | 1 | a0001c0001t0041g0254 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2424+1922C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123078684 | ||||||
| chr9:123078706
|
A | G | 1 | a0001c0001t0051g0067 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2424+1944A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123078706 | ||||||
| chr9:123078759
|
C | A | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2424+1997C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123078759 | ||||||
| chr9:123078902
|
C | T | 1 | a0001c0001t0056g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2424+2140C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123078902 | ||||||
| chr9:123079055
|
T | C | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2424+2293T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079055 | ||||||
| chr9:123079221
|
GTTT | G | 83 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2424+2464_2424+246 others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123079221 | |||||
| chr9:123079239
|
G | T | 2 | a0001c0001t0020g0088a0001c0001t0020g0089 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2424+2477G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079239 | ||||||
| chr9:123079239
|
GT | G | 9 | a0001c0001t0028g0240a0001c0001t0028g0244a0001c0001t0028g0246others(6): Show | 9 | HG01109.hp1 HG02818.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2424+2495delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123079239 | |||||
| chr9:123079239
|
GTTT | G | 82 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.2424+2493_2424+249 others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123079239 | |||||
| chr9:123079242
|
T | TTG | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2424+2481_2424+248 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123079242 | |||||
| chr9:123079244
|
T | G | 81 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(78): Show | 81 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.2424+2482T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079244 | ||||||
| chr9:123079247
|
T | G | 4 | a0001c0001t0001g0211a0001c0001t0097g0227a0001c0001t0107g0231others(1): Show | 4 | HG01070.hp1 NA18956.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.2424+2485T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079247 | ||||||
| chr9:123079248
|
T | G | 1 | a0001c0001t0036g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2424+2486T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079248 | ||||||
| chr9:123079249
|
T | G | 2 | a0001c0001t0007g0124a0001c0001t0094g0113 | 2 | HG02165.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2424+2487T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079249 | ||||||
| chr9:123079252
|
T | G | 1 | a0001c0001t0001g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2424+2490T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079252 | ||||||
| chr9:123079263
|
A | C | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2424+2501A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079263 | ||||||
| chr9:123079534
|
C | G | 1 | a0001c0001t0095g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2424+2772C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079534 | ||||||
| chr9:123079859
|
C | T | 1 | a0001c0001t0119g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2424+3097C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079859 | ||||||
| chr9:123079968
|
C | T | 1 | a0001c0001t0008g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2424+3206C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079968 | ||||||
| chr9:123080177
|
A | G | 134 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2424+3415A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123080177 | ||||||
| chr9:123080198
|
T | C | 29 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(26): Show | 29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.2424+3436T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123080198 | ||||||
| chr9:123080495
|
G | T | 1 | a0001c0001t0010g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2424+3733G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123080495 | ||||||
| chr9:123080761
|
A | G | 135 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.2424+3999A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123080761 | ||||||
| chr9:123080795
|
A | G | 3 | a0001c0001t0039g0171a0001c0001t0075g0208a0001c0001t0085g0189 | 3 | HG00280.hp2 HG00642.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.2424+4033A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123080795 | ||||||
| chr9:123080890
|
A | G | 3 | a0001c0001t0001g0211a0001c0001t0026g0181a0001c0001t0069g0210 | 3 | HG01070.hp1 HG01993.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2424+4128A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123080890 | ||||||
| chr9:123081515
|
C | G | 4 | a0001c0001t0028g0240a0001c0001t0028g0246a0001c0001t0084g0245others(1): Show | 4 | HG02055.hp2 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2424+4753C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081515 | ||||||
| chr9:123081533
|
C | T | 2 | a0001c0001t0031g0237a0001c0001t0078g0253 | 2 | HG02056.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.2424+4771C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081533 | ||||||
| chr9:123081565
|
T | G | 1 | a0001c0001t0025g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2424+4803T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081565 | ||||||
| chr9:123081614
|
T | C | 1 | a0001c0001t0004g0123 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2424+4852T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081614 | ||||||
| chr9:123081817
|
C | T | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2424+5055C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081817 | ||||||
| chr9:123081841
|
A | G | 1 | a0001c0001t0128g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2424+5079A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081841 | ||||||
| chr9:123081874
|
C | T | 3 | a0001c0001t0087g0084a0001c0001t0116g0120a0001c0001t0118g0116 | 3 | HG00558.hp2 HG02027.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.2424+5112C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081874 | ||||||
| chr9:123081946
|
G | A | 7 | a0001c0001t0028g0244a0001c0001t0059g0256a0001c0001t0061g0241others(4): Show | 7 | HG01109.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2424+5184G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081946 | ||||||
| chr9:123082247
|
A | T | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.2424+5485A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082247 | ||||||
| chr9:123082282
|
G | A | 1 | a0001c0001t0006g0149 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2424+5520G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082282 | ||||||
| chr9:123082303
|
G | A | 11 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0213others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2424+5541G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082303 | ||||||
| chr9:123082701
|
A | T | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.2424+5939A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082701 | ||||||
| chr9:123082706
|
G | T | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2424+5944G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082706 | ||||||
| chr9:123082727
|
G | GA | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.2424+5966dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123082727 | |||||
| chr9:123082750
|
T | A | 1 | a0001c0001t0061g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2424+5988T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082750 | ||||||
| chr9:123082913
|
C | T | 1 | a0001c0001t0008g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2424+6151C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082913 | ||||||
| chr9:123082930
|
G | A | 105 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2424+6168G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082930 | ||||||
| chr9:123082969
|
C | T | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2424+6207C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082969 | ||||||
| chr9:123083028
|
A | G | 105 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2424+6266A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123083028 | ||||||
| chr9:123083505
|
T | A | 1 | a0001c0001t0015g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2425-6253T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123083505 | ||||||
| chr9:123083842
|
C | T | 2 | a0001c0001t0015g0220a0001c0001t0030g0166 | 2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.2425-5916C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123083842 | ||||||
| chr9:123084117
|
T | C | 2 | a0001c0002t0050g0033a0001c0002t0050g0044 | 2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2425-5641T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123084117 | ||||||
| chr9:123084409
|
C | T | 1 | a0002c0003t0024g0079 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2425-5349C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123084409 | ||||||
| chr9:123084452
|
G | A | 1 | a0001c0001t0088g0130 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2425-5306G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123084452 | ||||||
| chr9:123084683
|
G | A | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2425-5075G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123084683 | ||||||
| chr9:123084817
|
T | C | 3 | a0001c0001t0014g0224a0001c0001t0014g0232a0001c0001t0027g0223 | 3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2425-4941T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123084817 | ||||||
| chr9:123084991
|
A | G | 2 | a0001c0001t0051g0067a0001c0001t0128g0065 | 2 | HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2425-4767A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123084991 | ||||||
| chr9:123085102
|
A | T | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2425-4656A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085102 | ||||||
| chr9:123085170
|
G | A | 1 | a0001c0007t0052g0035 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2425-4588G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085170 | ||||||
| chr9:123085181
|
A | G | 7 | a0001c0001t0095g0077a0002c0003t0024g0078a0002c0003t0024g0079others(4): Show | 7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2425-4577A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085181 | ||||||
| chr9:123085409
|
C | T | 6 | a0001c0001t0032g0006a0001c0001t0032g0007a0001c0001t0099g0003others(3): Show | 6 | HG02129.hp1 NA18970.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.2425-4349C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085409 | ||||||
| chr9:123085488
|
T | C | 3 | a0001c0001t0014g0224a0001c0001t0014g0232a0001c0001t0027g0223 | 3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2425-4270T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085488 | ||||||
| chr9:123085612
|
G | T | 1 | a0001c0001t0056g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2425-4146G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085612 | ||||||
| chr9:123085613
|
C | T | 8 | a0001c0001t0030g0169a0001c0001t0055g0188a0001c0001t0056g0086others(5): Show | 8 | HG00558.hp1 HG02040.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2425-4145C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085613 | ||||||
| chr9:123085615
|
G | A | 2 | a0001c0001t0013g0172a0001c0001t0013g0207 | 2 | HG01952.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2425-4143G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085615 | ||||||
| chr9:123085664
|
G | A | 1 | a0001c0001t0137g0198 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2425-4094G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085664 | ||||||
| chr9:123085710
|
C | A | 2 | a0001c0002t0050g0033a0001c0002t0050g0044 | 2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2425-4048C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085710 | ||||||
| chr9:123085742
|
T | G | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.2425-4016T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085742 | ||||||
| chr9:123085760
|
G | A | 246 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.2425-3998G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085760 | ||||||
| chr9:123085869
|
A | G | 2 | a0001c0001t0019g0185a0001c0001t0019g0186 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2425-3889A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085869 | ||||||
| chr9:123085931
|
ATTTG | A | 4 | a0001c0001t0045g0064a0001c0001t0051g0066a0001c0001t0051g0067others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2425-3823_2425-382 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123085931 | |||||
| chr9:123086203
|
G | A | 136 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.2425-3555G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123086203 | ||||||
| chr9:123086429
|
C | T | 1 | a0001c0001t0018g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2425-3329C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123086429 | ||||||
| chr9:123086621
|
C | A | 218 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.2425-3137C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123086621 | ||||||
| chr9:123086631
|
C | G | 1 | a0001c0001t0004g0119 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2425-3127C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123086631 | ||||||
| chr9:123086906
|
C | G | 1 | a0001c0001t0087g0084 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2425-2852C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123086906 | ||||||
| chr9:123087231
|
A | G | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2425-2527A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123087231 | ||||||
| chr9:123087413
|
A | G | 13 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(10): Show | 14 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2425-2345A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123087413 | ||||||
| chr9:123087430
|
G | C | 1 | a0001c0001t0045g0064 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2425-2328G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123087430 | ||||||
| chr9:123087523
|
C | G | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2425-2235C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123087523 | ||||||
| chr9:123087617
|
C | T | 110 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(107): Show | 111 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.2425-2141C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123087617 | ||||||
| chr9:123087638
|
C | A | 1 | a0001c0001t0007g0137 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2425-2120C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123087638 | ||||||
| chr9:123087992
|
T | C | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2425-1766T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123087992 | ||||||
| chr9:123088042
|
C | CT | 31 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(28): Show | 31 | HG00639.hp1 HG01069.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.2425-1703dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123088042 | |||||
| chr9:123088302
|
G | A | 26 | a0001c0001t0013g0192a0001c0001t0015g0225a0001c0001t0027g0194others(23): Show | 26 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.2425-1456G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123088302 | ||||||
| chr9:123088594
|
G | A | 2 | a0001c0001t0002g0110a0001c0001t0004g0123 | 2 | NA18970.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2425-1164G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123088594 | ||||||
| chr9:123088804
|
G | T | 12 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(9): Show | 13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.2425-954G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123088804 | ||||||
| chr9:123088924
|
A | G | 4 | a0002c0003t0024g0078a0002c0003t0024g0079a0002c0003t0072g0062others(1): Show | 4 | HG00544.hp1 HG02155.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.2425-834A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123088924 | ||||||
| chr9:123088935
|
A | C | 2 | a0001c0001t0022g0112a0001c0001t0022g0115 | 2 | NA18973.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2425-823A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123088935 | ||||||
| chr9:123089034
|
A | T | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2425-724A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123089034 | ||||||
| chr9:123089081
|
AAG | A | 81 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.2425-673_2425-672d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123089081 | |||||
| chr9:123089157
|
A | T | 27 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(24): Show | 27 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.2425-601A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123089157 | ||||||
| chr9:123089232
|
G | T | 2 | a0001c0001t0018g0071a0001c0001t0042g0098 | 2 | HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2425-526G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123089232 | ||||||
| chr9:123089909
|
C | T | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2517+59C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 20/25 | chr9 | 123089909 | ||||||
| chr9:123090574
|
C | G | 3 | a0001c0001t0007g0238a0001c0001t0031g0237a0001c0001t0078g0253 | 3 | HG02056.hp2 HG02132.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2628+189C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123090574 | ||||||
| chr9:123090589
|
T | G | 3 | a0001c0001t0017g0026a0001c0001t0017g0249a0001c0001t0017g0251 | 3 | HG01243.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2628+204T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123090589 | ||||||
| chr9:123090924
|
C | T | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2628+539C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123090924 | ||||||
| chr9:123090925
|
T | G | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2628+540T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123090925 | ||||||
| chr9:123091047
|
A | G | 1 | a0001c0001t0076g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2628+662A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123091047 | ||||||
| chr9:123091259
|
GT | G | 32 | a0001c0001t0028g0240a0001c0001t0028g0244a0001c0001t0028g0246others(29): Show | 32 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.2628+876delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123091259 | |||||
| chr9:123091414
|
A | G | 1 | a0001c0001t0020g0088 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2628+1029A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123091414 | ||||||
| chr9:123091578
|
C | G | 1 | a0001c0002t0129g0047 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2628+1193C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123091578 | ||||||
| chr9:123091637
|
A | C | 1 | a0001c0001t0025g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2628+1252A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123091637 | ||||||
| chr9:123092036
|
G | A | 84 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.2628+1651G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123092036 | ||||||
| chr9:123092038
|
A | G | 10 | a0001c0001t0008g0002a0001c0001t0008g0059a0001c0001t0008g0069others(7): Show | 11 | HG00323.hp1 HG00738.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2628+1653A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123092038 | ||||||
| chr9:123092079
|
C | G | 1 | a0001c0001t0026g0214 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2628+1694C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123092079 | ||||||
| chr9:123092086
|
G | A | 1 | a0001c0001t0038g0157 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2628+1701G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123092086 | ||||||
| chr9:123092204
|
C | T | 1 | a0001c0001t0007g0137 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2628+1819C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123092204 | ||||||
| chr9:123092560
|
C | CT | 40 | a0001c0001t0003g0159a0001c0001t0009g0009a0001c0001t0009g0015others(37): Show | 40 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.2628+2184dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123092560 | |||||
| chr9:123092586
|
T | A | 1 | a0001c0001t0108g0163 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2628+2201T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123092586 | ||||||
| chr9:123092592
|
G | A | 32 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(29): Show | 32 | HG01069.hp2 HG01099.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.2628+2207G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123092592 | ||||||
| chr9:123092643
|
A | ATG | 82 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.2628+2259_2628+226 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123092643 | |||||
| chr9:123093002
|
T | G | 1 | a0001c0001t0019g0111 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2628+2617T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123093002 | ||||||
| chr9:123093236
|
T | G | 1 | a0001c0001t0120g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2628+2851T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123093236 | ||||||
| chr9:123093410
|
C | G | 3 | a0001c0001t0018g0071a0001c0001t0018g0073a0001c0001t0044g0068 | 3 | HG01099.hp2 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2628+3025C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123093410 | ||||||
| chr9:123093432
|
C | T | 94 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(91): Show | 95 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.2628+3047C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123093432 | ||||||
| chr9:123093501
|
A | C | 249 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(246): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.2628+3116A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123093501 | ||||||
| chr9:123093546
|
T | G | 3 | a0001c0001t0015g0220a0001c0001t0030g0166a0001c0001t0108g0163 | 3 | HG00099.hp2 HG01934.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2628+3161T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123093546 | ||||||
| chr9:123093961
|
A | G | 84 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.2628+3576A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123093961 | ||||||
| chr9:123094180
|
C | G | 1 | a0001c0001t0074g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2629-3561C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094180 | ||||||
| chr9:123094255
|
T | C | 1 | a0001c0001t0068g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2629-3486T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094255 | ||||||
| chr9:123094451
|
T | C | 152 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.2629-3290T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094451 | ||||||
| chr9:123094456
|
C | T | 1 | a0001c0001t0027g0165 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2629-3285C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094456 | ||||||
| chr9:123094549
|
T | G | 3 | a0001c0001t0051g0066a0001c0001t0051g0067a0001c0001t0128g0065 | 3 | HG02109.hp2 HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2629-3192T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094549 | ||||||
| chr9:123094586
|
T | C | 3 | a0001c0001t0020g0088a0001c0001t0020g0089a0001c0001t0044g0090 | 3 | HG01109.hp2 HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2629-3155T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094586 | ||||||
| chr9:123094659
|
G | A | 247 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.2629-3082G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094659 | ||||||
| chr9:123094753
|
G | A | 86 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.2629-2988G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094753 | ||||||
| chr9:123094819
|
A | G | 2 | a0001c0001t0035g0129a0001c0001t0035g0134 | 2 | NA20300.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2629-2922A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094819 | ||||||
| chr9:123095226
|
C | CA | 11 | a0001c0001t0009g0015a0001c0001t0011g0014a0001c0001t0011g0020others(8): Show | 11 | HG00639.hp1 HG01069.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2629-2490dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123095226 | |||||
| chr9:123095226
|
CA | C | 84 | a0001c0001t0001g0179a0001c0001t0001g0211a0001c0001t0001g0213others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.2629-2490delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123095226 | |||||
| chr9:123095226
|
CAA | C | 85 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(82): Show | 85 | HG00544.hp1 HG00673.hp2 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.2629-2491_2629-249 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123095226 | |||||
| chr9:123095226
|
CAAA | C | 28 | a0001c0001t0007g0238a0001c0001t0008g0002a0001c0001t0008g0059others(25): Show | 29 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.2629-2492_2629-249 others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123095226 | |||||
| chr9:123095308
|
T | C | 22 | a0001c0002t0005g0032a0001c0002t0005g0034a0001c0002t0005g0036others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2629-2433T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123095308 | ||||||
| chr9:123095497
|
C | G | 1 | a0001c0001t0025g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2629-2244C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123095497 | ||||||
| chr9:123095624
|
C | T | 2 | a0001c0001t0022g0112a0001c0001t0022g0115 | 2 | NA18973.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2629-2117C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123095624 | ||||||
| chr9:123095642
|
T | C | 37 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(34): Show | 37 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.2629-2099T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123095642 | ||||||
| chr9:123095665
|
G | A | 7 | a0001c0001t0095g0077a0002c0003t0024g0078a0002c0003t0024g0079others(4): Show | 7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2629-2076G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123095665 | ||||||
| chr9:123095708
|
GA | G | 10 | a0001c0001t0021g0100a0001c0001t0034g0025a0001c0001t0068g0147others(7): Show | 10 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.2629-2019delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123095708 | |||||
| chr9:123095775
|
G | A | 2 | a0001c0001t0041g0254a0001c0001t0103g0184 | 2 | HG00597.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2629-1966G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123095775 | ||||||
| chr9:123096076
|
T | G | 3 | a0001c0001t0014g0224a0001c0001t0014g0232a0001c0001t0027g0223 | 3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2629-1665T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096076 | ||||||
| chr9:123096239
|
C | CATTTTGG others(66): Show |
8 | a0001c0001t0007g0137a0001c0001t0016g0138a0001c0001t0016g0140others(5): Show | 8 | HG01081.hp1 HG01106.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.2629-1441_2629-144 others(77): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123096239 | |||||
| chr9:123096315
|
C | G | 82 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.2629-1426C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096315 | ||||||
| chr9:123096351
|
T | G | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2629-1390T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096351 | ||||||
| chr9:123096500
|
G | T | 3 | a0001c0001t0011g0014a0001c0001t0011g0019a0001c0001t0011g0020 | 3 | HG02280.hp1 HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2629-1241G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096500 | ||||||
| chr9:123096600
|
G | A | 2 | a0001c0001t0021g0016a0001c0001t0021g0018 | 2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2629-1141G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096600 | ||||||
| chr9:123096631
|
C | T | 1 | a0001c0001t0017g0251 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2629-1110C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096631 | ||||||
| chr9:123096726
|
G | A | 1 | a0001c0001t0026g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2629-1015G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096726 | ||||||
| chr9:123096734
|
A | G | 1 | a0001c0001t0004g0132 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2629-1007A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096734 | ||||||
| chr9:123096772
|
A | T | 14 | a0001c0001t0003g0201a0001c0001t0013g0172a0001c0001t0013g0207others(11): Show | 14 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.2629-969A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096772 | ||||||
| chr9:123096940
|
A | C | 2 | a0001c0001t0002g0103a0001c0001t0002g0121 | 2 | HG02129.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2629-801A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096940 | ||||||
| chr9:123097166
|
C | G | 82 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.2629-575C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123097166 | ||||||
| chr9:123097943
|
C | G | 2 | a0001c0001t0036g0053a0001c0001t0059g0256 | 2 | HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2733+98C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 22/25 | chr9 | 123097943 | ||||||
| chr9:123098299
|
T | C | 249 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(246): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.2734-416T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 22/25 | chr9 | 123098299 | ||||||
| chr9:123098303
|
A | G | 247 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.2734-412A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 22/25 | chr9 | 123098303 | ||||||
| chr9:123098310
|
G | A | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2734-405G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 22/25 | chr9 | 123098310 | ||||||
| chr9:123098999
|
C | G | 5 | a0001c0001t0032g0006a0001c0001t0032g0007a0001c0001t0114g0005others(2): Show | 5 | NA18970.hp2 NA18979.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.2817+201C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 23/25 | chr9 | 123098999 | ||||||
| chr9:123099416
|
T | C | 123 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2818-62T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 23/25 | chr9 | 123099416 | ||||||
| chr9:123099462
|
A | C | 52 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(49): Show | 52 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.2818-16A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 23/25 | chr9 | 123099462 | ||||||
| chr9:123099584
|
A | G | 2 | a0001c0002t0005g0036a0001c0002t0005g0037 | 2 | NA18952.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2889+35A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | chr9 | 123099584 | ||||||
| chr9:123099609
|
A | G | 148 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0211others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.2889+60A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | chr9 | 123099609 | ||||||
| chr9:123099819
|
C | T | 2 | a0001c0001t0092g0239a0001c0001t0096g0248 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2889+270C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | chr9 | 123099819 | ||||||
| chr9:123100383
|
A | ATG | 17 | a0001c0001t0002g0083a0001c0001t0004g0123a0001c0001t0004g0125others(14): Show | 17 | HG01361.hp1 HG01943.hp1 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.2889+888_2889+889d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | |||||
| chr9:123100383
|
A | ATGTG | 5 | a0001c0001t0002g0122a0001c0001t0009g0030a0001c0001t0016g0257others(2): Show | 5 | HG01952.hp1 HG02055.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2889+886_2889+889d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | |||||
| chr9:123100383
|
A | ATGTGTG | 3 | a0001c0001t0004g0087a0001c0001t0010g0061a0001c0001t0047g0139 | 3 | HG00673.hp2 HG01106.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2889+884_2889+889d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | |||||
| chr9:123100383
|
A | ATGTGTGT others(3): Show |
4 | a0001c0001t0016g0138a0001c0001t0054g0252a0001c0001t0101g0135others(1): Show | 4 | HG01081.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2889+880_2889+889d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | |||||
| chr9:123100383
|
A | G | 1 | a0001c0001t0017g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2889+834A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | chr9 | 123100383 | ||||||
| chr9:123100383
|
ATG | A | 43 | a0001c0001t0002g0063a0001c0001t0004g0109a0001c0001t0004g0119others(40): Show | 43 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.2889+888_2889+889d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | |||||
| chr9:123100383
|
ATGTG | A | 26 | a0001c0001t0002g0121a0001c0001t0004g0143a0001c0001t0007g0124others(23): Show | 27 | HG00544.hp1 HG00558.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.2889+886_2889+889d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | |||||
| chr9:123100383
|
ATGTGTG | A | 16 | a0001c0001t0008g0069a0001c0001t0008g0070a0001c0001t0018g0054others(13): Show | 16 | HG01496.hp1 HG02055.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.2889+884_2889+889d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | |||||
| chr9:123100383
|
ATGTGTGT others(1): Show |
A | 8 | a0001c0001t0002g0103a0001c0001t0018g0073a0001c0001t0028g0240others(5): Show | 8 | HG00280.hp2 HG01099.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2889+882_2889+889d others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | |||||
| chr9:123100383
|
ATGTGTGT others(3): Show |
A | 14 | a0001c0001t0009g0009a0001c0001t0013g0192a0001c0001t0014g0224others(11): Show | 14 | HG00741.hp1 HG01258.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.2889+880_2889+889d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | |||||
| chr9:123100383
|
ATGTGTGT others(5): Show |
A | 8 | a0001c0001t0001g0182a0001c0001t0008g0002a0001c0001t0032g0007others(5): Show | 8 | HG01106.hp1 HG01167.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.2889+878_2889+889d others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | |||||
| chr9:123100383
|
ATGTGTGT others(7): Show |
A | 63 | a0001c0001t0001g0179a0001c0001t0001g0211a0001c0001t0001g0213others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.2889+876_2889+889d others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | |||||
| chr9:123100383
|
ATGTGTGT others(9): Show |
A | 4 | a0001c0001t0012g0217a0001c0001t0026g0181a0001c0001t0064g0212others(1): Show | 4 | HG00621.hp2 HG01069.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.2889+874_2889+889d others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | |||||
| chr9:123100508
|
C | T | 1 | a0001c0001t0018g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2889+959C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | chr9 | 123100508 | ||||||
| chr9:123100665
|
C | T | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2890-901C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | chr9 | 123100665 | ||||||
| chr9:123101071
|
A | G | 121 | a0001c0001t0002g0063a0001c0001t0002g0083a0001c0001t0002g0103others(118): Show | 122 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.2890-495A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | chr9 | 123101071 | ||||||
| chr9:123101784
|
A | G | 1 | a0001c0001t0012g0162 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3087+21A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123101784 | ||||||
| chr9:123101795
|
C | T | 1 | a0001c0001t0036g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3087+32C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123101795 | ||||||
| chr9:123101814
|
T | G | 37 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(34): Show | 37 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.3087+51T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123101814 | ||||||
| chr9:123101838
|
C | T | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0025g0144 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.3087+75C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123101838 | ||||||
| chr9:123101915
|
T | C | 1 | a0001c0001t0037g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3087+152T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123101915 | ||||||
| chr9:123102213
|
T | G | 37 | a0001c0001t0009g0009a0001c0001t0009g0015a0001c0001t0009g0017others(34): Show | 37 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.3087+450T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123102213 | ||||||
| chr9:123102410
|
C | T | 1 | a0001c0001t0062g0023 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3087+647C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123102410 | ||||||
| chr9:123102457
|
A | G | 1 | a0001c0001t0007g0117 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3088-634A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123102457 | ||||||
| chr9:123102470
|
T | G | 2 | a0001c0001t0105g0234a0001c0001t0121g0233 | 2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3088-621T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123102470 | ||||||
| chr9:123102989
|
C | T | 1 | a0001c0001t0009g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3088-102C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123102989 |